Ligand source activities (1 row/activity)





Ligands (move mouse cursor over ligand name to see structure) Receptor Activity Chemical information
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DOI

60096224 156636 None 0 Human Functional pEC50 = 9.8 9.8 43 2
Agonist activity at human mGlu3 receptor expressed in HEK cells assessed as inhibition of forskolin-stimulated cAMP formation after 20 mins by HTRF assayAgonist activity at human mGlu3 receptor expressed in HEK cells assessed as inhibition of forskolin-stimulated cAMP formation after 20 mins by HTRF assay
ChEMBL 320 4 5 5 -0.4 N[C@@]1(C(=O)O)C[C@H](NC(=O)c2ccccc2O)[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/acs.jmedchem.7b01481
CHEMBL4068189 156636 None 0 Human Functional pEC50 = 9.8 9.8 43 2
Agonist activity at human mGlu3 receptor expressed in HEK cells assessed as inhibition of forskolin-stimulated cAMP formation after 20 mins by HTRF assayAgonist activity at human mGlu3 receptor expressed in HEK cells assessed as inhibition of forskolin-stimulated cAMP formation after 20 mins by HTRF assay
ChEMBL 320 4 5 5 -0.4 N[C@@]1(C(=O)O)C[C@H](NC(=O)c2ccccc2O)[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/acs.jmedchem.7b01481
60096231 157747 None 19 Human Functional pEC50 = 9.3 9.3 48 4
Agonist activity at human mGlu3 receptor expressed in HEK cells assessed as inhibition of forskolin-stimulated cAMP formation after 20 mins by HTRF assayAgonist activity at human mGlu3 receptor expressed in HEK cells assessed as inhibition of forskolin-stimulated cAMP formation after 20 mins by HTRF assay
ChEMBL 334 5 4 5 -0.1 COc1cccc(C(=O)N[C@H]2C[C@@](N)(C(=O)O)[C@@H]3[C@@H](C(=O)O)[C@H]23)c1 10.1021/acs.jmedchem.7b01481
CHEMBL4081453 157747 None 19 Human Functional pEC50 = 9.3 9.3 48 4
Agonist activity at human mGlu3 receptor expressed in HEK cells assessed as inhibition of forskolin-stimulated cAMP formation after 20 mins by HTRF assayAgonist activity at human mGlu3 receptor expressed in HEK cells assessed as inhibition of forskolin-stimulated cAMP formation after 20 mins by HTRF assay
ChEMBL 334 5 4 5 -0.1 COc1cccc(C(=O)N[C@H]2C[C@@](N)(C(=O)O)[C@@H]3[C@@H](C(=O)O)[C@H]23)c1 10.1021/acs.jmedchem.7b01481
60096201 158660 None 0 Human Functional pEC50 = 9.2 9.2 5 2
Agonist activity at human mGlu3 receptor expressed in HEK cells assessed as inhibition of forskolin-stimulated cAMP formation after 20 mins by HTRF assayAgonist activity at human mGlu3 receptor expressed in HEK cells assessed as inhibition of forskolin-stimulated cAMP formation after 20 mins by HTRF assay
ChEMBL 320 4 5 5 -0.4 N[C@@]1(C(=O)O)C[C@H](NC(=O)c2cccc(O)c2)[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/acs.jmedchem.7b01481
CHEMBL4091735 158660 None 0 Human Functional pEC50 = 9.2 9.2 5 2
Agonist activity at human mGlu3 receptor expressed in HEK cells assessed as inhibition of forskolin-stimulated cAMP formation after 20 mins by HTRF assayAgonist activity at human mGlu3 receptor expressed in HEK cells assessed as inhibition of forskolin-stimulated cAMP formation after 20 mins by HTRF assay
ChEMBL 320 4 5 5 -0.4 N[C@@]1(C(=O)O)C[C@H](NC(=O)c2cccc(O)c2)[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/acs.jmedchem.7b01481
60096178 156973 None 0 Human Functional pEC50 = 9.1 9.1 10 2
Agonist activity at human mGlu3 receptor expressed in HEK cells assessed as inhibition of forskolin-stimulated cAMP formation after 20 mins by HTRF assayAgonist activity at human mGlu3 receptor expressed in HEK cells assessed as inhibition of forskolin-stimulated cAMP formation after 20 mins by HTRF assay
ChEMBL 338 4 4 4 0.6 N[C@@]1(C(=O)O)C[C@H](NC(=O)c2cccc(Cl)c2)[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/acs.jmedchem.7b01481
CHEMBL4071962 156973 None 0 Human Functional pEC50 = 9.1 9.1 10 2
Agonist activity at human mGlu3 receptor expressed in HEK cells assessed as inhibition of forskolin-stimulated cAMP formation after 20 mins by HTRF assayAgonist activity at human mGlu3 receptor expressed in HEK cells assessed as inhibition of forskolin-stimulated cAMP formation after 20 mins by HTRF assay
ChEMBL 338 4 4 4 0.6 N[C@@]1(C(=O)O)C[C@H](NC(=O)c2cccc(Cl)c2)[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/acs.jmedchem.7b01481
10353365 83279 None 1 Human Functional pEC50 = 8.9 8.9 -13 3
Agonist activity at human mGluR3 assessed as effect on cAMP production in RGT cellsAgonist activity at human mGluR3 assessed as effect on cAMP production in RGT cells
ChEMBL 219 2 3 4 -1.8 N[C@@]1(C(=O)O)C[S+]([O-])[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/jm060917u
CHEMBL218710 83279 None 1 Human Functional pEC50 = 8.9 8.9 -13 3
Agonist activity at human mGluR3 assessed as effect on cAMP production in RGT cellsAgonist activity at human mGluR3 assessed as effect on cAMP production in RGT cells
ChEMBL 219 2 3 4 -1.8 N[C@@]1(C(=O)O)C[S+]([O-])[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/jm060917u
10807972 35826 None 1 Rat Functional pEC50 = 7 7.0 -6 4
Agonist potency against cloned Metabotropic glutamate receptor 3Agonist potency against cloned Metabotropic glutamate receptor 3
ChEMBL 353 5 3 4 2.8 N[C@@](CC1c2ccccc2Oc2ccccc21)(C(=O)O)[C@H]1C[C@@H]1C(=O)O 10.1021/jm000346k
CHEMBL144151 35826 None 1 Rat Functional pEC50 = 7 7.0 -6 4
Agonist potency against cloned Metabotropic glutamate receptor 3Agonist potency against cloned Metabotropic glutamate receptor 3
ChEMBL 353 5 3 4 2.8 N[C@@](CC1c2ccccc2Oc2ccccc21)(C(=O)O)[C@H]1C[C@@H]1C(=O)O 10.1021/jm000346k
1310 2315 None 61 Human Functional pEC50 = 6 6.0 -251 17
Agonist activity at wild type human recombinant mGlu3 receptor expressed in AV12 cells assessed as stimulation of Ca2+ mobilization after 1 hr by FLIPR assayAgonist activity at wild type human recombinant mGlu3 receptor expressed in AV12 cells assessed as stimulation of Ca2+ mobilization after 1 hr by FLIPR assay
ChEMBL 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N 10.1021/acs.jmedchem.5b01124
1369 2315 None 61 Human Functional pEC50 = 6 6.0 -251 17
Agonist activity at wild type human recombinant mGlu3 receptor expressed in AV12 cells assessed as stimulation of Ca2+ mobilization after 1 hr by FLIPR assayAgonist activity at wild type human recombinant mGlu3 receptor expressed in AV12 cells assessed as stimulation of Ca2+ mobilization after 1 hr by FLIPR assay
ChEMBL 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N 10.1021/acs.jmedchem.5b01124
33032 2315 None 61 Human Functional pEC50 = 6 6.0 -251 17
Agonist activity at wild type human recombinant mGlu3 receptor expressed in AV12 cells assessed as stimulation of Ca2+ mobilization after 1 hr by FLIPR assayAgonist activity at wild type human recombinant mGlu3 receptor expressed in AV12 cells assessed as stimulation of Ca2+ mobilization after 1 hr by FLIPR assay
ChEMBL 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N 10.1021/acs.jmedchem.5b01124
44272391 2315 None 61 Human Functional pEC50 = 6 6.0 -251 17
Agonist activity at wild type human recombinant mGlu3 receptor expressed in AV12 cells assessed as stimulation of Ca2+ mobilization after 1 hr by FLIPR assayAgonist activity at wild type human recombinant mGlu3 receptor expressed in AV12 cells assessed as stimulation of Ca2+ mobilization after 1 hr by FLIPR assay
ChEMBL 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N 10.1021/acs.jmedchem.5b01124
88747398 2315 None 61 Human Functional pEC50 = 6 6.0 -251 17
Agonist activity at wild type human recombinant mGlu3 receptor expressed in AV12 cells assessed as stimulation of Ca2+ mobilization after 1 hr by FLIPR assayAgonist activity at wild type human recombinant mGlu3 receptor expressed in AV12 cells assessed as stimulation of Ca2+ mobilization after 1 hr by FLIPR assay
ChEMBL 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N 10.1021/acs.jmedchem.5b01124
CHEMBL575060 2315 None 61 Human Functional pEC50 = 6 6.0 -251 17
Agonist activity at wild type human recombinant mGlu3 receptor expressed in AV12 cells assessed as stimulation of Ca2+ mobilization after 1 hr by FLIPR assayAgonist activity at wild type human recombinant mGlu3 receptor expressed in AV12 cells assessed as stimulation of Ca2+ mobilization after 1 hr by FLIPR assay
ChEMBL 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N 10.1021/acs.jmedchem.5b01124
DB00142 2315 None 61 Human Functional pEC50 = 6 6.0 -251 17
Agonist activity at wild type human recombinant mGlu3 receptor expressed in AV12 cells assessed as stimulation of Ca2+ mobilization after 1 hr by FLIPR assayAgonist activity at wild type human recombinant mGlu3 receptor expressed in AV12 cells assessed as stimulation of Ca2+ mobilization after 1 hr by FLIPR assay
ChEMBL 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N 10.1021/acs.jmedchem.5b01124
71135411 123464 None 0 Human Functional pEC50 = 7.0 7.0 -5 2
Agonist activity at human recombinant mGlu3 receptor expressed in AV12 cells assessed as inhibition of forskolin-stimulated cAMP production after 1 hr by fluorescence assayAgonist activity at human recombinant mGlu3 receptor expressed in AV12 cells assessed as inhibition of forskolin-stimulated cAMP production after 1 hr by fluorescence assay
ChEMBL 298 4 4 6 -0.3 Cc1nnc(S[C@@H]2C[C@@](N)(C(=O)O)[C@@H]3[C@@H](C(=O)O)[C@H]23)[nH]1 10.1021/acs.jmedchem.5b01124
CHEMBL3616848 123464 None 0 Human Functional pEC50 = 7.0 7.0 -5 2
Agonist activity at human recombinant mGlu3 receptor expressed in AV12 cells assessed as inhibition of forskolin-stimulated cAMP production after 1 hr by fluorescence assayAgonist activity at human recombinant mGlu3 receptor expressed in AV12 cells assessed as inhibition of forskolin-stimulated cAMP production after 1 hr by fluorescence assay
ChEMBL 298 4 4 6 -0.3 Cc1nnc(S[C@@H]2C[C@@](N)(C(=O)O)[C@@H]3[C@@H](C(=O)O)[C@H]23)[nH]1 10.1021/acs.jmedchem.5b01124
49858118 1110 None 0 Human Functional pEC50 = 5.0 5.0 -10 2
Positive allosteric modulator activity at human mGluR3 expressed in HEK cells in presence of glutamate EC10 concentration by Ca2+ functional assayPositive allosteric modulator activity at human mGluR3 expressed in HEK cells in presence of glutamate EC10 concentration by Ca2+ functional assay
ChEMBL 324 3 2 5 2.7 O/N=C\1/c2ccccc2OC2(C1C2)C(=O)Nc1ccc(cc1)OC 10.1021/jm101069m
6224 1110 None 0 Human Functional pEC50 = 5.0 5.0 -10 2
Positive allosteric modulator activity at human mGluR3 expressed in HEK cells in presence of glutamate EC10 concentration by Ca2+ functional assayPositive allosteric modulator activity at human mGluR3 expressed in HEK cells in presence of glutamate EC10 concentration by Ca2+ functional assay
ChEMBL 324 3 2 5 2.7 O/N=C\1/c2ccccc2OC2(C1C2)C(=O)Nc1ccc(cc1)OC 10.1021/jm101069m
CHEMBL1630807 1110 None 0 Human Functional pEC50 = 5.0 5.0 -10 2
Positive allosteric modulator activity at human mGluR3 expressed in HEK cells in presence of glutamate EC10 concentration by Ca2+ functional assayPositive allosteric modulator activity at human mGluR3 expressed in HEK cells in presence of glutamate EC10 concentration by Ca2+ functional assay
ChEMBL 324 3 2 5 2.7 O/N=C\1/c2ccccc2OC2(C1C2)C(=O)Nc1ccc(cc1)OC 10.1021/jm101069m
71135411 123464 None 0 Human Functional pEC50 = 7.0 7.0 -5 2
Agonist activity at human recombinant mGlu3 receptor expressed in AV12 cells assessed as stimulation of Ca2+ mobilization after 1.5 hrs by FLIPR assayAgonist activity at human recombinant mGlu3 receptor expressed in AV12 cells assessed as stimulation of Ca2+ mobilization after 1.5 hrs by FLIPR assay
ChEMBL 298 4 4 6 -0.3 Cc1nnc(S[C@@H]2C[C@@](N)(C(=O)O)[C@@H]3[C@@H](C(=O)O)[C@H]23)[nH]1 10.1021/acs.jmedchem.5b01124
CHEMBL3616848 123464 None 0 Human Functional pEC50 = 7.0 7.0 -5 2
Agonist activity at human recombinant mGlu3 receptor expressed in AV12 cells assessed as stimulation of Ca2+ mobilization after 1.5 hrs by FLIPR assayAgonist activity at human recombinant mGlu3 receptor expressed in AV12 cells assessed as stimulation of Ca2+ mobilization after 1.5 hrs by FLIPR assay
ChEMBL 298 4 4 6 -0.3 Cc1nnc(S[C@@H]2C[C@@](N)(C(=O)O)[C@@H]3[C@@H](C(=O)O)[C@H]23)[nH]1 10.1021/acs.jmedchem.5b01124
44361401 31349 None 0 Rat Functional pEC50 = 8.0 8.0 -1 5
Metabotropic glutamate receptor 3 agonist activity against forskolin stimulated c-AMP formation in rat non neuronal cellsMetabotropic glutamate receptor 3 agonist activity against forskolin stimulated c-AMP formation in rat non neuronal cells
ChEMBL 175 3 4 4 -1.9 N[C@H](C(=O)O)[C@H]1[C@@H](O)[C@@H]1C(=O)O 10.1021/jm030967o
CHEMBL140197 31349 None 0 Rat Functional pEC50 = 8.0 8.0 -1 5
Metabotropic glutamate receptor 3 agonist activity against forskolin stimulated c-AMP formation in rat non neuronal cellsMetabotropic glutamate receptor 3 agonist activity against forskolin stimulated c-AMP formation in rat non neuronal cells
ChEMBL 175 3 4 4 -1.9 N[C@H](C(=O)O)[C@H]1[C@@H](O)[C@@H]1C(=O)O 10.1021/jm030967o
60096231 157747 None 19 Human Functional pEC50 = 7.9 7.9 48 4
Agonist activity at recombinant human mGlu3 receptor expressed in hamster AV12 cells co-expressing rat EAAT1/Galpha15 assessed as induction of increase in Ca2+ flux after 2.5 mins by Fluo-3 AM dye-based FLIPR assayAgonist activity at recombinant human mGlu3 receptor expressed in hamster AV12 cells co-expressing rat EAAT1/Galpha15 assessed as induction of increase in Ca2+ flux after 2.5 mins by Fluo-3 AM dye-based FLIPR assay
ChEMBL 334 5 4 5 -0.1 COc1cccc(C(=O)N[C@H]2C[C@@](N)(C(=O)O)[C@@H]3[C@@H](C(=O)O)[C@H]23)c1 10.1021/acs.jmedchem.7b01481
CHEMBL4081453 157747 None 19 Human Functional pEC50 = 7.9 7.9 48 4
Agonist activity at recombinant human mGlu3 receptor expressed in hamster AV12 cells co-expressing rat EAAT1/Galpha15 assessed as induction of increase in Ca2+ flux after 2.5 mins by Fluo-3 AM dye-based FLIPR assayAgonist activity at recombinant human mGlu3 receptor expressed in hamster AV12 cells co-expressing rat EAAT1/Galpha15 assessed as induction of increase in Ca2+ flux after 2.5 mins by Fluo-3 AM dye-based FLIPR assay
ChEMBL 334 5 4 5 -0.1 COc1cccc(C(=O)N[C@H]2C[C@@](N)(C(=O)O)[C@@H]3[C@@H](C(=O)O)[C@H]23)c1 10.1021/acs.jmedchem.7b01481
71137011 123474 None 0 Human Functional pEC50 = 7.0 7.0 -58 2
Agonist activity at human recombinant mGlu3 receptor expressed in AV12 cells assessed as inhibition of forskolin-stimulated cAMP production after 1 hr by fluorescence assayAgonist activity at human recombinant mGlu3 receptor expressed in AV12 cells assessed as inhibition of forskolin-stimulated cAMP production after 1 hr by fluorescence assay
ChEMBL 299 4 5 7 -1.0 Nc1nnc(S[C@H]2C[C@@](N)(C(=O)O)[C@@H]3[C@@H](C(=O)O)[C@H]23)[nH]1 10.1021/acs.jmedchem.5b01124
CHEMBL3616858 123474 None 0 Human Functional pEC50 = 7.0 7.0 -58 2
Agonist activity at human recombinant mGlu3 receptor expressed in AV12 cells assessed as inhibition of forskolin-stimulated cAMP production after 1 hr by fluorescence assayAgonist activity at human recombinant mGlu3 receptor expressed in AV12 cells assessed as inhibition of forskolin-stimulated cAMP production after 1 hr by fluorescence assay
ChEMBL 299 4 5 7 -1.0 Nc1nnc(S[C@H]2C[C@@](N)(C(=O)O)[C@@H]3[C@@H](C(=O)O)[C@H]23)[nH]1 10.1021/acs.jmedchem.5b01124
53240406 123463 None 21 Human Functional pEC50 = 5.9 5.9 -107 4
Agonist activity at human recombinant mGlu3 receptor D279E and Q306L mutant expressed in AV12 cells assessed as stimulation of Ca2+ mobilization after 1 hr by FLIPR assayAgonist activity at human recombinant mGlu3 receptor D279E and Q306L mutant expressed in AV12 cells assessed as stimulation of Ca2+ mobilization after 1 hr by FLIPR assay
ChEMBL 284 4 4 6 -0.6 N[C@@]1(C(=O)O)C[C@@H](Sc2nnc[nH]2)[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/acs.jmedchem.5b01124
CHEMBL3616847 123463 None 21 Human Functional pEC50 = 5.9 5.9 -107 4
Agonist activity at human recombinant mGlu3 receptor D279E and Q306L mutant expressed in AV12 cells assessed as stimulation of Ca2+ mobilization after 1 hr by FLIPR assayAgonist activity at human recombinant mGlu3 receptor D279E and Q306L mutant expressed in AV12 cells assessed as stimulation of Ca2+ mobilization after 1 hr by FLIPR assay
ChEMBL 284 4 4 6 -0.6 N[C@@]1(C(=O)O)C[C@@H](Sc2nnc[nH]2)[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/acs.jmedchem.5b01124
53240406 123463 None 21 Human Functional pEC50 = 6.9 6.9 -107 4
Agonist activity at human recombinant mGlu3 receptor expressed in AV12 cells assessed as inhibition of forskolin-stimulated cAMP production after 1 hr by fluorescence assayAgonist activity at human recombinant mGlu3 receptor expressed in AV12 cells assessed as inhibition of forskolin-stimulated cAMP production after 1 hr by fluorescence assay
ChEMBL 284 4 4 6 -0.6 N[C@@]1(C(=O)O)C[C@@H](Sc2nnc[nH]2)[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/acs.jmedchem.5b01124
CHEMBL3616847 123463 None 21 Human Functional pEC50 = 6.9 6.9 -107 4
Agonist activity at human recombinant mGlu3 receptor expressed in AV12 cells assessed as inhibition of forskolin-stimulated cAMP production after 1 hr by fluorescence assayAgonist activity at human recombinant mGlu3 receptor expressed in AV12 cells assessed as inhibition of forskolin-stimulated cAMP production after 1 hr by fluorescence assay
ChEMBL 284 4 4 6 -0.6 N[C@@]1(C(=O)O)C[C@@H](Sc2nnc[nH]2)[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/acs.jmedchem.5b01124
49836087 1061 None 0 Human Functional pEC50 = 4.9 4.9 -16 2
Positive allosteric modulator activity at human mGluR3 expressed in HEK cells in presence of glutamate EC10 concentration by Ca2+ functional assayPositive allosteric modulator activity at human mGluR3 expressed in HEK cells in presence of glutamate EC10 concentration by Ca2+ functional assay
ChEMBL 328 2 2 4 3.3 O/N=C\1/c2ccccc2OC2(C1C2)C(=O)Nc1ccc(cc1)Cl 10.1021/jm101069m
6222 1061 None 0 Human Functional pEC50 = 4.9 4.9 -16 2
Positive allosteric modulator activity at human mGluR3 expressed in HEK cells in presence of glutamate EC10 concentration by Ca2+ functional assayPositive allosteric modulator activity at human mGluR3 expressed in HEK cells in presence of glutamate EC10 concentration by Ca2+ functional assay
ChEMBL 328 2 2 4 3.3 O/N=C\1/c2ccccc2OC2(C1C2)C(=O)Nc1ccc(cc1)Cl 10.1021/jm101069m
CHEMBL1630805 1061 None 0 Human Functional pEC50 = 4.9 4.9 -16 2
Positive allosteric modulator activity at human mGluR3 expressed in HEK cells in presence of glutamate EC10 concentration by Ca2+ functional assayPositive allosteric modulator activity at human mGluR3 expressed in HEK cells in presence of glutamate EC10 concentration by Ca2+ functional assay
ChEMBL 328 2 2 4 3.3 O/N=C\1/c2ccccc2OC2(C1C2)C(=O)Nc1ccc(cc1)Cl 10.1021/jm101069m
1393 1539 None 42 Human Functional pEC50 = 6.9 6.9 -4 6
Agonist activity at human recombinant mGlu3 receptor expressed in AV12 cells assessed as stimulation of Ca2+ mobilization after 1.5 hrs by FLIPR assayAgonist activity at human recombinant mGlu3 receptor expressed in AV12 cells assessed as stimulation of Ca2+ mobilization after 1.5 hrs by FLIPR assay
ChEMBL 185 2 3 3 -0.5 OC(=O)[C@H]1[C@H]2[C@@H]1[C@](CC2)(N)C(=O)O 10.1021/acs.jmedchem.5b01124
1396 1539 None 42 Human Functional pEC50 = 6.9 6.9 -4 6
Agonist activity at human recombinant mGlu3 receptor expressed in AV12 cells assessed as stimulation of Ca2+ mobilization after 1.5 hrs by FLIPR assayAgonist activity at human recombinant mGlu3 receptor expressed in AV12 cells assessed as stimulation of Ca2+ mobilization after 1.5 hrs by FLIPR assay
ChEMBL 185 2 3 3 -0.5 OC(=O)[C@H]1[C@H]2[C@@H]1[C@](CC2)(N)C(=O)O 10.1021/acs.jmedchem.5b01124
213056 1539 None 42 Human Functional pEC50 = 6.9 6.9 -4 6
Agonist activity at human recombinant mGlu3 receptor expressed in AV12 cells assessed as stimulation of Ca2+ mobilization after 1.5 hrs by FLIPR assayAgonist activity at human recombinant mGlu3 receptor expressed in AV12 cells assessed as stimulation of Ca2+ mobilization after 1.5 hrs by FLIPR assay
ChEMBL 185 2 3 3 -0.5 OC(=O)[C@H]1[C@H]2[C@@H]1[C@](CC2)(N)C(=O)O 10.1021/acs.jmedchem.5b01124
CHEMBL8759 1539 None 42 Human Functional pEC50 = 6.9 6.9 -4 6
Agonist activity at human recombinant mGlu3 receptor expressed in AV12 cells assessed as stimulation of Ca2+ mobilization after 1.5 hrs by FLIPR assayAgonist activity at human recombinant mGlu3 receptor expressed in AV12 cells assessed as stimulation of Ca2+ mobilization after 1.5 hrs by FLIPR assay
ChEMBL 185 2 3 3 -0.5 OC(=O)[C@H]1[C@H]2[C@@H]1[C@](CC2)(N)C(=O)O 10.1021/acs.jmedchem.5b01124
1310 2315 None 61 Human Functional pEC50 = 5.8 5.8 -251 17
Agonist activity at human recombinant mGlu3 receptor Q306L mutant expressed in AV12 cells assessed as stimulation of Ca2+ mobilization after 1 hr by FLIPR assayAgonist activity at human recombinant mGlu3 receptor Q306L mutant expressed in AV12 cells assessed as stimulation of Ca2+ mobilization after 1 hr by FLIPR assay
ChEMBL 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N 10.1021/acs.jmedchem.5b01124
1369 2315 None 61 Human Functional pEC50 = 5.8 5.8 -251 17
Agonist activity at human recombinant mGlu3 receptor Q306L mutant expressed in AV12 cells assessed as stimulation of Ca2+ mobilization after 1 hr by FLIPR assayAgonist activity at human recombinant mGlu3 receptor Q306L mutant expressed in AV12 cells assessed as stimulation of Ca2+ mobilization after 1 hr by FLIPR assay
ChEMBL 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N 10.1021/acs.jmedchem.5b01124
33032 2315 None 61 Human Functional pEC50 = 5.8 5.8 -251 17
Agonist activity at human recombinant mGlu3 receptor Q306L mutant expressed in AV12 cells assessed as stimulation of Ca2+ mobilization after 1 hr by FLIPR assayAgonist activity at human recombinant mGlu3 receptor Q306L mutant expressed in AV12 cells assessed as stimulation of Ca2+ mobilization after 1 hr by FLIPR assay
ChEMBL 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N 10.1021/acs.jmedchem.5b01124
44272391 2315 None 61 Human Functional pEC50 = 5.8 5.8 -251 17
Agonist activity at human recombinant mGlu3 receptor Q306L mutant expressed in AV12 cells assessed as stimulation of Ca2+ mobilization after 1 hr by FLIPR assayAgonist activity at human recombinant mGlu3 receptor Q306L mutant expressed in AV12 cells assessed as stimulation of Ca2+ mobilization after 1 hr by FLIPR assay
ChEMBL 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N 10.1021/acs.jmedchem.5b01124
88747398 2315 None 61 Human Functional pEC50 = 5.8 5.8 -251 17
Agonist activity at human recombinant mGlu3 receptor Q306L mutant expressed in AV12 cells assessed as stimulation of Ca2+ mobilization after 1 hr by FLIPR assayAgonist activity at human recombinant mGlu3 receptor Q306L mutant expressed in AV12 cells assessed as stimulation of Ca2+ mobilization after 1 hr by FLIPR assay
ChEMBL 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N 10.1021/acs.jmedchem.5b01124
CHEMBL575060 2315 None 61 Human Functional pEC50 = 5.8 5.8 -251 17
Agonist activity at human recombinant mGlu3 receptor Q306L mutant expressed in AV12 cells assessed as stimulation of Ca2+ mobilization after 1 hr by FLIPR assayAgonist activity at human recombinant mGlu3 receptor Q306L mutant expressed in AV12 cells assessed as stimulation of Ca2+ mobilization after 1 hr by FLIPR assay
ChEMBL 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N 10.1021/acs.jmedchem.5b01124
DB00142 2315 None 61 Human Functional pEC50 = 5.8 5.8 -251 17
Agonist activity at human recombinant mGlu3 receptor Q306L mutant expressed in AV12 cells assessed as stimulation of Ca2+ mobilization after 1 hr by FLIPR assayAgonist activity at human recombinant mGlu3 receptor Q306L mutant expressed in AV12 cells assessed as stimulation of Ca2+ mobilization after 1 hr by FLIPR assay
ChEMBL 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N 10.1021/acs.jmedchem.5b01124
67973913 137162 None 0 Human Functional pEC50 = 6.8 6.8 -2 2
Antagonist activity at human mGlu3 expressed in HEK293 cells assessed as inhibition of glutamate-induced calcium mobilizationAntagonist activity at human mGlu3 expressed in HEK293 cells assessed as inhibition of glutamate-induced calcium mobilization
ChEMBL 333 4 0 4 3.4 Cc1ccc(N2CCn3nc(COc4ccccc4)cc3C2=O)cc1 10.1016/j.bmcl.2015.11.098
CHEMBL3747073 137162 None 0 Human Functional pEC50 = 6.8 6.8 -2 2
Antagonist activity at human mGlu3 expressed in HEK293 cells assessed as inhibition of glutamate-induced calcium mobilizationAntagonist activity at human mGlu3 expressed in HEK293 cells assessed as inhibition of glutamate-induced calcium mobilization
ChEMBL 333 4 0 4 3.4 Cc1ccc(N2CCn3nc(COc4ccccc4)cc3C2=O)cc1 10.1016/j.bmcl.2015.11.098
1392 73 None 32 Rat Functional pEC50 = 5.8 5.8 -5 4
Effective concentration required for agonistic activity at Metabotropic glutamate receptor 3Effective concentration required for agonistic activity at Metabotropic glutamate receptor 3
ChEMBL 174 2 4 4 -1.8 OC(=O)[C@@H]1NC[C@@](C1)(N)C(=O)O 10.1016/s0960-894x(01)00329-8
5310984 73 None 32 Rat Functional pEC50 = 5.8 5.8 -5 4
Effective concentration required for agonistic activity at Metabotropic glutamate receptor 3Effective concentration required for agonistic activity at Metabotropic glutamate receptor 3
ChEMBL 174 2 4 4 -1.8 OC(=O)[C@@H]1NC[C@@](C1)(N)C(=O)O 10.1016/s0960-894x(01)00329-8
CHEMBL40086 73 None 32 Rat Functional pEC50 = 5.8 5.8 -5 4
Effective concentration required for agonistic activity at Metabotropic glutamate receptor 3Effective concentration required for agonistic activity at Metabotropic glutamate receptor 3
ChEMBL 174 2 4 4 -1.8 OC(=O)[C@@H]1NC[C@@](C1)(N)C(=O)O 10.1016/s0960-894x(01)00329-8
90643858 111929 None 0 Rat Functional pEC50 = 5.8 5.8 -25 2
Positive allosteric modulation of rat mGluR3 receptor expressed in TREx293 cells by calcium mobilization assayPositive allosteric modulation of rat mGluR3 receptor expressed in TREx293 cells by calcium mobilization assay
ChEMBL 430 12 2 6 4.9 COc1cc(C(=O)O)ccc1OCCCCOc1ccc(C(=O)CC(C)C)c(O)c1C 10.1021/jm5000563
CHEMBL3287695 111929 None 0 Rat Functional pEC50 = 5.8 5.8 -25 2
Positive allosteric modulation of rat mGluR3 receptor expressed in TREx293 cells by calcium mobilization assayPositive allosteric modulation of rat mGluR3 receptor expressed in TREx293 cells by calcium mobilization assay
ChEMBL 430 12 2 6 4.9 COc1cc(C(=O)O)ccc1OCCCCOc1ccc(C(=O)CC(C)C)c(O)c1C 10.1021/jm5000563
60096211 90093 None 0 Human Functional pEC50 = 6.7 6.7 1 4
Agonist activity at human mGlu3 receptor expressed in HEK cells assessed as inhibition of forskolin-stimulated cAMP formation after 20 mins by HTRF assayAgonist activity at human mGlu3 receptor expressed in HEK cells assessed as inhibition of forskolin-stimulated cAMP formation after 20 mins by HTRF assay
ChEMBL 242 3 4 4 -1.4 CC(=O)N[C@H]1C[C@@](N)(C(=O)O)[C@@H]2[C@@H](C(=O)O)[C@H]12 10.1021/acs.jmedchem.7b01481
CHEMBL2381649 90093 None 0 Human Functional pEC50 = 6.7 6.7 1 4
Agonist activity at human mGlu3 receptor expressed in HEK cells assessed as inhibition of forskolin-stimulated cAMP formation after 20 mins by HTRF assayAgonist activity at human mGlu3 receptor expressed in HEK cells assessed as inhibition of forskolin-stimulated cAMP formation after 20 mins by HTRF assay
ChEMBL 242 3 4 4 -1.4 CC(=O)N[C@H]1C[C@@](N)(C(=O)O)[C@@H]2[C@@H](C(=O)O)[C@H]12 10.1021/acs.jmedchem.7b01481
60096190 158605 None 0 Human Functional pEC50 = 8.7 8.7 9 2
Agonist activity at human mGlu3 receptor expressed in HEK cells assessed as inhibition of forskolin-stimulated cAMP formation after 20 mins by HTRF assayAgonist activity at human mGlu3 receptor expressed in HEK cells assessed as inhibition of forskolin-stimulated cAMP formation after 20 mins by HTRF assay
ChEMBL 322 4 4 4 0.1 N[C@@]1(C(=O)O)C[C@H](NC(=O)c2cccc(F)c2)[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/acs.jmedchem.7b01481
CHEMBL4091203 158605 None 0 Human Functional pEC50 = 8.7 8.7 9 2
Agonist activity at human mGlu3 receptor expressed in HEK cells assessed as inhibition of forskolin-stimulated cAMP formation after 20 mins by HTRF assayAgonist activity at human mGlu3 receptor expressed in HEK cells assessed as inhibition of forskolin-stimulated cAMP formation after 20 mins by HTRF assay
ChEMBL 322 4 4 4 0.1 N[C@@]1(C(=O)O)C[C@H](NC(=O)c2cccc(F)c2)[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/acs.jmedchem.7b01481
1395 2528 None 14 Human Functional pEC50 = 8.7 8.7 -3 4
Agonist activity at mGLUR3 expressed in CHO cellsAgonist activity at mGLUR3 expressed in CHO cells
ChEMBL 217 2 3 4 -1.2 O=C1C[C@@]([C@H]2[C@@H]1[C@]2(F)C(=O)O)(N)C(=O)O 10.1016/j.bmcl.2012.01.039
9837317 2528 None 14 Human Functional pEC50 = 8.7 8.7 -3 4
Agonist activity at mGLUR3 expressed in CHO cellsAgonist activity at mGLUR3 expressed in CHO cells
ChEMBL 217 2 3 4 -1.2 O=C1C[C@@]([C@H]2[C@@H]1[C@]2(F)C(=O)O)(N)C(=O)O 10.1016/j.bmcl.2012.01.039
CHEMBL121053 2528 None 14 Human Functional pEC50 = 8.7 8.7 -3 4
Agonist activity at mGLUR3 expressed in CHO cellsAgonist activity at mGLUR3 expressed in CHO cells
ChEMBL 217 2 3 4 -1.2 O=C1C[C@@]([C@H]2[C@@H]1[C@]2(F)C(=O)O)(N)C(=O)O 10.1016/j.bmcl.2012.01.039
1395 2528 None 14 Rat Functional pEC50 = 8.7 8.7 -3 4
Agonist potency against cloned Metabotropic glutamate receptor 3Agonist potency against cloned Metabotropic glutamate receptor 3
ChEMBL 217 2 3 4 -1.2 O=C1C[C@@]([C@H]2[C@@H]1[C@]2(F)C(=O)O)(N)C(=O)O 10.1021/jm000346k
9837317 2528 None 14 Rat Functional pEC50 = 8.7 8.7 -3 4
Agonist potency against cloned Metabotropic glutamate receptor 3Agonist potency against cloned Metabotropic glutamate receptor 3
ChEMBL 217 2 3 4 -1.2 O=C1C[C@@]([C@H]2[C@@H]1[C@]2(F)C(=O)O)(N)C(=O)O 10.1021/jm000346k
CHEMBL121053 2528 None 14 Rat Functional pEC50 = 8.7 8.7 -3 4
Agonist potency against cloned Metabotropic glutamate receptor 3Agonist potency against cloned Metabotropic glutamate receptor 3
ChEMBL 217 2 3 4 -1.2 O=C1C[C@@]([C@H]2[C@@H]1[C@]2(F)C(=O)O)(N)C(=O)O 10.1021/jm000346k
60096228 156879 None 0 Human Functional pEC50 = 8.7 8.7 2 2
Agonist activity at human mGlu3 receptor expressed in HEK cells assessed as inhibition of forskolin-stimulated cAMP formation after 20 mins by HTRF assayAgonist activity at human mGlu3 receptor expressed in HEK cells assessed as inhibition of forskolin-stimulated cAMP formation after 20 mins by HTRF assay
ChEMBL 320 4 5 5 -0.4 N[C@@]1(C(=O)O)C[C@H](NC(=O)c2ccc(O)cc2)[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/acs.jmedchem.7b01481
CHEMBL4070866 156879 None 0 Human Functional pEC50 = 8.7 8.7 2 2
Agonist activity at human mGlu3 receptor expressed in HEK cells assessed as inhibition of forskolin-stimulated cAMP formation after 20 mins by HTRF assayAgonist activity at human mGlu3 receptor expressed in HEK cells assessed as inhibition of forskolin-stimulated cAMP formation after 20 mins by HTRF assay
ChEMBL 320 4 5 5 -0.4 N[C@@]1(C(=O)O)C[C@H](NC(=O)c2ccc(O)cc2)[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/acs.jmedchem.7b01481
60096246 156037 None 0 Human Functional pEC50 = 8.6 8.6 6 2
Agonist activity at human mGlu3 receptor expressed in HEK cells assessed as inhibition of forskolin-stimulated cAMP formation after 20 mins by HTRF assayAgonist activity at human mGlu3 receptor expressed in HEK cells assessed as inhibition of forskolin-stimulated cAMP formation after 20 mins by HTRF assay
ChEMBL 334 5 4 5 -0.1 COc1ccc(C(=O)N[C@H]2C[C@@](N)(C(=O)O)[C@@H]3[C@@H](C(=O)O)[C@H]23)cc1 10.1021/acs.jmedchem.7b01481
CHEMBL4061162 156037 None 0 Human Functional pEC50 = 8.6 8.6 6 2
Agonist activity at human mGlu3 receptor expressed in HEK cells assessed as inhibition of forskolin-stimulated cAMP formation after 20 mins by HTRF assayAgonist activity at human mGlu3 receptor expressed in HEK cells assessed as inhibition of forskolin-stimulated cAMP formation after 20 mins by HTRF assay
ChEMBL 334 5 4 5 -0.1 COc1ccc(C(=O)N[C@H]2C[C@@](N)(C(=O)O)[C@@H]3[C@@H](C(=O)O)[C@H]23)cc1 10.1021/acs.jmedchem.7b01481
1377 1340 None 23 Rat Functional pEC50 = 6.7 6.7 -1 8
Metabotropic glutamate receptor 3 agonist activity against forskolin stimulated c-AMP formation in rat non neuronal cellsMetabotropic glutamate receptor 3 agonist activity against forskolin stimulated c-AMP formation in rat non neuronal cells
ChEMBL 203 4 4 4 -1.6 N[C@@H](C1[C@H]([C@@H]1C(=O)O)C(=O)O)C(=O)O 10.1021/jm030967o
5310979 1340 None 23 Rat Functional pEC50 = 6.7 6.7 -1 8
Metabotropic glutamate receptor 3 agonist activity against forskolin stimulated c-AMP formation in rat non neuronal cellsMetabotropic glutamate receptor 3 agonist activity against forskolin stimulated c-AMP formation in rat non neuronal cells
ChEMBL 203 4 4 4 -1.6 N[C@@H](C1[C@H]([C@@H]1C(=O)O)C(=O)O)C(=O)O 10.1021/jm030967o
CHEMBL284193 1340 None 23 Rat Functional pEC50 = 6.7 6.7 -1 8
Metabotropic glutamate receptor 3 agonist activity against forskolin stimulated c-AMP formation in rat non neuronal cellsMetabotropic glutamate receptor 3 agonist activity against forskolin stimulated c-AMP formation in rat non neuronal cells
ChEMBL 203 4 4 4 -1.6 N[C@@H](C1[C@H]([C@@H]1C(=O)O)C(=O)O)C(=O)O 10.1021/jm030967o
10353365 83279 None 1 Human Functional pEC50 = 6.7 6.7 -13 3
Agonist activity at human mGluR3 assessed as effect on cAMP production in RGT cellsAgonist activity at human mGluR3 assessed as effect on cAMP production in RGT cells
ChEMBL 219 2 3 4 -1.8 N[C@@]1(C(=O)O)C[S+]([O-])[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/jm060917u
CHEMBL218710 83279 None 1 Human Functional pEC50 = 6.7 6.7 -13 3
Agonist activity at human mGluR3 assessed as effect on cAMP production in RGT cellsAgonist activity at human mGluR3 assessed as effect on cAMP production in RGT cells
ChEMBL 219 2 3 4 -1.8 N[C@@]1(C(=O)O)C[S+]([O-])[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/jm060917u
53240406 123463 None 21 Human Functional pEC50 = 5.7 5.7 -107 4
Agonist activity at human recombinant mGlu3 receptor D279E mutant expressed in AV12 cells assessed as stimulation of Ca2+ mobilization after 1 hr by FLIPR assayAgonist activity at human recombinant mGlu3 receptor D279E mutant expressed in AV12 cells assessed as stimulation of Ca2+ mobilization after 1 hr by FLIPR assay
ChEMBL 284 4 4 6 -0.6 N[C@@]1(C(=O)O)C[C@@H](Sc2nnc[nH]2)[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/acs.jmedchem.5b01124
CHEMBL3616847 123463 None 21 Human Functional pEC50 = 5.7 5.7 -107 4
Agonist activity at human recombinant mGlu3 receptor D279E mutant expressed in AV12 cells assessed as stimulation of Ca2+ mobilization after 1 hr by FLIPR assayAgonist activity at human recombinant mGlu3 receptor D279E mutant expressed in AV12 cells assessed as stimulation of Ca2+ mobilization after 1 hr by FLIPR assay
ChEMBL 284 4 4 6 -0.6 N[C@@]1(C(=O)O)C[C@@H](Sc2nnc[nH]2)[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/acs.jmedchem.5b01124
71136653 123470 None 0 Human Functional pEC50 = 6.6 6.6 -51 2
Agonist activity at human recombinant mGlu3 receptor expressed in AV12 cells assessed as inhibition of forskolin-stimulated cAMP production after 1 hr by fluorescence assayAgonist activity at human recombinant mGlu3 receptor expressed in AV12 cells assessed as inhibition of forskolin-stimulated cAMP production after 1 hr by fluorescence assay
ChEMBL 284 4 4 6 -0.6 N[C@@]1(C(=O)O)C[C@H](Sc2nnc[nH]2)[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/acs.jmedchem.5b01124
CHEMBL3616854 123470 None 0 Human Functional pEC50 = 6.6 6.6 -51 2
Agonist activity at human recombinant mGlu3 receptor expressed in AV12 cells assessed as inhibition of forskolin-stimulated cAMP production after 1 hr by fluorescence assayAgonist activity at human recombinant mGlu3 receptor expressed in AV12 cells assessed as inhibition of forskolin-stimulated cAMP production after 1 hr by fluorescence assay
ChEMBL 284 4 4 6 -0.6 N[C@@]1(C(=O)O)C[C@H](Sc2nnc[nH]2)[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/acs.jmedchem.5b01124
71136640 123469 None 0 Human Functional pEC50 = 6.6 6.6 -60 2
Agonist activity at human recombinant mGlu3 receptor expressed in AV12 cells assessed as inhibition of forskolin-stimulated cAMP production after 1 hr by fluorescence assayAgonist activity at human recombinant mGlu3 receptor expressed in AV12 cells assessed as inhibition of forskolin-stimulated cAMP production after 1 hr by fluorescence assay
ChEMBL 284 4 4 6 -0.6 N[C@@]1(C(=O)O)C[C@@H](Sc2c[nH]nn2)[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/acs.jmedchem.5b01124
CHEMBL3616853 123469 None 0 Human Functional pEC50 = 6.6 6.6 -60 2
Agonist activity at human recombinant mGlu3 receptor expressed in AV12 cells assessed as inhibition of forskolin-stimulated cAMP production after 1 hr by fluorescence assayAgonist activity at human recombinant mGlu3 receptor expressed in AV12 cells assessed as inhibition of forskolin-stimulated cAMP production after 1 hr by fluorescence assay
ChEMBL 284 4 4 6 -0.6 N[C@@]1(C(=O)O)C[C@@H](Sc2c[nH]nn2)[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/acs.jmedchem.5b01124
1393 1539 None 42 Human Functional pEC50 = 7.6 7.6 -4 6
Agonistic activity against Human Metabotropic glutamate receptor 3Agonistic activity against Human Metabotropic glutamate receptor 3
ChEMBL 185 2 3 3 -0.5 OC(=O)[C@H]1[C@H]2[C@@H]1[C@](CC2)(N)C(=O)O 10.1021/jm970719q
1396 1539 None 42 Human Functional pEC50 = 7.6 7.6 -4 6
Agonistic activity against Human Metabotropic glutamate receptor 3Agonistic activity against Human Metabotropic glutamate receptor 3
ChEMBL 185 2 3 3 -0.5 OC(=O)[C@H]1[C@H]2[C@@H]1[C@](CC2)(N)C(=O)O 10.1021/jm970719q
213056 1539 None 42 Human Functional pEC50 = 7.6 7.6 -4 6
Agonistic activity against Human Metabotropic glutamate receptor 3Agonistic activity against Human Metabotropic glutamate receptor 3
ChEMBL 185 2 3 3 -0.5 OC(=O)[C@H]1[C@H]2[C@@H]1[C@](CC2)(N)C(=O)O 10.1021/jm970719q
CHEMBL8759 1539 None 42 Human Functional pEC50 = 7.6 7.6 -4 6
Agonistic activity against Human Metabotropic glutamate receptor 3Agonistic activity against Human Metabotropic glutamate receptor 3
ChEMBL 185 2 3 3 -0.5 OC(=O)[C@H]1[C@H]2[C@@H]1[C@](CC2)(N)C(=O)O 10.1021/jm970719q
11275666 90091 None 1 Human Functional pEC50 = 7.6 7.6 -1 3
Agonist activity at human mGlu3 receptor expressed in HEK cells assessed as inhibition of forskolin-stimulated cAMP formation after 20 mins by HTRF assayAgonist activity at human mGlu3 receptor expressed in HEK cells assessed as inhibition of forskolin-stimulated cAMP formation after 20 mins by HTRF assay
ChEMBL 200 2 4 4 -1.6 N[C@H]1C[C@@](N)(C(=O)O)[C@@H]2[C@@H](C(=O)O)[C@H]12 10.1021/acs.jmedchem.7b01481
CHEMBL2381647 90091 None 1 Human Functional pEC50 = 7.6 7.6 -1 3
Agonist activity at human mGlu3 receptor expressed in HEK cells assessed as inhibition of forskolin-stimulated cAMP formation after 20 mins by HTRF assayAgonist activity at human mGlu3 receptor expressed in HEK cells assessed as inhibition of forskolin-stimulated cAMP formation after 20 mins by HTRF assay
ChEMBL 200 2 4 4 -1.6 N[C@H]1C[C@@](N)(C(=O)O)[C@@H]2[C@@H](C(=O)O)[C@H]12 10.1021/acs.jmedchem.7b01481
1310 2315 None 61 Human Functional pEC50 = 5.6 5.6 -251 17
Agonistic activity evaluated in CHO(Chinese hamster ovary) cells expressing chimeric mGluR3/1a receptorAgonistic activity evaluated in CHO(Chinese hamster ovary) cells expressing chimeric mGluR3/1a receptor
ChEMBL 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N 10.1016/s0960-894x(99)00266-8
1369 2315 None 61 Human Functional pEC50 = 5.6 5.6 -251 17
Agonistic activity evaluated in CHO(Chinese hamster ovary) cells expressing chimeric mGluR3/1a receptorAgonistic activity evaluated in CHO(Chinese hamster ovary) cells expressing chimeric mGluR3/1a receptor
ChEMBL 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N 10.1016/s0960-894x(99)00266-8
33032 2315 None 61 Human Functional pEC50 = 5.6 5.6 -251 17
Agonistic activity evaluated in CHO(Chinese hamster ovary) cells expressing chimeric mGluR3/1a receptorAgonistic activity evaluated in CHO(Chinese hamster ovary) cells expressing chimeric mGluR3/1a receptor
ChEMBL 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N 10.1016/s0960-894x(99)00266-8
44272391 2315 None 61 Human Functional pEC50 = 5.6 5.6 -251 17
Agonistic activity evaluated in CHO(Chinese hamster ovary) cells expressing chimeric mGluR3/1a receptorAgonistic activity evaluated in CHO(Chinese hamster ovary) cells expressing chimeric mGluR3/1a receptor
ChEMBL 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N 10.1016/s0960-894x(99)00266-8
88747398 2315 None 61 Human Functional pEC50 = 5.6 5.6 -251 17
Agonistic activity evaluated in CHO(Chinese hamster ovary) cells expressing chimeric mGluR3/1a receptorAgonistic activity evaluated in CHO(Chinese hamster ovary) cells expressing chimeric mGluR3/1a receptor
ChEMBL 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N 10.1016/s0960-894x(99)00266-8
CHEMBL575060 2315 None 61 Human Functional pEC50 = 5.6 5.6 -251 17
Agonistic activity evaluated in CHO(Chinese hamster ovary) cells expressing chimeric mGluR3/1a receptorAgonistic activity evaluated in CHO(Chinese hamster ovary) cells expressing chimeric mGluR3/1a receptor
ChEMBL 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N 10.1016/s0960-894x(99)00266-8
DB00142 2315 None 61 Human Functional pEC50 = 5.6 5.6 -251 17
Agonistic activity evaluated in CHO(Chinese hamster ovary) cells expressing chimeric mGluR3/1a receptorAgonistic activity evaluated in CHO(Chinese hamster ovary) cells expressing chimeric mGluR3/1a receptor
ChEMBL 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N 10.1016/s0960-894x(99)00266-8
71131322 123473 None 0 Human Functional pEC50 = 7.6 7.6 -43 2
Agonist activity at human recombinant mGlu3 receptor expressed in AV12 cells assessed as inhibition of forskolin-stimulated cAMP production after 1 hr by fluorescence assayAgonist activity at human recombinant mGlu3 receptor expressed in AV12 cells assessed as inhibition of forskolin-stimulated cAMP production after 1 hr by fluorescence assay
ChEMBL 334 5 4 6 0.3 N[C@@]1(C(=O)O)C[C@H](Sc2nnc(C(F)F)[nH]2)[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/acs.jmedchem.5b01124
CHEMBL3616857 123473 None 0 Human Functional pEC50 = 7.6 7.6 -43 2
Agonist activity at human recombinant mGlu3 receptor expressed in AV12 cells assessed as inhibition of forskolin-stimulated cAMP production after 1 hr by fluorescence assayAgonist activity at human recombinant mGlu3 receptor expressed in AV12 cells assessed as inhibition of forskolin-stimulated cAMP production after 1 hr by fluorescence assay
ChEMBL 334 5 4 6 0.3 N[C@@]1(C(=O)O)C[C@H](Sc2nnc(C(F)F)[nH]2)[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/acs.jmedchem.5b01124
1393 1539 None 42 Human Functional pEC50 = 7.6 7.6 -4 6
Agonist activity at human mGlu3 receptor expressed in HEK cells assessed as inhibition of forskolin-stimulated cAMP formation after 20 mins by HTRF assayAgonist activity at human mGlu3 receptor expressed in HEK cells assessed as inhibition of forskolin-stimulated cAMP formation after 20 mins by HTRF assay
ChEMBL 185 2 3 3 -0.5 OC(=O)[C@H]1[C@H]2[C@@H]1[C@](CC2)(N)C(=O)O 10.1021/acs.jmedchem.7b01481
1396 1539 None 42 Human Functional pEC50 = 7.6 7.6 -4 6
Agonist activity at human mGlu3 receptor expressed in HEK cells assessed as inhibition of forskolin-stimulated cAMP formation after 20 mins by HTRF assayAgonist activity at human mGlu3 receptor expressed in HEK cells assessed as inhibition of forskolin-stimulated cAMP formation after 20 mins by HTRF assay
ChEMBL 185 2 3 3 -0.5 OC(=O)[C@H]1[C@H]2[C@@H]1[C@](CC2)(N)C(=O)O 10.1021/acs.jmedchem.7b01481
213056 1539 None 42 Human Functional pEC50 = 7.6 7.6 -4 6
Agonist activity at human mGlu3 receptor expressed in HEK cells assessed as inhibition of forskolin-stimulated cAMP formation after 20 mins by HTRF assayAgonist activity at human mGlu3 receptor expressed in HEK cells assessed as inhibition of forskolin-stimulated cAMP formation after 20 mins by HTRF assay
ChEMBL 185 2 3 3 -0.5 OC(=O)[C@H]1[C@H]2[C@@H]1[C@](CC2)(N)C(=O)O 10.1021/acs.jmedchem.7b01481
CHEMBL8759 1539 None 42 Human Functional pEC50 = 7.6 7.6 -4 6
Agonist activity at human mGlu3 receptor expressed in HEK cells assessed as inhibition of forskolin-stimulated cAMP formation after 20 mins by HTRF assayAgonist activity at human mGlu3 receptor expressed in HEK cells assessed as inhibition of forskolin-stimulated cAMP formation after 20 mins by HTRF assay
ChEMBL 185 2 3 3 -0.5 OC(=O)[C@H]1[C@H]2[C@@H]1[C@](CC2)(N)C(=O)O 10.1021/acs.jmedchem.7b01481
1393 1539 None 42 Human Functional pEC50 = 7.6 7.6 -4 6
Agonist activity at human recombinant mGlu3 receptor expressed in AV12 cells assessed as inhibition of forskolin-stimulated cAMP production after 1 hr by fluorescence assayAgonist activity at human recombinant mGlu3 receptor expressed in AV12 cells assessed as inhibition of forskolin-stimulated cAMP production after 1 hr by fluorescence assay
ChEMBL 185 2 3 3 -0.5 OC(=O)[C@H]1[C@H]2[C@@H]1[C@](CC2)(N)C(=O)O 10.1021/acs.jmedchem.5b01124
1396 1539 None 42 Human Functional pEC50 = 7.6 7.6 -4 6
Agonist activity at human recombinant mGlu3 receptor expressed in AV12 cells assessed as inhibition of forskolin-stimulated cAMP production after 1 hr by fluorescence assayAgonist activity at human recombinant mGlu3 receptor expressed in AV12 cells assessed as inhibition of forskolin-stimulated cAMP production after 1 hr by fluorescence assay
ChEMBL 185 2 3 3 -0.5 OC(=O)[C@H]1[C@H]2[C@@H]1[C@](CC2)(N)C(=O)O 10.1021/acs.jmedchem.5b01124
213056 1539 None 42 Human Functional pEC50 = 7.6 7.6 -4 6
Agonist activity at human recombinant mGlu3 receptor expressed in AV12 cells assessed as inhibition of forskolin-stimulated cAMP production after 1 hr by fluorescence assayAgonist activity at human recombinant mGlu3 receptor expressed in AV12 cells assessed as inhibition of forskolin-stimulated cAMP production after 1 hr by fluorescence assay
ChEMBL 185 2 3 3 -0.5 OC(=O)[C@H]1[C@H]2[C@@H]1[C@](CC2)(N)C(=O)O 10.1021/acs.jmedchem.5b01124
CHEMBL8759 1539 None 42 Human Functional pEC50 = 7.6 7.6 -4 6
Agonist activity at human recombinant mGlu3 receptor expressed in AV12 cells assessed as inhibition of forskolin-stimulated cAMP production after 1 hr by fluorescence assayAgonist activity at human recombinant mGlu3 receptor expressed in AV12 cells assessed as inhibition of forskolin-stimulated cAMP production after 1 hr by fluorescence assay
ChEMBL 185 2 3 3 -0.5 OC(=O)[C@H]1[C@H]2[C@@H]1[C@](CC2)(N)C(=O)O 10.1021/acs.jmedchem.5b01124
71136655 123468 None 0 Human Functional pEC50 = 6.6 6.6 -12 2
Agonist activity at human recombinant mGlu3 receptor expressed in AV12 cells assessed as inhibition of forskolin-stimulated cAMP production after 1 hr by fluorescence assayAgonist activity at human recombinant mGlu3 receptor expressed in AV12 cells assessed as inhibition of forskolin-stimulated cAMP production after 1 hr by fluorescence assay
ChEMBL 326 5 4 6 0.5 CC(C)c1nnc(S[C@@H]2C[C@@](N)(C(=O)O)[C@@H]3[C@@H](C(=O)O)[C@H]23)[nH]1 10.1021/acs.jmedchem.5b01124
CHEMBL3616852 123468 None 0 Human Functional pEC50 = 6.6 6.6 -12 2
Agonist activity at human recombinant mGlu3 receptor expressed in AV12 cells assessed as inhibition of forskolin-stimulated cAMP production after 1 hr by fluorescence assayAgonist activity at human recombinant mGlu3 receptor expressed in AV12 cells assessed as inhibition of forskolin-stimulated cAMP production after 1 hr by fluorescence assay
ChEMBL 326 5 4 6 0.5 CC(C)c1nnc(S[C@@H]2C[C@@](N)(C(=O)O)[C@@H]3[C@@H](C(=O)O)[C@H]23)[nH]1 10.1021/acs.jmedchem.5b01124
53240406 123463 None 21 Human Functional pEC50 = 5.6 5.6 -107 4
Agonist activity at human recombinant mGlu3 receptor Q306L mutant expressed in AV12 cells assessed as stimulation of Ca2+ mobilization after 1 hr by FLIPR assayAgonist activity at human recombinant mGlu3 receptor Q306L mutant expressed in AV12 cells assessed as stimulation of Ca2+ mobilization after 1 hr by FLIPR assay
ChEMBL 284 4 4 6 -0.6 N[C@@]1(C(=O)O)C[C@@H](Sc2nnc[nH]2)[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/acs.jmedchem.5b01124
CHEMBL3616847 123463 None 21 Human Functional pEC50 = 5.6 5.6 -107 4
Agonist activity at human recombinant mGlu3 receptor Q306L mutant expressed in AV12 cells assessed as stimulation of Ca2+ mobilization after 1 hr by FLIPR assayAgonist activity at human recombinant mGlu3 receptor Q306L mutant expressed in AV12 cells assessed as stimulation of Ca2+ mobilization after 1 hr by FLIPR assay
ChEMBL 284 4 4 6 -0.6 N[C@@]1(C(=O)O)C[C@@H](Sc2nnc[nH]2)[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/acs.jmedchem.5b01124
67973779 137191 None 0 Human Functional pEC50 = 6.5 6.5 1 2
Antagonist activity at human mGlu3 expressed in HEK293 cells assessed as inhibition of glutamate-induced calcium mobilizationAntagonist activity at human mGlu3 expressed in HEK293 cells assessed as inhibition of glutamate-induced calcium mobilization
ChEMBL 338 4 0 5 2.7 O=C1c2cc(COc3ccccn3)nn2CCN1c1ccc(F)cc1 10.1016/j.bmcl.2015.11.098
CHEMBL3747522 137191 None 0 Human Functional pEC50 = 6.5 6.5 1 2
Antagonist activity at human mGlu3 expressed in HEK293 cells assessed as inhibition of glutamate-induced calcium mobilizationAntagonist activity at human mGlu3 expressed in HEK293 cells assessed as inhibition of glutamate-induced calcium mobilization
ChEMBL 338 4 0 5 2.7 O=C1c2cc(COc3ccccn3)nn2CCN1c1ccc(F)cc1 10.1016/j.bmcl.2015.11.098
90098428 123472 None 0 Human Functional pEC50 = 7.5 7.5 -60 2
Agonist activity at human recombinant mGlu3 receptor expressed in AV12 cells assessed as inhibition of forskolin-stimulated cAMP production after 1 hr by fluorescence assayAgonist activity at human recombinant mGlu3 receptor expressed in AV12 cells assessed as inhibition of forskolin-stimulated cAMP production after 1 hr by fluorescence assay
ChEMBL 352 4 4 6 0.4 N[C@@]1(C(=O)O)C[C@H](Sc2nnc(C(F)(F)F)[nH]2)[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/acs.jmedchem.5b01124
CHEMBL3616856 123472 None 0 Human Functional pEC50 = 7.5 7.5 -60 2
Agonist activity at human recombinant mGlu3 receptor expressed in AV12 cells assessed as inhibition of forskolin-stimulated cAMP production after 1 hr by fluorescence assayAgonist activity at human recombinant mGlu3 receptor expressed in AV12 cells assessed as inhibition of forskolin-stimulated cAMP production after 1 hr by fluorescence assay
ChEMBL 352 4 4 6 0.4 N[C@@]1(C(=O)O)C[C@H](Sc2nnc(C(F)(F)F)[nH]2)[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/acs.jmedchem.5b01124
1392 73 None 32 Human Functional pEC50 = 5.5 5.5 -9 4
Agonistic activity evaluated in CHO(Chinese hamster ovary) cells expressing chimeric mGluR3/1a receptorAgonistic activity evaluated in CHO(Chinese hamster ovary) cells expressing chimeric mGluR3/1a receptor
ChEMBL 174 2 4 4 -1.8 OC(=O)[C@@H]1NC[C@@](C1)(N)C(=O)O 10.1016/s0960-894x(99)00266-8
5310984 73 None 32 Human Functional pEC50 = 5.5 5.5 -9 4
Agonistic activity evaluated in CHO(Chinese hamster ovary) cells expressing chimeric mGluR3/1a receptorAgonistic activity evaluated in CHO(Chinese hamster ovary) cells expressing chimeric mGluR3/1a receptor
ChEMBL 174 2 4 4 -1.8 OC(=O)[C@@H]1NC[C@@](C1)(N)C(=O)O 10.1016/s0960-894x(99)00266-8
CHEMBL40086 73 None 32 Human Functional pEC50 = 5.5 5.5 -9 4
Agonistic activity evaluated in CHO(Chinese hamster ovary) cells expressing chimeric mGluR3/1a receptorAgonistic activity evaluated in CHO(Chinese hamster ovary) cells expressing chimeric mGluR3/1a receptor
ChEMBL 174 2 4 4 -1.8 OC(=O)[C@@H]1NC[C@@](C1)(N)C(=O)O 10.1016/s0960-894x(99)00266-8
104766 33 None 30 Human Functional pEC50 = 4.5 4.5 -8 14
Agonistic activity evaluated in CHO(Chinese hamster ovary) cells expressing chimeric mGluR3/1a receptorAgonistic activity evaluated in CHO(Chinese hamster ovary) cells expressing chimeric mGluR3/1a receptor
ChEMBL 173 2 3 3 -0.3 OC(=O)[C@@H]1CC[C@@](C1)(N)C(=O)O 10.1016/s0960-894x(99)00266-8
1365 33 None 30 Human Functional pEC50 = 4.5 4.5 -8 14
Agonistic activity evaluated in CHO(Chinese hamster ovary) cells expressing chimeric mGluR3/1a receptorAgonistic activity evaluated in CHO(Chinese hamster ovary) cells expressing chimeric mGluR3/1a receptor
ChEMBL 173 2 3 3 -0.3 OC(=O)[C@@H]1CC[C@@](C1)(N)C(=O)O 10.1016/s0960-894x(99)00266-8
CHEMBL34453 33 None 30 Human Functional pEC50 = 4.5 4.5 -8 14
Agonistic activity evaluated in CHO(Chinese hamster ovary) cells expressing chimeric mGluR3/1a receptorAgonistic activity evaluated in CHO(Chinese hamster ovary) cells expressing chimeric mGluR3/1a receptor
ChEMBL 173 2 3 3 -0.3 OC(=O)[C@@H]1CC[C@@](C1)(N)C(=O)O 10.1016/s0960-894x(99)00266-8
44378268 120189 None 0 Human Functional pEC50 = 4.5 4.5 - 1
Agonist potency against cloned Metabotropic glutamate receptor 3Agonist potency against cloned Metabotropic glutamate receptor 3
ChEMBL 354 12 5 5 0.4 O=C(O)CC[C@H](CP(=O)(O)C[C@H](CCC(=O)O)C(=O)O)C(=O)O 10.1021/jm9905559
CHEMBL351166 120189 None 0 Human Functional pEC50 = 4.5 4.5 - 1
Agonist potency against cloned Metabotropic glutamate receptor 3Agonist potency against cloned Metabotropic glutamate receptor 3
ChEMBL 354 12 5 5 0.4 O=C(O)CC[C@H](CP(=O)(O)C[C@H](CCC(=O)O)C(=O)O)C(=O)O 10.1021/jm9905559
72714783 137168 None 0 Human Functional pEC50 = 5.5 5.5 -21 2
Antagonist activity at human mGlu3 expressed in HEK293 cells assessed as inhibition of glutamate-induced calcium mobilizationAntagonist activity at human mGlu3 expressed in HEK293 cells assessed as inhibition of glutamate-induced calcium mobilization
ChEMBL 337 4 0 4 3.3 O=C1c2cc(OCc3ccccc3)nn2CCN1c1ccc(F)cc1 10.1016/j.bmcl.2015.11.098
CHEMBL3747116 137168 None 0 Human Functional pEC50 = 5.5 5.5 -21 2
Antagonist activity at human mGlu3 expressed in HEK293 cells assessed as inhibition of glutamate-induced calcium mobilizationAntagonist activity at human mGlu3 expressed in HEK293 cells assessed as inhibition of glutamate-induced calcium mobilization
ChEMBL 337 4 0 4 3.3 O=C1c2cc(OCc3ccccc3)nn2CCN1c1ccc(F)cc1 10.1016/j.bmcl.2015.11.098
67974346 137068 None 0 Human Functional pEC50 = 7.5 7.5 3 2
Antagonist activity at human mGlu3 expressed in HEK293 cells assessed as inhibition of glutamate-induced calcium mobilizationAntagonist activity at human mGlu3 expressed in HEK293 cells assessed as inhibition of glutamate-induced calcium mobilization
ChEMBL 355 4 0 4 3.4 O=C1c2cc(COc3ccc(F)cc3)nn2CCN1c1ccc(F)cc1 10.1016/j.bmcl.2015.11.098
CHEMBL3745812 137068 None 0 Human Functional pEC50 = 7.5 7.5 3 2
Antagonist activity at human mGlu3 expressed in HEK293 cells assessed as inhibition of glutamate-induced calcium mobilizationAntagonist activity at human mGlu3 expressed in HEK293 cells assessed as inhibition of glutamate-induced calcium mobilization
ChEMBL 355 4 0 4 3.4 O=C1c2cc(COc3ccc(F)cc3)nn2CCN1c1ccc(F)cc1 10.1016/j.bmcl.2015.11.098
11344646 126844 None 0 Human Functional pEC50 = 7.5 7.5 -2 3
Evaluation of the functional effect on cAMP responses in RGT cells expressing human mGlu3 receptorEvaluation of the functional effect on cAMP responses in RGT cells expressing human mGlu3 receptor
ChEMBL 199 2 3 3 -0.2 C[C@H]1C[C@@](N)(C(=O)O)[C@@H]2[C@@H](C(=O)O)[C@H]12 10.1021/jm040222y
CHEMBL365368 126844 None 0 Human Functional pEC50 = 7.5 7.5 -2 3
Evaluation of the functional effect on cAMP responses in RGT cells expressing human mGlu3 receptorEvaluation of the functional effect on cAMP responses in RGT cells expressing human mGlu3 receptor
ChEMBL 199 2 3 3 -0.2 C[C@H]1C[C@@](N)(C(=O)O)[C@@H]2[C@@H](C(=O)O)[C@H]12 10.1021/jm040222y
60096194 156679 None 0 Human Functional pEC50 = 6.5 6.5 1 2
Agonist activity at human mGlu3 receptor expressed in HEK cells assessed as inhibition of forskolin-stimulated cAMP formation after 20 mins by HTRF assayAgonist activity at human mGlu3 receptor expressed in HEK cells assessed as inhibition of forskolin-stimulated cAMP formation after 20 mins by HTRF assay
ChEMBL 290 5 4 4 0.3 N[C@@]1(C(=O)O)C[C@H](NCc2ccccc2)[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/acs.jmedchem.7b01481
CHEMBL4068679 156679 None 0 Human Functional pEC50 = 6.5 6.5 1 2
Agonist activity at human mGlu3 receptor expressed in HEK cells assessed as inhibition of forskolin-stimulated cAMP formation after 20 mins by HTRF assayAgonist activity at human mGlu3 receptor expressed in HEK cells assessed as inhibition of forskolin-stimulated cAMP formation after 20 mins by HTRF assay
ChEMBL 290 5 4 4 0.3 N[C@@]1(C(=O)O)C[C@H](NCc2ccccc2)[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/acs.jmedchem.7b01481
44300820 13383 None 0 Rat Functional pEC50 = 4.4 4.4 1 2
Effective concentration required for agonistic activity at Metabotropic glutamate receptor 3Effective concentration required for agonistic activity at Metabotropic glutamate receptor 3
ChEMBL 265 4 3 5 -0.5 N[C@]1(C(=O)O)C[C@H](C(=O)O)N(Cc2ccccn2)C1 10.1016/s0960-894x(01)00329-8
CHEMBL1192558 13383 None 0 Rat Functional pEC50 = 4.4 4.4 1 2
Effective concentration required for agonistic activity at Metabotropic glutamate receptor 3Effective concentration required for agonistic activity at Metabotropic glutamate receptor 3
ChEMBL 265 4 3 5 -0.5 N[C@]1(C(=O)O)C[C@H](C(=O)O)N(Cc2ccccn2)C1 10.1016/s0960-894x(01)00329-8
CHEMBL543811 13383 None 0 Rat Functional pEC50 = 4.4 4.4 1 2
Effective concentration required for agonistic activity at Metabotropic glutamate receptor 3Effective concentration required for agonistic activity at Metabotropic glutamate receptor 3
ChEMBL 265 4 3 5 -0.5 N[C@]1(C(=O)O)C[C@H](C(=O)O)N(Cc2ccccn2)C1 10.1016/s0960-894x(01)00329-8
1393 1539 None 42 Human Functional pEC50 = 7.4 7.4 -4 6
Agonist activity at human mGluR3 assessed as effect on cAMP production in RGT cellsAgonist activity at human mGluR3 assessed as effect on cAMP production in RGT cells
ChEMBL 185 2 3 3 -0.5 OC(=O)[C@H]1[C@H]2[C@@H]1[C@](CC2)(N)C(=O)O 10.1021/jm060917u
1396 1539 None 42 Human Functional pEC50 = 7.4 7.4 -4 6
Agonist activity at human mGluR3 assessed as effect on cAMP production in RGT cellsAgonist activity at human mGluR3 assessed as effect on cAMP production in RGT cells
ChEMBL 185 2 3 3 -0.5 OC(=O)[C@H]1[C@H]2[C@@H]1[C@](CC2)(N)C(=O)O 10.1021/jm060917u
213056 1539 None 42 Human Functional pEC50 = 7.4 7.4 -4 6
Agonist activity at human mGluR3 assessed as effect on cAMP production in RGT cellsAgonist activity at human mGluR3 assessed as effect on cAMP production in RGT cells
ChEMBL 185 2 3 3 -0.5 OC(=O)[C@H]1[C@H]2[C@@H]1[C@](CC2)(N)C(=O)O 10.1021/jm060917u
CHEMBL8759 1539 None 42 Human Functional pEC50 = 7.4 7.4 -4 6
Agonist activity at human mGluR3 assessed as effect on cAMP production in RGT cellsAgonist activity at human mGluR3 assessed as effect on cAMP production in RGT cells
ChEMBL 185 2 3 3 -0.5 OC(=O)[C@H]1[C@H]2[C@@H]1[C@](CC2)(N)C(=O)O 10.1021/jm060917u
1393 1539 None 42 Rat Functional pEC50 = 7.4 7.4 -5 6
Agonist activity at mGLUR3 in rat cerebral cortex assessed as inhibition of forskolin-stimulated cAMP productionAgonist activity at mGLUR3 in rat cerebral cortex assessed as inhibition of forskolin-stimulated cAMP production
ChEMBL 185 2 3 3 -0.5 OC(=O)[C@H]1[C@H]2[C@@H]1[C@](CC2)(N)C(=O)O 10.1016/j.bmcl.2012.01.039
1396 1539 None 42 Rat Functional pEC50 = 7.4 7.4 -5 6
Agonist activity at mGLUR3 in rat cerebral cortex assessed as inhibition of forskolin-stimulated cAMP productionAgonist activity at mGLUR3 in rat cerebral cortex assessed as inhibition of forskolin-stimulated cAMP production
ChEMBL 185 2 3 3 -0.5 OC(=O)[C@H]1[C@H]2[C@@H]1[C@](CC2)(N)C(=O)O 10.1016/j.bmcl.2012.01.039
213056 1539 None 42 Rat Functional pEC50 = 7.4 7.4 -5 6
Agonist activity at mGLUR3 in rat cerebral cortex assessed as inhibition of forskolin-stimulated cAMP productionAgonist activity at mGLUR3 in rat cerebral cortex assessed as inhibition of forskolin-stimulated cAMP production
ChEMBL 185 2 3 3 -0.5 OC(=O)[C@H]1[C@H]2[C@@H]1[C@](CC2)(N)C(=O)O 10.1016/j.bmcl.2012.01.039
CHEMBL8759 1539 None 42 Rat Functional pEC50 = 7.4 7.4 -5 6
Agonist activity at mGLUR3 in rat cerebral cortex assessed as inhibition of forskolin-stimulated cAMP productionAgonist activity at mGLUR3 in rat cerebral cortex assessed as inhibition of forskolin-stimulated cAMP production
ChEMBL 185 2 3 3 -0.5 OC(=O)[C@H]1[C@H]2[C@@H]1[C@](CC2)(N)C(=O)O 10.1016/j.bmcl.2012.01.039
1393 1539 None 42 Human Functional pEC50 = 7.4 7.4 -4 6
Evaluation of the functional effect on cAMP responses in RGT cells expressing human mGlu3 receptorEvaluation of the functional effect on cAMP responses in RGT cells expressing human mGlu3 receptor
ChEMBL 185 2 3 3 -0.5 OC(=O)[C@H]1[C@H]2[C@@H]1[C@](CC2)(N)C(=O)O 10.1021/jm040222y
1396 1539 None 42 Human Functional pEC50 = 7.4 7.4 -4 6
Evaluation of the functional effect on cAMP responses in RGT cells expressing human mGlu3 receptorEvaluation of the functional effect on cAMP responses in RGT cells expressing human mGlu3 receptor
ChEMBL 185 2 3 3 -0.5 OC(=O)[C@H]1[C@H]2[C@@H]1[C@](CC2)(N)C(=O)O 10.1021/jm040222y
213056 1539 None 42 Human Functional pEC50 = 7.4 7.4 -4 6
Evaluation of the functional effect on cAMP responses in RGT cells expressing human mGlu3 receptorEvaluation of the functional effect on cAMP responses in RGT cells expressing human mGlu3 receptor
ChEMBL 185 2 3 3 -0.5 OC(=O)[C@H]1[C@H]2[C@@H]1[C@](CC2)(N)C(=O)O 10.1021/jm040222y
CHEMBL8759 1539 None 42 Human Functional pEC50 = 7.4 7.4 -4 6
Evaluation of the functional effect on cAMP responses in RGT cells expressing human mGlu3 receptorEvaluation of the functional effect on cAMP responses in RGT cells expressing human mGlu3 receptor
ChEMBL 185 2 3 3 -0.5 OC(=O)[C@H]1[C@H]2[C@@H]1[C@](CC2)(N)C(=O)O 10.1021/jm040222y
1393 1539 None 42 Human Functional pEC50 = 7.4 7.4 -4 6
Inhibition of forskolin stimulated cAMP production in RGT cells expressing recombinant human Metabotropic glutamate receptor 3Inhibition of forskolin stimulated cAMP production in RGT cells expressing recombinant human Metabotropic glutamate receptor 3
ChEMBL 185 2 3 3 -0.5 OC(=O)[C@H]1[C@H]2[C@@H]1[C@](CC2)(N)C(=O)O 10.1021/jm980616n
1396 1539 None 42 Human Functional pEC50 = 7.4 7.4 -4 6
Inhibition of forskolin stimulated cAMP production in RGT cells expressing recombinant human Metabotropic glutamate receptor 3Inhibition of forskolin stimulated cAMP production in RGT cells expressing recombinant human Metabotropic glutamate receptor 3
ChEMBL 185 2 3 3 -0.5 OC(=O)[C@H]1[C@H]2[C@@H]1[C@](CC2)(N)C(=O)O 10.1021/jm980616n
213056 1539 None 42 Human Functional pEC50 = 7.4 7.4 -4 6
Inhibition of forskolin stimulated cAMP production in RGT cells expressing recombinant human Metabotropic glutamate receptor 3Inhibition of forskolin stimulated cAMP production in RGT cells expressing recombinant human Metabotropic glutamate receptor 3
ChEMBL 185 2 3 3 -0.5 OC(=O)[C@H]1[C@H]2[C@@H]1[C@](CC2)(N)C(=O)O 10.1021/jm980616n
CHEMBL8759 1539 None 42 Human Functional pEC50 = 7.4 7.4 -4 6
Inhibition of forskolin stimulated cAMP production in RGT cells expressing recombinant human Metabotropic glutamate receptor 3Inhibition of forskolin stimulated cAMP production in RGT cells expressing recombinant human Metabotropic glutamate receptor 3
ChEMBL 185 2 3 3 -0.5 OC(=O)[C@H]1[C@H]2[C@@H]1[C@](CC2)(N)C(=O)O 10.1021/jm980616n
10176324 114891 None 1 Rat Functional pEC50 = 7.4 7.4 -4 4
Metabotropic glutamate receptor 3 agonist activity against forskolin stimulated c-AMP formation in rat non neuronal cellsMetabotropic glutamate receptor 3 agonist activity against forskolin stimulated c-AMP formation in rat non neuronal cells
ChEMBL 173 3 3 3 -0.6 C[C@H]1[C@H](C(=O)O)[C@H]1[C@H](N)C(=O)O 10.1021/jm030967o
CHEMBL334160 114891 None 1 Rat Functional pEC50 = 7.4 7.4 -4 4
Metabotropic glutamate receptor 3 agonist activity against forskolin stimulated c-AMP formation in rat non neuronal cellsMetabotropic glutamate receptor 3 agonist activity against forskolin stimulated c-AMP formation in rat non neuronal cells
ChEMBL 173 3 3 3 -0.6 C[C@H]1[C@H](C(=O)O)[C@H]1[C@H](N)C(=O)O 10.1021/jm030967o
4408 25142 None 12 Human Functional pEC50 = 4.4 4.4 - 1
Agonist potency against cloned Metabotropic glutamate receptor 3Agonist potency against cloned Metabotropic glutamate receptor 3
ChEMBL 354 12 5 5 0.4 O=C(O)CCC(CP(=O)(O)CC(CCC(=O)O)C(=O)O)C(=O)O 10.1021/jm9905559
CHEMBL134749 25142 None 12 Human Functional pEC50 = 4.4 4.4 - 1
Agonist potency against cloned Metabotropic glutamate receptor 3Agonist potency against cloned Metabotropic glutamate receptor 3
ChEMBL 354 12 5 5 0.4 O=C(O)CCC(CP(=O)(O)CC(CCC(=O)O)C(=O)O)C(=O)O 10.1021/jm9905559
10197984 2421 None 36 Human Functional pEC50 = 8.3 8.3 -1 5
Agonist activity at human mGLUR3 assessed as inhibition of forskolin-stimulated cAMP production by cell-based assayAgonist activity at human mGLUR3 assessed as inhibition of forskolin-stimulated cAMP production by cell-based assay
ChEMBL 187 2 3 4 -1.5 OC(=O)[C@H]1[C@H]2[C@@H]1[C@](CO2)(N)C(=O)O 10.1016/j.bmcl.2012.01.039
1394 2421 None 36 Human Functional pEC50 = 8.3 8.3 -1 5
Agonist activity at human mGLUR3 assessed as inhibition of forskolin-stimulated cAMP production by cell-based assayAgonist activity at human mGLUR3 assessed as inhibition of forskolin-stimulated cAMP production by cell-based assay
ChEMBL 187 2 3 4 -1.5 OC(=O)[C@H]1[C@H]2[C@@H]1[C@](CO2)(N)C(=O)O 10.1016/j.bmcl.2012.01.039
CHEMBL275079 2421 None 36 Human Functional pEC50 = 8.3 8.3 -1 5
Agonist activity at human mGLUR3 assessed as inhibition of forskolin-stimulated cAMP production by cell-based assayAgonist activity at human mGLUR3 assessed as inhibition of forskolin-stimulated cAMP production by cell-based assay
ChEMBL 187 2 3 4 -1.5 OC(=O)[C@H]1[C@H]2[C@@H]1[C@](CO2)(N)C(=O)O 10.1016/j.bmcl.2012.01.039
10197984 2421 None 36 Human Functional pEC50 = 8.3 8.3 -1 5
Inhibition of forskolin stimulated cAMP production in RGT cells expressing recombinant human Metabotropic glutamate receptor 3Inhibition of forskolin stimulated cAMP production in RGT cells expressing recombinant human Metabotropic glutamate receptor 3
ChEMBL 187 2 3 4 -1.5 OC(=O)[C@H]1[C@H]2[C@@H]1[C@](CO2)(N)C(=O)O 10.1021/jm980616n
1394 2421 None 36 Human Functional pEC50 = 8.3 8.3 -1 5
Inhibition of forskolin stimulated cAMP production in RGT cells expressing recombinant human Metabotropic glutamate receptor 3Inhibition of forskolin stimulated cAMP production in RGT cells expressing recombinant human Metabotropic glutamate receptor 3
ChEMBL 187 2 3 4 -1.5 OC(=O)[C@H]1[C@H]2[C@@H]1[C@](CO2)(N)C(=O)O 10.1021/jm980616n
CHEMBL275079 2421 None 36 Human Functional pEC50 = 8.3 8.3 -1 5
Inhibition of forskolin stimulated cAMP production in RGT cells expressing recombinant human Metabotropic glutamate receptor 3Inhibition of forskolin stimulated cAMP production in RGT cells expressing recombinant human Metabotropic glutamate receptor 3
ChEMBL 187 2 3 4 -1.5 OC(=O)[C@H]1[C@H]2[C@@H]1[C@](CO2)(N)C(=O)O 10.1021/jm980616n
10197984 2421 None 36 Human Functional pEC50 = 8.3 8.3 -1 5
Agonist activity at human mGluR3 assessed as effect on cAMP production in RGT cellsAgonist activity at human mGluR3 assessed as effect on cAMP production in RGT cells
ChEMBL 187 2 3 4 -1.5 OC(=O)[C@H]1[C@H]2[C@@H]1[C@](CO2)(N)C(=O)O 10.1021/jm060917u
1394 2421 None 36 Human Functional pEC50 = 8.3 8.3 -1 5
Agonist activity at human mGluR3 assessed as effect on cAMP production in RGT cellsAgonist activity at human mGluR3 assessed as effect on cAMP production in RGT cells
ChEMBL 187 2 3 4 -1.5 OC(=O)[C@H]1[C@H]2[C@@H]1[C@](CO2)(N)C(=O)O 10.1021/jm060917u
CHEMBL275079 2421 None 36 Human Functional pEC50 = 8.3 8.3 -1 5
Agonist activity at human mGluR3 assessed as effect on cAMP production in RGT cellsAgonist activity at human mGluR3 assessed as effect on cAMP production in RGT cells
ChEMBL 187 2 3 4 -1.5 OC(=O)[C@H]1[C@H]2[C@@H]1[C@](CO2)(N)C(=O)O 10.1021/jm060917u
11220424 159053 None 0 Human Functional pEC50 = 8.3 8.3 3 2
Agonist activity at human mGlu3 receptor expressed in HEK cells assessed as inhibition of forskolin-stimulated cAMP formation after 20 mins by HTRF assayAgonist activity at human mGlu3 receptor expressed in HEK cells assessed as inhibition of forskolin-stimulated cAMP formation after 20 mins by HTRF assay
ChEMBL 304 4 4 4 -0.1 N[C@@]1(C(=O)O)C[C@H](NC(=O)c2ccccc2)[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/acs.jmedchem.7b01481
CHEMBL4095995 159053 None 0 Human Functional pEC50 = 8.3 8.3 3 2
Agonist activity at human mGlu3 receptor expressed in HEK cells assessed as inhibition of forskolin-stimulated cAMP formation after 20 mins by HTRF assayAgonist activity at human mGlu3 receptor expressed in HEK cells assessed as inhibition of forskolin-stimulated cAMP formation after 20 mins by HTRF assay
ChEMBL 304 4 4 4 -0.1 N[C@@]1(C(=O)O)C[C@H](NC(=O)c2ccccc2)[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/acs.jmedchem.7b01481
137659992 159329 None 0 Human Functional pEC50 = 8.3 8.3 8 2
Agonist activity at human mGlu3 receptor expressed in HEK cells assessed as inhibition of forskolin-stimulated cAMP formation after 20 mins by HTRF assayAgonist activity at human mGlu3 receptor expressed in HEK cells assessed as inhibition of forskolin-stimulated cAMP formation after 20 mins by HTRF assay
ChEMBL 338 4 4 4 0.6 N[C@@]1(C(=O)O)C[C@H](NC(=O)c2ccccc2Cl)[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/acs.jmedchem.7b01481
CHEMBL4098939 159329 None 0 Human Functional pEC50 = 8.3 8.3 8 2
Agonist activity at human mGlu3 receptor expressed in HEK cells assessed as inhibition of forskolin-stimulated cAMP formation after 20 mins by HTRF assayAgonist activity at human mGlu3 receptor expressed in HEK cells assessed as inhibition of forskolin-stimulated cAMP formation after 20 mins by HTRF assay
ChEMBL 338 4 4 4 0.6 N[C@@]1(C(=O)O)C[C@H](NC(=O)c2ccccc2Cl)[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/acs.jmedchem.7b01481
1310 2315 None 61 Human Functional pEC50 = 5.4 5.4 -251 17
Agonist activity at human recombinant mGlu3 receptor D279E mutant expressed in AV12 cells assessed as stimulation of Ca2+ mobilization after 1 hr by FLIPR assayAgonist activity at human recombinant mGlu3 receptor D279E mutant expressed in AV12 cells assessed as stimulation of Ca2+ mobilization after 1 hr by FLIPR assay
ChEMBL 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N 10.1021/acs.jmedchem.5b01124
1369 2315 None 61 Human Functional pEC50 = 5.4 5.4 -251 17
Agonist activity at human recombinant mGlu3 receptor D279E mutant expressed in AV12 cells assessed as stimulation of Ca2+ mobilization after 1 hr by FLIPR assayAgonist activity at human recombinant mGlu3 receptor D279E mutant expressed in AV12 cells assessed as stimulation of Ca2+ mobilization after 1 hr by FLIPR assay
ChEMBL 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N 10.1021/acs.jmedchem.5b01124
33032 2315 None 61 Human Functional pEC50 = 5.4 5.4 -251 17
Agonist activity at human recombinant mGlu3 receptor D279E mutant expressed in AV12 cells assessed as stimulation of Ca2+ mobilization after 1 hr by FLIPR assayAgonist activity at human recombinant mGlu3 receptor D279E mutant expressed in AV12 cells assessed as stimulation of Ca2+ mobilization after 1 hr by FLIPR assay
ChEMBL 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N 10.1021/acs.jmedchem.5b01124
44272391 2315 None 61 Human Functional pEC50 = 5.4 5.4 -251 17
Agonist activity at human recombinant mGlu3 receptor D279E mutant expressed in AV12 cells assessed as stimulation of Ca2+ mobilization after 1 hr by FLIPR assayAgonist activity at human recombinant mGlu3 receptor D279E mutant expressed in AV12 cells assessed as stimulation of Ca2+ mobilization after 1 hr by FLIPR assay
ChEMBL 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N 10.1021/acs.jmedchem.5b01124
88747398 2315 None 61 Human Functional pEC50 = 5.4 5.4 -251 17
Agonist activity at human recombinant mGlu3 receptor D279E mutant expressed in AV12 cells assessed as stimulation of Ca2+ mobilization after 1 hr by FLIPR assayAgonist activity at human recombinant mGlu3 receptor D279E mutant expressed in AV12 cells assessed as stimulation of Ca2+ mobilization after 1 hr by FLIPR assay
ChEMBL 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N 10.1021/acs.jmedchem.5b01124
CHEMBL575060 2315 None 61 Human Functional pEC50 = 5.4 5.4 -251 17
Agonist activity at human recombinant mGlu3 receptor D279E mutant expressed in AV12 cells assessed as stimulation of Ca2+ mobilization after 1 hr by FLIPR assayAgonist activity at human recombinant mGlu3 receptor D279E mutant expressed in AV12 cells assessed as stimulation of Ca2+ mobilization after 1 hr by FLIPR assay
ChEMBL 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N 10.1021/acs.jmedchem.5b01124
DB00142 2315 None 61 Human Functional pEC50 = 5.4 5.4 -251 17
Agonist activity at human recombinant mGlu3 receptor D279E mutant expressed in AV12 cells assessed as stimulation of Ca2+ mobilization after 1 hr by FLIPR assayAgonist activity at human recombinant mGlu3 receptor D279E mutant expressed in AV12 cells assessed as stimulation of Ca2+ mobilization after 1 hr by FLIPR assay
ChEMBL 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N 10.1021/acs.jmedchem.5b01124
9815616 114864 None 4 Rat Functional pEC50 = 7.3 7.3 1 4
Agonist potency against cloned Metabotropic glutamate receptor 3Agonist potency against cloned Metabotropic glutamate receptor 3
ChEMBL 203 2 3 3 -0.5 N[C@@]1(C(=O)O)[C@@H](F)C[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/jm000346k
CHEMBL334014 114864 None 4 Rat Functional pEC50 = 7.3 7.3 1 4
Agonist potency against cloned Metabotropic glutamate receptor 3Agonist potency against cloned Metabotropic glutamate receptor 3
ChEMBL 203 2 3 3 -0.5 N[C@@]1(C(=O)O)[C@@H](F)C[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/jm000346k
4408 25142 None 12 Human Functional pEC50 = 4.4 4.4 - 1
Agonist potency against cloned Metabotropic glutamate receptor 3Agonist potency against cloned Metabotropic glutamate receptor 3
ChEMBL 354 12 5 5 0.4 O=C(O)CCC(CP(=O)(O)CC(CCC(=O)O)C(=O)O)C(=O)O 10.1021/jm9905559
CHEMBL134749 25142 None 12 Human Functional pEC50 = 4.4 4.4 - 1
Agonist potency against cloned Metabotropic glutamate receptor 3Agonist potency against cloned Metabotropic glutamate receptor 3
ChEMBL 354 12 5 5 0.4 O=C(O)CCC(CP(=O)(O)CC(CCC(=O)O)C(=O)O)C(=O)O 10.1021/jm9905559
9834591 137687 None 46 Human Functional pEC50 = 7.3 7.3 -2 3
Agonist activity at human mGluR3 assessed as effect on cAMP production in RGT cellsAgonist activity at human mGluR3 assessed as effect on cAMP production in RGT cells
ChEMBL 235 2 3 5 -2.1 N[C@@]1(C(=O)O)CS(=O)(=O)[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/jm060917u
CHEMBL375611 137687 None 46 Human Functional pEC50 = 7.3 7.3 -2 3
Agonist activity at human mGluR3 assessed as effect on cAMP production in RGT cellsAgonist activity at human mGluR3 assessed as effect on cAMP production in RGT cells
ChEMBL 235 2 3 5 -2.1 N[C@@]1(C(=O)O)CS(=O)(=O)[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/jm060917u
60096236 158514 None 0 Human Functional pEC50 = 8.3 8.3 3 2
Agonist activity at human mGlu3 receptor expressed in HEK cells assessed as inhibition of forskolin-stimulated cAMP formation after 20 mins by HTRF assayAgonist activity at human mGlu3 receptor expressed in HEK cells assessed as inhibition of forskolin-stimulated cAMP formation after 20 mins by HTRF assay
ChEMBL 322 4 4 4 0.1 N[C@@]1(C(=O)O)C[C@H](NC(=O)c2ccccc2F)[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/acs.jmedchem.7b01481
CHEMBL4090293 158514 None 0 Human Functional pEC50 = 8.3 8.3 3 2
Agonist activity at human mGlu3 receptor expressed in HEK cells assessed as inhibition of forskolin-stimulated cAMP formation after 20 mins by HTRF assayAgonist activity at human mGlu3 receptor expressed in HEK cells assessed as inhibition of forskolin-stimulated cAMP formation after 20 mins by HTRF assay
ChEMBL 322 4 4 4 0.1 N[C@@]1(C(=O)O)C[C@H](NC(=O)c2ccccc2F)[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/acs.jmedchem.7b01481
60096250 159013 None 0 Human Functional pEC50 = 8.3 8.3 1 2
Agonist activity at human mGlu3 receptor expressed in HEK cells assessed as inhibition of forskolin-stimulated cAMP formation after 20 mins by HTRF assayAgonist activity at human mGlu3 receptor expressed in HEK cells assessed as inhibition of forskolin-stimulated cAMP formation after 20 mins by HTRF assay
ChEMBL 338 4 4 4 0.6 N[C@@]1(C(=O)O)C[C@H](NC(=O)c2ccc(Cl)cc2)[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/acs.jmedchem.7b01481
CHEMBL4095567 159013 None 0 Human Functional pEC50 = 8.3 8.3 1 2
Agonist activity at human mGlu3 receptor expressed in HEK cells assessed as inhibition of forskolin-stimulated cAMP formation after 20 mins by HTRF assayAgonist activity at human mGlu3 receptor expressed in HEK cells assessed as inhibition of forskolin-stimulated cAMP formation after 20 mins by HTRF assay
ChEMBL 338 4 4 4 0.6 N[C@@]1(C(=O)O)C[C@H](NC(=O)c2ccc(Cl)cc2)[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/acs.jmedchem.7b01481
4408 25142 None 12 Human Functional pEC50 = 4.3 4.3 - 1
Agonist potency against cloned Metabotropic glutamate receptor 3Agonist potency against cloned Metabotropic glutamate receptor 3
ChEMBL 354 12 5 5 0.4 O=C(O)CCC(CP(=O)(O)CC(CCC(=O)O)C(=O)O)C(=O)O 10.1021/jm9905559
CHEMBL134749 25142 None 12 Human Functional pEC50 = 4.3 4.3 - 1
Agonist potency against cloned Metabotropic glutamate receptor 3Agonist potency against cloned Metabotropic glutamate receptor 3
ChEMBL 354 12 5 5 0.4 O=C(O)CCC(CP(=O)(O)CC(CCC(=O)O)C(=O)O)C(=O)O 10.1021/jm9905559
1310 2315 None 61 Human Functional pEC50 = 5.3 5.3 -251 17
Agonist activity at human recombinant mGlu3 receptor D279E and Q306L mutant expressed in AV12 cells assessed as stimulation of Ca2+ mobilization after 1 hr by FLIPR assayAgonist activity at human recombinant mGlu3 receptor D279E and Q306L mutant expressed in AV12 cells assessed as stimulation of Ca2+ mobilization after 1 hr by FLIPR assay
ChEMBL 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N 10.1021/acs.jmedchem.5b01124
1369 2315 None 61 Human Functional pEC50 = 5.3 5.3 -251 17
Agonist activity at human recombinant mGlu3 receptor D279E and Q306L mutant expressed in AV12 cells assessed as stimulation of Ca2+ mobilization after 1 hr by FLIPR assayAgonist activity at human recombinant mGlu3 receptor D279E and Q306L mutant expressed in AV12 cells assessed as stimulation of Ca2+ mobilization after 1 hr by FLIPR assay
ChEMBL 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N 10.1021/acs.jmedchem.5b01124
33032 2315 None 61 Human Functional pEC50 = 5.3 5.3 -251 17
Agonist activity at human recombinant mGlu3 receptor D279E and Q306L mutant expressed in AV12 cells assessed as stimulation of Ca2+ mobilization after 1 hr by FLIPR assayAgonist activity at human recombinant mGlu3 receptor D279E and Q306L mutant expressed in AV12 cells assessed as stimulation of Ca2+ mobilization after 1 hr by FLIPR assay
ChEMBL 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N 10.1021/acs.jmedchem.5b01124
44272391 2315 None 61 Human Functional pEC50 = 5.3 5.3 -251 17
Agonist activity at human recombinant mGlu3 receptor D279E and Q306L mutant expressed in AV12 cells assessed as stimulation of Ca2+ mobilization after 1 hr by FLIPR assayAgonist activity at human recombinant mGlu3 receptor D279E and Q306L mutant expressed in AV12 cells assessed as stimulation of Ca2+ mobilization after 1 hr by FLIPR assay
ChEMBL 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N 10.1021/acs.jmedchem.5b01124
88747398 2315 None 61 Human Functional pEC50 = 5.3 5.3 -251 17
Agonist activity at human recombinant mGlu3 receptor D279E and Q306L mutant expressed in AV12 cells assessed as stimulation of Ca2+ mobilization after 1 hr by FLIPR assayAgonist activity at human recombinant mGlu3 receptor D279E and Q306L mutant expressed in AV12 cells assessed as stimulation of Ca2+ mobilization after 1 hr by FLIPR assay
ChEMBL 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N 10.1021/acs.jmedchem.5b01124
CHEMBL575060 2315 None 61 Human Functional pEC50 = 5.3 5.3 -251 17
Agonist activity at human recombinant mGlu3 receptor D279E and Q306L mutant expressed in AV12 cells assessed as stimulation of Ca2+ mobilization after 1 hr by FLIPR assayAgonist activity at human recombinant mGlu3 receptor D279E and Q306L mutant expressed in AV12 cells assessed as stimulation of Ca2+ mobilization after 1 hr by FLIPR assay
ChEMBL 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N 10.1021/acs.jmedchem.5b01124
DB00142 2315 None 61 Human Functional pEC50 = 5.3 5.3 -251 17
Agonist activity at human recombinant mGlu3 receptor D279E and Q306L mutant expressed in AV12 cells assessed as stimulation of Ca2+ mobilization after 1 hr by FLIPR assayAgonist activity at human recombinant mGlu3 receptor D279E and Q306L mutant expressed in AV12 cells assessed as stimulation of Ca2+ mobilization after 1 hr by FLIPR assay
ChEMBL 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N 10.1021/acs.jmedchem.5b01124
10330132 101437 None 1 Human Functional pEC50 = 4.3 4.3 -10 2
Agonistic activity evaluated in CHO(Chinese hamster ovary) cells expressing chimeric mGluR3/1a receptorAgonistic activity evaluated in CHO(Chinese hamster ovary) cells expressing chimeric mGluR3/1a receptor
ChEMBL 189 2 4 5 -2.2 NN1C[C@@](N)(C(=O)O)C[C@@H]1C(=O)O 10.1016/s0960-894x(99)00266-8
CHEMBL297150 101437 None 1 Human Functional pEC50 = 4.3 4.3 -10 2
Agonistic activity evaluated in CHO(Chinese hamster ovary) cells expressing chimeric mGluR3/1a receptorAgonistic activity evaluated in CHO(Chinese hamster ovary) cells expressing chimeric mGluR3/1a receptor
ChEMBL 189 2 4 5 -2.2 NN1C[C@@](N)(C(=O)O)C[C@@H]1C(=O)O 10.1016/s0960-894x(99)00266-8
127039660 137111 None 0 Human Functional pEC50 = 6.3 6.3 -3 2
Antagonist activity at human mGlu3 expressed in HEK293 cells assessed as inhibition of glutamate-induced calcium mobilizationAntagonist activity at human mGlu3 expressed in HEK293 cells assessed as inhibition of glutamate-induced calcium mobilization
ChEMBL 351 4 0 4 3.7 O=C1c2cc(COc3ccccc3)nn2CCCN1c1ccc(F)cc1 10.1016/j.bmcl.2015.11.098
CHEMBL3746344 137111 None 0 Human Functional pEC50 = 6.3 6.3 -3 2
Antagonist activity at human mGlu3 expressed in HEK293 cells assessed as inhibition of glutamate-induced calcium mobilizationAntagonist activity at human mGlu3 expressed in HEK293 cells assessed as inhibition of glutamate-induced calcium mobilization
ChEMBL 351 4 0 4 3.7 O=C1c2cc(COc3ccccc3)nn2CCCN1c1ccc(F)cc1 10.1016/j.bmcl.2015.11.098
53240406 123463 None 21 Human Functional pEC50 = 5.3 5.3 -107 4
Agonist activity at wild type human recombinant mGlu3 receptor expressed in AV12 cells assessed as stimulation of Ca2+ mobilization after 1 hr by FLIPR assayAgonist activity at wild type human recombinant mGlu3 receptor expressed in AV12 cells assessed as stimulation of Ca2+ mobilization after 1 hr by FLIPR assay
ChEMBL 284 4 4 6 -0.6 N[C@@]1(C(=O)O)C[C@@H](Sc2nnc[nH]2)[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/acs.jmedchem.5b01124
CHEMBL3616847 123463 None 21 Human Functional pEC50 = 5.3 5.3 -107 4
Agonist activity at wild type human recombinant mGlu3 receptor expressed in AV12 cells assessed as stimulation of Ca2+ mobilization after 1 hr by FLIPR assayAgonist activity at wild type human recombinant mGlu3 receptor expressed in AV12 cells assessed as stimulation of Ca2+ mobilization after 1 hr by FLIPR assay
ChEMBL 284 4 4 6 -0.6 N[C@@]1(C(=O)O)C[C@@H](Sc2nnc[nH]2)[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/acs.jmedchem.5b01124
60096204 156215 None 0 Human Functional pEC50 = 8.2 8.2 2 2
Agonist activity at human mGlu3 receptor expressed in HEK cells assessed as inhibition of forskolin-stimulated cAMP formation after 20 mins by HTRF assayAgonist activity at human mGlu3 receptor expressed in HEK cells assessed as inhibition of forskolin-stimulated cAMP formation after 20 mins by HTRF assay
ChEMBL 322 4 4 4 0.1 N[C@@]1(C(=O)O)C[C@H](NC(=O)c2ccc(F)cc2)[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/acs.jmedchem.7b01481
CHEMBL4063336 156215 None 0 Human Functional pEC50 = 8.2 8.2 2 2
Agonist activity at human mGlu3 receptor expressed in HEK cells assessed as inhibition of forskolin-stimulated cAMP formation after 20 mins by HTRF assayAgonist activity at human mGlu3 receptor expressed in HEK cells assessed as inhibition of forskolin-stimulated cAMP formation after 20 mins by HTRF assay
ChEMBL 322 4 4 4 0.1 N[C@@]1(C(=O)O)C[C@H](NC(=O)c2ccc(F)cc2)[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/acs.jmedchem.7b01481
1368 2290 None 30 Rat Functional pEC50 = 6.2 6.2 -1 11
Metabotropic glutamate receptor 3 agonist activity against forskolin stimulated c-AMP formation in rat non neuronal cellsMetabotropic glutamate receptor 3 agonist activity against forskolin stimulated c-AMP formation in rat non neuronal cells
ChEMBL 159 3 3 3 -0.9 N[C@@H]([C@H]1C[C@@H]1C(=O)O)C(=O)O 10.1021/jm030967o
5310956 2290 None 30 Rat Functional pEC50 = 6.2 6.2 -1 11
Metabotropic glutamate receptor 3 agonist activity against forskolin stimulated c-AMP formation in rat non neuronal cellsMetabotropic glutamate receptor 3 agonist activity against forskolin stimulated c-AMP formation in rat non neuronal cells
ChEMBL 159 3 3 3 -0.9 N[C@@H]([C@H]1C[C@@H]1C(=O)O)C(=O)O 10.1021/jm030967o
CHEMBL280563 2290 None 30 Rat Functional pEC50 = 6.2 6.2 -1 11
Metabotropic glutamate receptor 3 agonist activity against forskolin stimulated c-AMP formation in rat non neuronal cellsMetabotropic glutamate receptor 3 agonist activity against forskolin stimulated c-AMP formation in rat non neuronal cells
ChEMBL 159 3 3 3 -0.9 N[C@@H]([C@H]1C[C@@H]1C(=O)O)C(=O)O 10.1021/jm030967o
1393 1539 None 42 Rat Functional pEC50 = 7.2 7.2 -5 6
Agonist potency against cloned Metabotropic glutamate receptor 3Agonist potency against cloned Metabotropic glutamate receptor 3
ChEMBL 185 2 3 3 -0.5 OC(=O)[C@H]1[C@H]2[C@@H]1[C@](CC2)(N)C(=O)O 10.1021/jm000346k
1396 1539 None 42 Rat Functional pEC50 = 7.2 7.2 -5 6
Agonist potency against cloned Metabotropic glutamate receptor 3Agonist potency against cloned Metabotropic glutamate receptor 3
ChEMBL 185 2 3 3 -0.5 OC(=O)[C@H]1[C@H]2[C@@H]1[C@](CC2)(N)C(=O)O 10.1021/jm000346k
213056 1539 None 42 Rat Functional pEC50 = 7.2 7.2 -5 6
Agonist potency against cloned Metabotropic glutamate receptor 3Agonist potency against cloned Metabotropic glutamate receptor 3
ChEMBL 185 2 3 3 -0.5 OC(=O)[C@H]1[C@H]2[C@@H]1[C@](CC2)(N)C(=O)O 10.1021/jm000346k
CHEMBL8759 1539 None 42 Rat Functional pEC50 = 7.2 7.2 -5 6
Agonist potency against cloned Metabotropic glutamate receptor 3Agonist potency against cloned Metabotropic glutamate receptor 3
ChEMBL 185 2 3 3 -0.5 OC(=O)[C@H]1[C@H]2[C@@H]1[C@](CC2)(N)C(=O)O 10.1021/jm000346k
155518933 170449 None 0 Human Functional pEC50 = 6.2 6.2 1 3
Allosteric agonist activity at human mGlu3 expressed in CHO cells assessed as reduction in forskolin-induced cAMP production after 30 mins by cAMP reagent-based assayAllosteric agonist activity at human mGlu3 expressed in CHO cells assessed as reduction in forskolin-induced cAMP production after 30 mins by cAMP reagent-based assay
ChEMBL 421 6 1 3 4.3 CNC(=O)N1CCCC(CN2CCC(OC(c3ccccc3)c3ccccc3)CC2)C1 10.1039/C8MD00524A
CHEMBL4447269 170449 None 0 Human Functional pEC50 = 6.2 6.2 1 3
Allosteric agonist activity at human mGlu3 expressed in CHO cells assessed as reduction in forskolin-induced cAMP production after 30 mins by cAMP reagent-based assayAllosteric agonist activity at human mGlu3 expressed in CHO cells assessed as reduction in forskolin-induced cAMP production after 30 mins by cAMP reagent-based assay
ChEMBL 421 6 1 3 4.3 CNC(=O)N1CCCC(CN2CCC(OC(c3ccccc3)c3ccccc3)CC2)C1 10.1039/C8MD00524A
67974411 137116 None 0 Human Functional pEC50 = 5.2 5.2 -52 2
Antagonist activity at human mGlu3 expressed in HEK293 cells assessed as inhibition of glutamate-induced calcium mobilizationAntagonist activity at human mGlu3 expressed in HEK293 cells assessed as inhibition of glutamate-induced calcium mobilization
ChEMBL 338 4 0 5 2.7 O=C1c2cc(COc3ccccc3)nn2CCN1c1ccc(F)cn1 10.1016/j.bmcl.2015.11.098
CHEMBL3746457 137116 None 0 Human Functional pEC50 = 5.2 5.2 -52 2
Antagonist activity at human mGlu3 expressed in HEK293 cells assessed as inhibition of glutamate-induced calcium mobilizationAntagonist activity at human mGlu3 expressed in HEK293 cells assessed as inhibition of glutamate-induced calcium mobilization
ChEMBL 338 4 0 5 2.7 O=C1c2cc(COc3ccccc3)nn2CCN1c1ccc(F)cn1 10.1016/j.bmcl.2015.11.098
10474978 13464 None 0 Rat Functional pEC50 = 5.2 5.2 -1 2
Effective concentration required for agonistic activity at Metabotropic glutamate receptor 3Effective concentration required for agonistic activity at Metabotropic glutamate receptor 3
ChEMBL 309 5 3 6 0.0 N[C@]1(C(=O)O)C[C@H](C(=O)O)N(Cc2ccccc2[N+](=O)[O-])C1 10.1016/s0960-894x(01)00329-8
CHEMBL1193146 13464 None 0 Rat Functional pEC50 = 5.2 5.2 -1 2
Effective concentration required for agonistic activity at Metabotropic glutamate receptor 3Effective concentration required for agonistic activity at Metabotropic glutamate receptor 3
ChEMBL 309 5 3 6 0.0 N[C@]1(C(=O)O)C[C@H](C(=O)O)N(Cc2ccccc2[N+](=O)[O-])C1 10.1016/s0960-894x(01)00329-8
CHEMBL544508 13464 None 0 Rat Functional pEC50 = 5.2 5.2 -1 2
Effective concentration required for agonistic activity at Metabotropic glutamate receptor 3Effective concentration required for agonistic activity at Metabotropic glutamate receptor 3
ChEMBL 309 5 3 6 0.0 N[C@]1(C(=O)O)C[C@H](C(=O)O)N(Cc2ccccc2[N+](=O)[O-])C1 10.1016/s0960-894x(01)00329-8
44361401 31349 None 0 Rat Functional pEC50 = 8.2 8.2 -1 5
Metabotropic glutamate receptor 3 agonist activity against forskolin stimulated c-AMP formation in rat non neuronal cellsMetabotropic glutamate receptor 3 agonist activity against forskolin stimulated c-AMP formation in rat non neuronal cells
ChEMBL 175 3 4 4 -1.9 N[C@H](C(=O)O)[C@H]1[C@@H](O)[C@@H]1C(=O)O 10.1021/jm030967o
CHEMBL140197 31349 None 0 Rat Functional pEC50 = 8.2 8.2 -1 5
Metabotropic glutamate receptor 3 agonist activity against forskolin stimulated c-AMP formation in rat non neuronal cellsMetabotropic glutamate receptor 3 agonist activity against forskolin stimulated c-AMP formation in rat non neuronal cells
ChEMBL 175 3 4 4 -1.9 N[C@H](C(=O)O)[C@H]1[C@@H](O)[C@@H]1C(=O)O 10.1021/jm030967o
60096183 159377 None 0 Human Functional pEC50 = 8.2 8.2 3 2
Agonist activity at human mGlu3 receptor expressed in HEK cells assessed as inhibition of forskolin-stimulated cAMP formation after 20 mins by HTRF assayAgonist activity at human mGlu3 receptor expressed in HEK cells assessed as inhibition of forskolin-stimulated cAMP formation after 20 mins by HTRF assay
ChEMBL 334 5 4 5 -0.1 COc1ccccc1C(=O)N[C@H]1C[C@@](N)(C(=O)O)[C@@H]2[C@@H](C(=O)O)[C@H]12 10.1021/acs.jmedchem.7b01481
CHEMBL4099470 159377 None 0 Human Functional pEC50 = 8.2 8.2 3 2
Agonist activity at human mGlu3 receptor expressed in HEK cells assessed as inhibition of forskolin-stimulated cAMP formation after 20 mins by HTRF assayAgonist activity at human mGlu3 receptor expressed in HEK cells assessed as inhibition of forskolin-stimulated cAMP formation after 20 mins by HTRF assay
ChEMBL 334 5 4 5 -0.1 COc1ccccc1C(=O)N[C@H]1C[C@@](N)(C(=O)O)[C@@H]2[C@@H](C(=O)O)[C@H]12 10.1021/acs.jmedchem.7b01481
10198133 208966 None 10 Human Functional pEC50 = 8.1 8.1 -1 4
Agonist activity at human mGluR3 assessed as effect on cAMP production in RGT cellsAgonist activity at human mGluR3 assessed as effect on cAMP production in RGT cells
ChEMBL 203 2 3 4 -0.8 N[C@@]1(C(=O)O)CS[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/jm060917u
CHEMBL8839 208966 None 10 Human Functional pEC50 = 8.1 8.1 -1 4
Agonist activity at human mGluR3 assessed as effect on cAMP production in RGT cellsAgonist activity at human mGluR3 assessed as effect on cAMP production in RGT cells
ChEMBL 203 2 3 4 -0.8 N[C@@]1(C(=O)O)CS[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/jm060917u
10198133 208966 None 10 Human Functional pEC50 = 8.1 8.1 -1 4
Inhibition of forskolin stimulated cAMP production in RGT cells expressing recombinant human Metabotropic glutamate receptor 3Inhibition of forskolin stimulated cAMP production in RGT cells expressing recombinant human Metabotropic glutamate receptor 3
ChEMBL 203 2 3 4 -0.8 N[C@@]1(C(=O)O)CS[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/jm980616n
CHEMBL8839 208966 None 10 Human Functional pEC50 = 8.1 8.1 -1 4
Inhibition of forskolin stimulated cAMP production in RGT cells expressing recombinant human Metabotropic glutamate receptor 3Inhibition of forskolin stimulated cAMP production in RGT cells expressing recombinant human Metabotropic glutamate receptor 3
ChEMBL 203 2 3 4 -0.8 N[C@@]1(C(=O)O)CS[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/jm980616n
71137012 123467 None 0 Human Functional pEC50 = 7.1 7.1 -11 2
Agonist activity at human recombinant mGlu3 receptor expressed in AV12 cells assessed as inhibition of forskolin-stimulated cAMP production after 1 hr by fluorescence assayAgonist activity at human recombinant mGlu3 receptor expressed in AV12 cells assessed as inhibition of forskolin-stimulated cAMP production after 1 hr by fluorescence assay
ChEMBL 299 4 5 7 -1.0 Nc1nnc(S[C@@H]2C[C@@](N)(C(=O)O)[C@@H]3[C@@H](C(=O)O)[C@H]23)[nH]1 10.1021/acs.jmedchem.5b01124
CHEMBL3616851 123467 None 0 Human Functional pEC50 = 7.1 7.1 -11 2
Agonist activity at human recombinant mGlu3 receptor expressed in AV12 cells assessed as inhibition of forskolin-stimulated cAMP production after 1 hr by fluorescence assayAgonist activity at human recombinant mGlu3 receptor expressed in AV12 cells assessed as inhibition of forskolin-stimulated cAMP production after 1 hr by fluorescence assay
ChEMBL 299 4 5 7 -1.0 Nc1nnc(S[C@@H]2C[C@@](N)(C(=O)O)[C@@H]3[C@@H](C(=O)O)[C@H]23)[nH]1 10.1021/acs.jmedchem.5b01124
67974644 137209 None 0 Human Functional pEC50 = 7.1 7.1 -1 2
Antagonist activity at human mGlu3 expressed in HEK293 cells assessed as inhibition of glutamate-induced calcium mobilizationAntagonist activity at human mGlu3 expressed in HEK293 cells assessed as inhibition of glutamate-induced calcium mobilization
ChEMBL 337 4 0 4 3.3 O=C1c2cc(COc3ccccc3)nn2CCN1c1ccc(F)cc1 10.1016/j.bmcl.2015.11.098
CHEMBL3747735 137209 None 0 Human Functional pEC50 = 7.1 7.1 -1 2
Antagonist activity at human mGlu3 expressed in HEK293 cells assessed as inhibition of glutamate-induced calcium mobilizationAntagonist activity at human mGlu3 expressed in HEK293 cells assessed as inhibition of glutamate-induced calcium mobilization
ChEMBL 337 4 0 4 3.3 O=C1c2cc(COc3ccccc3)nn2CCN1c1ccc(F)cc1 10.1016/j.bmcl.2015.11.098
9815616 114864 None 4 Human Functional pEC50 = 7.1 7.1 -1 4
Agonist activity at human mGlu3 receptor expressed in CHO cell membranes by GTPgammaS binding assayAgonist activity at human mGlu3 receptor expressed in CHO cell membranes by GTPgammaS binding assay
ChEMBL 203 2 3 3 -0.5 N[C@@]1(C(=O)O)[C@@H](F)C[C@H]2[C@H](C(=O)O)[C@H]21 10.1016/j.ejmech.2020.112521
CHEMBL334014 114864 None 4 Human Functional pEC50 = 7.1 7.1 -1 4
Agonist activity at human mGlu3 receptor expressed in CHO cell membranes by GTPgammaS binding assayAgonist activity at human mGlu3 receptor expressed in CHO cell membranes by GTPgammaS binding assay
ChEMBL 203 2 3 3 -0.5 N[C@@]1(C(=O)O)[C@@H](F)C[C@H]2[C@H](C(=O)O)[C@H]21 10.1016/j.ejmech.2020.112521
44300605 13360 None 0 Rat Functional pEC50 = 5.1 5.1 3 3
Effective concentration required for partial agonistic activity at Metabotropic glutamate receptor 3; Partial agonistEffective concentration required for partial agonistic activity at Metabotropic glutamate receptor 3; Partial agonist
ChEMBL 280 4 4 5 -0.2 N[C@]1(C(=O)O)C[C@H](C(=O)O)N(Cc2ccc(O)cc2)C1 10.1016/s0960-894x(01)00329-8
CHEMBL1192345 13360 None 0 Rat Functional pEC50 = 5.1 5.1 3 3
Effective concentration required for partial agonistic activity at Metabotropic glutamate receptor 3; Partial agonistEffective concentration required for partial agonistic activity at Metabotropic glutamate receptor 3; Partial agonist
ChEMBL 280 4 4 5 -0.2 N[C@]1(C(=O)O)C[C@H](C(=O)O)N(Cc2ccc(O)cc2)C1 10.1016/s0960-894x(01)00329-8
CHEMBL543568 13360 None 0 Rat Functional pEC50 = 5.1 5.1 3 3
Effective concentration required for partial agonistic activity at Metabotropic glutamate receptor 3; Partial agonistEffective concentration required for partial agonistic activity at Metabotropic glutamate receptor 3; Partial agonist
ChEMBL 280 4 4 5 -0.2 N[C@]1(C(=O)O)C[C@H](C(=O)O)N(Cc2ccc(O)cc2)C1 10.1016/s0960-894x(01)00329-8
71137034 123466 None 0 Human Functional pEC50 = 7.1 7.1 -7 2
Agonist activity at human recombinant mGlu3 receptor expressed in AV12 cells assessed as inhibition of forskolin-stimulated cAMP production after 1 hr by fluorescence assayAgonist activity at human recombinant mGlu3 receptor expressed in AV12 cells assessed as inhibition of forskolin-stimulated cAMP production after 1 hr by fluorescence assay
ChEMBL 334 5 4 6 0.3 N[C@@]1(C(=O)O)C[C@@H](Sc2nnc(C(F)F)[nH]2)[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/acs.jmedchem.5b01124
CHEMBL3616850 123466 None 0 Human Functional pEC50 = 7.1 7.1 -7 2
Agonist activity at human recombinant mGlu3 receptor expressed in AV12 cells assessed as inhibition of forskolin-stimulated cAMP production after 1 hr by fluorescence assayAgonist activity at human recombinant mGlu3 receptor expressed in AV12 cells assessed as inhibition of forskolin-stimulated cAMP production after 1 hr by fluorescence assay
ChEMBL 334 5 4 6 0.3 N[C@@]1(C(=O)O)C[C@@H](Sc2nnc(C(F)F)[nH]2)[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/acs.jmedchem.5b01124
71136654 123475 None 0 Human Functional pEC50 = 7.1 7.1 -3 2
Agonist activity at human recombinant mGlu3 receptor expressed in AV12 cells assessed as inhibition of forskolin-stimulated cAMP production after 1 hr by fluorescence assayAgonist activity at human recombinant mGlu3 receptor expressed in AV12 cells assessed as inhibition of forskolin-stimulated cAMP production after 1 hr by fluorescence assay
ChEMBL 326 5 4 6 0.5 CC(C)c1nnc(S[C@H]2C[C@@](N)(C(=O)O)[C@@H]3[C@@H](C(=O)O)[C@H]23)[nH]1 10.1021/acs.jmedchem.5b01124
CHEMBL3616859 123475 None 0 Human Functional pEC50 = 7.1 7.1 -3 2
Agonist activity at human recombinant mGlu3 receptor expressed in AV12 cells assessed as inhibition of forskolin-stimulated cAMP production after 1 hr by fluorescence assayAgonist activity at human recombinant mGlu3 receptor expressed in AV12 cells assessed as inhibition of forskolin-stimulated cAMP production after 1 hr by fluorescence assay
ChEMBL 326 5 4 6 0.5 CC(C)c1nnc(S[C@H]2C[C@@](N)(C(=O)O)[C@@H]3[C@@H](C(=O)O)[C@H]23)[nH]1 10.1021/acs.jmedchem.5b01124
71137010 123465 None 0 Human Functional pEC50 = 7.1 7.1 -5 2
Agonist activity at human recombinant mGlu3 receptor expressed in AV12 cells assessed as inhibition of forskolin-stimulated cAMP production after 1 hr by fluorescence assayAgonist activity at human recombinant mGlu3 receptor expressed in AV12 cells assessed as inhibition of forskolin-stimulated cAMP production after 1 hr by fluorescence assay
ChEMBL 352 4 4 6 0.4 N[C@@]1(C(=O)O)C[C@@H](Sc2nnc(C(F)(F)F)[nH]2)[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/acs.jmedchem.5b01124
CHEMBL3616849 123465 None 0 Human Functional pEC50 = 7.1 7.1 -5 2
Agonist activity at human recombinant mGlu3 receptor expressed in AV12 cells assessed as inhibition of forskolin-stimulated cAMP production after 1 hr by fluorescence assayAgonist activity at human recombinant mGlu3 receptor expressed in AV12 cells assessed as inhibition of forskolin-stimulated cAMP production after 1 hr by fluorescence assay
ChEMBL 352 4 4 6 0.4 N[C@@]1(C(=O)O)C[C@@H](Sc2nnc(C(F)(F)F)[nH]2)[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/acs.jmedchem.5b01124
9815617 114563 None 3 Rat Functional pEC50 = 7.1 7.1 1 2
Agonist potency against cloned Metabotropic glutamate receptor 3Agonist potency against cloned Metabotropic glutamate receptor 3
ChEMBL 203 2 3 3 -0.4 N[C@@]1(C(=O)O)CC[C@@H]2[C@H]1[C@@]2(F)C(=O)O 10.1021/jm000346k
CHEMBL333519 114563 None 3 Rat Functional pEC50 = 7.1 7.1 1 2
Agonist potency against cloned Metabotropic glutamate receptor 3Agonist potency against cloned Metabotropic glutamate receptor 3
ChEMBL 203 2 3 3 -0.4 N[C@@]1(C(=O)O)CC[C@@H]2[C@H]1[C@@]2(F)C(=O)O 10.1021/jm000346k
71137010 123465 None 0 Human Functional pEC50 = 7.1 7.1 -5 2
Agonist activity at human recombinant mGlu3 receptor expressed in AV12 cells assessed as stimulation of Ca2+ mobilization after 1.5 hrs by FLIPR assayAgonist activity at human recombinant mGlu3 receptor expressed in AV12 cells assessed as stimulation of Ca2+ mobilization after 1.5 hrs by FLIPR assay
ChEMBL 352 4 4 6 0.4 N[C@@]1(C(=O)O)C[C@@H](Sc2nnc(C(F)(F)F)[nH]2)[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/acs.jmedchem.5b01124
CHEMBL3616849 123465 None 0 Human Functional pEC50 = 7.1 7.1 -5 2
Agonist activity at human recombinant mGlu3 receptor expressed in AV12 cells assessed as stimulation of Ca2+ mobilization after 1.5 hrs by FLIPR assayAgonist activity at human recombinant mGlu3 receptor expressed in AV12 cells assessed as stimulation of Ca2+ mobilization after 1.5 hrs by FLIPR assay
ChEMBL 352 4 4 6 0.4 N[C@@]1(C(=O)O)C[C@@H](Sc2nnc(C(F)(F)F)[nH]2)[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/acs.jmedchem.5b01124
117972250 142399 None 4 Human Functional pEC50 = 6.1 6.1 -32 2
Positive allosteric modulation of human mGlu3 receptor expressed in HEK293 cells assessed as inhibition of forskolin-stimulated cAMP production measured after 30 mins in presence of orthosteric antagonist LY341495 by FLIPR assayPositive allosteric modulation of human mGlu3 receptor expressed in HEK293 cells assessed as inhibition of forskolin-stimulated cAMP production measured after 30 mins in presence of orthosteric antagonist LY341495 by FLIPR assay
ChEMBL 421 6 0 4 5.5 FC(F)(F)c1c(OC[C@H]2C[C@@H]2c2ccc(Cl)cc2)ccn2c(CC3CC3)nnc12 10.1016/j.bmc.2016.11.018
CHEMBL3885379 142399 None 4 Human Functional pEC50 = 6.1 6.1 -32 2
Positive allosteric modulation of human mGlu3 receptor expressed in HEK293 cells assessed as inhibition of forskolin-stimulated cAMP production measured after 30 mins in presence of orthosteric antagonist LY341495 by FLIPR assayPositive allosteric modulation of human mGlu3 receptor expressed in HEK293 cells assessed as inhibition of forskolin-stimulated cAMP production measured after 30 mins in presence of orthosteric antagonist LY341495 by FLIPR assay
ChEMBL 421 6 0 4 5.5 FC(F)(F)c1c(OC[C@H]2C[C@@H]2c2ccc(Cl)cc2)ccn2c(CC3CC3)nnc12 10.1016/j.bmc.2016.11.018
49858117 1089 None 4 Human Functional pEC50 = 5.1 5.1 -5 2
Positive allosteric modulator activity at human mGluR3 expressed in HEK cells in presence of glutamate EC10 concentration by Ca2+ functional assayPositive allosteric modulator activity at human mGluR3 expressed in HEK cells in presence of glutamate EC10 concentration by Ca2+ functional assay
ChEMBL 308 2 2 4 3.0 O/N=C\1/c2ccccc2OC2(C1C2)C(=O)Nc1ccc(cc1)C 10.1021/jm101069m
6223 1089 None 4 Human Functional pEC50 = 5.1 5.1 -5 2
Positive allosteric modulator activity at human mGluR3 expressed in HEK cells in presence of glutamate EC10 concentration by Ca2+ functional assayPositive allosteric modulator activity at human mGluR3 expressed in HEK cells in presence of glutamate EC10 concentration by Ca2+ functional assay
ChEMBL 308 2 2 4 3.0 O/N=C\1/c2ccccc2OC2(C1C2)C(=O)Nc1ccc(cc1)C 10.1021/jm101069m
CHEMBL1630806 1089 None 4 Human Functional pEC50 = 5.1 5.1 -5 2
Positive allosteric modulator activity at human mGluR3 expressed in HEK cells in presence of glutamate EC10 concentration by Ca2+ functional assayPositive allosteric modulator activity at human mGluR3 expressed in HEK cells in presence of glutamate EC10 concentration by Ca2+ functional assay
ChEMBL 308 2 2 4 3.0 O/N=C\1/c2ccccc2OC2(C1C2)C(=O)Nc1ccc(cc1)C 10.1021/jm101069m
71476419 123476 None 0 Human Functional pEC50 = 7.0 7.0 -51 2
Agonist activity at human recombinant mGlu3 receptor expressed in AV12 cells assessed as inhibition of forskolin-stimulated cAMP production after 1 hr by fluorescence assayAgonist activity at human recombinant mGlu3 receptor expressed in AV12 cells assessed as inhibition of forskolin-stimulated cAMP production after 1 hr by fluorescence assay
ChEMBL 284 4 4 6 -0.6 N[C@@]1(C(=O)O)C[C@H](Sc2c[nH]nn2)[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/acs.jmedchem.5b01124
CHEMBL3616860 123476 None 0 Human Functional pEC50 = 7.0 7.0 -51 2
Agonist activity at human recombinant mGlu3 receptor expressed in AV12 cells assessed as inhibition of forskolin-stimulated cAMP production after 1 hr by fluorescence assayAgonist activity at human recombinant mGlu3 receptor expressed in AV12 cells assessed as inhibition of forskolin-stimulated cAMP production after 1 hr by fluorescence assay
ChEMBL 284 4 4 6 -0.6 N[C@@]1(C(=O)O)C[C@H](Sc2c[nH]nn2)[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/acs.jmedchem.5b01124
71137008 123471 None 0 Human Functional pEC50 = 7.0 7.0 -7 2
Agonist activity at human recombinant mGlu3 receptor expressed in AV12 cells assessed as inhibition of forskolin-stimulated cAMP production after 1 hr by fluorescence assayAgonist activity at human recombinant mGlu3 receptor expressed in AV12 cells assessed as inhibition of forskolin-stimulated cAMP production after 1 hr by fluorescence assay
ChEMBL 298 4 4 6 -0.3 Cc1nnc(S[C@H]2C[C@@](N)(C(=O)O)[C@@H]3[C@@H](C(=O)O)[C@H]23)[nH]1 10.1021/acs.jmedchem.5b01124
CHEMBL3616855 123471 None 0 Human Functional pEC50 = 7.0 7.0 -7 2
Agonist activity at human recombinant mGlu3 receptor expressed in AV12 cells assessed as inhibition of forskolin-stimulated cAMP production after 1 hr by fluorescence assayAgonist activity at human recombinant mGlu3 receptor expressed in AV12 cells assessed as inhibition of forskolin-stimulated cAMP production after 1 hr by fluorescence assay
ChEMBL 298 4 4 6 -0.3 Cc1nnc(S[C@H]2C[C@@](N)(C(=O)O)[C@@H]3[C@@H](C(=O)O)[C@H]23)[nH]1 10.1021/acs.jmedchem.5b01124
9815616 114864 None 4 Rat Functional pEC50 = 7.0 7.0 1 4
Agonist activity at rat mGlu3 receptor expressed in CHO cell membranes by GTPgammaS binding assayAgonist activity at rat mGlu3 receptor expressed in CHO cell membranes by GTPgammaS binding assay
ChEMBL 203 2 3 3 -0.5 N[C@@]1(C(=O)O)[C@@H](F)C[C@H]2[C@H](C(=O)O)[C@H]21 10.1016/j.ejmech.2020.112521
CHEMBL334014 114864 None 4 Rat Functional pEC50 = 7.0 7.0 1 4
Agonist activity at rat mGlu3 receptor expressed in CHO cell membranes by GTPgammaS binding assayAgonist activity at rat mGlu3 receptor expressed in CHO cell membranes by GTPgammaS binding assay
ChEMBL 203 2 3 3 -0.5 N[C@@]1(C(=O)O)[C@@H](F)C[C@H]2[C@H](C(=O)O)[C@H]21 10.1016/j.ejmech.2020.112521
1378 2417 None 39 Human Functional pIC50 = 8 8.0 2 14
Effect on 1S,3R-ACPD-induced inhibition of forskolin stimulated cyclic-AMP in RGT cells expressing human Metabotropic glutamate receptor 3Effect on 1S,3R-ACPD-induced inhibition of forskolin stimulated cyclic-AMP in RGT cells expressing human Metabotropic glutamate receptor 3
ChEMBL 353 5 3 4 2.8 OC(=O)[C@H]1C[C@@H]1[C@](C(=O)O)(CC1c2ccccc2Oc2c1cccc2)N 10.1021/jm970498o
1399 2417 None 39 Human Functional pIC50 = 8 8.0 2 14
Effect on 1S,3R-ACPD-induced inhibition of forskolin stimulated cyclic-AMP in RGT cells expressing human Metabotropic glutamate receptor 3Effect on 1S,3R-ACPD-induced inhibition of forskolin stimulated cyclic-AMP in RGT cells expressing human Metabotropic glutamate receptor 3
ChEMBL 353 5 3 4 2.8 OC(=O)[C@H]1C[C@@H]1[C@](C(=O)O)(CC1c2ccccc2Oc2c1cccc2)N 10.1021/jm970498o
9819927 2417 None 39 Human Functional pIC50 = 8 8.0 2 14
Effect on 1S,3R-ACPD-induced inhibition of forskolin stimulated cyclic-AMP in RGT cells expressing human Metabotropic glutamate receptor 3Effect on 1S,3R-ACPD-induced inhibition of forskolin stimulated cyclic-AMP in RGT cells expressing human Metabotropic glutamate receptor 3
ChEMBL 353 5 3 4 2.8 OC(=O)[C@H]1C[C@@H]1[C@](C(=O)O)(CC1c2ccccc2Oc2c1cccc2)N 10.1021/jm970498o
CHEMBL432038 2417 None 39 Human Functional pIC50 = 8 8.0 2 14
Effect on 1S,3R-ACPD-induced inhibition of forskolin stimulated cyclic-AMP in RGT cells expressing human Metabotropic glutamate receptor 3Effect on 1S,3R-ACPD-induced inhibition of forskolin stimulated cyclic-AMP in RGT cells expressing human Metabotropic glutamate receptor 3
ChEMBL 353 5 3 4 2.8 OC(=O)[C@H]1C[C@@H]1[C@](C(=O)O)(CC1c2ccccc2Oc2c1cccc2)N 10.1021/jm970498o
44329032 112607 None 0 Rat Functional pIC50 = 7 7.0 3 5
Antagonistic activity against metabotropic glutamate receptor 3 (mGluR3) was evaluatedAntagonistic activity against metabotropic glutamate receptor 3 (mGluR3) was evaluated
ChEMBL 423 9 3 4 4.6 CCCCC[C@@H]1[C@H](C(=O)O)[C@H]1C(N)(CC1c2ccccc2Oc2ccccc21)C(=O)O 10.1016/s0960-894x(98)00510-1
CHEMBL329920 112607 None 0 Rat Functional pIC50 = 7 7.0 3 5
Antagonistic activity against metabotropic glutamate receptor 3 (mGluR3) was evaluatedAntagonistic activity against metabotropic glutamate receptor 3 (mGluR3) was evaluated
ChEMBL 423 9 3 4 4.6 CCCCC[C@@H]1[C@H](C(=O)O)[C@H]1C(N)(CC1c2ccccc2Oc2ccccc21)C(=O)O 10.1016/s0960-894x(98)00510-1
44328850 210510 None 0 Rat Functional pIC50 = 6 6.0 1 4
Antagonistic activity against metabotropic glutamate receptor 3 (mGluR3) was evaluatedAntagonistic activity against metabotropic glutamate receptor 3 (mGluR3) was evaluated
ChEMBL 367 5 3 4 3.1 C[C@@H]1[C@H](C(=O)O)[C@H]1C(N)(CC1c2ccccc2Oc2ccccc21)C(=O)O 10.1016/s0960-894x(98)00510-1
CHEMBL97574 210510 None 0 Rat Functional pIC50 = 6 6.0 1 4
Antagonistic activity against metabotropic glutamate receptor 3 (mGluR3) was evaluatedAntagonistic activity against metabotropic glutamate receptor 3 (mGluR3) was evaluated
ChEMBL 367 5 3 4 3.1 C[C@@H]1[C@H](C(=O)O)[C@H]1C(N)(CC1c2ccccc2Oc2ccccc21)C(=O)O 10.1016/s0960-894x(98)00510-1
122456191 163041 None 0 Rat Functional pIC50 = 6.0 6.0 -2 2
Negative allosteric modulation of rat mGlu3 receptor expressed in TREX cells coexpressing Galpha15 assessed as inhibition of glutamate induced-calcium mobilization preincubated for 2.3 mins followed by glutamate addition measured for 2.6 mins by Fluo-4 AM dye based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor expressed in TREX cells coexpressing Galpha15 assessed as inhibition of glutamate induced-calcium mobilization preincubated for 2.3 mins followed by glutamate addition measured for 2.6 mins by Fluo-4 AM dye based fluorescence assay
ChEMBL 344 6 0 5 3.0 O=c1nc(OCCOc2ccccc2)ccn1-c1ccc(F)c(F)c1 10.1021/acsmedchemlett.7b00249
CHEMBL4174544 163041 None 0 Rat Functional pIC50 = 6.0 6.0 -2 2
Negative allosteric modulation of rat mGlu3 receptor expressed in TREX cells coexpressing Galpha15 assessed as inhibition of glutamate induced-calcium mobilization preincubated for 2.3 mins followed by glutamate addition measured for 2.6 mins by Fluo-4 AM dye based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor expressed in TREX cells coexpressing Galpha15 assessed as inhibition of glutamate induced-calcium mobilization preincubated for 2.3 mins followed by glutamate addition measured for 2.6 mins by Fluo-4 AM dye based fluorescence assay
ChEMBL 344 6 0 5 3.0 O=c1nc(OCCOc2ccccc2)ccn1-c1ccc(F)c(F)c1 10.1021/acsmedchemlett.7b00249
122456191 163041 None 0 Rat Functional pIC50 = 6.0 6.0 -2 2
Negative allosteric modulation of rat mGlu3 receptor expressed in TREX cells coexpressing Galpha15 assessed as inhibition of glutamate induced-calcium mobilization preincubated for 2.3 mins followed by glutamate addition measured for 2.6 mins by Fluo-4 AM dye based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor expressed in TREX cells coexpressing Galpha15 assessed as inhibition of glutamate induced-calcium mobilization preincubated for 2.3 mins followed by glutamate addition measured for 2.6 mins by Fluo-4 AM dye based fluorescence assay
ChEMBL 344 6 0 5 3.0 O=c1nc(OCCOc2ccccc2)ccn1-c1ccc(F)c(F)c1 10.1021/acsmedchemlett.7b00249
CHEMBL4174544 163041 None 0 Rat Functional pIC50 = 6.0 6.0 -2 2
Negative allosteric modulation of rat mGlu3 receptor expressed in TREX cells coexpressing Galpha15 assessed as inhibition of glutamate induced-calcium mobilization preincubated for 2.3 mins followed by glutamate addition measured for 2.6 mins by Fluo-4 AM dye based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor expressed in TREX cells coexpressing Galpha15 assessed as inhibition of glutamate induced-calcium mobilization preincubated for 2.3 mins followed by glutamate addition measured for 2.6 mins by Fluo-4 AM dye based fluorescence assay
ChEMBL 344 6 0 5 3.0 O=c1nc(OCCOc2ccccc2)ccn1-c1ccc(F)c(F)c1 10.1021/acsmedchemlett.7b00249
60210837 90361 None 0 Rat Functional pIC50 = 5.0 5.0 - 1
Negative allosteric modulation of rat mGlu3 receptor transfected in human TREX cells assessed as inhibition of glutamate-induced calcium mobilization after 2.5 minsNegative allosteric modulation of rat mGlu3 receptor transfected in human TREX cells assessed as inhibition of glutamate-induced calcium mobilization after 2.5 mins
ChEMBL 321 2 1 3 2.3 COc1ccc(C#Cc2ccc(C(=O)N3CC[C@@H](O)C3)cc2)cc1 10.1021/jm400439t
CHEMBL2385881 90361 None 0 Rat Functional pIC50 = 5.0 5.0 - 1
Negative allosteric modulation of rat mGlu3 receptor transfected in human TREX cells assessed as inhibition of glutamate-induced calcium mobilization after 2.5 minsNegative allosteric modulation of rat mGlu3 receptor transfected in human TREX cells assessed as inhibition of glutamate-induced calcium mobilization after 2.5 mins
ChEMBL 321 2 1 3 2.3 COc1ccc(C#Cc2ccc(C(=O)N3CC[C@@H](O)C3)cc2)cc1 10.1021/jm400439t
122190324 123520 None 0 Rat Functional pIC50 = 6.0 6.0 1 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 381 5 0 5 3.8 COc1ccc(OCc2cc3n(n2)[C@H](C)CN(c2ccc(F)cc2)C3=O)cc1 10.1021/acs.jmedchem.5b01005
CHEMBL3617508 123520 None 0 Rat Functional pIC50 = 6.0 6.0 1 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 381 5 0 5 3.8 COc1ccc(OCc2cc3n(n2)[C@H](C)CN(c2ccc(F)cc2)C3=O)cc1 10.1021/acs.jmedchem.5b01005
122190324 123520 None 0 Rat Functional pIC50 = 6.0 6.0 1 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 381 5 0 5 3.8 COc1ccc(OCc2cc3n(n2)[C@H](C)CN(c2ccc(F)cc2)C3=O)cc1 10.1021/acs.jmedchem.5b01005
CHEMBL3617508 123520 None 0 Rat Functional pIC50 = 6.0 6.0 1 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 381 5 0 5 3.8 COc1ccc(OCc2cc3n(n2)[C@H](C)CN(c2ccc(F)cc2)C3=O)cc1 10.1021/acs.jmedchem.5b01005
11310142 2422 None 14 Human Functional pIC50 = 6.0 6.0 -13 3
Evaluation of the functional effect on cAMP responses in RGT cells expressing human mGlu3 receptorEvaluation of the functional effect on cAMP responses in RGT cells expressing human mGlu3 receptor
ChEMBL 199 2 3 3 -0.2 C[C@@H]1C[C@@]([C@H]2[C@@H]1[C@@H]2C(=O)O)(N)C(=O)O 10.1021/jm040222y
11614 2422 None 14 Human Functional pIC50 = 6.0 6.0 -13 3
Evaluation of the functional effect on cAMP responses in RGT cells expressing human mGlu3 receptorEvaluation of the functional effect on cAMP responses in RGT cells expressing human mGlu3 receptor
ChEMBL 199 2 3 3 -0.2 C[C@@H]1C[C@@]([C@H]2[C@@H]1[C@@H]2C(=O)O)(N)C(=O)O 10.1021/jm040222y
CHEMBL192051 2422 None 14 Human Functional pIC50 = 6.0 6.0 -13 3
Evaluation of the functional effect on cAMP responses in RGT cells expressing human mGlu3 receptorEvaluation of the functional effect on cAMP responses in RGT cells expressing human mGlu3 receptor
ChEMBL 199 2 3 3 -0.2 C[C@@H]1C[C@@]([C@H]2[C@@H]1[C@@H]2C(=O)O)(N)C(=O)O 10.1021/jm040222y
10979251 90094 None 0 Human Functional pIC50 = 6.0 6.0 -1 3
Antagonist activity at human recombinant mGlu3 receptor expressed in AV12 cells assessed as reversal of DCG-4-inhibited, forskolin-stimulated cAMP production after 1 hr by fluorescence assayAntagonist activity at human recombinant mGlu3 receptor expressed in AV12 cells assessed as reversal of DCG-4-inhibited, forskolin-stimulated cAMP production after 1 hr by fluorescence assay
ChEMBL 293 4 3 4 1.3 N[C@@]1(C(=O)O)C[C@@H](Sc2ccccc2)[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/acs.jmedchem.5b01124
CHEMBL2381650 90094 None 0 Human Functional pIC50 = 6.0 6.0 -1 3
Antagonist activity at human recombinant mGlu3 receptor expressed in AV12 cells assessed as reversal of DCG-4-inhibited, forskolin-stimulated cAMP production after 1 hr by fluorescence assayAntagonist activity at human recombinant mGlu3 receptor expressed in AV12 cells assessed as reversal of DCG-4-inhibited, forskolin-stimulated cAMP production after 1 hr by fluorescence assay
ChEMBL 293 4 3 4 1.3 N[C@@]1(C(=O)O)C[C@@H](Sc2ccccc2)[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/acs.jmedchem.5b01124
134138062 147588 None 0 Human Functional pIC50 = 6.0 6.0 1 2
Antagonist activity at recombinant human mGlu3 receptor expressed in hamster AV12 cells co-expressing human EAAT1 assessed as reduction of DCG-4-inhibited forskolin-stimulated cAMP formation after 20 mins by HTRF assayAntagonist activity at recombinant human mGlu3 receptor expressed in hamster AV12 cells co-expressing human EAAT1 assessed as reduction of DCG-4-inhibited forskolin-stimulated cAMP formation after 20 mins by HTRF assay
ChEMBL 374 5 4 5 0.9 N[C@H]1[C@H]2[C@H](C(=O)O)[C@H]2[C@](N)(C(=O)O)[C@@H]1OCc1ccc(Cl)c(Cl)c1 10.1016/j.bmcl.2016.10.067
CHEMBL3930511 147588 None 0 Human Functional pIC50 = 6.0 6.0 1 2
Antagonist activity at recombinant human mGlu3 receptor expressed in hamster AV12 cells co-expressing human EAAT1 assessed as reduction of DCG-4-inhibited forskolin-stimulated cAMP formation after 20 mins by HTRF assayAntagonist activity at recombinant human mGlu3 receptor expressed in hamster AV12 cells co-expressing human EAAT1 assessed as reduction of DCG-4-inhibited forskolin-stimulated cAMP formation after 20 mins by HTRF assay
ChEMBL 374 5 4 5 0.9 N[C@H]1[C@H]2[C@H](C(=O)O)[C@H]2[C@](N)(C(=O)O)[C@@H]1OCc1ccc(Cl)c(Cl)c1 10.1016/j.bmcl.2016.10.067
122190330 123526 None 0 Rat Functional pIC50 = 6.0 6.0 3 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 370 4 0 5 3.4 C[C@@H]1CN(c2ccc(F)cc2)C(=O)c2cc(COc3ncccc3F)nn21 10.1021/acs.jmedchem.5b01005
CHEMBL3617514 123526 None 0 Rat Functional pIC50 = 6.0 6.0 3 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 370 4 0 5 3.4 C[C@@H]1CN(c2ccc(F)cc2)C(=O)c2cc(COc3ncccc3F)nn21 10.1021/acs.jmedchem.5b01005
60204019 90363 None 0 Rat Functional pIC50 = 6.0 6.0 - 1
Negative allosteric modulation of rat mGlu3 receptor transfected in human TREX cells assessed as inhibition of glutamate-induced calcium mobilization after 2.5 minsNegative allosteric modulation of rat mGlu3 receptor transfected in human TREX cells assessed as inhibition of glutamate-induced calcium mobilization after 2.5 mins
ChEMBL 349 2 1 3 3.1 COc1ccc(C#Cc2ccc(C(=O)N3CCCC(C)(O)C3)cc2)cc1 10.1021/jm400439t
CHEMBL2385883 90363 None 0 Rat Functional pIC50 = 6.0 6.0 - 1
Negative allosteric modulation of rat mGlu3 receptor transfected in human TREX cells assessed as inhibition of glutamate-induced calcium mobilization after 2.5 minsNegative allosteric modulation of rat mGlu3 receptor transfected in human TREX cells assessed as inhibition of glutamate-induced calcium mobilization after 2.5 mins
ChEMBL 349 2 1 3 3.1 COc1ccc(C#Cc2ccc(C(=O)N3CCCC(C)(O)C3)cc2)cc1 10.1021/jm400439t
21309795 150912 None 0 Human Functional pIC50 = 7.0 7.0 3 2
Antagonist activity at human recombinant mGlu3 receptor stably expressed in golden hamster AV12 cells co-expressing rat EAAT1 assessed as reduction in DCG IV-induced inhibition of forskolin-stimulated cAMP accumulation preincubated for 20 mins followed by incubation with cAMP-d2 conjugate and anti-cAMP cryptate for 1 hr by HTRF assayAntagonist activity at human recombinant mGlu3 receptor stably expressed in golden hamster AV12 cells co-expressing rat EAAT1 assessed as reduction in DCG IV-induced inhibition of forskolin-stimulated cAMP accumulation preincubated for 20 mins followed by incubation with cAMP-d2 conjugate and anti-cAMP cryptate for 1 hr by HTRF assay
ChEMBL 327 4 3 3 1.8 N[C@@]1(C(=O)O)[C@H](Cc2ccc(F)c(Cl)c2)C[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/acs.jmedchem.6b01119
CHEMBL3956934 150912 None 0 Human Functional pIC50 = 7.0 7.0 3 2
Antagonist activity at human recombinant mGlu3 receptor stably expressed in golden hamster AV12 cells co-expressing rat EAAT1 assessed as reduction in DCG IV-induced inhibition of forskolin-stimulated cAMP accumulation preincubated for 20 mins followed by incubation with cAMP-d2 conjugate and anti-cAMP cryptate for 1 hr by HTRF assayAntagonist activity at human recombinant mGlu3 receptor stably expressed in golden hamster AV12 cells co-expressing rat EAAT1 assessed as reduction in DCG IV-induced inhibition of forskolin-stimulated cAMP accumulation preincubated for 20 mins followed by incubation with cAMP-d2 conjugate and anti-cAMP cryptate for 1 hr by HTRF assay
ChEMBL 327 4 3 3 1.8 N[C@@]1(C(=O)O)[C@H](Cc2ccc(F)c(Cl)c2)C[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/acs.jmedchem.6b01119
122190330 123526 None 0 Rat Functional pIC50 = 6.0 6.0 3 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 370 4 0 5 3.4 C[C@@H]1CN(c2ccc(F)cc2)C(=O)c2cc(COc3ncccc3F)nn21 10.1021/acs.jmedchem.5b01005
CHEMBL3617514 123526 None 0 Rat Functional pIC50 = 6.0 6.0 3 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 370 4 0 5 3.4 C[C@@H]1CN(c2ccc(F)cc2)C(=O)c2cc(COc3ncccc3F)nn21 10.1021/acs.jmedchem.5b01005
60210864 90357 None 0 Rat Functional pIC50 = 6.0 6.0 - 1
Negative allosteric modulation of rat mGlu3 receptor transfected in human TREX cells assessed as inhibition of glutamate-induced calcium mobilization after 2.5 minsNegative allosteric modulation of rat mGlu3 receptor transfected in human TREX cells assessed as inhibition of glutamate-induced calcium mobilization after 2.5 mins
ChEMBL 335 2 1 3 2.7 COc1ccc(C#Cc2ccc(C(=O)N3CCC[C@H](O)C3)cc2)cc1 10.1021/jm400439t
CHEMBL2385877 90357 None 0 Rat Functional pIC50 = 6.0 6.0 - 1
Negative allosteric modulation of rat mGlu3 receptor transfected in human TREX cells assessed as inhibition of glutamate-induced calcium mobilization after 2.5 minsNegative allosteric modulation of rat mGlu3 receptor transfected in human TREX cells assessed as inhibition of glutamate-induced calcium mobilization after 2.5 mins
ChEMBL 335 2 1 3 2.7 COc1ccc(C#Cc2ccc(C(=O)N3CCC[C@H](O)C3)cc2)cc1 10.1021/jm400439t
122190328 123524 None 0 Rat Functional pIC50 = 5.9 5.9 - 1
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 395 6 0 5 4.2 CCOc1ccc(OCc2cc3n(n2)[C@H](C)CN(c2ccc(F)cc2)C3=O)cc1 10.1021/acs.jmedchem.5b01005
CHEMBL3617512 123524 None 0 Rat Functional pIC50 = 5.9 5.9 - 1
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 395 6 0 5 4.2 CCOc1ccc(OCc2cc3n(n2)[C@H](C)CN(c2ccc(F)cc2)C3=O)cc1 10.1021/acs.jmedchem.5b01005
122190328 123524 None 0 Rat Functional pIC50 = 5.9 5.9 - 1
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 395 6 0 5 4.2 CCOc1ccc(OCc2cc3n(n2)[C@H](C)CN(c2ccc(F)cc2)C3=O)cc1 10.1021/acs.jmedchem.5b01005
CHEMBL3617512 123524 None 0 Rat Functional pIC50 = 5.9 5.9 - 1
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 395 6 0 5 4.2 CCOc1ccc(OCc2cc3n(n2)[C@H](C)CN(c2ccc(F)cc2)C3=O)cc1 10.1021/acs.jmedchem.5b01005
122190321 123517 None 0 Rat Functional pIC50 = 5.9 5.9 -1 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 385 4 0 4 4.5 C[C@@H]1CN(c2ccc(F)cc2)C(=O)c2cc(COc3ccc(Cl)cc3)nn21 10.1021/acs.jmedchem.5b01005
CHEMBL3617505 123517 None 0 Rat Functional pIC50 = 5.9 5.9 -1 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 385 4 0 4 4.5 C[C@@H]1CN(c2ccc(F)cc2)C(=O)c2cc(COc3ccc(Cl)cc3)nn21 10.1021/acs.jmedchem.5b01005
122190321 123517 None 0 Rat Functional pIC50 = 5.9 5.9 -1 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 385 4 0 4 4.5 C[C@@H]1CN(c2ccc(F)cc2)C(=O)c2cc(COc3ccc(Cl)cc3)nn21 10.1021/acs.jmedchem.5b01005
CHEMBL3617505 123517 None 0 Rat Functional pIC50 = 5.9 5.9 -1 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 385 4 0 4 4.5 C[C@@H]1CN(c2ccc(F)cc2)C(=O)c2cc(COc3ccc(Cl)cc3)nn21 10.1021/acs.jmedchem.5b01005
90643961 112057 None 0 Rat Functional pIC50 = 5.9 5.9 2 2
Inhibition of rat mGlu3 receptor transfected in HEK293 cells coexpressing mouse Galpha15 assessed as decrease in glutamate-induced calcium signaling by fluorescence plate reader analysis in presence of glutamate at EC87 concentrationInhibition of rat mGlu3 receptor transfected in HEK293 cells coexpressing mouse Galpha15 assessed as decrease in glutamate-induced calcium signaling by fluorescence plate reader analysis in presence of glutamate at EC87 concentration
ChEMBL 382 3 0 6 3.9 COc1cccc(-c2cc3n(C)c(=O)c4ccc(-c5cccnc5)cc4n3n2)c1 10.1016/j.bmcl.2014.04.051
CHEMBL3288649 112057 None 0 Rat Functional pIC50 = 5.9 5.9 2 2
Inhibition of rat mGlu3 receptor transfected in HEK293 cells coexpressing mouse Galpha15 assessed as decrease in glutamate-induced calcium signaling by fluorescence plate reader analysis in presence of glutamate at EC87 concentrationInhibition of rat mGlu3 receptor transfected in HEK293 cells coexpressing mouse Galpha15 assessed as decrease in glutamate-induced calcium signaling by fluorescence plate reader analysis in presence of glutamate at EC87 concentration
ChEMBL 382 3 0 6 3.9 COc1cccc(-c2cc3n(C)c(=O)c4ccc(-c5cccnc5)cc4n3n2)c1 10.1016/j.bmcl.2014.04.051
122190318 123514 None 0 Rat Functional pIC50 = 5.9 5.9 -1 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 365 4 0 4 4.1 Cc1ccc(OCc2cc3n(n2)[C@H](C)CN(c2ccc(F)cc2)C3=O)cc1 10.1021/acs.jmedchem.5b01005
CHEMBL3617502 123514 None 0 Rat Functional pIC50 = 5.9 5.9 -1 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 365 4 0 4 4.1 Cc1ccc(OCc2cc3n(n2)[C@H](C)CN(c2ccc(F)cc2)C3=O)cc1 10.1021/acs.jmedchem.5b01005
69669820 183746 None 0 Human Functional pIC50 = 7.9 7.9 2 2
Antagonist activity at human recombinant mGlu3 receptor stably expressed in golden hamster AV12 cells co-expressing rat EAAT1 assessed as reduction in DCG IV-induced inhibition of forskolin-stimulated cAMP accumulation preincubated for 20 mins followed by incubation with cAMP-d2 conjugate and anti-cAMP cryptate for 1 hr by HTRF assayAntagonist activity at human recombinant mGlu3 receptor stably expressed in golden hamster AV12 cells co-expressing rat EAAT1 assessed as reduction in DCG IV-induced inhibition of forskolin-stimulated cAMP accumulation preincubated for 20 mins followed by incubation with cAMP-d2 conjugate and anti-cAMP cryptate for 1 hr by HTRF assay
ChEMBL 396 6 4 5 1.1 CC(=O)N[C@H]1[C@H]2[C@H](C(=O)O)[C@H]2[C@](N)(C(=O)O)[C@@H]1CSc1ccc(F)c(C)c1 10.1021/acs.jmedchem.6b01119
CHEMBL4746125 183746 None 0 Human Functional pIC50 = 7.9 7.9 2 2
Antagonist activity at human recombinant mGlu3 receptor stably expressed in golden hamster AV12 cells co-expressing rat EAAT1 assessed as reduction in DCG IV-induced inhibition of forskolin-stimulated cAMP accumulation preincubated for 20 mins followed by incubation with cAMP-d2 conjugate and anti-cAMP cryptate for 1 hr by HTRF assayAntagonist activity at human recombinant mGlu3 receptor stably expressed in golden hamster AV12 cells co-expressing rat EAAT1 assessed as reduction in DCG IV-induced inhibition of forskolin-stimulated cAMP accumulation preincubated for 20 mins followed by incubation with cAMP-d2 conjugate and anti-cAMP cryptate for 1 hr by HTRF assay
ChEMBL 396 6 4 5 1.1 CC(=O)N[C@H]1[C@H]2[C@H](C(=O)O)[C@H]2[C@](N)(C(=O)O)[C@@H]1CSc1ccc(F)c(C)c1 10.1021/acs.jmedchem.6b01119
CHEMBL4802570 183746 None 0 Human Functional pIC50 = 7.9 7.9 2 2
Antagonist activity at human recombinant mGlu3 receptor stably expressed in golden hamster AV12 cells co-expressing rat EAAT1 assessed as reduction in DCG IV-induced inhibition of forskolin-stimulated cAMP accumulation preincubated for 20 mins followed by incubation with cAMP-d2 conjugate and anti-cAMP cryptate for 1 hr by HTRF assayAntagonist activity at human recombinant mGlu3 receptor stably expressed in golden hamster AV12 cells co-expressing rat EAAT1 assessed as reduction in DCG IV-induced inhibition of forskolin-stimulated cAMP accumulation preincubated for 20 mins followed by incubation with cAMP-d2 conjugate and anti-cAMP cryptate for 1 hr by HTRF assay
ChEMBL 396 6 4 5 1.1 CC(=O)N[C@H]1[C@H]2[C@H](C(=O)O)[C@H]2[C@](N)(C(=O)O)[C@@H]1CSc1ccc(F)c(C)c1 10.1021/acs.jmedchem.6b01119
10710505 78769 None 0 Human Functional pIC50 = 5.9 5.9 1 2
Ability to block 1S,3R-ACPD-induced inhibition of forskolin stimulated cyclic-AMP in non-neuronal cell line expressing human Metabotropic glutamate receptor 3Ability to block 1S,3R-ACPD-induced inhibition of forskolin stimulated cyclic-AMP in non-neuronal cell line expressing human Metabotropic glutamate receptor 3
ChEMBL 316 6 3 4 1.6 Cn1cc(CCC(N)(C(=O)O)[C@H]2C[C@@H]2C(=O)O)c2ccccc21 10.1021/jm970497w
CHEMBL2112580 78769 None 0 Human Functional pIC50 = 5.9 5.9 1 2
Ability to block 1S,3R-ACPD-induced inhibition of forskolin stimulated cyclic-AMP in non-neuronal cell line expressing human Metabotropic glutamate receptor 3Ability to block 1S,3R-ACPD-induced inhibition of forskolin stimulated cyclic-AMP in non-neuronal cell line expressing human Metabotropic glutamate receptor 3
ChEMBL 316 6 3 4 1.6 Cn1cc(CCC(N)(C(=O)O)[C@H]2C[C@@H]2C(=O)O)c2ccccc21 10.1021/jm970497w
122190318 123514 None 0 Rat Functional pIC50 = 5.9 5.9 -1 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 365 4 0 4 4.1 Cc1ccc(OCc2cc3n(n2)[C@H](C)CN(c2ccc(F)cc2)C3=O)cc1 10.1021/acs.jmedchem.5b01005
CHEMBL3617502 123514 None 0 Rat Functional pIC50 = 5.9 5.9 -1 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 365 4 0 4 4.1 Cc1ccc(OCc2cc3n(n2)[C@H](C)CN(c2ccc(F)cc2)C3=O)cc1 10.1021/acs.jmedchem.5b01005
22448579 155868 None 0 Rat Functional pIC50 = 6.9 6.9 -4 2
Antagonist activity at rat mGluR3 expressed in CHO cells assessed as inhibition of glutamate-induced GIRK currentAntagonist activity at rat mGluR3 expressed in CHO cells assessed as inhibition of glutamate-induced GIRK current
ChEMBL 412 3 2 5 4.8 O=C1CC(c2cccc(-n3ccnc3)c2)=Nc2cc(O)c(-c3ccccc3F)cc2N1 10.1016/j.bmcl.2008.02.076
CHEMBL405895 155868 None 0 Rat Functional pIC50 = 6.9 6.9 -4 2
Antagonist activity at rat mGluR3 expressed in CHO cells assessed as inhibition of glutamate-induced GIRK currentAntagonist activity at rat mGluR3 expressed in CHO cells assessed as inhibition of glutamate-induced GIRK current
ChEMBL 412 3 2 5 4.8 O=C1CC(c2cccc(-n3ccnc3)c2)=Nc2cc(O)c(-c3ccccc3F)cc2N1 10.1016/j.bmcl.2008.02.076
44329031 108330 None 0 Rat Functional pIC50 = 6.9 6.9 6 7
Antagonistic activity against metabotropic glutamate receptor 3 (mGluR3) was evaluatedAntagonistic activity against metabotropic glutamate receptor 3 (mGluR3) was evaluated
ChEMBL 437 10 3 4 5.0 CCCCCC[C@@H]1[C@H](C(=O)O)[C@H]1C(N)(CC1c2ccccc2Oc2ccccc21)C(=O)O 10.1016/s0960-894x(98)00510-1
CHEMBL319732 108330 None 0 Rat Functional pIC50 = 6.9 6.9 6 7
Antagonistic activity against metabotropic glutamate receptor 3 (mGluR3) was evaluatedAntagonistic activity against metabotropic glutamate receptor 3 (mGluR3) was evaluated
ChEMBL 437 10 3 4 5.0 CCCCCC[C@@H]1[C@H](C(=O)O)[C@H]1C(N)(CC1c2ccccc2Oc2ccccc21)C(=O)O 10.1016/s0960-894x(98)00510-1
122190401 123577 None 0 Rat Functional pIC50 = 6.9 6.9 - 1
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 388 4 0 5 3.5 C[C@@H]1CN(c2cc(F)ccc2F)C(=O)c2cc(COc3ccc(F)cn3)nn21 10.1021/acs.jmedchem.5b01005
CHEMBL3617624 123577 None 0 Rat Functional pIC50 = 6.9 6.9 - 1
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 388 4 0 5 3.5 C[C@@H]1CN(c2cc(F)ccc2F)C(=O)c2cc(COc3ccc(F)cn3)nn21 10.1021/acs.jmedchem.5b01005
122190401 123577 None 0 Rat Functional pIC50 = 6.9 6.9 - 1
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 388 4 0 5 3.5 C[C@@H]1CN(c2cc(F)ccc2F)C(=O)c2cc(COc3ccc(F)cn3)nn21 10.1021/acs.jmedchem.5b01005
CHEMBL3617624 123577 None 0 Rat Functional pIC50 = 6.9 6.9 - 1
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 388 4 0 5 3.5 C[C@@H]1CN(c2cc(F)ccc2F)C(=O)c2cc(COc3ccc(F)cn3)nn21 10.1021/acs.jmedchem.5b01005
122190411 123587 None 0 Rat Functional pIC50 = 5.9 5.9 2 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 402 4 0 5 4.4 C[C@@H]1CN(c2ccc(Cl)cc2)C(=O)c2cc(COc3ccc(Cl)cn3)nn21 10.1021/acs.jmedchem.5b01005
CHEMBL3617634 123587 None 0 Rat Functional pIC50 = 5.9 5.9 2 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 402 4 0 5 4.4 C[C@@H]1CN(c2ccc(Cl)cc2)C(=O)c2cc(COc3ccc(Cl)cn3)nn21 10.1021/acs.jmedchem.5b01005
122456006 162388 None 0 Rat Functional pIC50 = 5.9 5.9 - 1
Negative allosteric modulation of rat mGlu3 receptor expressed in TREX cells coexpressing Galpha15 assessed as inhibition of glutamate induced-calcium mobilization preincubated for 2.3 mins followed by glutamate addition measured for 2.6 mins by Fluo-4 AM dye based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor expressed in TREX cells coexpressing Galpha15 assessed as inhibition of glutamate induced-calcium mobilization preincubated for 2.3 mins followed by glutamate addition measured for 2.6 mins by Fluo-4 AM dye based fluorescence assay
ChEMBL 339 6 0 4 3.8 CC(COc1ccn(-c2ccc(F)cc2)c(=O)c1)Oc1ccccc1 10.1021/acsmedchemlett.7b00249
CHEMBL4164219 162388 None 0 Rat Functional pIC50 = 5.9 5.9 - 1
Negative allosteric modulation of rat mGlu3 receptor expressed in TREX cells coexpressing Galpha15 assessed as inhibition of glutamate induced-calcium mobilization preincubated for 2.3 mins followed by glutamate addition measured for 2.6 mins by Fluo-4 AM dye based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor expressed in TREX cells coexpressing Galpha15 assessed as inhibition of glutamate induced-calcium mobilization preincubated for 2.3 mins followed by glutamate addition measured for 2.6 mins by Fluo-4 AM dye based fluorescence assay
ChEMBL 339 6 0 4 3.8 CC(COc1ccn(-c2ccc(F)cc2)c(=O)c1)Oc1ccccc1 10.1021/acsmedchemlett.7b00249
122190411 123587 None 0 Rat Functional pIC50 = 5.9 5.9 2 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 402 4 0 5 4.4 C[C@@H]1CN(c2ccc(Cl)cc2)C(=O)c2cc(COc3ccc(Cl)cn3)nn21 10.1021/acs.jmedchem.5b01005
CHEMBL3617634 123587 None 0 Rat Functional pIC50 = 5.9 5.9 2 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 402 4 0 5 4.4 C[C@@H]1CN(c2ccc(Cl)cc2)C(=O)c2cc(COc3ccc(Cl)cn3)nn21 10.1021/acs.jmedchem.5b01005
122456006 162388 None 0 Rat Functional pIC50 = 5.9 5.9 - 1
Negative allosteric modulation of rat mGlu3 receptor expressed in TREX cells coexpressing Galpha15 assessed as inhibition of glutamate induced-calcium mobilization preincubated for 2.3 mins followed by glutamate addition measured for 2.6 mins by Fluo-4 AM dye based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor expressed in TREX cells coexpressing Galpha15 assessed as inhibition of glutamate induced-calcium mobilization preincubated for 2.3 mins followed by glutamate addition measured for 2.6 mins by Fluo-4 AM dye based fluorescence assay
ChEMBL 339 6 0 4 3.8 CC(COc1ccn(-c2ccc(F)cc2)c(=O)c1)Oc1ccccc1 10.1021/acsmedchemlett.7b00249
CHEMBL4164219 162388 None 0 Rat Functional pIC50 = 5.9 5.9 - 1
Negative allosteric modulation of rat mGlu3 receptor expressed in TREX cells coexpressing Galpha15 assessed as inhibition of glutamate induced-calcium mobilization preincubated for 2.3 mins followed by glutamate addition measured for 2.6 mins by Fluo-4 AM dye based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor expressed in TREX cells coexpressing Galpha15 assessed as inhibition of glutamate induced-calcium mobilization preincubated for 2.3 mins followed by glutamate addition measured for 2.6 mins by Fluo-4 AM dye based fluorescence assay
ChEMBL 339 6 0 4 3.8 CC(COc1ccn(-c2ccc(F)cc2)c(=O)c1)Oc1ccccc1 10.1021/acsmedchemlett.7b00249
10456810 107935 None 0 Rat Functional pIC50 = 6.9 6.9 7 5
Antagonistic activity against metabotropic glutamate receptor 3 (mGluR3) was evaluatedAntagonistic activity against metabotropic glutamate receptor 3 (mGluR3) was evaluated
ChEMBL 457 8 3 4 4.7 NC(CC1c2ccccc2Oc2ccccc21)(C(=O)O)[C@H]1[C@H](CCc2ccccc2)[C@@H]1C(=O)O 10.1016/s0960-894x(98)00510-1
CHEMBL319279 107935 None 0 Rat Functional pIC50 = 6.9 6.9 7 5
Antagonistic activity against metabotropic glutamate receptor 3 (mGluR3) was evaluatedAntagonistic activity against metabotropic glutamate receptor 3 (mGluR3) was evaluated
ChEMBL 457 8 3 4 4.7 NC(CC1c2ccccc2Oc2ccccc21)(C(=O)O)[C@H]1[C@H](CCc2ccccc2)[C@@H]1C(=O)O 10.1016/s0960-894x(98)00510-1
90643970 112063 None 0 Rat Functional pIC50 = 5.9 5.9 -1 2
Inhibition of rat mGlu3 receptor transfected in HEK293 cells coexpressing mouse Galpha15 assessed as decrease in glutamate-induced calcium signaling by fluorescence plate reader analysis in presence of glutamate at EC87 concentrationInhibition of rat mGlu3 receptor transfected in HEK293 cells coexpressing mouse Galpha15 assessed as decrease in glutamate-induced calcium signaling by fluorescence plate reader analysis in presence of glutamate at EC87 concentration
ChEMBL 464 3 1 6 3.8 Cn1c(=O)c2ccc(-c3cccc(S(N)(=O)=O)c3)cc2n2nc(-c3ccc(Cl)cc3)cc12 10.1016/j.bmcl.2014.04.051
CHEMBL3288664 112063 None 0 Rat Functional pIC50 = 5.9 5.9 -1 2
Inhibition of rat mGlu3 receptor transfected in HEK293 cells coexpressing mouse Galpha15 assessed as decrease in glutamate-induced calcium signaling by fluorescence plate reader analysis in presence of glutamate at EC87 concentrationInhibition of rat mGlu3 receptor transfected in HEK293 cells coexpressing mouse Galpha15 assessed as decrease in glutamate-induced calcium signaling by fluorescence plate reader analysis in presence of glutamate at EC87 concentration
ChEMBL 464 3 1 6 3.8 Cn1c(=O)c2ccc(-c3cccc(S(N)(=O)=O)c3)cc2n2nc(-c3ccc(Cl)cc3)cc12 10.1016/j.bmcl.2014.04.051
134129940 142533 None 0 Human Functional pIC50 = 6.9 6.9 1 2
Antagonist activity at recombinant human mGlu3 receptor expressed in hamster AV12 cells co-expressing human EAAT1 assessed as reduction of DCG-4-inhibited forskolin-stimulated cAMP formation after 20 mins by HTRF assayAntagonist activity at recombinant human mGlu3 receptor expressed in hamster AV12 cells co-expressing human EAAT1 assessed as reduction of DCG-4-inhibited forskolin-stimulated cAMP formation after 20 mins by HTRF assay
ChEMBL 359 5 4 5 0.5 N[C@@]1(C(=O)O)[C@H](OCc2ccc(Cl)c(F)c2)[C@H](O)[C@@H]2[C@H]1[C@H]2C(=O)O 10.1016/j.bmcl.2016.10.067
CHEMBL3890112 142533 None 0 Human Functional pIC50 = 6.9 6.9 1 2
Antagonist activity at recombinant human mGlu3 receptor expressed in hamster AV12 cells co-expressing human EAAT1 assessed as reduction of DCG-4-inhibited forskolin-stimulated cAMP formation after 20 mins by HTRF assayAntagonist activity at recombinant human mGlu3 receptor expressed in hamster AV12 cells co-expressing human EAAT1 assessed as reduction of DCG-4-inhibited forskolin-stimulated cAMP formation after 20 mins by HTRF assay
ChEMBL 359 5 4 5 0.5 N[C@@]1(C(=O)O)[C@H](OCc2ccc(Cl)c(F)c2)[C@H](O)[C@@H]2[C@H]1[C@H]2C(=O)O 10.1016/j.bmcl.2016.10.067
122190323 123519 None 0 Rat Functional pIC50 = 5.9 5.9 1 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 381 5 0 5 3.8 COc1cccc(OCc2cc3n(n2)[C@H](C)CN(c2ccc(F)cc2)C3=O)c1 10.1021/acs.jmedchem.5b01005
CHEMBL3617507 123519 None 0 Rat Functional pIC50 = 5.9 5.9 1 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 381 5 0 5 3.8 COc1cccc(OCc2cc3n(n2)[C@H](C)CN(c2ccc(F)cc2)C3=O)c1 10.1021/acs.jmedchem.5b01005
122190323 123519 None 0 Rat Functional pIC50 = 5.9 5.9 1 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 381 5 0 5 3.8 COc1cccc(OCc2cc3n(n2)[C@H](C)CN(c2ccc(F)cc2)C3=O)c1 10.1021/acs.jmedchem.5b01005
CHEMBL3617507 123519 None 0 Rat Functional pIC50 = 5.9 5.9 1 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 381 5 0 5 3.8 COc1cccc(OCc2cc3n(n2)[C@H](C)CN(c2ccc(F)cc2)C3=O)c1 10.1021/acs.jmedchem.5b01005
53393854 83635 None 0 Rat Functional pIC50 = 5.9 5.9 2 2
Negative allosteric modulation of rat mGlu3 receptor transfected in human TREX cells assessed as inhibition of glutamate-induced calcium mobilization after 2.5 minsNegative allosteric modulation of rat mGlu3 receptor transfected in human TREX cells assessed as inhibition of glutamate-induced calcium mobilization after 2.5 mins
ChEMBL 335 2 1 3 2.7 COc1ccc(C#Cc2ccc(C(=O)N3CCCC(O)C3)cc2)cc1 10.1021/jm400439t
CHEMBL2204439 83635 None 0 Rat Functional pIC50 = 5.9 5.9 2 2
Negative allosteric modulation of rat mGlu3 receptor transfected in human TREX cells assessed as inhibition of glutamate-induced calcium mobilization after 2.5 minsNegative allosteric modulation of rat mGlu3 receptor transfected in human TREX cells assessed as inhibition of glutamate-induced calcium mobilization after 2.5 mins
ChEMBL 335 2 1 3 2.7 COc1ccc(C#Cc2ccc(C(=O)N3CCCC(O)C3)cc2)cc1 10.1021/jm400439t
1378 2417 None 39 Human Functional pIC50 = 7.9 7.9 2 14
Antagonist activity at human mGLUR3 expressed in RGT cells assessed as inhibition of (1S,3R)-1-aminocyclopentane-1,3-dicarboxylic acid-induced inhibition of forskolin stimulated cyclic-AMPAntagonist activity at human mGLUR3 expressed in RGT cells assessed as inhibition of (1S,3R)-1-aminocyclopentane-1,3-dicarboxylic acid-induced inhibition of forskolin stimulated cyclic-AMP
ChEMBL 353 5 3 4 2.8 OC(=O)[C@H]1C[C@@H]1[C@](C(=O)O)(CC1c2ccccc2Oc2c1cccc2)N 10.1016/j.bmcl.2012.01.039
1399 2417 None 39 Human Functional pIC50 = 7.9 7.9 2 14
Antagonist activity at human mGLUR3 expressed in RGT cells assessed as inhibition of (1S,3R)-1-aminocyclopentane-1,3-dicarboxylic acid-induced inhibition of forskolin stimulated cyclic-AMPAntagonist activity at human mGLUR3 expressed in RGT cells assessed as inhibition of (1S,3R)-1-aminocyclopentane-1,3-dicarboxylic acid-induced inhibition of forskolin stimulated cyclic-AMP
ChEMBL 353 5 3 4 2.8 OC(=O)[C@H]1C[C@@H]1[C@](C(=O)O)(CC1c2ccccc2Oc2c1cccc2)N 10.1016/j.bmcl.2012.01.039
9819927 2417 None 39 Human Functional pIC50 = 7.9 7.9 2 14
Antagonist activity at human mGLUR3 expressed in RGT cells assessed as inhibition of (1S,3R)-1-aminocyclopentane-1,3-dicarboxylic acid-induced inhibition of forskolin stimulated cyclic-AMPAntagonist activity at human mGLUR3 expressed in RGT cells assessed as inhibition of (1S,3R)-1-aminocyclopentane-1,3-dicarboxylic acid-induced inhibition of forskolin stimulated cyclic-AMP
ChEMBL 353 5 3 4 2.8 OC(=O)[C@H]1C[C@@H]1[C@](C(=O)O)(CC1c2ccccc2Oc2c1cccc2)N 10.1016/j.bmcl.2012.01.039
CHEMBL432038 2417 None 39 Human Functional pIC50 = 7.9 7.9 2 14
Antagonist activity at human mGLUR3 expressed in RGT cells assessed as inhibition of (1S,3R)-1-aminocyclopentane-1,3-dicarboxylic acid-induced inhibition of forskolin stimulated cyclic-AMPAntagonist activity at human mGLUR3 expressed in RGT cells assessed as inhibition of (1S,3R)-1-aminocyclopentane-1,3-dicarboxylic acid-induced inhibition of forskolin stimulated cyclic-AMP
ChEMBL 353 5 3 4 2.8 OC(=O)[C@H]1C[C@@H]1[C@](C(=O)O)(CC1c2ccccc2Oc2c1cccc2)N 10.1016/j.bmcl.2012.01.039
11281280 56424 None 0 Rat Functional pIC50 = 7.9 7.9 -1 3
Antagonist activity at rat mGluR3 receptor expressed in CHO cells assessed as inhibition of GIRK currentAntagonist activity at rat mGluR3 receptor expressed in CHO cells assessed as inhibition of GIRK current
ChEMBL 409 2 1 3 5.8 Cc1cc(-c2cccc(C3=Nc4cc(C)c(C(F)(F)F)cc4NC(=O)C3)c2)ccn1 10.1016/j.bmcl.2010.09.125
CHEMBL1631859 56424 None 0 Rat Functional pIC50 = 7.9 7.9 -1 3
Antagonist activity at rat mGluR3 receptor expressed in CHO cells assessed as inhibition of GIRK currentAntagonist activity at rat mGluR3 receptor expressed in CHO cells assessed as inhibition of GIRK current
ChEMBL 409 2 1 3 5.8 Cc1cc(-c2cccc(C3=Nc4cc(C)c(C(F)(F)F)cc4NC(=O)C3)c2)ccn1 10.1016/j.bmcl.2010.09.125
67705376 145427 None 0 Human Functional pIC50 = 7.8 7.8 1 2
Antagonist activity at recombinant human mGlu3 receptor expressed in hamster AV12 cells co-expressing human EAAT1 assessed as reduction of DCG-4-inhibited forskolin-stimulated cAMP formation after 20 mins by HTRF assayAntagonist activity at recombinant human mGlu3 receptor expressed in hamster AV12 cells co-expressing human EAAT1 assessed as reduction of DCG-4-inhibited forskolin-stimulated cAMP formation after 20 mins by HTRF assay
ChEMBL 416 6 4 5 1.1 CC(=O)N[C@H]1[C@H]2[C@H](C(=O)O)[C@H]2[C@](N)(C(=O)O)[C@@H]1OCc1ccc(Cl)c(Cl)c1 10.1016/j.bmcl.2016.10.067
CHEMBL3913414 145427 None 0 Human Functional pIC50 = 7.8 7.8 1 2
Antagonist activity at recombinant human mGlu3 receptor expressed in hamster AV12 cells co-expressing human EAAT1 assessed as reduction of DCG-4-inhibited forskolin-stimulated cAMP formation after 20 mins by HTRF assayAntagonist activity at recombinant human mGlu3 receptor expressed in hamster AV12 cells co-expressing human EAAT1 assessed as reduction of DCG-4-inhibited forskolin-stimulated cAMP formation after 20 mins by HTRF assay
ChEMBL 416 6 4 5 1.1 CC(=O)N[C@H]1[C@H]2[C@H](C(=O)O)[C@H]2[C@](N)(C(=O)O)[C@@H]1OCc1ccc(Cl)c(Cl)c1 10.1016/j.bmcl.2016.10.067
10515174 78762 None 0 Human Functional pIC50 = 5.9 5.9 -1 2
Ability to block 1S,3R-ACPD-induced inhibition of forskolin stimulated cyclic-AMP in non-neuronal cell line expressing human Metabotropic glutamate receptor 3Ability to block 1S,3R-ACPD-induced inhibition of forskolin stimulated cyclic-AMP in non-neuronal cell line expressing human Metabotropic glutamate receptor 3
ChEMBL 255 5 3 3 1.5 NC(CC1CCCCC1)(C(=O)O)[C@H]1C[C@@H]1C(=O)O 10.1021/jm970497w
CHEMBL2112574 78762 None 0 Human Functional pIC50 = 5.9 5.9 -1 2
Ability to block 1S,3R-ACPD-induced inhibition of forskolin stimulated cyclic-AMP in non-neuronal cell line expressing human Metabotropic glutamate receptor 3Ability to block 1S,3R-ACPD-induced inhibition of forskolin stimulated cyclic-AMP in non-neuronal cell line expressing human Metabotropic glutamate receptor 3
ChEMBL 255 5 3 3 1.5 NC(CC1CCCCC1)(C(=O)O)[C@H]1C[C@@H]1C(=O)O 10.1021/jm970497w
122190391 123567 None 0 Rat Functional pIC50 = 6.9 6.9 7 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 386 4 0 5 3.9 C[C@@H]1CN(c2ccccc2Cl)C(=O)c2cc(COc3ccc(F)cn3)nn21 10.1021/acs.jmedchem.5b01005
CHEMBL3617614 123567 None 0 Rat Functional pIC50 = 6.9 6.9 7 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 386 4 0 5 3.9 C[C@@H]1CN(c2ccccc2Cl)C(=O)c2cc(COc3ccc(F)cn3)nn21 10.1021/acs.jmedchem.5b01005
122190391 123567 None 0 Rat Functional pIC50 = 6.9 6.9 7 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 386 4 0 5 3.9 C[C@@H]1CN(c2ccccc2Cl)C(=O)c2cc(COc3ccc(F)cn3)nn21 10.1021/acs.jmedchem.5b01005
CHEMBL3617614 123567 None 0 Rat Functional pIC50 = 6.9 6.9 7 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 386 4 0 5 3.9 C[C@@H]1CN(c2ccccc2Cl)C(=O)c2cc(COc3ccc(F)cn3)nn21 10.1021/acs.jmedchem.5b01005
122190392 123568 None 0 Rat Functional pIC50 = 6.8 6.8 12 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 386 4 0 5 3.9 C[C@@H]1CN(c2cccc(Cl)c2)C(=O)c2cc(COc3ccc(F)cn3)nn21 10.1021/acs.jmedchem.5b01005
CHEMBL3617615 123568 None 0 Rat Functional pIC50 = 6.8 6.8 12 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 386 4 0 5 3.9 C[C@@H]1CN(c2cccc(Cl)c2)C(=O)c2cc(COc3ccc(F)cn3)nn21 10.1021/acs.jmedchem.5b01005
122190317 123513 None 0 Rat Functional pIC50 = 5.8 5.8 - 1
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 365 4 0 4 4.1 Cc1cccc(OCc2cc3n(n2)[C@H](C)CN(c2ccc(F)cc2)C3=O)c1 10.1021/acs.jmedchem.5b01005
CHEMBL3617501 123513 None 0 Rat Functional pIC50 = 5.8 5.8 - 1
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 365 4 0 4 4.1 Cc1cccc(OCc2cc3n(n2)[C@H](C)CN(c2ccc(F)cc2)C3=O)c1 10.1021/acs.jmedchem.5b01005
122190317 123513 None 0 Rat Functional pIC50 = 5.8 5.8 - 1
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 365 4 0 4 4.1 Cc1cccc(OCc2cc3n(n2)[C@H](C)CN(c2ccc(F)cc2)C3=O)c1 10.1021/acs.jmedchem.5b01005
CHEMBL3617501 123513 None 0 Rat Functional pIC50 = 5.8 5.8 - 1
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 365 4 0 4 4.1 Cc1cccc(OCc2cc3n(n2)[C@H](C)CN(c2ccc(F)cc2)C3=O)c1 10.1021/acs.jmedchem.5b01005
122455999 163061 None 0 Rat Functional pIC50 = 5.8 5.8 5 2
Negative allosteric modulation of rat mGlu3 receptor expressed in TREX cells coexpressing Galpha15 assessed as inhibition of glutamate induced-calcium mobilization preincubated for 2.3 mins followed by glutamate addition measured for 2.6 mins by Fluo-4 AM dye based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor expressed in TREX cells coexpressing Galpha15 assessed as inhibition of glutamate induced-calcium mobilization preincubated for 2.3 mins followed by glutamate addition measured for 2.6 mins by Fluo-4 AM dye based fluorescence assay
ChEMBL 360 6 0 5 3.5 O=c1cc(OCCOc2cc(Cl)ccn2)ccn1-c1ccc(F)cc1 10.1021/acsmedchemlett.7b00249
CHEMBL4174878 163061 None 0 Rat Functional pIC50 = 5.8 5.8 5 2
Negative allosteric modulation of rat mGlu3 receptor expressed in TREX cells coexpressing Galpha15 assessed as inhibition of glutamate induced-calcium mobilization preincubated for 2.3 mins followed by glutamate addition measured for 2.6 mins by Fluo-4 AM dye based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor expressed in TREX cells coexpressing Galpha15 assessed as inhibition of glutamate induced-calcium mobilization preincubated for 2.3 mins followed by glutamate addition measured for 2.6 mins by Fluo-4 AM dye based fluorescence assay
ChEMBL 360 6 0 5 3.5 O=c1cc(OCCOc2cc(Cl)ccn2)ccn1-c1ccc(F)cc1 10.1021/acsmedchemlett.7b00249
134154496 152599 None 0 Human Functional pIC50 = 6.8 6.8 1 2
Antagonist activity at recombinant human mGlu3 receptor expressed in hamster AV12 cells co-expressing human EAAT1 assessed as reduction of DCG-4-inhibited forskolin-stimulated cAMP formation after 20 mins by HTRF assayAntagonist activity at recombinant human mGlu3 receptor expressed in hamster AV12 cells co-expressing human EAAT1 assessed as reduction of DCG-4-inhibited forskolin-stimulated cAMP formation after 20 mins by HTRF assay
ChEMBL 341 5 4 5 0.3 N[C@@]1(C(=O)O)[C@H](OCc2ccc(Cl)cc2)[C@H](O)[C@@H]2[C@H]1[C@H]2C(=O)O 10.1016/j.bmcl.2016.10.067
CHEMBL3971347 152599 None 0 Human Functional pIC50 = 6.8 6.8 1 2
Antagonist activity at recombinant human mGlu3 receptor expressed in hamster AV12 cells co-expressing human EAAT1 assessed as reduction of DCG-4-inhibited forskolin-stimulated cAMP formation after 20 mins by HTRF assayAntagonist activity at recombinant human mGlu3 receptor expressed in hamster AV12 cells co-expressing human EAAT1 assessed as reduction of DCG-4-inhibited forskolin-stimulated cAMP formation after 20 mins by HTRF assay
ChEMBL 341 5 4 5 0.3 N[C@@]1(C(=O)O)[C@H](OCc2ccc(Cl)cc2)[C@H](O)[C@@H]2[C@H]1[C@H]2C(=O)O 10.1016/j.bmcl.2016.10.067
122190392 123568 None 0 Rat Functional pIC50 = 6.8 6.8 12 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 386 4 0 5 3.9 C[C@@H]1CN(c2cccc(Cl)c2)C(=O)c2cc(COc3ccc(F)cn3)nn21 10.1021/acs.jmedchem.5b01005
CHEMBL3617615 123568 None 0 Rat Functional pIC50 = 6.8 6.8 12 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 386 4 0 5 3.9 C[C@@H]1CN(c2cccc(Cl)c2)C(=O)c2cc(COc3ccc(F)cn3)nn21 10.1021/acs.jmedchem.5b01005
122455999 163061 None 0 Rat Functional pIC50 = 5.8 5.8 5 2
Negative allosteric modulation of rat mGlu3 receptor expressed in TREX cells coexpressing Galpha15 assessed as inhibition of glutamate induced-calcium mobilization preincubated for 2.3 mins followed by glutamate addition measured for 2.6 mins by Fluo-4 AM dye based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor expressed in TREX cells coexpressing Galpha15 assessed as inhibition of glutamate induced-calcium mobilization preincubated for 2.3 mins followed by glutamate addition measured for 2.6 mins by Fluo-4 AM dye based fluorescence assay
ChEMBL 360 6 0 5 3.5 O=c1cc(OCCOc2cc(Cl)ccn2)ccn1-c1ccc(F)cc1 10.1021/acsmedchemlett.7b00249
CHEMBL4174878 163061 None 0 Rat Functional pIC50 = 5.8 5.8 5 2
Negative allosteric modulation of rat mGlu3 receptor expressed in TREX cells coexpressing Galpha15 assessed as inhibition of glutamate induced-calcium mobilization preincubated for 2.3 mins followed by glutamate addition measured for 2.6 mins by Fluo-4 AM dye based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor expressed in TREX cells coexpressing Galpha15 assessed as inhibition of glutamate induced-calcium mobilization preincubated for 2.3 mins followed by glutamate addition measured for 2.6 mins by Fluo-4 AM dye based fluorescence assay
ChEMBL 360 6 0 5 3.5 O=c1cc(OCCOc2cc(Cl)ccn2)ccn1-c1ccc(F)cc1 10.1021/acsmedchemlett.7b00249
134132133 144877 None 0 Human Functional pIC50 = 6.8 6.8 1 2
Antagonist activity at recombinant human mGlu3 receptor expressed in hamster AV12 cells co-expressing human EAAT1 assessed as reduction of DCG-4-inhibited forskolin-stimulated cAMP formation after 20 mins by HTRF assayAntagonist activity at recombinant human mGlu3 receptor expressed in hamster AV12 cells co-expressing human EAAT1 assessed as reduction of DCG-4-inhibited forskolin-stimulated cAMP formation after 20 mins by HTRF assay
ChEMBL 375 5 4 5 1.0 N[C@@]1(C(=O)O)[C@H](OCc2ccc(Cl)c(Cl)c2)[C@H](O)[C@@H]2[C@H]1[C@H]2C(=O)O 10.1016/j.bmcl.2016.10.067
CHEMBL3909237 144877 None 0 Human Functional pIC50 = 6.8 6.8 1 2
Antagonist activity at recombinant human mGlu3 receptor expressed in hamster AV12 cells co-expressing human EAAT1 assessed as reduction of DCG-4-inhibited forskolin-stimulated cAMP formation after 20 mins by HTRF assayAntagonist activity at recombinant human mGlu3 receptor expressed in hamster AV12 cells co-expressing human EAAT1 assessed as reduction of DCG-4-inhibited forskolin-stimulated cAMP formation after 20 mins by HTRF assay
ChEMBL 375 5 4 5 1.0 N[C@@]1(C(=O)O)[C@H](OCc2ccc(Cl)c(Cl)c2)[C@H](O)[C@@H]2[C@H]1[C@H]2C(=O)O 10.1016/j.bmcl.2016.10.067
71137034 123466 None 0 Human Functional pIC50 = 6.8 6.8 -7 2
Antagonist activity at human recombinant mGlu3 receptor expressed in AV12 cells assessed as inhibition of glutamate-stimulated Ca2+ mobilization after 1.5 hrs by FLIPR assayAntagonist activity at human recombinant mGlu3 receptor expressed in AV12 cells assessed as inhibition of glutamate-stimulated Ca2+ mobilization after 1.5 hrs by FLIPR assay
ChEMBL 334 5 4 6 0.3 N[C@@]1(C(=O)O)C[C@@H](Sc2nnc(C(F)F)[nH]2)[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/acs.jmedchem.5b01124
CHEMBL3616850 123466 None 0 Human Functional pIC50 = 6.8 6.8 -7 2
Antagonist activity at human recombinant mGlu3 receptor expressed in AV12 cells assessed as inhibition of glutamate-stimulated Ca2+ mobilization after 1.5 hrs by FLIPR assayAntagonist activity at human recombinant mGlu3 receptor expressed in AV12 cells assessed as inhibition of glutamate-stimulated Ca2+ mobilization after 1.5 hrs by FLIPR assay
ChEMBL 334 5 4 6 0.3 N[C@@]1(C(=O)O)C[C@@H](Sc2nnc(C(F)F)[nH]2)[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/acs.jmedchem.5b01124
122190340 123536 None 0 Rat Functional pIC50 = 5.8 5.8 - 1
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 382 5 0 6 3.2 COc1cccc(OCc2cc3n(n2)[C@H](C)CN(c2ccc(F)cc2)C3=O)n1 10.1021/acs.jmedchem.5b01005
CHEMBL3617524 123536 None 0 Rat Functional pIC50 = 5.8 5.8 - 1
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 382 5 0 6 3.2 COc1cccc(OCc2cc3n(n2)[C@H](C)CN(c2ccc(F)cc2)C3=O)n1 10.1021/acs.jmedchem.5b01005
122190340 123536 None 0 Rat Functional pIC50 = 5.8 5.8 - 1
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 382 5 0 6 3.2 COc1cccc(OCc2cc3n(n2)[C@H](C)CN(c2ccc(F)cc2)C3=O)n1 10.1021/acs.jmedchem.5b01005
CHEMBL3617524 123536 None 0 Rat Functional pIC50 = 5.8 5.8 - 1
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 382 5 0 6 3.2 COc1cccc(OCc2cc3n(n2)[C@H](C)CN(c2ccc(F)cc2)C3=O)n1 10.1021/acs.jmedchem.5b01005
10807972 35826 None 1 Human Functional pIC50 = 7.8 7.8 3 4
Ability to block 1S,3R-ACPD-induced inhibition of forskolin stimulated cyclic-AMP in non-neuronal cell line expressing human Metabotropic glutamate receptor 3Ability to block 1S,3R-ACPD-induced inhibition of forskolin stimulated cyclic-AMP in non-neuronal cell line expressing human Metabotropic glutamate receptor 3
ChEMBL 353 5 3 4 2.8 N[C@@](CC1c2ccccc2Oc2ccccc21)(C(=O)O)[C@H]1C[C@@H]1C(=O)O 10.1021/jm970497w
CHEMBL144151 35826 None 1 Human Functional pIC50 = 7.8 7.8 3 4
Ability to block 1S,3R-ACPD-induced inhibition of forskolin stimulated cyclic-AMP in non-neuronal cell line expressing human Metabotropic glutamate receptor 3Ability to block 1S,3R-ACPD-induced inhibition of forskolin stimulated cyclic-AMP in non-neuronal cell line expressing human Metabotropic glutamate receptor 3
ChEMBL 353 5 3 4 2.8 N[C@@](CC1c2ccccc2Oc2ccccc21)(C(=O)O)[C@H]1C[C@@H]1C(=O)O 10.1021/jm970497w
1378 2417 None 39 Rat Functional pIC50 = 7.8 7.8 -2 14
Antagonistic activity against metabotropic glutamate receptor 3 (mGluR3) was evaluatedAntagonistic activity against metabotropic glutamate receptor 3 (mGluR3) was evaluated
ChEMBL 353 5 3 4 2.8 OC(=O)[C@H]1C[C@@H]1[C@](C(=O)O)(CC1c2ccccc2Oc2c1cccc2)N 10.1016/s0960-894x(98)00510-1
1399 2417 None 39 Rat Functional pIC50 = 7.8 7.8 -2 14
Antagonistic activity against metabotropic glutamate receptor 3 (mGluR3) was evaluatedAntagonistic activity against metabotropic glutamate receptor 3 (mGluR3) was evaluated
ChEMBL 353 5 3 4 2.8 OC(=O)[C@H]1C[C@@H]1[C@](C(=O)O)(CC1c2ccccc2Oc2c1cccc2)N 10.1016/s0960-894x(98)00510-1
9819927 2417 None 39 Rat Functional pIC50 = 7.8 7.8 -2 14
Antagonistic activity against metabotropic glutamate receptor 3 (mGluR3) was evaluatedAntagonistic activity against metabotropic glutamate receptor 3 (mGluR3) was evaluated
ChEMBL 353 5 3 4 2.8 OC(=O)[C@H]1C[C@@H]1[C@](C(=O)O)(CC1c2ccccc2Oc2c1cccc2)N 10.1016/s0960-894x(98)00510-1
CHEMBL432038 2417 None 39 Rat Functional pIC50 = 7.8 7.8 -2 14
Antagonistic activity against metabotropic glutamate receptor 3 (mGluR3) was evaluatedAntagonistic activity against metabotropic glutamate receptor 3 (mGluR3) was evaluated
ChEMBL 353 5 3 4 2.8 OC(=O)[C@H]1C[C@@H]1[C@](C(=O)O)(CC1c2ccccc2Oc2c1cccc2)N 10.1016/s0960-894x(98)00510-1
67637415 183793 None 0 Human Functional pIC50 = 7.8 7.8 -2 2
Antagonist activity at human recombinant mGlu3 receptor stably expressed in golden hamster AV12 cells co-expressing rat EAAT1 assessed as reduction in DCG IV-induced inhibition of forskolin-stimulated cAMP accumulation preincubated for 20 mins followed by incubation with cAMP-d2 conjugate and anti-cAMP cryptate for 1 hr by HTRF assayAntagonist activity at human recombinant mGlu3 receptor stably expressed in golden hamster AV12 cells co-expressing rat EAAT1 assessed as reduction in DCG IV-induced inhibition of forskolin-stimulated cAMP accumulation preincubated for 20 mins followed by incubation with cAMP-d2 conjugate and anti-cAMP cryptate for 1 hr by HTRF assay
ChEMBL 438 7 4 7 1.9 Cc1cc(SC[C@@H]2[C@@H](Sc3nc[nH]n3)[C@H]3[C@H](C(=O)O)[C@H]3[C@]2(N)C(=O)O)ccc1F 10.1021/acs.jmedchem.6b01119
CHEMBL4759992 183793 None 0 Human Functional pIC50 = 7.8 7.8 -2 2
Antagonist activity at human recombinant mGlu3 receptor stably expressed in golden hamster AV12 cells co-expressing rat EAAT1 assessed as reduction in DCG IV-induced inhibition of forskolin-stimulated cAMP accumulation preincubated for 20 mins followed by incubation with cAMP-d2 conjugate and anti-cAMP cryptate for 1 hr by HTRF assayAntagonist activity at human recombinant mGlu3 receptor stably expressed in golden hamster AV12 cells co-expressing rat EAAT1 assessed as reduction in DCG IV-induced inhibition of forskolin-stimulated cAMP accumulation preincubated for 20 mins followed by incubation with cAMP-d2 conjugate and anti-cAMP cryptate for 1 hr by HTRF assay
ChEMBL 438 7 4 7 1.9 Cc1cc(SC[C@@H]2[C@@H](Sc3nc[nH]n3)[C@H]3[C@H](C(=O)O)[C@H]3[C@]2(N)C(=O)O)ccc1F 10.1021/acs.jmedchem.6b01119
CHEMBL4803099 183793 None 0 Human Functional pIC50 = 7.8 7.8 -2 2
Antagonist activity at human recombinant mGlu3 receptor stably expressed in golden hamster AV12 cells co-expressing rat EAAT1 assessed as reduction in DCG IV-induced inhibition of forskolin-stimulated cAMP accumulation preincubated for 20 mins followed by incubation with cAMP-d2 conjugate and anti-cAMP cryptate for 1 hr by HTRF assayAntagonist activity at human recombinant mGlu3 receptor stably expressed in golden hamster AV12 cells co-expressing rat EAAT1 assessed as reduction in DCG IV-induced inhibition of forskolin-stimulated cAMP accumulation preincubated for 20 mins followed by incubation with cAMP-d2 conjugate and anti-cAMP cryptate for 1 hr by HTRF assay
ChEMBL 438 7 4 7 1.9 Cc1cc(SC[C@@H]2[C@@H](Sc3nc[nH]n3)[C@H]3[C@H](C(=O)O)[C@H]3[C@]2(N)C(=O)O)ccc1F 10.1021/acs.jmedchem.6b01119
44348939 118558 None 0 Human Functional pIC50 = 6.8 6.8 2 2
Effect on 1S,3R-ACPD-induced inhibition of forskolin stimulated cyclic-AMP in RGT cells expressing human Metabotropic glutamate receptor 3Effect on 1S,3R-ACPD-induced inhibition of forskolin stimulated cyclic-AMP in RGT cells expressing human Metabotropic glutamate receptor 3
ChEMBL 293 7 3 4 1.1 COc1cccc(CC[C@](N)(C(=O)O)C2C[C@@H]2C(=O)O)c1 10.1021/jm970498o
CHEMBL341457 118558 None 0 Human Functional pIC50 = 6.8 6.8 2 2
Effect on 1S,3R-ACPD-induced inhibition of forskolin stimulated cyclic-AMP in RGT cells expressing human Metabotropic glutamate receptor 3Effect on 1S,3R-ACPD-induced inhibition of forskolin stimulated cyclic-AMP in RGT cells expressing human Metabotropic glutamate receptor 3
ChEMBL 293 7 3 4 1.1 COc1cccc(CC[C@](N)(C(=O)O)C2C[C@@H]2C(=O)O)c1 10.1021/jm970498o
44302608 100900 None 0 Human Functional pIC50 = 4.8 4.8 2 2
In vitro antagonist activity at recombinant human Metabotropic glutamate receptor 3 expressed in RGT cells.In vitro antagonist activity at recombinant human Metabotropic glutamate receptor 3 expressed in RGT cells.
ChEMBL 340 5 3 4 1.8 N[C@]1(C(=O)O)C[C@H](C(=O)O)N(Cc2ccccc2-c2ccccc2)C1 10.1016/s0960-894x(98)00352-7
CHEMBL293434 100900 None 0 Human Functional pIC50 = 4.8 4.8 2 2
In vitro antagonist activity at recombinant human Metabotropic glutamate receptor 3 expressed in RGT cells.In vitro antagonist activity at recombinant human Metabotropic glutamate receptor 3 expressed in RGT cells.
ChEMBL 340 5 3 4 1.8 N[C@]1(C(=O)O)C[C@H](C(=O)O)N(Cc2ccccc2-c2ccccc2)C1 10.1016/s0960-894x(98)00352-7
122190389 123565 None 0 Rat Functional pIC50 = 6.8 6.8 - 1
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 370 4 0 5 3.4 C[C@@H]1CN(c2ccccc2F)C(=O)c2cc(COc3ccc(F)cn3)nn21 10.1021/acs.jmedchem.5b01005
CHEMBL3617612 123565 None 0 Rat Functional pIC50 = 6.8 6.8 - 1
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 370 4 0 5 3.4 C[C@@H]1CN(c2ccccc2F)C(=O)c2cc(COc3ccc(F)cn3)nn21 10.1021/acs.jmedchem.5b01005
122190389 123565 None 0 Rat Functional pIC50 = 6.8 6.8 - 1
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 370 4 0 5 3.4 C[C@@H]1CN(c2ccccc2F)C(=O)c2cc(COc3ccc(F)cn3)nn21 10.1021/acs.jmedchem.5b01005
CHEMBL3617612 123565 None 0 Rat Functional pIC50 = 6.8 6.8 - 1
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 370 4 0 5 3.4 C[C@@H]1CN(c2ccccc2F)C(=O)c2cc(COc3ccc(F)cn3)nn21 10.1021/acs.jmedchem.5b01005
122190320 123516 None 0 Rat Functional pIC50 = 5.8 5.8 - 1
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 385 4 0 4 4.5 C[C@@H]1CN(c2ccc(F)cc2)C(=O)c2cc(COc3cccc(Cl)c3)nn21 10.1021/acs.jmedchem.5b01005
CHEMBL3617504 123516 None 0 Rat Functional pIC50 = 5.8 5.8 - 1
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 385 4 0 4 4.5 C[C@@H]1CN(c2ccc(F)cc2)C(=O)c2cc(COc3cccc(Cl)c3)nn21 10.1021/acs.jmedchem.5b01005
122190320 123516 None 0 Rat Functional pIC50 = 5.8 5.8 - 1
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 385 4 0 4 4.5 C[C@@H]1CN(c2ccc(F)cc2)C(=O)c2cc(COc3cccc(Cl)c3)nn21 10.1021/acs.jmedchem.5b01005
CHEMBL3617504 123516 None 0 Rat Functional pIC50 = 5.8 5.8 - 1
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 385 4 0 4 4.5 C[C@@H]1CN(c2ccc(F)cc2)C(=O)c2cc(COc3cccc(Cl)c3)nn21 10.1021/acs.jmedchem.5b01005
69669702 183781 None 0 Human Functional pIC50 = 6.8 6.8 -3 2
Antagonist activity at human recombinant mGlu3 receptor stably expressed in golden hamster AV12 cells co-expressing rat EAAT1 assessed as reduction in DCG IV-induced inhibition of forskolin-stimulated cAMP accumulation preincubated for 20 mins followed by incubation with cAMP-d2 conjugate and anti-cAMP cryptate for 1 hr by HTRF assayAntagonist activity at human recombinant mGlu3 receptor stably expressed in golden hamster AV12 cells co-expressing rat EAAT1 assessed as reduction in DCG IV-induced inhibition of forskolin-stimulated cAMP accumulation preincubated for 20 mins followed by incubation with cAMP-d2 conjugate and anti-cAMP cryptate for 1 hr by HTRF assay
ChEMBL 354 5 4 5 0.9 Cc1cc(SC[C@@H]2[C@@H](N)[C@H]3[C@H](C(=O)O)[C@H]3[C@]2(N)C(=O)O)ccc1F 10.1021/acs.jmedchem.6b01119
CHEMBL4756556 183781 None 0 Human Functional pIC50 = 6.8 6.8 -3 2
Antagonist activity at human recombinant mGlu3 receptor stably expressed in golden hamster AV12 cells co-expressing rat EAAT1 assessed as reduction in DCG IV-induced inhibition of forskolin-stimulated cAMP accumulation preincubated for 20 mins followed by incubation with cAMP-d2 conjugate and anti-cAMP cryptate for 1 hr by HTRF assayAntagonist activity at human recombinant mGlu3 receptor stably expressed in golden hamster AV12 cells co-expressing rat EAAT1 assessed as reduction in DCG IV-induced inhibition of forskolin-stimulated cAMP accumulation preincubated for 20 mins followed by incubation with cAMP-d2 conjugate and anti-cAMP cryptate for 1 hr by HTRF assay
ChEMBL 354 5 4 5 0.9 Cc1cc(SC[C@@H]2[C@@H](N)[C@H]3[C@H](C(=O)O)[C@H]3[C@]2(N)C(=O)O)ccc1F 10.1021/acs.jmedchem.6b01119
CHEMBL4802948 183781 None 0 Human Functional pIC50 = 6.8 6.8 -3 2
Antagonist activity at human recombinant mGlu3 receptor stably expressed in golden hamster AV12 cells co-expressing rat EAAT1 assessed as reduction in DCG IV-induced inhibition of forskolin-stimulated cAMP accumulation preincubated for 20 mins followed by incubation with cAMP-d2 conjugate and anti-cAMP cryptate for 1 hr by HTRF assayAntagonist activity at human recombinant mGlu3 receptor stably expressed in golden hamster AV12 cells co-expressing rat EAAT1 assessed as reduction in DCG IV-induced inhibition of forskolin-stimulated cAMP accumulation preincubated for 20 mins followed by incubation with cAMP-d2 conjugate and anti-cAMP cryptate for 1 hr by HTRF assay
ChEMBL 354 5 4 5 0.9 Cc1cc(SC[C@@H]2[C@@H](N)[C@H]3[C@H](C(=O)O)[C@H]3[C@]2(N)C(=O)O)ccc1F 10.1021/acs.jmedchem.6b01119
90643956 112054 None 0 Rat Functional pIC50 = 6.8 6.8 5 2
Inhibition of rat mGlu3 receptor transfected in HEK293 cells coexpressing mouse Galpha15 assessed as decrease in glutamate-induced calcium signaling by fluorescence plate reader analysis in presence of glutamate at EC87 concentrationInhibition of rat mGlu3 receptor transfected in HEK293 cells coexpressing mouse Galpha15 assessed as decrease in glutamate-induced calcium signaling by fluorescence plate reader analysis in presence of glutamate at EC87 concentration
ChEMBL 352 2 0 5 3.9 Cn1c(=O)c2ccc(-c3cccnc3)cc2n2nc(-c3ccccc3)cc12 10.1016/j.bmcl.2014.04.051
CHEMBL3288639 112054 None 0 Rat Functional pIC50 = 6.8 6.8 5 2
Inhibition of rat mGlu3 receptor transfected in HEK293 cells coexpressing mouse Galpha15 assessed as decrease in glutamate-induced calcium signaling by fluorescence plate reader analysis in presence of glutamate at EC87 concentrationInhibition of rat mGlu3 receptor transfected in HEK293 cells coexpressing mouse Galpha15 assessed as decrease in glutamate-induced calcium signaling by fluorescence plate reader analysis in presence of glutamate at EC87 concentration
ChEMBL 352 2 0 5 3.9 Cn1c(=O)c2ccc(-c3cccnc3)cc2n2nc(-c3ccccc3)cc12 10.1016/j.bmcl.2014.04.051
122190334 123530 None 0 Rat Functional pIC50 = 5.8 5.8 - 1
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 420 4 0 5 4.2 C[C@@H]1CN(c2ccc(F)cc2)C(=O)c2cc(COc3cc(C(F)(F)F)ccn3)nn21 10.1021/acs.jmedchem.5b01005
CHEMBL3617518 123530 None 0 Rat Functional pIC50 = 5.8 5.8 - 1
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 420 4 0 5 4.2 C[C@@H]1CN(c2ccc(F)cc2)C(=O)c2cc(COc3cc(C(F)(F)F)ccn3)nn21 10.1021/acs.jmedchem.5b01005
122190334 123530 None 0 Rat Functional pIC50 = 5.8 5.8 - 1
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 420 4 0 5 4.2 C[C@@H]1CN(c2ccc(F)cc2)C(=O)c2cc(COc3cc(C(F)(F)F)ccn3)nn21 10.1021/acs.jmedchem.5b01005
CHEMBL3617518 123530 None 0 Rat Functional pIC50 = 5.8 5.8 - 1
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 420 4 0 5 4.2 C[C@@H]1CN(c2ccc(F)cc2)C(=O)c2cc(COc3cc(C(F)(F)F)ccn3)nn21 10.1021/acs.jmedchem.5b01005
60210864 90357 None 0 Rat Functional pIC50 = 5.8 5.8 - 1
Negative allosteric modulation of rat mGlu3 receptor transfected in human TREX cells assessed as inhibition of glutamate-induced calcium mobilization after 2.5 minsNegative allosteric modulation of rat mGlu3 receptor transfected in human TREX cells assessed as inhibition of glutamate-induced calcium mobilization after 2.5 mins
ChEMBL 335 2 1 3 2.7 COc1ccc(C#Cc2ccc(C(=O)N3CCC[C@H](O)C3)cc2)cc1 10.1021/jm400439t
CHEMBL2385877 90357 None 0 Rat Functional pIC50 = 5.8 5.8 - 1
Negative allosteric modulation of rat mGlu3 receptor transfected in human TREX cells assessed as inhibition of glutamate-induced calcium mobilization after 2.5 minsNegative allosteric modulation of rat mGlu3 receptor transfected in human TREX cells assessed as inhibition of glutamate-induced calcium mobilization after 2.5 mins
ChEMBL 335 2 1 3 2.7 COc1ccc(C#Cc2ccc(C(=O)N3CCC[C@H](O)C3)cc2)cc1 10.1021/jm400439t
22224852 95917 None 0 Rat Functional pIC50 = 7.8 7.8 2 2
Antagonist activity at rat mGluR3 expressed in CHO cells assessed as inhibition of glutamate-induced GIRK currentAntagonist activity at rat mGluR3 expressed in CHO cells assessed as inhibition of glutamate-induced GIRK current
ChEMBL 396 3 1 4 5.1 O=C1CC(c2cccc(-n3ccnc3)c2)=Nc2ccc(-c3ccc(F)cc3)cc2N1 10.1016/j.bmcl.2008.02.076
CHEMBL259054 95917 None 0 Rat Functional pIC50 = 7.8 7.8 2 2
Antagonist activity at rat mGluR3 expressed in CHO cells assessed as inhibition of glutamate-induced GIRK currentAntagonist activity at rat mGluR3 expressed in CHO cells assessed as inhibition of glutamate-induced GIRK current
ChEMBL 396 3 1 4 5.1 O=C1CC(c2cccc(-n3ccnc3)c2)=Nc2ccc(-c3ccc(F)cc3)cc2N1 10.1016/j.bmcl.2008.02.076
11211597 56324 None 0 Rat Functional pIC50 = 7.8 7.8 1 3
Antagonist activity at rat mGluR3 receptor expressed in CHO cells assessed as inhibition of GIRK currentAntagonist activity at rat mGluR3 receptor expressed in CHO cells assessed as inhibition of GIRK current
ChEMBL 395 2 1 3 5.5 Cc1cc(-c2cccc(C3=Nc4ccc(C(F)(F)F)cc4NC(=O)C3)c2)ccn1 10.1016/j.bmcl.2010.09.125
CHEMBL1629865 56324 None 0 Rat Functional pIC50 = 7.8 7.8 1 3
Antagonist activity at rat mGluR3 receptor expressed in CHO cells assessed as inhibition of GIRK currentAntagonist activity at rat mGluR3 receptor expressed in CHO cells assessed as inhibition of GIRK current
ChEMBL 395 2 1 3 5.5 Cc1cc(-c2cccc(C3=Nc4ccc(C(F)(F)F)cc4NC(=O)C3)c2)ccn1 10.1016/j.bmcl.2010.09.125
10688450 16611 None 0 Human Functional pIC50 = 6.8 6.8 1 2
Effect on 1S,3R-ACPD-induced inhibition of forskolin stimulated cyclic-AMP in RGT cells expressing human Metabotropic glutamate receptor 3Effect on 1S,3R-ACPD-induced inhibition of forskolin stimulated cyclic-AMP in RGT cells expressing human Metabotropic glutamate receptor 3
ChEMBL 339 7 3 3 2.7 N[C@](CC(c1ccccc1)c1ccccc1)(C(=O)O)[C@H]1C[C@@H]1C(=O)O 10.1021/jm970498o
CHEMBL124078 16611 None 0 Human Functional pIC50 = 6.8 6.8 1 2
Effect on 1S,3R-ACPD-induced inhibition of forskolin stimulated cyclic-AMP in RGT cells expressing human Metabotropic glutamate receptor 3Effect on 1S,3R-ACPD-induced inhibition of forskolin stimulated cyclic-AMP in RGT cells expressing human Metabotropic glutamate receptor 3
ChEMBL 339 7 3 3 2.7 N[C@](CC(c1ccccc1)c1ccccc1)(C(=O)O)[C@H]1C[C@@H]1C(=O)O 10.1021/jm970498o
134144441 150482 None 0 Human Functional pIC50 = 6.8 6.8 1 2
Antagonist activity at recombinant human mGlu3 receptor expressed in hamster AV12 cells co-expressing human EAAT1 assessed as reduction of DCG-4-inhibited forskolin-stimulated cAMP formation after 20 mins by HTRF assayAntagonist activity at recombinant human mGlu3 receptor expressed in hamster AV12 cells co-expressing human EAAT1 assessed as reduction of DCG-4-inhibited forskolin-stimulated cAMP formation after 20 mins by HTRF assay
ChEMBL 341 5 4 5 0.3 N[C@@]1(C(=O)O)[C@H](OCc2cccc(Cl)c2)[C@H](O)[C@@H]2[C@H]1[C@H]2C(=O)O 10.1016/j.bmcl.2016.10.067
CHEMBL3953570 150482 None 0 Human Functional pIC50 = 6.8 6.8 1 2
Antagonist activity at recombinant human mGlu3 receptor expressed in hamster AV12 cells co-expressing human EAAT1 assessed as reduction of DCG-4-inhibited forskolin-stimulated cAMP formation after 20 mins by HTRF assayAntagonist activity at recombinant human mGlu3 receptor expressed in hamster AV12 cells co-expressing human EAAT1 assessed as reduction of DCG-4-inhibited forskolin-stimulated cAMP formation after 20 mins by HTRF assay
ChEMBL 341 5 4 5 0.3 N[C@@]1(C(=O)O)[C@H](OCc2cccc(Cl)c2)[C@H](O)[C@@H]2[C@H]1[C@H]2C(=O)O 10.1016/j.bmcl.2016.10.067
44348993 114649 None 0 Human Functional pIC50 = 6.8 6.8 -1 2
Effect on 1S,3R-ACPD-induced inhibition of forskolin stimulated cyclic-AMP in RGT cells expressing human Metabotropic glutamate receptor 3Effect on 1S,3R-ACPD-induced inhibition of forskolin stimulated cyclic-AMP in RGT cells expressing human Metabotropic glutamate receptor 3
ChEMBL 297 6 3 3 1.8 N[C@@](CCc1cccc(Cl)c1)(C(=O)O)C1C[C@@H]1C(=O)O 10.1021/jm970498o
CHEMBL333771 114649 None 0 Human Functional pIC50 = 6.8 6.8 -1 2
Effect on 1S,3R-ACPD-induced inhibition of forskolin stimulated cyclic-AMP in RGT cells expressing human Metabotropic glutamate receptor 3Effect on 1S,3R-ACPD-induced inhibition of forskolin stimulated cyclic-AMP in RGT cells expressing human Metabotropic glutamate receptor 3
ChEMBL 297 6 3 3 1.8 N[C@@](CCc1cccc(Cl)c1)(C(=O)O)C1C[C@@H]1C(=O)O 10.1021/jm970498o
44348846 117076 None 0 Human Functional pIC50 = 6.8 6.8 1 2
Effect on 1S,3R-ACPD-induced inhibition of forskolin stimulated cyclic-AMP in RGT cells expressing human Metabotropic glutamate receptor 3Effect on 1S,3R-ACPD-induced inhibition of forskolin stimulated cyclic-AMP in RGT cells expressing human Metabotropic glutamate receptor 3
ChEMBL 341 7 3 5 0.5 CS(=O)(=O)c1cccc(CC[C@](N)(C(=O)O)C2C[C@@H]2C(=O)O)c1 10.1021/jm970498o
CHEMBL2111822 117076 None 0 Human Functional pIC50 = 6.8 6.8 1 2
Effect on 1S,3R-ACPD-induced inhibition of forskolin stimulated cyclic-AMP in RGT cells expressing human Metabotropic glutamate receptor 3Effect on 1S,3R-ACPD-induced inhibition of forskolin stimulated cyclic-AMP in RGT cells expressing human Metabotropic glutamate receptor 3
ChEMBL 341 7 3 5 0.5 CS(=O)(=O)c1cccc(CC[C@](N)(C(=O)O)C2C[C@@H]2C(=O)O)c1 10.1021/jm970498o
CHEMBL338911 117076 None 0 Human Functional pIC50 = 6.8 6.8 1 2
Effect on 1S,3R-ACPD-induced inhibition of forskolin stimulated cyclic-AMP in RGT cells expressing human Metabotropic glutamate receptor 3Effect on 1S,3R-ACPD-induced inhibition of forskolin stimulated cyclic-AMP in RGT cells expressing human Metabotropic glutamate receptor 3
ChEMBL 341 7 3 5 0.5 CS(=O)(=O)c1cccc(CC[C@](N)(C(=O)O)C2C[C@@H]2C(=O)O)c1 10.1021/jm970498o
122456206 162320 None 0 Rat Functional pIC50 = 6.8 6.8 1 2
Negative allosteric modulation of rat mGlu3 receptor expressed in TREX cells coexpressing Galpha15 assessed as inhibition of glutamate induced-calcium mobilization preincubated for 2.3 mins followed by glutamate addition measured for 2.6 mins by Fluo-4 AM dye based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor expressed in TREX cells coexpressing Galpha15 assessed as inhibition of glutamate induced-calcium mobilization preincubated for 2.3 mins followed by glutamate addition measured for 2.6 mins by Fluo-4 AM dye based fluorescence assay
ChEMBL 343 6 0 4 3.6 O=c1cc(OCCOc2ccccc2)ccn1-c1ccc(F)c(F)c1 10.1021/acsmedchemlett.7b00249
CHEMBL4163186 162320 None 0 Rat Functional pIC50 = 6.8 6.8 1 2
Negative allosteric modulation of rat mGlu3 receptor expressed in TREX cells coexpressing Galpha15 assessed as inhibition of glutamate induced-calcium mobilization preincubated for 2.3 mins followed by glutamate addition measured for 2.6 mins by Fluo-4 AM dye based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor expressed in TREX cells coexpressing Galpha15 assessed as inhibition of glutamate induced-calcium mobilization preincubated for 2.3 mins followed by glutamate addition measured for 2.6 mins by Fluo-4 AM dye based fluorescence assay
ChEMBL 343 6 0 4 3.6 O=c1cc(OCCOc2ccccc2)ccn1-c1ccc(F)c(F)c1 10.1021/acsmedchemlett.7b00249
44345358 113413 None 0 Human Functional pIC50 = 5.8 5.8 -1 2
Ability to block 1S,3R-ACPD-induced inhibition of forskolin stimulated cyclic-AMP in non-neuronal cell line expressing human Metabotropic glutamate receptor 3Ability to block 1S,3R-ACPD-induced inhibition of forskolin stimulated cyclic-AMP in non-neuronal cell line expressing human Metabotropic glutamate receptor 3
ChEMBL 215 5 3 3 0.5 CC(C)C[C@](N)(C(=O)O)C1C[C@@H]1C(=O)O 10.1021/jm970497w
CHEMBL331753 113413 None 0 Human Functional pIC50 = 5.8 5.8 -1 2
Ability to block 1S,3R-ACPD-induced inhibition of forskolin stimulated cyclic-AMP in non-neuronal cell line expressing human Metabotropic glutamate receptor 3Ability to block 1S,3R-ACPD-induced inhibition of forskolin stimulated cyclic-AMP in non-neuronal cell line expressing human Metabotropic glutamate receptor 3
ChEMBL 215 5 3 3 0.5 CC(C)C[C@](N)(C(=O)O)C1C[C@@H]1C(=O)O 10.1021/jm970497w
122190402 123578 None 0 Rat Functional pIC50 = 6.7 6.7 6 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 388 4 0 5 3.5 C[C@@H]1CN(c2c(F)cccc2F)C(=O)c2cc(COc3ccc(F)cn3)nn21 10.1021/acs.jmedchem.5b01005
CHEMBL3617625 123578 None 0 Rat Functional pIC50 = 6.7 6.7 6 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 388 4 0 5 3.5 C[C@@H]1CN(c2c(F)cccc2F)C(=O)c2cc(COc3ccc(F)cn3)nn21 10.1021/acs.jmedchem.5b01005
122190402 123578 None 0 Rat Functional pIC50 = 6.7 6.7 6 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 388 4 0 5 3.5 C[C@@H]1CN(c2c(F)cccc2F)C(=O)c2cc(COc3ccc(F)cn3)nn21 10.1021/acs.jmedchem.5b01005
CHEMBL3617625 123578 None 0 Rat Functional pIC50 = 6.7 6.7 6 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 388 4 0 5 3.5 C[C@@H]1CN(c2c(F)cccc2F)C(=O)c2cc(COc3ccc(F)cn3)nn21 10.1021/acs.jmedchem.5b01005
122456206 162320 None 0 Rat Functional pIC50 = 6.7 6.7 1 2
Negative allosteric modulation of rat mGlu3 receptor expressed in TREX cells coexpressing Galpha15 assessed as inhibition of glutamate induced-calcium mobilization preincubated for 2.3 mins followed by glutamate addition measured for 2.6 mins by Fluo-4 AM dye based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor expressed in TREX cells coexpressing Galpha15 assessed as inhibition of glutamate induced-calcium mobilization preincubated for 2.3 mins followed by glutamate addition measured for 2.6 mins by Fluo-4 AM dye based fluorescence assay
ChEMBL 343 6 0 4 3.6 O=c1cc(OCCOc2ccccc2)ccn1-c1ccc(F)c(F)c1 10.1021/acsmedchemlett.7b00249
CHEMBL4163186 162320 None 0 Rat Functional pIC50 = 6.7 6.7 1 2
Negative allosteric modulation of rat mGlu3 receptor expressed in TREX cells coexpressing Galpha15 assessed as inhibition of glutamate induced-calcium mobilization preincubated for 2.3 mins followed by glutamate addition measured for 2.6 mins by Fluo-4 AM dye based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor expressed in TREX cells coexpressing Galpha15 assessed as inhibition of glutamate induced-calcium mobilization preincubated for 2.3 mins followed by glutamate addition measured for 2.6 mins by Fluo-4 AM dye based fluorescence assay
ChEMBL 343 6 0 4 3.6 O=c1cc(OCCOc2ccccc2)ccn1-c1ccc(F)c(F)c1 10.1021/acsmedchemlett.7b00249
122190400 123576 None 0 Rat Functional pIC50 = 6.7 6.7 11 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 388 4 0 5 3.5 C[C@@H]1CN(c2cccc(F)c2F)C(=O)c2cc(COc3ccc(F)cn3)nn21 10.1021/acs.jmedchem.5b01005
CHEMBL3617623 123576 None 0 Rat Functional pIC50 = 6.7 6.7 11 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 388 4 0 5 3.5 C[C@@H]1CN(c2cccc(F)c2F)C(=O)c2cc(COc3ccc(F)cn3)nn21 10.1021/acs.jmedchem.5b01005
134152341 153552 None 0 Human Functional pIC50 = 6.7 6.7 2 2
Antagonist activity at recombinant human mGlu3 receptor expressed in hamster AV12 cells co-expressing human EAAT1 assessed as reduction of DCG-4-inhibited forskolin-stimulated cAMP formation after 20 mins by HTRF assayAntagonist activity at recombinant human mGlu3 receptor expressed in hamster AV12 cells co-expressing human EAAT1 assessed as reduction of DCG-4-inhibited forskolin-stimulated cAMP formation after 20 mins by HTRF assay
ChEMBL 375 5 4 5 1.0 N[C@@]1(C(=O)O)[C@H](OCc2cc(Cl)ccc2Cl)[C@H](O)[C@@H]2[C@H]1[C@H]2C(=O)O 10.1016/j.bmcl.2016.10.067
CHEMBL3979475 153552 None 0 Human Functional pIC50 = 6.7 6.7 2 2
Antagonist activity at recombinant human mGlu3 receptor expressed in hamster AV12 cells co-expressing human EAAT1 assessed as reduction of DCG-4-inhibited forskolin-stimulated cAMP formation after 20 mins by HTRF assayAntagonist activity at recombinant human mGlu3 receptor expressed in hamster AV12 cells co-expressing human EAAT1 assessed as reduction of DCG-4-inhibited forskolin-stimulated cAMP formation after 20 mins by HTRF assay
ChEMBL 375 5 4 5 1.0 N[C@@]1(C(=O)O)[C@H](OCc2cc(Cl)ccc2Cl)[C@H](O)[C@@H]2[C@H]1[C@H]2C(=O)O 10.1016/j.bmcl.2016.10.067
122190325 123521 None 0 Rat Functional pIC50 = 5.7 5.7 - 1
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 419 4 0 4 4.8 C[C@@H]1CN(c2ccc(F)cc2)C(=O)c2cc(COc3ccc(C(F)(F)F)cc3)nn21 10.1021/acs.jmedchem.5b01005
CHEMBL3617509 123521 None 0 Rat Functional pIC50 = 5.7 5.7 - 1
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 419 4 0 4 4.8 C[C@@H]1CN(c2ccc(F)cc2)C(=O)c2cc(COc3ccc(C(F)(F)F)cc3)nn21 10.1021/acs.jmedchem.5b01005
122190400 123576 None 0 Rat Functional pIC50 = 6.7 6.7 11 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 388 4 0 5 3.5 C[C@@H]1CN(c2cccc(F)c2F)C(=O)c2cc(COc3ccc(F)cn3)nn21 10.1021/acs.jmedchem.5b01005
CHEMBL3617623 123576 None 0 Rat Functional pIC50 = 6.7 6.7 11 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 388 4 0 5 3.5 C[C@@H]1CN(c2cccc(F)c2F)C(=O)c2cc(COc3ccc(F)cn3)nn21 10.1021/acs.jmedchem.5b01005
122190325 123521 None 0 Rat Functional pIC50 = 5.7 5.7 - 1
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 419 4 0 4 4.8 C[C@@H]1CN(c2ccc(F)cc2)C(=O)c2cc(COc3ccc(C(F)(F)F)cc3)nn21 10.1021/acs.jmedchem.5b01005
CHEMBL3617509 123521 None 0 Rat Functional pIC50 = 5.7 5.7 - 1
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 419 4 0 4 4.8 C[C@@H]1CN(c2ccc(F)cc2)C(=O)c2cc(COc3ccc(C(F)(F)F)cc3)nn21 10.1021/acs.jmedchem.5b01005
122190390 123566 None 0 Rat Functional pIC50 = 6.7 6.7 14 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 370 4 0 5 3.4 C[C@@H]1CN(c2cccc(F)c2)C(=O)c2cc(COc3ccc(F)cn3)nn21 10.1021/acs.jmedchem.5b01005
CHEMBL3617613 123566 None 0 Rat Functional pIC50 = 6.7 6.7 14 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 370 4 0 5 3.4 C[C@@H]1CN(c2cccc(F)c2)C(=O)c2cc(COc3ccc(F)cn3)nn21 10.1021/acs.jmedchem.5b01005
122190390 123566 None 0 Rat Functional pIC50 = 6.7 6.7 14 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 370 4 0 5 3.4 C[C@@H]1CN(c2cccc(F)c2)C(=O)c2cc(COc3ccc(F)cn3)nn21 10.1021/acs.jmedchem.5b01005
CHEMBL3617613 123566 None 0 Rat Functional pIC50 = 6.7 6.7 14 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 370 4 0 5 3.4 C[C@@H]1CN(c2cccc(F)c2)C(=O)c2cc(COc3ccc(F)cn3)nn21 10.1021/acs.jmedchem.5b01005
122190393 123569 None 0 Rat Functional pIC50 = 6.7 6.7 1 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 386 4 0 5 3.9 C[C@@H]1CN(c2ccc(Cl)cc2)C(=O)c2cc(COc3ccc(F)cn3)nn21 10.1021/acs.jmedchem.5b01005
CHEMBL3617616 123569 None 0 Rat Functional pIC50 = 6.7 6.7 1 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 386 4 0 5 3.9 C[C@@H]1CN(c2ccc(Cl)cc2)C(=O)c2cc(COc3ccc(F)cn3)nn21 10.1021/acs.jmedchem.5b01005
44329024 210817 None 0 Rat Functional pIC50 = 6.7 6.7 11 3
Antagonistic activity against metabotropic glutamate receptor 3 (mGluR3) was evaluatedAntagonistic activity against metabotropic glutamate receptor 3 (mGluR3) was evaluated
ChEMBL 395 7 3 4 3.8 CCC[C@@H]1[C@H](C(=O)O)[C@H]1C(N)(CC1c2ccccc2Oc2ccccc21)C(=O)O 10.1016/s0960-894x(98)00510-1
CHEMBL99462 210817 None 0 Rat Functional pIC50 = 6.7 6.7 11 3
Antagonistic activity against metabotropic glutamate receptor 3 (mGluR3) was evaluatedAntagonistic activity against metabotropic glutamate receptor 3 (mGluR3) was evaluated
ChEMBL 395 7 3 4 3.8 CCC[C@@H]1[C@H](C(=O)O)[C@H]1C(N)(CC1c2ccccc2Oc2ccccc21)C(=O)O 10.1016/s0960-894x(98)00510-1
122190393 123569 None 0 Rat Functional pIC50 = 6.7 6.7 1 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 386 4 0 5 3.9 C[C@@H]1CN(c2ccc(Cl)cc2)C(=O)c2cc(COc3ccc(F)cn3)nn21 10.1021/acs.jmedchem.5b01005
CHEMBL3617616 123569 None 0 Rat Functional pIC50 = 6.7 6.7 1 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 386 4 0 5 3.9 C[C@@H]1CN(c2ccc(Cl)cc2)C(=O)c2cc(COc3ccc(F)cn3)nn21 10.1021/acs.jmedchem.5b01005
122190398 123574 None 0 Rat Functional pIC50 = 6.7 6.7 - 1
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 382 5 0 6 3.2 COc1cccc(N2C[C@@H](C)n3nc(COc4ccc(F)cn4)cc3C2=O)c1 10.1021/acs.jmedchem.5b01005
CHEMBL3617621 123574 None 0 Rat Functional pIC50 = 6.7 6.7 - 1
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 382 5 0 6 3.2 COc1cccc(N2C[C@@H](C)n3nc(COc4ccc(F)cn4)cc3C2=O)c1 10.1021/acs.jmedchem.5b01005
122190398 123574 None 0 Rat Functional pIC50 = 6.7 6.7 - 1
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 382 5 0 6 3.2 COc1cccc(N2C[C@@H](C)n3nc(COc4ccc(F)cn4)cc3C2=O)c1 10.1021/acs.jmedchem.5b01005
CHEMBL3617621 123574 None 0 Rat Functional pIC50 = 6.7 6.7 - 1
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 382 5 0 6 3.2 COc1cccc(N2C[C@@H](C)n3nc(COc4ccc(F)cn4)cc3C2=O)c1 10.1021/acs.jmedchem.5b01005
90643966 112061 None 0 Rat Functional pIC50 = 5.7 5.7 1 2
Inhibition of rat mGlu3 receptor transfected in HEK293 cells coexpressing mouse Galpha15 assessed as decrease in glutamate-induced calcium signaling by fluorescence plate reader analysis in presence of glutamate at EC87 concentrationInhibition of rat mGlu3 receptor transfected in HEK293 cells coexpressing mouse Galpha15 assessed as decrease in glutamate-induced calcium signaling by fluorescence plate reader analysis in presence of glutamate at EC87 concentration
ChEMBL 448 3 1 6 3.3 Cn1c(=O)c2ccc(-c3cccc(S(N)(=O)=O)c3)cc2n2nc(-c3ccc(F)cc3)cc12 10.1016/j.bmcl.2014.04.051
CHEMBL3288660 112061 None 0 Rat Functional pIC50 = 5.7 5.7 1 2
Inhibition of rat mGlu3 receptor transfected in HEK293 cells coexpressing mouse Galpha15 assessed as decrease in glutamate-induced calcium signaling by fluorescence plate reader analysis in presence of glutamate at EC87 concentrationInhibition of rat mGlu3 receptor transfected in HEK293 cells coexpressing mouse Galpha15 assessed as decrease in glutamate-induced calcium signaling by fluorescence plate reader analysis in presence of glutamate at EC87 concentration
ChEMBL 448 3 1 6 3.3 Cn1c(=O)c2ccc(-c3cccc(S(N)(=O)=O)c3)cc2n2nc(-c3ccc(F)cc3)cc12 10.1016/j.bmcl.2014.04.051
69669747 183759 None 14 Human Functional pIC50 = 8.6 8.6 2 4
Antagonist activity at human recombinant mGlu3 stably expressed in golden hamster AV12 cell membrane co-expressing Galpha15 assessed as assessed as reduction in glutamate-induced calcium influx incubated for 90 to 120 min by Fluo-4-AM dye based FLIPR assayAntagonist activity at human recombinant mGlu3 stably expressed in golden hamster AV12 cell membrane co-expressing Galpha15 assessed as assessed as reduction in glutamate-induced calcium influx incubated for 90 to 120 min by Fluo-4-AM dye based FLIPR assay
ChEMBL 359 5 4 5 0.8 N[C@@]1(C(=O)O)[C@H](CSc2ccc(F)c(F)c2)[C@@H](O)[C@@H]2[C@H]1[C@H]2C(=O)O 10.1021/acs.jmedchem.6b01119
CHEMBL4751065 183759 None 14 Human Functional pIC50 = 8.6 8.6 2 4
Antagonist activity at human recombinant mGlu3 stably expressed in golden hamster AV12 cell membrane co-expressing Galpha15 assessed as assessed as reduction in glutamate-induced calcium influx incubated for 90 to 120 min by Fluo-4-AM dye based FLIPR assayAntagonist activity at human recombinant mGlu3 stably expressed in golden hamster AV12 cell membrane co-expressing Galpha15 assessed as assessed as reduction in glutamate-induced calcium influx incubated for 90 to 120 min by Fluo-4-AM dye based FLIPR assay
ChEMBL 359 5 4 5 0.8 N[C@@]1(C(=O)O)[C@H](CSc2ccc(F)c(F)c2)[C@@H](O)[C@@H]2[C@H]1[C@H]2C(=O)O 10.1021/acs.jmedchem.6b01119
CHEMBL4802733 183759 None 14 Human Functional pIC50 = 8.6 8.6 2 4
Antagonist activity at human recombinant mGlu3 stably expressed in golden hamster AV12 cell membrane co-expressing Galpha15 assessed as assessed as reduction in glutamate-induced calcium influx incubated for 90 to 120 min by Fluo-4-AM dye based FLIPR assayAntagonist activity at human recombinant mGlu3 stably expressed in golden hamster AV12 cell membrane co-expressing Galpha15 assessed as assessed as reduction in glutamate-induced calcium influx incubated for 90 to 120 min by Fluo-4-AM dye based FLIPR assay
ChEMBL 359 5 4 5 0.8 N[C@@]1(C(=O)O)[C@H](CSc2ccc(F)c(F)c2)[C@@H](O)[C@@H]2[C@H]1[C@H]2C(=O)O 10.1021/acs.jmedchem.6b01119
1378 2417 None 39 Human Functional pIC50 = 8.6 8.6 2 14
Antagonist activity at human recombinant mGlu3 stably expressed in golden hamster AV12 cell membrane co-expressing Galpha15 assessed as assessed as reduction in glutamate-induced calcium influx incubated for 90 to 120 min by Fluo-4-AM dye based FLIPR assayAntagonist activity at human recombinant mGlu3 stably expressed in golden hamster AV12 cell membrane co-expressing Galpha15 assessed as assessed as reduction in glutamate-induced calcium influx incubated for 90 to 120 min by Fluo-4-AM dye based FLIPR assay
ChEMBL 353 5 3 4 2.8 OC(=O)[C@H]1C[C@@H]1[C@](C(=O)O)(CC1c2ccccc2Oc2c1cccc2)N 10.1021/acs.jmedchem.6b01119
1399 2417 None 39 Human Functional pIC50 = 8.6 8.6 2 14
Antagonist activity at human recombinant mGlu3 stably expressed in golden hamster AV12 cell membrane co-expressing Galpha15 assessed as assessed as reduction in glutamate-induced calcium influx incubated for 90 to 120 min by Fluo-4-AM dye based FLIPR assayAntagonist activity at human recombinant mGlu3 stably expressed in golden hamster AV12 cell membrane co-expressing Galpha15 assessed as assessed as reduction in glutamate-induced calcium influx incubated for 90 to 120 min by Fluo-4-AM dye based FLIPR assay
ChEMBL 353 5 3 4 2.8 OC(=O)[C@H]1C[C@@H]1[C@](C(=O)O)(CC1c2ccccc2Oc2c1cccc2)N 10.1021/acs.jmedchem.6b01119
9819927 2417 None 39 Human Functional pIC50 = 8.6 8.6 2 14
Antagonist activity at human recombinant mGlu3 stably expressed in golden hamster AV12 cell membrane co-expressing Galpha15 assessed as assessed as reduction in glutamate-induced calcium influx incubated for 90 to 120 min by Fluo-4-AM dye based FLIPR assayAntagonist activity at human recombinant mGlu3 stably expressed in golden hamster AV12 cell membrane co-expressing Galpha15 assessed as assessed as reduction in glutamate-induced calcium influx incubated for 90 to 120 min by Fluo-4-AM dye based FLIPR assay
ChEMBL 353 5 3 4 2.8 OC(=O)[C@H]1C[C@@H]1[C@](C(=O)O)(CC1c2ccccc2Oc2c1cccc2)N 10.1021/acs.jmedchem.6b01119
CHEMBL432038 2417 None 39 Human Functional pIC50 = 8.6 8.6 2 14
Antagonist activity at human recombinant mGlu3 stably expressed in golden hamster AV12 cell membrane co-expressing Galpha15 assessed as assessed as reduction in glutamate-induced calcium influx incubated for 90 to 120 min by Fluo-4-AM dye based FLIPR assayAntagonist activity at human recombinant mGlu3 stably expressed in golden hamster AV12 cell membrane co-expressing Galpha15 assessed as assessed as reduction in glutamate-induced calcium influx incubated for 90 to 120 min by Fluo-4-AM dye based FLIPR assay
ChEMBL 353 5 3 4 2.8 OC(=O)[C@H]1C[C@@H]1[C@](C(=O)O)(CC1c2ccccc2Oc2c1cccc2)N 10.1021/acs.jmedchem.6b01119
67707808 148730 None 0 Human Functional pIC50 = 7.7 7.7 -1 2
Antagonist activity at recombinant human mGlu3 receptor expressed in hamster AV12 cells co-expressing human EAAT1 assessed as reduction of DCG-4-inhibited forskolin-stimulated cAMP formation after 20 mins by HTRF assayAntagonist activity at recombinant human mGlu3 receptor expressed in hamster AV12 cells co-expressing human EAAT1 assessed as reduction of DCG-4-inhibited forskolin-stimulated cAMP formation after 20 mins by HTRF assay
ChEMBL 432 6 4 6 1.3 COC(=O)N[C@H]1[C@H]2[C@H](C(=O)O)[C@H]2[C@](N)(C(=O)O)[C@@H]1OCc1ccc(Cl)c(Cl)c1 10.1016/j.bmcl.2016.10.067
CHEMBL3939492 148730 None 0 Human Functional pIC50 = 7.7 7.7 -1 2
Antagonist activity at recombinant human mGlu3 receptor expressed in hamster AV12 cells co-expressing human EAAT1 assessed as reduction of DCG-4-inhibited forskolin-stimulated cAMP formation after 20 mins by HTRF assayAntagonist activity at recombinant human mGlu3 receptor expressed in hamster AV12 cells co-expressing human EAAT1 assessed as reduction of DCG-4-inhibited forskolin-stimulated cAMP formation after 20 mins by HTRF assay
ChEMBL 432 6 4 6 1.3 COC(=O)N[C@H]1[C@H]2[C@H](C(=O)O)[C@H]2[C@](N)(C(=O)O)[C@@H]1OCc1ccc(Cl)c(Cl)c1 10.1016/j.bmcl.2016.10.067
44348859 16571 None 0 Human Functional pIC50 = 6.7 6.7 15 2
Effect on 1S,3R-ACPD-induced inhibition of forskolin stimulated cyclic-AMP in RGT cells expressing human Metabotropic glutamate receptor 3Effect on 1S,3R-ACPD-induced inhibition of forskolin stimulated cyclic-AMP in RGT cells expressing human Metabotropic glutamate receptor 3
ChEMBL 278 6 4 4 0.7 Nc1cccc(CC[C@](N)(C(=O)O)C2C[C@@H]2C(=O)O)c1 10.1021/jm970498o
CHEMBL123842 16571 None 0 Human Functional pIC50 = 6.7 6.7 15 2
Effect on 1S,3R-ACPD-induced inhibition of forskolin stimulated cyclic-AMP in RGT cells expressing human Metabotropic glutamate receptor 3Effect on 1S,3R-ACPD-induced inhibition of forskolin stimulated cyclic-AMP in RGT cells expressing human Metabotropic glutamate receptor 3
ChEMBL 278 6 4 4 0.7 Nc1cccc(CC[C@](N)(C(=O)O)C2C[C@@H]2C(=O)O)c1 10.1021/jm970498o
162658781 183797 None 0 Human Functional pIC50 = 6.7 6.7 -1 2
Antagonist activity at human recombinant mGlu3 receptor stably expressed in golden hamster AV12 cells co-expressing rat EAAT1 assessed as reduction in DCG IV-induced inhibition of forskolin-stimulated cAMP accumulation preincubated for 20 mins followed by incubation with cAMP-d2 conjugate and anti-cAMP cryptate for 1 hr by HTRF assayAntagonist activity at human recombinant mGlu3 receptor stably expressed in golden hamster AV12 cells co-expressing rat EAAT1 assessed as reduction in DCG IV-induced inhibition of forskolin-stimulated cAMP accumulation preincubated for 20 mins followed by incubation with cAMP-d2 conjugate and anti-cAMP cryptate for 1 hr by HTRF assay
ChEMBL 323 5 4 5 0.5 N[C@@]1(C(=O)O)[C@H](CSc2ccccc2)[C@@H](O)[C@@H]2[C@H]1[C@H]2C(=O)O 10.1021/acs.jmedchem.6b01119
CHEMBL4759209 183797 None 0 Human Functional pIC50 = 6.7 6.7 -1 2
Antagonist activity at human recombinant mGlu3 receptor stably expressed in golden hamster AV12 cells co-expressing rat EAAT1 assessed as reduction in DCG IV-induced inhibition of forskolin-stimulated cAMP accumulation preincubated for 20 mins followed by incubation with cAMP-d2 conjugate and anti-cAMP cryptate for 1 hr by HTRF assayAntagonist activity at human recombinant mGlu3 receptor stably expressed in golden hamster AV12 cells co-expressing rat EAAT1 assessed as reduction in DCG IV-induced inhibition of forskolin-stimulated cAMP accumulation preincubated for 20 mins followed by incubation with cAMP-d2 conjugate and anti-cAMP cryptate for 1 hr by HTRF assay
ChEMBL 323 5 4 5 0.5 N[C@@]1(C(=O)O)[C@H](CSc2ccccc2)[C@@H](O)[C@@H]2[C@H]1[C@H]2C(=O)O 10.1021/acs.jmedchem.6b01119
CHEMBL4803105 183797 None 0 Human Functional pIC50 = 6.7 6.7 -1 2
Antagonist activity at human recombinant mGlu3 receptor stably expressed in golden hamster AV12 cells co-expressing rat EAAT1 assessed as reduction in DCG IV-induced inhibition of forskolin-stimulated cAMP accumulation preincubated for 20 mins followed by incubation with cAMP-d2 conjugate and anti-cAMP cryptate for 1 hr by HTRF assayAntagonist activity at human recombinant mGlu3 receptor stably expressed in golden hamster AV12 cells co-expressing rat EAAT1 assessed as reduction in DCG IV-induced inhibition of forskolin-stimulated cAMP accumulation preincubated for 20 mins followed by incubation with cAMP-d2 conjugate and anti-cAMP cryptate for 1 hr by HTRF assay
ChEMBL 323 5 4 5 0.5 N[C@@]1(C(=O)O)[C@H](CSc2ccccc2)[C@@H](O)[C@@H]2[C@H]1[C@H]2C(=O)O 10.1021/acs.jmedchem.6b01119
122190408 123584 None 0 Rat Functional pIC50 = 6.7 6.7 29 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 386 4 0 5 3.9 C[C@@H]1CN(c2cccc(F)c2)C(=O)c2cc(COc3ccc(Cl)cn3)nn21 10.1021/acs.jmedchem.5b01005
CHEMBL3617631 123584 None 0 Rat Functional pIC50 = 6.7 6.7 29 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 386 4 0 5 3.9 C[C@@H]1CN(c2cccc(F)c2)C(=O)c2cc(COc3ccc(Cl)cn3)nn21 10.1021/acs.jmedchem.5b01005
137634033 156732 None 0 Human Functional pIC50 = 5.7 5.7 1 2
Antagonist activity at human mGlu3 receptor expressed in HEK cells assessed as reversal of DCG-4 inhibited forskolin-stimulated cAMP formation after 20 mins by HTRF assayAntagonist activity at human mGlu3 receptor expressed in HEK cells assessed as reversal of DCG-4 inhibited forskolin-stimulated cAMP formation after 20 mins by HTRF assay
ChEMBL 332 6 4 4 0.2 N[C@@]1(C(=O)O)C[C@H](NC(=O)CCc2ccccc2)[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/acs.jmedchem.7b01481
CHEMBL4069251 156732 None 0 Human Functional pIC50 = 5.7 5.7 1 2
Antagonist activity at human mGlu3 receptor expressed in HEK cells assessed as reversal of DCG-4 inhibited forskolin-stimulated cAMP formation after 20 mins by HTRF assayAntagonist activity at human mGlu3 receptor expressed in HEK cells assessed as reversal of DCG-4 inhibited forskolin-stimulated cAMP formation after 20 mins by HTRF assay
ChEMBL 332 6 4 4 0.2 N[C@@]1(C(=O)O)C[C@H](NC(=O)CCc2ccccc2)[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/acs.jmedchem.7b01481
122190408 123584 None 0 Rat Functional pIC50 = 6.7 6.7 29 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 386 4 0 5 3.9 C[C@@H]1CN(c2cccc(F)c2)C(=O)c2cc(COc3ccc(Cl)cn3)nn21 10.1021/acs.jmedchem.5b01005
CHEMBL3617631 123584 None 0 Rat Functional pIC50 = 6.7 6.7 29 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 386 4 0 5 3.9 C[C@@H]1CN(c2cccc(F)c2)C(=O)c2cc(COc3ccc(Cl)cn3)nn21 10.1021/acs.jmedchem.5b01005
122190333 123529 None 0 Rat Functional pIC50 = 5.7 5.7 - 1
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 366 4 0 5 3.5 Cc1ccnc(OCc2cc3n(n2)[C@H](C)CN(c2ccc(F)cc2)C3=O)c1 10.1021/acs.jmedchem.5b01005
CHEMBL3617517 123529 None 0 Rat Functional pIC50 = 5.7 5.7 - 1
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 366 4 0 5 3.5 Cc1ccnc(OCc2cc3n(n2)[C@H](C)CN(c2ccc(F)cc2)C3=O)c1 10.1021/acs.jmedchem.5b01005
122190333 123529 None 0 Rat Functional pIC50 = 5.7 5.7 - 1
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 366 4 0 5 3.5 Cc1ccnc(OCc2cc3n(n2)[C@H](C)CN(c2ccc(F)cc2)C3=O)c1 10.1021/acs.jmedchem.5b01005
CHEMBL3617517 123529 None 0 Rat Functional pIC50 = 5.7 5.7 - 1
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 366 4 0 5 3.5 Cc1ccnc(OCc2cc3n(n2)[C@H](C)CN(c2ccc(F)cc2)C3=O)c1 10.1021/acs.jmedchem.5b01005
44348706 116946 None 0 Human Functional pIC50 = 6.7 6.7 -1 2
Effect on 1S,3R-ACPD-induced inhibition of forskolin stimulated cyclic-AMP in RGT cells expressing human Metabotropic glutamate receptor 3Effect on 1S,3R-ACPD-induced inhibition of forskolin stimulated cyclic-AMP in RGT cells expressing human Metabotropic glutamate receptor 3
ChEMBL 281 6 3 3 1.3 N[C@@](CCc1ccc(F)cc1)(C(=O)O)C1C[C@@H]1C(=O)O 10.1021/jm970498o
CHEMBL338282 116946 None 0 Human Functional pIC50 = 6.7 6.7 -1 2
Effect on 1S,3R-ACPD-induced inhibition of forskolin stimulated cyclic-AMP in RGT cells expressing human Metabotropic glutamate receptor 3Effect on 1S,3R-ACPD-induced inhibition of forskolin stimulated cyclic-AMP in RGT cells expressing human Metabotropic glutamate receptor 3
ChEMBL 281 6 3 3 1.3 N[C@@](CCc1ccc(F)cc1)(C(=O)O)C1C[C@@H]1C(=O)O 10.1021/jm970498o
10091203 12956 None 0 Rat Functional pIC50 = 4.7 4.7 1 3
Inhibitory concentration required for antagonistic activity at Metabotropic glutamate receptor 3Inhibitory concentration required for antagonistic activity at Metabotropic glutamate receptor 3
ChEMBL 308 5 4 5 -0.2 N[C@]1(C(=O)O)C[C@H](C(=O)O)N(C(C(=O)O)c2ccccc2)C1 10.1016/s0960-894x(01)00329-8
CHEMBL1189303 12956 None 0 Rat Functional pIC50 = 4.7 4.7 1 3
Inhibitory concentration required for antagonistic activity at Metabotropic glutamate receptor 3Inhibitory concentration required for antagonistic activity at Metabotropic glutamate receptor 3
ChEMBL 308 5 4 5 -0.2 N[C@]1(C(=O)O)C[C@H](C(=O)O)N(C(C(=O)O)c2ccccc2)C1 10.1016/s0960-894x(01)00329-8
CHEMBL538489 12956 None 0 Rat Functional pIC50 = 4.7 4.7 1 3
Inhibitory concentration required for antagonistic activity at Metabotropic glutamate receptor 3Inhibitory concentration required for antagonistic activity at Metabotropic glutamate receptor 3
ChEMBL 308 5 4 5 -0.2 N[C@]1(C(=O)O)C[C@H](C(=O)O)N(C(C(=O)O)c2ccccc2)C1 10.1016/s0960-894x(01)00329-8
122190395 123571 None 0 Rat Functional pIC50 = 6.7 6.7 - 1
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 366 4 0 5 3.5 Cc1cccc(N2C[C@@H](C)n3nc(COc4ccc(F)cn4)cc3C2=O)c1 10.1021/acs.jmedchem.5b01005
CHEMBL3617618 123571 None 0 Rat Functional pIC50 = 6.7 6.7 - 1
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 366 4 0 5 3.5 Cc1cccc(N2C[C@@H](C)n3nc(COc4ccc(F)cn4)cc3C2=O)c1 10.1021/acs.jmedchem.5b01005
122190395 123571 None 0 Rat Functional pIC50 = 6.7 6.7 - 1
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 366 4 0 5 3.5 Cc1cccc(N2C[C@@H](C)n3nc(COc4ccc(F)cn4)cc3C2=O)c1 10.1021/acs.jmedchem.5b01005
CHEMBL3617618 123571 None 0 Rat Functional pIC50 = 6.7 6.7 - 1
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 366 4 0 5 3.5 Cc1cccc(N2C[C@@H](C)n3nc(COc4ccc(F)cn4)cc3C2=O)c1 10.1021/acs.jmedchem.5b01005
162663798 183825 None 0 Human Functional pIC50 = 5.7 5.7 -1 2
Antagonist activity at human recombinant mGlu3 receptor stably expressed in golden hamster AV12 cells co-expressing rat EAAT1 assessed as reduction in DCG IV-induced inhibition of forskolin-stimulated cAMP accumulation preincubated for 20 mins followed by incubation with cAMP-d2 conjugate and anti-cAMP cryptate for 1 hr by HTRF assayAntagonist activity at human recombinant mGlu3 receptor stably expressed in golden hamster AV12 cells co-expressing rat EAAT1 assessed as reduction in DCG IV-induced inhibition of forskolin-stimulated cAMP accumulation preincubated for 20 mins followed by incubation with cAMP-d2 conjugate and anti-cAMP cryptate for 1 hr by HTRF assay
ChEMBL 323 5 4 5 0.5 N[C@]1(C(=O)O)[C@@H]2[C@@H](C(=O)O)[C@@H]2[C@@H](O)[C@@H]1CSc1ccccc1 10.1021/acs.jmedchem.6b01119
CHEMBL4779554 183825 None 0 Human Functional pIC50 = 5.7 5.7 -1 2
Antagonist activity at human recombinant mGlu3 receptor stably expressed in golden hamster AV12 cells co-expressing rat EAAT1 assessed as reduction in DCG IV-induced inhibition of forskolin-stimulated cAMP accumulation preincubated for 20 mins followed by incubation with cAMP-d2 conjugate and anti-cAMP cryptate for 1 hr by HTRF assayAntagonist activity at human recombinant mGlu3 receptor stably expressed in golden hamster AV12 cells co-expressing rat EAAT1 assessed as reduction in DCG IV-induced inhibition of forskolin-stimulated cAMP accumulation preincubated for 20 mins followed by incubation with cAMP-d2 conjugate and anti-cAMP cryptate for 1 hr by HTRF assay
ChEMBL 323 5 4 5 0.5 N[C@]1(C(=O)O)[C@@H]2[C@@H](C(=O)O)[C@@H]2[C@@H](O)[C@@H]1CSc1ccccc1 10.1021/acs.jmedchem.6b01119
CHEMBL4803378 183825 None 0 Human Functional pIC50 = 5.7 5.7 -1 2
Antagonist activity at human recombinant mGlu3 receptor stably expressed in golden hamster AV12 cells co-expressing rat EAAT1 assessed as reduction in DCG IV-induced inhibition of forskolin-stimulated cAMP accumulation preincubated for 20 mins followed by incubation with cAMP-d2 conjugate and anti-cAMP cryptate for 1 hr by HTRF assayAntagonist activity at human recombinant mGlu3 receptor stably expressed in golden hamster AV12 cells co-expressing rat EAAT1 assessed as reduction in DCG IV-induced inhibition of forskolin-stimulated cAMP accumulation preincubated for 20 mins followed by incubation with cAMP-d2 conjugate and anti-cAMP cryptate for 1 hr by HTRF assay
ChEMBL 323 5 4 5 0.5 N[C@]1(C(=O)O)[C@@H]2[C@@H](C(=O)O)[C@@H]2[C@@H](O)[C@@H]1CSc1ccccc1 10.1021/acs.jmedchem.6b01119
122190407 123583 None 0 Rat Functional pIC50 = 6.7 6.7 14 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 386 4 0 5 3.9 C[C@@H]1CN(c2ccccc2F)C(=O)c2cc(COc3ccc(Cl)cn3)nn21 10.1021/acs.jmedchem.5b01005
CHEMBL3617630 123583 None 0 Rat Functional pIC50 = 6.7 6.7 14 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 386 4 0 5 3.9 C[C@@H]1CN(c2ccccc2F)C(=O)c2cc(COc3ccc(Cl)cn3)nn21 10.1021/acs.jmedchem.5b01005
122190423 123599 None 0 Rat Functional pIC50 = 6.7 6.7 6 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 404 4 0 5 4.0 C[C@@H]1CN(c2c(F)cccc2F)C(=O)c2cc(COc3ccc(Cl)cn3)nn21 10.1021/acs.jmedchem.5b01005
CHEMBL3617646 123599 None 0 Rat Functional pIC50 = 6.7 6.7 6 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 404 4 0 5 4.0 C[C@@H]1CN(c2c(F)cccc2F)C(=O)c2cc(COc3ccc(Cl)cn3)nn21 10.1021/acs.jmedchem.5b01005
122190423 123599 None 0 Rat Functional pIC50 = 6.7 6.7 6 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 404 4 0 5 4.0 C[C@@H]1CN(c2c(F)cccc2F)C(=O)c2cc(COc3ccc(Cl)cn3)nn21 10.1021/acs.jmedchem.5b01005
CHEMBL3617646 123599 None 0 Rat Functional pIC50 = 6.7 6.7 6 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 404 4 0 5 4.0 C[C@@H]1CN(c2c(F)cccc2F)C(=O)c2cc(COc3ccc(Cl)cn3)nn21 10.1021/acs.jmedchem.5b01005
122190407 123583 None 0 Rat Functional pIC50 = 6.7 6.7 14 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 386 4 0 5 3.9 C[C@@H]1CN(c2ccccc2F)C(=O)c2cc(COc3ccc(Cl)cn3)nn21 10.1021/acs.jmedchem.5b01005
CHEMBL3617630 123583 None 0 Rat Functional pIC50 = 6.7 6.7 14 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 386 4 0 5 3.9 C[C@@H]1CN(c2ccccc2F)C(=O)c2cc(COc3ccc(Cl)cn3)nn21 10.1021/acs.jmedchem.5b01005
67705089 152344 None 0 Human Functional pIC50 = 7.6 7.6 -1 2
Antagonist activity at recombinant human mGlu3 receptor expressed in hamster AV12 cells co-expressing human EAAT1 assessed as reduction of DCG-4-inhibited forskolin-stimulated cAMP formation after 20 mins by HTRF assayAntagonist activity at recombinant human mGlu3 receptor expressed in hamster AV12 cells co-expressing human EAAT1 assessed as reduction of DCG-4-inhibited forskolin-stimulated cAMP formation after 20 mins by HTRF assay
ChEMBL 458 7 4 7 1.9 N[C@@]1(C(=O)O)[C@H](OCc2ccc(Cl)c(Cl)c2)[C@@H](Sc2nc[nH]n2)[C@H]2[C@H](C(=O)O)[C@H]21 10.1016/j.bmcl.2016.10.067
CHEMBL3969063 152344 None 0 Human Functional pIC50 = 7.6 7.6 -1 2
Antagonist activity at recombinant human mGlu3 receptor expressed in hamster AV12 cells co-expressing human EAAT1 assessed as reduction of DCG-4-inhibited forskolin-stimulated cAMP formation after 20 mins by HTRF assayAntagonist activity at recombinant human mGlu3 receptor expressed in hamster AV12 cells co-expressing human EAAT1 assessed as reduction of DCG-4-inhibited forskolin-stimulated cAMP formation after 20 mins by HTRF assay
ChEMBL 458 7 4 7 1.9 N[C@@]1(C(=O)O)[C@H](OCc2ccc(Cl)c(Cl)c2)[C@@H](Sc2nc[nH]n2)[C@H]2[C@H](C(=O)O)[C@H]21 10.1016/j.bmcl.2016.10.067
10250423 13018 None 0 Rat Functional pIC50 = 4.6 4.6 1 2
Inhibitory concentration required for antagonistic activity at Metabotropic glutamate receptor 3Inhibitory concentration required for antagonistic activity at Metabotropic glutamate receptor 3
ChEMBL 364 4 3 4 1.5 N[C@]1(C(=O)O)C[C@H](C(=O)O)N(Cc2ccccc2C#Cc2ccccc2)C1 10.1016/s0960-894x(01)00329-8
CHEMBL1189797 13018 None 0 Rat Functional pIC50 = 4.6 4.6 1 2
Inhibitory concentration required for antagonistic activity at Metabotropic glutamate receptor 3Inhibitory concentration required for antagonistic activity at Metabotropic glutamate receptor 3
ChEMBL 364 4 3 4 1.5 N[C@]1(C(=O)O)C[C@H](C(=O)O)N(Cc2ccccc2C#Cc2ccccc2)C1 10.1016/s0960-894x(01)00329-8
CHEMBL539516 13018 None 0 Rat Functional pIC50 = 4.6 4.6 1 2
Inhibitory concentration required for antagonistic activity at Metabotropic glutamate receptor 3Inhibitory concentration required for antagonistic activity at Metabotropic glutamate receptor 3
ChEMBL 364 4 3 4 1.5 N[C@]1(C(=O)O)C[C@H](C(=O)O)N(Cc2ccccc2C#Cc2ccccc2)C1 10.1016/s0960-894x(01)00329-8
122190339 123535 None 0 Rat Functional pIC50 = 5.6 5.6 - 1
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 420 4 0 5 4.2 C[C@@H]1CN(c2ccc(F)cc2)C(=O)c2cc(COc3cccc(C(F)(F)F)n3)nn21 10.1021/acs.jmedchem.5b01005
CHEMBL3617523 123535 None 0 Rat Functional pIC50 = 5.6 5.6 - 1
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 420 4 0 5 4.2 C[C@@H]1CN(c2ccc(F)cc2)C(=O)c2cc(COc3cccc(C(F)(F)F)n3)nn21 10.1021/acs.jmedchem.5b01005
71136654 123475 None 0 Human Functional pIC50 = 5.6 5.6 -3 2
Antagonist activity at human recombinant mGlu3 receptor expressed in AV12 cells assessed as inhibition of glutamate-stimulated Ca2+ mobilization after 1.5 hrs by FLIPR assayAntagonist activity at human recombinant mGlu3 receptor expressed in AV12 cells assessed as inhibition of glutamate-stimulated Ca2+ mobilization after 1.5 hrs by FLIPR assay
ChEMBL 326 5 4 6 0.5 CC(C)c1nnc(S[C@H]2C[C@@](N)(C(=O)O)[C@@H]3[C@@H](C(=O)O)[C@H]23)[nH]1 10.1021/acs.jmedchem.5b01124
CHEMBL3616859 123475 None 0 Human Functional pIC50 = 5.6 5.6 -3 2
Antagonist activity at human recombinant mGlu3 receptor expressed in AV12 cells assessed as inhibition of glutamate-stimulated Ca2+ mobilization after 1.5 hrs by FLIPR assayAntagonist activity at human recombinant mGlu3 receptor expressed in AV12 cells assessed as inhibition of glutamate-stimulated Ca2+ mobilization after 1.5 hrs by FLIPR assay
ChEMBL 326 5 4 6 0.5 CC(C)c1nnc(S[C@H]2C[C@@](N)(C(=O)O)[C@@H]3[C@@H](C(=O)O)[C@H]23)[nH]1 10.1021/acs.jmedchem.5b01124
122190339 123535 None 0 Rat Functional pIC50 = 5.6 5.6 - 1
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 420 4 0 5 4.2 C[C@@H]1CN(c2ccc(F)cc2)C(=O)c2cc(COc3cccc(C(F)(F)F)n3)nn21 10.1021/acs.jmedchem.5b01005
CHEMBL3617523 123535 None 0 Rat Functional pIC50 = 5.6 5.6 - 1
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 420 4 0 5 4.2 C[C@@H]1CN(c2ccc(F)cc2)C(=O)c2cc(COc3cccc(C(F)(F)F)n3)nn21 10.1021/acs.jmedchem.5b01005
122190338 123534 None 0 Rat Functional pIC50 = 5.6 5.6 -1 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 366 4 0 5 3.5 Cc1cccc(OCc2cc3n(n2)[C@H](C)CN(c2ccc(F)cc2)C3=O)n1 10.1021/acs.jmedchem.5b01005
CHEMBL3617522 123534 None 0 Rat Functional pIC50 = 5.6 5.6 -1 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 366 4 0 5 3.5 Cc1cccc(OCc2cc3n(n2)[C@H](C)CN(c2ccc(F)cc2)C3=O)n1 10.1021/acs.jmedchem.5b01005
71136640 123469 None 0 Human Functional pIC50 = 5.6 5.6 -60 2
Antagonist activity at human recombinant mGlu3 receptor expressed in AV12 cells assessed as reversal of DCG-4-inhibited, forskolin-stimulated cAMP production after 1 hr by fluorescence assayAntagonist activity at human recombinant mGlu3 receptor expressed in AV12 cells assessed as reversal of DCG-4-inhibited, forskolin-stimulated cAMP production after 1 hr by fluorescence assay
ChEMBL 284 4 4 6 -0.6 N[C@@]1(C(=O)O)C[C@@H](Sc2c[nH]nn2)[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/acs.jmedchem.5b01124
CHEMBL3616853 123469 None 0 Human Functional pIC50 = 5.6 5.6 -60 2
Antagonist activity at human recombinant mGlu3 receptor expressed in AV12 cells assessed as reversal of DCG-4-inhibited, forskolin-stimulated cAMP production after 1 hr by fluorescence assayAntagonist activity at human recombinant mGlu3 receptor expressed in AV12 cells assessed as reversal of DCG-4-inhibited, forskolin-stimulated cAMP production after 1 hr by fluorescence assay
ChEMBL 284 4 4 6 -0.6 N[C@@]1(C(=O)O)C[C@@H](Sc2c[nH]nn2)[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/acs.jmedchem.5b01124
134144056 150725 None 0 Human Functional pIC50 = 6.6 6.6 1 2
Antagonist activity at recombinant human mGlu3 receptor expressed in hamster AV12 cells co-expressing human EAAT1 assessed as reduction of DCG-4-inhibited forskolin-stimulated cAMP formation after 20 mins by HTRF assayAntagonist activity at recombinant human mGlu3 receptor expressed in hamster AV12 cells co-expressing human EAAT1 assessed as reduction of DCG-4-inhibited forskolin-stimulated cAMP formation after 20 mins by HTRF assay
ChEMBL 307 5 4 5 -0.3 N[C@@]1(C(=O)O)[C@H](OCc2ccccc2)[C@H](O)[C@@H]2[C@H]1[C@H]2C(=O)O 10.1016/j.bmcl.2016.10.067
CHEMBL3955458 150725 None 0 Human Functional pIC50 = 6.6 6.6 1 2
Antagonist activity at recombinant human mGlu3 receptor expressed in hamster AV12 cells co-expressing human EAAT1 assessed as reduction of DCG-4-inhibited forskolin-stimulated cAMP formation after 20 mins by HTRF assayAntagonist activity at recombinant human mGlu3 receptor expressed in hamster AV12 cells co-expressing human EAAT1 assessed as reduction of DCG-4-inhibited forskolin-stimulated cAMP formation after 20 mins by HTRF assay
ChEMBL 307 5 4 5 -0.3 N[C@@]1(C(=O)O)[C@H](OCc2ccccc2)[C@H](O)[C@@H]2[C@H]1[C@H]2C(=O)O 10.1016/j.bmcl.2016.10.067
122190338 123534 None 0 Rat Functional pIC50 = 5.6 5.6 -1 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 366 4 0 5 3.5 Cc1cccc(OCc2cc3n(n2)[C@H](C)CN(c2ccc(F)cc2)C3=O)n1 10.1021/acs.jmedchem.5b01005
CHEMBL3617522 123534 None 0 Rat Functional pIC50 = 5.6 5.6 -1 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 366 4 0 5 3.5 Cc1cccc(OCc2cc3n(n2)[C@H](C)CN(c2ccc(F)cc2)C3=O)n1 10.1021/acs.jmedchem.5b01005
1397 2529 None 15 Human Functional pIC50 = 7.6 7.6 -1 8
Antagonist activity at mGLUR3 expressed in CHO cells assessed as inhibition of glutamate-induced inhibition of forskolin-stimulated cAMP productionAntagonist activity at mGLUR3 expressed in CHO cells assessed as inhibition of glutamate-induced inhibition of forskolin-stimulated cAMP production
ChEMBL 377 5 3 4 2.1 OC(=O)[C@]1(N)[C@H](OCc2ccc(c(c2)Cl)Cl)C[C@@H]2[C@H]1[C@@]2(F)C(=O)O 10.1016/j.bmcl.2012.01.039
9886034 2529 None 15 Human Functional pIC50 = 7.6 7.6 -1 8
Antagonist activity at mGLUR3 expressed in CHO cells assessed as inhibition of glutamate-induced inhibition of forskolin-stimulated cAMP productionAntagonist activity at mGLUR3 expressed in CHO cells assessed as inhibition of glutamate-induced inhibition of forskolin-stimulated cAMP production
ChEMBL 377 5 3 4 2.1 OC(=O)[C@]1(N)[C@H](OCc2ccc(c(c2)Cl)Cl)C[C@@H]2[C@H]1[C@@]2(F)C(=O)O 10.1016/j.bmcl.2012.01.039
CHEMBL186453 2529 None 15 Human Functional pIC50 = 7.6 7.6 -1 8
Antagonist activity at mGLUR3 expressed in CHO cells assessed as inhibition of glutamate-induced inhibition of forskolin-stimulated cAMP productionAntagonist activity at mGLUR3 expressed in CHO cells assessed as inhibition of glutamate-induced inhibition of forskolin-stimulated cAMP production
ChEMBL 377 5 3 4 2.1 OC(=O)[C@]1(N)[C@H](OCc2ccc(c(c2)Cl)Cl)C[C@@H]2[C@H]1[C@@]2(F)C(=O)O 10.1016/j.bmcl.2012.01.039
162644419 183728 None 0 Human Functional pIC50 = 5.6 5.6 -186 2
Antagonist activity at human recombinant mGlu3 receptor stably expressed in golden hamster AV12 cells co-expressing rat EAAT1 assessed as reduction in DCG IV-induced inhibition of forskolin-stimulated cAMP accumulation preincubated for 20 mins followed by incubation with cAMP-d2 conjugate and anti-cAMP cryptate for 1 hr by HTRF assayAntagonist activity at human recombinant mGlu3 receptor stably expressed in golden hamster AV12 cells co-expressing rat EAAT1 assessed as reduction in DCG IV-induced inhibition of forskolin-stimulated cAMP accumulation preincubated for 20 mins followed by incubation with cAMP-d2 conjugate and anti-cAMP cryptate for 1 hr by HTRF assay
ChEMBL 323 5 4 5 0.5 N[C@]1(C(=O)O)[C@@H]2[C@@H](C(=O)O)[C@@H]2[C@H](O)[C@@H]1CSc1ccccc1 10.1021/acs.jmedchem.6b01119
CHEMBL4778355 183728 None 0 Human Functional pIC50 = 5.6 5.6 -186 2
Antagonist activity at human recombinant mGlu3 receptor stably expressed in golden hamster AV12 cells co-expressing rat EAAT1 assessed as reduction in DCG IV-induced inhibition of forskolin-stimulated cAMP accumulation preincubated for 20 mins followed by incubation with cAMP-d2 conjugate and anti-cAMP cryptate for 1 hr by HTRF assayAntagonist activity at human recombinant mGlu3 receptor stably expressed in golden hamster AV12 cells co-expressing rat EAAT1 assessed as reduction in DCG IV-induced inhibition of forskolin-stimulated cAMP accumulation preincubated for 20 mins followed by incubation with cAMP-d2 conjugate and anti-cAMP cryptate for 1 hr by HTRF assay
ChEMBL 323 5 4 5 0.5 N[C@]1(C(=O)O)[C@@H]2[C@@H](C(=O)O)[C@@H]2[C@H](O)[C@@H]1CSc1ccccc1 10.1021/acs.jmedchem.6b01119
CHEMBL4802356 183728 None 0 Human Functional pIC50 = 5.6 5.6 -186 2
Antagonist activity at human recombinant mGlu3 receptor stably expressed in golden hamster AV12 cells co-expressing rat EAAT1 assessed as reduction in DCG IV-induced inhibition of forskolin-stimulated cAMP accumulation preincubated for 20 mins followed by incubation with cAMP-d2 conjugate and anti-cAMP cryptate for 1 hr by HTRF assayAntagonist activity at human recombinant mGlu3 receptor stably expressed in golden hamster AV12 cells co-expressing rat EAAT1 assessed as reduction in DCG IV-induced inhibition of forskolin-stimulated cAMP accumulation preincubated for 20 mins followed by incubation with cAMP-d2 conjugate and anti-cAMP cryptate for 1 hr by HTRF assay
ChEMBL 323 5 4 5 0.5 N[C@]1(C(=O)O)[C@@H]2[C@@H](C(=O)O)[C@@H]2[C@H](O)[C@@H]1CSc1ccccc1 10.1021/acs.jmedchem.6b01119
71131322 123473 None 0 Human Functional pIC50 = 6.6 6.6 -43 2
Antagonist activity at human recombinant mGlu3 receptor expressed in AV12 cells assessed as inhibition of glutamate-stimulated Ca2+ mobilization after 1.5 hrs by FLIPR assayAntagonist activity at human recombinant mGlu3 receptor expressed in AV12 cells assessed as inhibition of glutamate-stimulated Ca2+ mobilization after 1.5 hrs by FLIPR assay
ChEMBL 334 5 4 6 0.3 N[C@@]1(C(=O)O)C[C@H](Sc2nnc(C(F)F)[nH]2)[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/acs.jmedchem.5b01124
CHEMBL3616857 123473 None 0 Human Functional pIC50 = 6.6 6.6 -43 2
Antagonist activity at human recombinant mGlu3 receptor expressed in AV12 cells assessed as inhibition of glutamate-stimulated Ca2+ mobilization after 1.5 hrs by FLIPR assayAntagonist activity at human recombinant mGlu3 receptor expressed in AV12 cells assessed as inhibition of glutamate-stimulated Ca2+ mobilization after 1.5 hrs by FLIPR assay
ChEMBL 334 5 4 6 0.3 N[C@@]1(C(=O)O)C[C@H](Sc2nnc(C(F)F)[nH]2)[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/acs.jmedchem.5b01124
145949267 162912 None 11 Rat Functional pIC50 = 6.6 6.6 - 1
Negative allosteric modulation of rat mGlu3 receptor expressed in TREX cells coexpressing Galpha15 assessed as inhibition of glutamate induced-calcium mobilization preincubated for 2.3 mins followed by glutamate addition measured for 2.6 mins by Fluo-4 AM dye based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor expressed in TREX cells coexpressing Galpha15 assessed as inhibition of glutamate induced-calcium mobilization preincubated for 2.3 mins followed by glutamate addition measured for 2.6 mins by Fluo-4 AM dye based fluorescence assay
ChEMBL 339 6 0 4 3.8 C[C@@H](COc1ccn(-c2ccc(F)cc2)c(=O)c1)Oc1ccccc1 10.1021/acsmedchemlett.7b00249
CHEMBL4172540 162912 None 11 Rat Functional pIC50 = 6.6 6.6 - 1
Negative allosteric modulation of rat mGlu3 receptor expressed in TREX cells coexpressing Galpha15 assessed as inhibition of glutamate induced-calcium mobilization preincubated for 2.3 mins followed by glutamate addition measured for 2.6 mins by Fluo-4 AM dye based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor expressed in TREX cells coexpressing Galpha15 assessed as inhibition of glutamate induced-calcium mobilization preincubated for 2.3 mins followed by glutamate addition measured for 2.6 mins by Fluo-4 AM dye based fluorescence assay
ChEMBL 339 6 0 4 3.8 C[C@@H](COc1ccn(-c2ccc(F)cc2)c(=O)c1)Oc1ccccc1 10.1021/acsmedchemlett.7b00249
145949267 162912 None 11 Rat Functional pIC50 = 6.6 6.6 - 1
Negative allosteric modulation of rat mGlu3R expressed in HEK293 cells co-expressing Galpha15 assessed as decrease in glutamate-induced calcium mobilization preincubated for 2.5 mins followed by glutamate addition by S3 Fluo-4-AM dye based fluorescence assayNegative allosteric modulation of rat mGlu3R expressed in HEK293 cells co-expressing Galpha15 assessed as decrease in glutamate-induced calcium mobilization preincubated for 2.5 mins followed by glutamate addition by S3 Fluo-4-AM dye based fluorescence assay
ChEMBL 339 6 0 4 3.8 C[C@@H](COc1ccn(-c2ccc(F)cc2)c(=O)c1)Oc1ccccc1 10.1016/j.bmcl.2019.07.030
CHEMBL4172540 162912 None 11 Rat Functional pIC50 = 6.6 6.6 - 1
Negative allosteric modulation of rat mGlu3R expressed in HEK293 cells co-expressing Galpha15 assessed as decrease in glutamate-induced calcium mobilization preincubated for 2.5 mins followed by glutamate addition by S3 Fluo-4-AM dye based fluorescence assayNegative allosteric modulation of rat mGlu3R expressed in HEK293 cells co-expressing Galpha15 assessed as decrease in glutamate-induced calcium mobilization preincubated for 2.5 mins followed by glutamate addition by S3 Fluo-4-AM dye based fluorescence assay
ChEMBL 339 6 0 4 3.8 C[C@@H](COc1ccn(-c2ccc(F)cc2)c(=O)c1)Oc1ccccc1 10.1016/j.bmcl.2019.07.030
145949267 162912 None 11 Rat Functional pIC50 = 6.6 6.6 - 1
Negative allosteric modulation of rat mGlu3 receptor expressed in TREX cells coexpressing Galpha15 assessed as inhibition of glutamate induced-calcium mobilization preincubated for 2.3 mins followed by glutamate addition measured for 2.6 mins by Fluo-4 AM dye based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor expressed in TREX cells coexpressing Galpha15 assessed as inhibition of glutamate induced-calcium mobilization preincubated for 2.3 mins followed by glutamate addition measured for 2.6 mins by Fluo-4 AM dye based fluorescence assay
ChEMBL 339 6 0 4 3.8 C[C@@H](COc1ccn(-c2ccc(F)cc2)c(=O)c1)Oc1ccccc1 10.1021/acsmedchemlett.7b00249
CHEMBL4172540 162912 None 11 Rat Functional pIC50 = 6.6 6.6 - 1
Negative allosteric modulation of rat mGlu3 receptor expressed in TREX cells coexpressing Galpha15 assessed as inhibition of glutamate induced-calcium mobilization preincubated for 2.3 mins followed by glutamate addition measured for 2.6 mins by Fluo-4 AM dye based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor expressed in TREX cells coexpressing Galpha15 assessed as inhibition of glutamate induced-calcium mobilization preincubated for 2.3 mins followed by glutamate addition measured for 2.6 mins by Fluo-4 AM dye based fluorescence assay
ChEMBL 339 6 0 4 3.8 C[C@@H](COc1ccn(-c2ccc(F)cc2)c(=O)c1)Oc1ccccc1 10.1021/acsmedchemlett.7b00249
90643958 112055 None 0 Rat Functional pIC50 = 6.6 6.6 6 2
Inhibition of rat mGlu3 receptor transfected in HEK293 cells coexpressing mouse Galpha15 assessed as decrease in glutamate-induced calcium signaling by fluorescence plate reader analysis in presence of glutamate at EC87 concentrationInhibition of rat mGlu3 receptor transfected in HEK293 cells coexpressing mouse Galpha15 assessed as decrease in glutamate-induced calcium signaling by fluorescence plate reader analysis in presence of glutamate at EC87 concentration
ChEMBL 370 2 0 5 4.1 Cn1c(=O)c2ccc(-c3cccnc3)cc2n2nc(-c3cccc(F)c3)cc12 10.1016/j.bmcl.2014.04.051
CHEMBL3288644 112055 None 0 Rat Functional pIC50 = 6.6 6.6 6 2
Inhibition of rat mGlu3 receptor transfected in HEK293 cells coexpressing mouse Galpha15 assessed as decrease in glutamate-induced calcium signaling by fluorescence plate reader analysis in presence of glutamate at EC87 concentrationInhibition of rat mGlu3 receptor transfected in HEK293 cells coexpressing mouse Galpha15 assessed as decrease in glutamate-induced calcium signaling by fluorescence plate reader analysis in presence of glutamate at EC87 concentration
ChEMBL 370 2 0 5 4.1 Cn1c(=O)c2ccc(-c3cccnc3)cc2n2nc(-c3cccc(F)c3)cc12 10.1016/j.bmcl.2014.04.051
10607617 78767 None 0 Human Functional pIC50 = 5.6 5.6 2 2
Ability to block 1S,3R-ACPD-induced inhibition of forskolin stimulated cyclic-AMP in non-neuronal cell line expressing human Metabotropic glutamate receptor 3Ability to block 1S,3R-ACPD-induced inhibition of forskolin stimulated cyclic-AMP in non-neuronal cell line expressing human Metabotropic glutamate receptor 3
ChEMBL 187 4 3 3 -0.1 CCC(N)(C(=O)O)[C@H]1C[C@@H]1C(=O)O 10.1021/jm970497w
CHEMBL2112579 78767 None 0 Human Functional pIC50 = 5.6 5.6 2 2
Ability to block 1S,3R-ACPD-induced inhibition of forskolin stimulated cyclic-AMP in non-neuronal cell line expressing human Metabotropic glutamate receptor 3Ability to block 1S,3R-ACPD-induced inhibition of forskolin stimulated cyclic-AMP in non-neuronal cell line expressing human Metabotropic glutamate receptor 3
ChEMBL 187 4 3 3 -0.1 CCC(N)(C(=O)O)[C@H]1C[C@@H]1C(=O)O 10.1021/jm970497w
53240406 123463 None 21 Human Functional pIC50 = 4.6 4.6 -107 4
Antagonist activity at human recombinant mGlu3 receptor expressed in AV12 cells assessed as inhibition of glutamate-stimulated Ca2+ mobilization after 1.5 hrs by FLIPR assayAntagonist activity at human recombinant mGlu3 receptor expressed in AV12 cells assessed as inhibition of glutamate-stimulated Ca2+ mobilization after 1.5 hrs by FLIPR assay
ChEMBL 284 4 4 6 -0.6 N[C@@]1(C(=O)O)C[C@@H](Sc2nnc[nH]2)[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/acs.jmedchem.5b01124
CHEMBL3616847 123463 None 21 Human Functional pIC50 = 4.6 4.6 -107 4
Antagonist activity at human recombinant mGlu3 receptor expressed in AV12 cells assessed as inhibition of glutamate-stimulated Ca2+ mobilization after 1.5 hrs by FLIPR assayAntagonist activity at human recombinant mGlu3 receptor expressed in AV12 cells assessed as inhibition of glutamate-stimulated Ca2+ mobilization after 1.5 hrs by FLIPR assay
ChEMBL 284 4 4 6 -0.6 N[C@@]1(C(=O)O)C[C@@H](Sc2nnc[nH]2)[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/acs.jmedchem.5b01124
122190322 123518 None 0 Rat Functional pIC50 = 5.6 5.6 - 1
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 381 5 0 5 3.8 COc1ccccc1OCc1cc2n(n1)[C@H](C)CN(c1ccc(F)cc1)C2=O 10.1021/acs.jmedchem.5b01005
CHEMBL3617506 123518 None 0 Rat Functional pIC50 = 5.6 5.6 - 1
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 381 5 0 5 3.8 COc1ccccc1OCc1cc2n(n1)[C@H](C)CN(c1ccc(F)cc1)C2=O 10.1021/acs.jmedchem.5b01005
122190431 123607 None 0 Rat Functional pIC50 = 6.6 6.6 - 1
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 387 4 0 6 3.3 C[C@@H]1CN(c2ccc(F)cn2)C(=O)c2cc(COc3ccc(Cl)cn3)nn21 10.1021/acs.jmedchem.5b01005
CHEMBL3617654 123607 None 0 Rat Functional pIC50 = 6.6 6.6 - 1
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 387 4 0 6 3.3 C[C@@H]1CN(c2ccc(F)cn2)C(=O)c2cc(COc3ccc(Cl)cn3)nn21 10.1021/acs.jmedchem.5b01005
122190322 123518 None 0 Rat Functional pIC50 = 5.6 5.6 - 1
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 381 5 0 5 3.8 COc1ccccc1OCc1cc2n(n1)[C@H](C)CN(c1ccc(F)cc1)C2=O 10.1021/acs.jmedchem.5b01005
CHEMBL3617506 123518 None 0 Rat Functional pIC50 = 5.6 5.6 - 1
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 381 5 0 5 3.8 COc1ccccc1OCc1cc2n(n1)[C@H](C)CN(c1ccc(F)cc1)C2=O 10.1021/acs.jmedchem.5b01005
44348769 16788 None 0 Human Functional pIC50 = 6.6 6.6 3 2
Effect on 1S,3R-ACPD-induced inhibition of forskolin stimulated cyclic-AMP in RGT cells expressing human Metabotropic glutamate receptor 3Effect on 1S,3R-ACPD-induced inhibition of forskolin stimulated cyclic-AMP in RGT cells expressing human Metabotropic glutamate receptor 3
ChEMBL 279 6 4 4 0.8 N[C@@](CCc1cccc(O)c1)(C(=O)O)C1C[C@@H]1C(=O)O 10.1021/jm970498o
CHEMBL124483 16788 None 0 Human Functional pIC50 = 6.6 6.6 3 2
Effect on 1S,3R-ACPD-induced inhibition of forskolin stimulated cyclic-AMP in RGT cells expressing human Metabotropic glutamate receptor 3Effect on 1S,3R-ACPD-induced inhibition of forskolin stimulated cyclic-AMP in RGT cells expressing human Metabotropic glutamate receptor 3
ChEMBL 279 6 4 4 0.8 N[C@@](CCc1cccc(O)c1)(C(=O)O)C1C[C@@H]1C(=O)O 10.1021/jm970498o
122190431 123607 None 0 Rat Functional pIC50 = 6.6 6.6 - 1
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 387 4 0 6 3.3 C[C@@H]1CN(c2ccc(F)cn2)C(=O)c2cc(COc3ccc(Cl)cn3)nn21 10.1021/acs.jmedchem.5b01005
CHEMBL3617654 123607 None 0 Rat Functional pIC50 = 6.6 6.6 - 1
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 387 4 0 6 3.3 C[C@@H]1CN(c2ccc(F)cn2)C(=O)c2cc(COc3ccc(Cl)cn3)nn21 10.1021/acs.jmedchem.5b01005
118575176 123507 None 0 Rat Functional pIC50 = 6.6 6.6 -5 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 351 4 0 4 3.8 C[C@@H]1CN(c2ccc(F)cc2)C(=O)c2cc(COc3ccccc3)nn21 10.1021/acs.jmedchem.5b01005
CHEMBL3617495 123507 None 0 Rat Functional pIC50 = 6.6 6.6 -5 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 351 4 0 4 3.8 C[C@@H]1CN(c2ccc(F)cc2)C(=O)c2cc(COc3ccccc3)nn21 10.1021/acs.jmedchem.5b01005
122190396 123572 None 0 Rat Functional pIC50 = 6.6 6.6 - 1
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 366 4 0 5 3.5 Cc1ccc(N2C[C@@H](C)n3nc(COc4ccc(F)cn4)cc3C2=O)cc1 10.1021/acs.jmedchem.5b01005
CHEMBL3617619 123572 None 0 Rat Functional pIC50 = 6.6 6.6 - 1
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 366 4 0 5 3.5 Cc1ccc(N2C[C@@H](C)n3nc(COc4ccc(F)cn4)cc3C2=O)cc1 10.1021/acs.jmedchem.5b01005
118575176 123507 None 0 Rat Functional pIC50 = 6.6 6.6 -5 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 351 4 0 4 3.8 C[C@@H]1CN(c2ccc(F)cc2)C(=O)c2cc(COc3ccccc3)nn21 10.1021/acs.jmedchem.5b01005
CHEMBL3617495 123507 None 0 Rat Functional pIC50 = 6.6 6.6 -5 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 351 4 0 4 3.8 C[C@@H]1CN(c2ccc(F)cc2)C(=O)c2cc(COc3ccccc3)nn21 10.1021/acs.jmedchem.5b01005
122190396 123572 None 0 Rat Functional pIC50 = 6.6 6.6 - 1
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 366 4 0 5 3.5 Cc1ccc(N2C[C@@H](C)n3nc(COc4ccc(F)cn4)cc3C2=O)cc1 10.1021/acs.jmedchem.5b01005
CHEMBL3617619 123572 None 0 Rat Functional pIC50 = 6.6 6.6 - 1
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 366 4 0 5 3.5 Cc1ccc(N2C[C@@H](C)n3nc(COc4ccc(F)cn4)cc3C2=O)cc1 10.1021/acs.jmedchem.5b01005
140839138 162978 None 0 Rat Functional pIC50 = 6.6 6.6 4 2
Negative allosteric modulation of rat mGlu3 receptor expressed in TREX cells coexpressing Galpha15 assessed as inhibition of glutamate induced-calcium mobilization preincubated for 2.3 mins followed by glutamate addition measured for 2.6 mins by Fluo-4 AM dye based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor expressed in TREX cells coexpressing Galpha15 assessed as inhibition of glutamate induced-calcium mobilization preincubated for 2.3 mins followed by glutamate addition measured for 2.6 mins by Fluo-4 AM dye based fluorescence assay
ChEMBL 350 6 0 5 3.3 N#Cc1cc(F)cc(-n2ccc(OCCOc3ccccc3)cc2=O)c1 10.1021/acsmedchemlett.7b00249
CHEMBL4173490 162978 None 0 Rat Functional pIC50 = 6.6 6.6 4 2
Negative allosteric modulation of rat mGlu3 receptor expressed in TREX cells coexpressing Galpha15 assessed as inhibition of glutamate induced-calcium mobilization preincubated for 2.3 mins followed by glutamate addition measured for 2.6 mins by Fluo-4 AM dye based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor expressed in TREX cells coexpressing Galpha15 assessed as inhibition of glutamate induced-calcium mobilization preincubated for 2.3 mins followed by glutamate addition measured for 2.6 mins by Fluo-4 AM dye based fluorescence assay
ChEMBL 350 6 0 5 3.3 N#Cc1cc(F)cc(-n2ccc(OCCOc3ccccc3)cc2=O)c1 10.1021/acsmedchemlett.7b00249
67633340 183827 None 0 Human Functional pIC50 = 7.6 7.6 -1 2
Antagonist activity at human recombinant mGlu3 receptor stably expressed in golden hamster AV12 cells co-expressing rat EAAT1 assessed as reduction in DCG IV-induced inhibition of forskolin-stimulated cAMP accumulation preincubated for 20 mins followed by incubation with cAMP-d2 conjugate and anti-cAMP cryptate for 1 hr by HTRF assayAntagonist activity at human recombinant mGlu3 receptor stably expressed in golden hamster AV12 cells co-expressing rat EAAT1 assessed as reduction in DCG IV-induced inhibition of forskolin-stimulated cAMP accumulation preincubated for 20 mins followed by incubation with cAMP-d2 conjugate and anti-cAMP cryptate for 1 hr by HTRF assay
ChEMBL 355 5 4 5 0.9 Cc1cc(SC[C@@H]2[C@@H](O)[C@@H]3[C@@H]([C@H]3C(=O)O)[C@]2(N)C(=O)O)ccc1F 10.1021/acs.jmedchem.6b01119
CHEMBL4780402 183827 None 0 Human Functional pIC50 = 7.6 7.6 -1 2
Antagonist activity at human recombinant mGlu3 receptor stably expressed in golden hamster AV12 cells co-expressing rat EAAT1 assessed as reduction in DCG IV-induced inhibition of forskolin-stimulated cAMP accumulation preincubated for 20 mins followed by incubation with cAMP-d2 conjugate and anti-cAMP cryptate for 1 hr by HTRF assayAntagonist activity at human recombinant mGlu3 receptor stably expressed in golden hamster AV12 cells co-expressing rat EAAT1 assessed as reduction in DCG IV-induced inhibition of forskolin-stimulated cAMP accumulation preincubated for 20 mins followed by incubation with cAMP-d2 conjugate and anti-cAMP cryptate for 1 hr by HTRF assay
ChEMBL 355 5 4 5 0.9 Cc1cc(SC[C@@H]2[C@@H](O)[C@@H]3[C@@H]([C@H]3C(=O)O)[C@]2(N)C(=O)O)ccc1F 10.1021/acs.jmedchem.6b01119
CHEMBL4803381 183827 None 0 Human Functional pIC50 = 7.6 7.6 -1 2
Antagonist activity at human recombinant mGlu3 receptor stably expressed in golden hamster AV12 cells co-expressing rat EAAT1 assessed as reduction in DCG IV-induced inhibition of forskolin-stimulated cAMP accumulation preincubated for 20 mins followed by incubation with cAMP-d2 conjugate and anti-cAMP cryptate for 1 hr by HTRF assayAntagonist activity at human recombinant mGlu3 receptor stably expressed in golden hamster AV12 cells co-expressing rat EAAT1 assessed as reduction in DCG IV-induced inhibition of forskolin-stimulated cAMP accumulation preincubated for 20 mins followed by incubation with cAMP-d2 conjugate and anti-cAMP cryptate for 1 hr by HTRF assay
ChEMBL 355 5 4 5 0.9 Cc1cc(SC[C@@H]2[C@@H](O)[C@@H]3[C@@H]([C@H]3C(=O)O)[C@]2(N)C(=O)O)ccc1F 10.1021/acs.jmedchem.6b01119
140839138 162978 None 0 Rat Functional pIC50 = 6.6 6.6 4 2
Negative allosteric modulation of rat mGlu3 receptor expressed in TREX cells coexpressing Galpha15 assessed as inhibition of glutamate induced-calcium mobilization preincubated for 2.3 mins followed by glutamate addition measured for 2.6 mins by Fluo-4 AM dye based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor expressed in TREX cells coexpressing Galpha15 assessed as inhibition of glutamate induced-calcium mobilization preincubated for 2.3 mins followed by glutamate addition measured for 2.6 mins by Fluo-4 AM dye based fluorescence assay
ChEMBL 350 6 0 5 3.3 N#Cc1cc(F)cc(-n2ccc(OCCOc3ccccc3)cc2=O)c1 10.1021/acsmedchemlett.7b00249
CHEMBL4173490 162978 None 0 Rat Functional pIC50 = 6.6 6.6 4 2
Negative allosteric modulation of rat mGlu3 receptor expressed in TREX cells coexpressing Galpha15 assessed as inhibition of glutamate induced-calcium mobilization preincubated for 2.3 mins followed by glutamate addition measured for 2.6 mins by Fluo-4 AM dye based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor expressed in TREX cells coexpressing Galpha15 assessed as inhibition of glutamate induced-calcium mobilization preincubated for 2.3 mins followed by glutamate addition measured for 2.6 mins by Fluo-4 AM dye based fluorescence assay
ChEMBL 350 6 0 5 3.3 N#Cc1cc(F)cc(-n2ccc(OCCOc3ccccc3)cc2=O)c1 10.1021/acsmedchemlett.7b00249
10473248 14191 None 0 Rat Functional pIC50 = 4.6 4.6 -4 3
Inhibitory concentration required for antagonistic activity at Metabotropic glutamate receptor 3Inhibitory concentration required for antagonistic activity at Metabotropic glutamate receptor 3
ChEMBL 280 4 4 5 -0.2 N[C@]1(C(=O)O)C[C@H](C(=O)O)N(Cc2ccccc2O)C1 10.1016/s0960-894x(01)00329-8
CHEMBL1198741 14191 None 0 Rat Functional pIC50 = 4.6 4.6 -4 3
Inhibitory concentration required for antagonistic activity at Metabotropic glutamate receptor 3Inhibitory concentration required for antagonistic activity at Metabotropic glutamate receptor 3
ChEMBL 280 4 4 5 -0.2 N[C@]1(C(=O)O)C[C@H](C(=O)O)N(Cc2ccccc2O)C1 10.1016/s0960-894x(01)00329-8
CHEMBL540015 14191 None 0 Rat Functional pIC50 = 4.6 4.6 -4 3
Inhibitory concentration required for antagonistic activity at Metabotropic glutamate receptor 3Inhibitory concentration required for antagonistic activity at Metabotropic glutamate receptor 3
ChEMBL 280 4 4 5 -0.2 N[C@]1(C(=O)O)C[C@H](C(=O)O)N(Cc2ccccc2O)C1 10.1016/s0960-894x(01)00329-8
162666357 183837 None 0 Human Functional pIC50 = 6.6 6.6 -3 2
Antagonist activity at human recombinant mGlu3 receptor stably expressed in golden hamster AV12 cells co-expressing rat EAAT1 assessed as reduction in DCG IV-induced inhibition of forskolin-stimulated cAMP accumulation preincubated for 20 mins followed by incubation with cAMP-d2 conjugate and anti-cAMP cryptate for 1 hr by HTRF assayAntagonist activity at human recombinant mGlu3 receptor stably expressed in golden hamster AV12 cells co-expressing rat EAAT1 assessed as reduction in DCG IV-induced inhibition of forskolin-stimulated cAMP accumulation preincubated for 20 mins followed by incubation with cAMP-d2 conjugate and anti-cAMP cryptate for 1 hr by HTRF assay
ChEMBL 341 5 4 5 0.6 N[C@@]1(C(=O)O)[C@H](CSc2cccc(F)c2)[C@@H](O)[C@@H]2[C@H]1[C@H]2C(=O)O 10.1021/acs.jmedchem.6b01119
CHEMBL4784701 183837 None 0 Human Functional pIC50 = 6.6 6.6 -3 2
Antagonist activity at human recombinant mGlu3 receptor stably expressed in golden hamster AV12 cells co-expressing rat EAAT1 assessed as reduction in DCG IV-induced inhibition of forskolin-stimulated cAMP accumulation preincubated for 20 mins followed by incubation with cAMP-d2 conjugate and anti-cAMP cryptate for 1 hr by HTRF assayAntagonist activity at human recombinant mGlu3 receptor stably expressed in golden hamster AV12 cells co-expressing rat EAAT1 assessed as reduction in DCG IV-induced inhibition of forskolin-stimulated cAMP accumulation preincubated for 20 mins followed by incubation with cAMP-d2 conjugate and anti-cAMP cryptate for 1 hr by HTRF assay
ChEMBL 341 5 4 5 0.6 N[C@@]1(C(=O)O)[C@H](CSc2cccc(F)c2)[C@@H](O)[C@@H]2[C@H]1[C@H]2C(=O)O 10.1021/acs.jmedchem.6b01119
CHEMBL4803523 183837 None 0 Human Functional pIC50 = 6.6 6.6 -3 2
Antagonist activity at human recombinant mGlu3 receptor stably expressed in golden hamster AV12 cells co-expressing rat EAAT1 assessed as reduction in DCG IV-induced inhibition of forskolin-stimulated cAMP accumulation preincubated for 20 mins followed by incubation with cAMP-d2 conjugate and anti-cAMP cryptate for 1 hr by HTRF assayAntagonist activity at human recombinant mGlu3 receptor stably expressed in golden hamster AV12 cells co-expressing rat EAAT1 assessed as reduction in DCG IV-induced inhibition of forskolin-stimulated cAMP accumulation preincubated for 20 mins followed by incubation with cAMP-d2 conjugate and anti-cAMP cryptate for 1 hr by HTRF assay
ChEMBL 341 5 4 5 0.6 N[C@@]1(C(=O)O)[C@H](CSc2cccc(F)c2)[C@@H](O)[C@@H]2[C@H]1[C@H]2C(=O)O 10.1021/acs.jmedchem.6b01119
53240406 123463 None 21 Human Functional pIC50 = 5.6 5.6 -107 4
Antagonist activity at human recombinant mGlu3 receptor expressed in AV12 cells assessed as reversal of DCG-4-inhibited, forskolin-stimulated cAMP production after 1 hr by fluorescence assayAntagonist activity at human recombinant mGlu3 receptor expressed in AV12 cells assessed as reversal of DCG-4-inhibited, forskolin-stimulated cAMP production after 1 hr by fluorescence assay
ChEMBL 284 4 4 6 -0.6 N[C@@]1(C(=O)O)C[C@@H](Sc2nnc[nH]2)[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/acs.jmedchem.5b01124
CHEMBL3616847 123463 None 21 Human Functional pIC50 = 5.6 5.6 -107 4
Antagonist activity at human recombinant mGlu3 receptor expressed in AV12 cells assessed as reversal of DCG-4-inhibited, forskolin-stimulated cAMP production after 1 hr by fluorescence assayAntagonist activity at human recombinant mGlu3 receptor expressed in AV12 cells assessed as reversal of DCG-4-inhibited, forskolin-stimulated cAMP production after 1 hr by fluorescence assay
ChEMBL 284 4 4 6 -0.6 N[C@@]1(C(=O)O)C[C@@H](Sc2nnc[nH]2)[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/acs.jmedchem.5b01124
60210850 90364 None 0 Rat Functional pIC50 = 5.6 5.6 - 1
Negative allosteric modulation of rat mGlu3 receptor transfected in human TREX cells assessed as inhibition of glutamate-induced calcium mobilization after 2.5 minsNegative allosteric modulation of rat mGlu3 receptor transfected in human TREX cells assessed as inhibition of glutamate-induced calcium mobilization after 2.5 mins
ChEMBL 359 2 0 3 3.1 COc1ccc(C#Cc2ccc(C(=O)N3CC4CCC(=O)C4C3)cc2)cc1 10.1021/jm400439t
CHEMBL2385884 90364 None 0 Rat Functional pIC50 = 5.6 5.6 - 1
Negative allosteric modulation of rat mGlu3 receptor transfected in human TREX cells assessed as inhibition of glutamate-induced calcium mobilization after 2.5 minsNegative allosteric modulation of rat mGlu3 receptor transfected in human TREX cells assessed as inhibition of glutamate-induced calcium mobilization after 2.5 mins
ChEMBL 359 2 0 3 3.1 COc1ccc(C#Cc2ccc(C(=O)N3CC4CCC(=O)C4C3)cc2)cc1 10.1021/jm400439t
60210794 90360 None 0 Rat Functional pIC50 = 4.6 4.6 - 1
Negative allosteric modulation of rat mGlu3 receptor transfected in human TREX cells assessed as inhibition of glutamate-induced calcium mobilization after 2.5 minsNegative allosteric modulation of rat mGlu3 receptor transfected in human TREX cells assessed as inhibition of glutamate-induced calcium mobilization after 2.5 mins
ChEMBL 321 2 1 3 2.3 COc1ccc(C#Cc2ccc(C(=O)N3CC[C@H](O)C3)cc2)cc1 10.1021/jm400439t
CHEMBL2385880 90360 None 0 Rat Functional pIC50 = 4.6 4.6 - 1
Negative allosteric modulation of rat mGlu3 receptor transfected in human TREX cells assessed as inhibition of glutamate-induced calcium mobilization after 2.5 minsNegative allosteric modulation of rat mGlu3 receptor transfected in human TREX cells assessed as inhibition of glutamate-induced calcium mobilization after 2.5 mins
ChEMBL 321 2 1 3 2.3 COc1ccc(C#Cc2ccc(C(=O)N3CC[C@H](O)C3)cc2)cc1 10.1021/jm400439t
71476419 123476 None 0 Human Functional pIC50 = 5.6 5.6 -51 2
Antagonist activity at human recombinant mGlu3 receptor expressed in AV12 cells assessed as inhibition of glutamate-stimulated Ca2+ mobilization after 1.5 hrs by FLIPR assayAntagonist activity at human recombinant mGlu3 receptor expressed in AV12 cells assessed as inhibition of glutamate-stimulated Ca2+ mobilization after 1.5 hrs by FLIPR assay
ChEMBL 284 4 4 6 -0.6 N[C@@]1(C(=O)O)C[C@H](Sc2c[nH]nn2)[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/acs.jmedchem.5b01124
CHEMBL3616860 123476 None 0 Human Functional pIC50 = 5.6 5.6 -51 2
Antagonist activity at human recombinant mGlu3 receptor expressed in AV12 cells assessed as inhibition of glutamate-stimulated Ca2+ mobilization after 1.5 hrs by FLIPR assayAntagonist activity at human recombinant mGlu3 receptor expressed in AV12 cells assessed as inhibition of glutamate-stimulated Ca2+ mobilization after 1.5 hrs by FLIPR assay
ChEMBL 284 4 4 6 -0.6 N[C@@]1(C(=O)O)C[C@H](Sc2c[nH]nn2)[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/acs.jmedchem.5b01124
10783272 86156 None 0 Human Functional pIC50 = 6.6 6.6 15 2
Ability to block 1S,3R-ACPD-induced inhibition of forskolin stimulated cyclic-AMP in non-neuronal cell line expressing human Metabotropic glutamate receptor 3Ability to block 1S,3R-ACPD-induced inhibition of forskolin stimulated cyclic-AMP in non-neuronal cell line expressing human Metabotropic glutamate receptor 3
ChEMBL 339 7 3 3 2.7 N[C@@](CC(c1ccccc1)c1ccccc1)(C(=O)O)[C@H]1C[C@@H]1C(=O)O 10.1021/jm970497w
CHEMBL2311086 86156 None 0 Human Functional pIC50 = 6.6 6.6 15 2
Ability to block 1S,3R-ACPD-induced inhibition of forskolin stimulated cyclic-AMP in non-neuronal cell line expressing human Metabotropic glutamate receptor 3Ability to block 1S,3R-ACPD-induced inhibition of forskolin stimulated cyclic-AMP in non-neuronal cell line expressing human Metabotropic glutamate receptor 3
ChEMBL 339 7 3 3 2.7 N[C@@](CC(c1ccccc1)c1ccccc1)(C(=O)O)[C@H]1C[C@@H]1C(=O)O 10.1021/jm970497w
122190422 123598 None 0 Rat Functional pIC50 = 6.6 6.6 9 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 404 4 0 5 4.0 C[C@@H]1CN(c2ccc(F)cc2F)C(=O)c2cc(COc3ccc(Cl)cn3)nn21 10.1021/acs.jmedchem.5b01005
CHEMBL3617645 123598 None 0 Rat Functional pIC50 = 6.6 6.6 9 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 404 4 0 5 4.0 C[C@@H]1CN(c2ccc(F)cc2F)C(=O)c2cc(COc3ccc(Cl)cn3)nn21 10.1021/acs.jmedchem.5b01005
10732318 78774 None 0 Human Functional pIC50 = 5.6 5.6 -6 2
Ability to block 1S,3R-ACPD-induced inhibition of forskolin stimulated cyclic-AMP in non-neuronal cell line expressing human Metabotropic glutamate receptor 3Ability to block 1S,3R-ACPD-induced inhibition of forskolin stimulated cyclic-AMP in non-neuronal cell line expressing human Metabotropic glutamate receptor 3
ChEMBL 291 8 3 3 1.9 NC(CCCCc1ccccc1)(C(=O)O)[C@H]1C[C@@H]1C(=O)O 10.1021/jm970497w
CHEMBL2112585 78774 None 0 Human Functional pIC50 = 5.6 5.6 -6 2
Ability to block 1S,3R-ACPD-induced inhibition of forskolin stimulated cyclic-AMP in non-neuronal cell line expressing human Metabotropic glutamate receptor 3Ability to block 1S,3R-ACPD-induced inhibition of forskolin stimulated cyclic-AMP in non-neuronal cell line expressing human Metabotropic glutamate receptor 3
ChEMBL 291 8 3 3 1.9 NC(CCCCc1ccccc1)(C(=O)O)[C@H]1C[C@@H]1C(=O)O 10.1021/jm970497w
122190422 123598 None 0 Rat Functional pIC50 = 6.6 6.6 9 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 404 4 0 5 4.0 C[C@@H]1CN(c2ccc(F)cc2F)C(=O)c2cc(COc3ccc(Cl)cn3)nn21 10.1021/acs.jmedchem.5b01005
CHEMBL3617645 123598 None 0 Rat Functional pIC50 = 6.6 6.6 9 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 404 4 0 5 4.0 C[C@@H]1CN(c2ccc(F)cc2F)C(=O)c2cc(COc3ccc(Cl)cn3)nn21 10.1021/acs.jmedchem.5b01005
11269030 56320 None 0 Rat Functional pIC50 = 7.5 7.5 1 3
Antagonist activity at rat mGluR3 receptor expressed in CHO cells assessed as inhibition of GIRK currentAntagonist activity at rat mGluR3 receptor expressed in CHO cells assessed as inhibition of GIRK current
ChEMBL 381 2 1 3 5.2 O=C1CC(c2cccc(-c3ccncc3)c2)=Nc2ccc(C(F)(F)F)cc2N1 10.1016/j.bmcl.2010.09.125
CHEMBL1629861 56320 None 0 Rat Functional pIC50 = 7.5 7.5 1 3
Antagonist activity at rat mGluR3 receptor expressed in CHO cells assessed as inhibition of GIRK currentAntagonist activity at rat mGluR3 receptor expressed in CHO cells assessed as inhibition of GIRK current
ChEMBL 381 2 1 3 5.2 O=C1CC(c2cccc(-c3ccncc3)c2)=Nc2ccc(C(F)(F)F)cc2N1 10.1016/j.bmcl.2010.09.125
44328753 210213 None 0 Rat Functional pIC50 = 7.5 7.5 16 6
Antagonistic activity against metabotropic glutamate receptor 3 (mGluR3) was evaluatedAntagonistic activity against metabotropic glutamate receptor 3 (mGluR3) was evaluated
ChEMBL 409 8 3 4 4.2 CCCC[C@@H]1[C@H](C(=O)O)[C@H]1C(N)(CC1c2ccccc2Oc2ccccc21)C(=O)O 10.1016/s0960-894x(98)00510-1
CHEMBL95868 210213 None 0 Rat Functional pIC50 = 7.5 7.5 16 6
Antagonistic activity against metabotropic glutamate receptor 3 (mGluR3) was evaluatedAntagonistic activity against metabotropic glutamate receptor 3 (mGluR3) was evaluated
ChEMBL 409 8 3 4 4.2 CCCC[C@@H]1[C@H](C(=O)O)[C@H]1C(N)(CC1c2ccccc2Oc2ccccc21)C(=O)O 10.1016/s0960-894x(98)00510-1
86695984 149853 None 0 Human Functional pIC50 = 7.5 7.5 -1 2
Antagonist activity at recombinant human mGlu3 receptor expressed in hamster AV12 cells co-expressing human EAAT1 assessed as reduction of DCG-4-inhibited forskolin-stimulated cAMP formation after 20 mins by HTRF assayAntagonist activity at recombinant human mGlu3 receptor expressed in hamster AV12 cells co-expressing human EAAT1 assessed as reduction of DCG-4-inhibited forskolin-stimulated cAMP formation after 20 mins by HTRF assay
ChEMBL 472 7 3 8 1.9 Cn1ncnc1S[C@@H]1[C@@H](OCc2ccc(Cl)c(Cl)c2)[C@@](N)(C(=O)O)[C@@H]2[C@@H](C(=O)O)[C@H]12 10.1016/j.bmcl.2016.10.067
CHEMBL3948272 149853 None 0 Human Functional pIC50 = 7.5 7.5 -1 2
Antagonist activity at recombinant human mGlu3 receptor expressed in hamster AV12 cells co-expressing human EAAT1 assessed as reduction of DCG-4-inhibited forskolin-stimulated cAMP formation after 20 mins by HTRF assayAntagonist activity at recombinant human mGlu3 receptor expressed in hamster AV12 cells co-expressing human EAAT1 assessed as reduction of DCG-4-inhibited forskolin-stimulated cAMP formation after 20 mins by HTRF assay
ChEMBL 472 7 3 8 1.9 Cn1ncnc1S[C@@H]1[C@@H](OCc2ccc(Cl)c(Cl)c2)[C@@](N)(C(=O)O)[C@@H]2[C@@H](C(=O)O)[C@H]12 10.1016/j.bmcl.2016.10.067
122455994 162393 None 0 Rat Functional pIC50 = 6.5 6.5 4 2
Negative allosteric modulation of rat mGlu3 receptor expressed in TREX cells coexpressing Galpha15 assessed as inhibition of glutamate induced-calcium mobilization preincubated for 2.3 mins followed by glutamate addition measured for 2.6 mins by Fluo-4 AM dye based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor expressed in TREX cells coexpressing Galpha15 assessed as inhibition of glutamate induced-calcium mobilization preincubated for 2.3 mins followed by glutamate addition measured for 2.6 mins by Fluo-4 AM dye based fluorescence assay
ChEMBL 326 6 0 5 2.8 O=c1nc(OCCOc2ccccc2)ccn1-c1ccc(F)cc1 10.1021/acsmedchemlett.7b00249
CHEMBL4164285 162393 None 0 Rat Functional pIC50 = 6.5 6.5 4 2
Negative allosteric modulation of rat mGlu3 receptor expressed in TREX cells coexpressing Galpha15 assessed as inhibition of glutamate induced-calcium mobilization preincubated for 2.3 mins followed by glutamate addition measured for 2.6 mins by Fluo-4 AM dye based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor expressed in TREX cells coexpressing Galpha15 assessed as inhibition of glutamate induced-calcium mobilization preincubated for 2.3 mins followed by glutamate addition measured for 2.6 mins by Fluo-4 AM dye based fluorescence assay
ChEMBL 326 6 0 5 2.8 O=c1nc(OCCOc2ccccc2)ccn1-c1ccc(F)cc1 10.1021/acsmedchemlett.7b00249
90643964 112059 None 0 Rat Functional pIC50 = 6.5 6.5 1 2
Inhibition of rat mGlu3 receptor transfected in HEK293 cells coexpressing mouse Galpha15 assessed as decrease in glutamate-induced calcium signaling by fluorescence plate reader analysis in presence of glutamate at EC87 concentrationInhibition of rat mGlu3 receptor transfected in HEK293 cells coexpressing mouse Galpha15 assessed as decrease in glutamate-induced calcium signaling by fluorescence plate reader analysis in presence of glutamate at EC87 concentration
ChEMBL 386 2 0 5 4.6 Cn1c(=O)c2ccc(-c3cccnc3)cc2n2nc(-c3cccc(Cl)c3)cc12 10.1016/j.bmcl.2014.04.051
CHEMBL3288656 112059 None 0 Rat Functional pIC50 = 6.5 6.5 1 2
Inhibition of rat mGlu3 receptor transfected in HEK293 cells coexpressing mouse Galpha15 assessed as decrease in glutamate-induced calcium signaling by fluorescence plate reader analysis in presence of glutamate at EC87 concentrationInhibition of rat mGlu3 receptor transfected in HEK293 cells coexpressing mouse Galpha15 assessed as decrease in glutamate-induced calcium signaling by fluorescence plate reader analysis in presence of glutamate at EC87 concentration
ChEMBL 386 2 0 5 4.6 Cn1c(=O)c2ccc(-c3cccnc3)cc2n2nc(-c3cccc(Cl)c3)cc12 10.1016/j.bmcl.2014.04.051
122190432 123398 None 0 Rat Functional pIC50 = 6.5 6.5 - 1
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 387 4 0 6 3.3 C[C@@H]1CN(c2cccc(F)n2)C(=O)c2cc(COc3ccc(Cl)cn3)nn21 10.1021/acs.jmedchem.5b01005
CHEMBL3616489 123398 None 0 Rat Functional pIC50 = 6.5 6.5 - 1
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 387 4 0 6 3.3 C[C@@H]1CN(c2cccc(F)n2)C(=O)c2cc(COc3ccc(Cl)cn3)nn21 10.1021/acs.jmedchem.5b01005
11310142 2422 None 14 Human Functional pIC50 = 5.5 5.5 -13 3
Evaluation of the functional effect on cAMP responses in RGT cells expressing human mGlu3 receptorEvaluation of the functional effect on cAMP responses in RGT cells expressing human mGlu3 receptor
ChEMBL 199 2 3 3 -0.2 C[C@@H]1C[C@@]([C@H]2[C@@H]1[C@@H]2C(=O)O)(N)C(=O)O 10.1021/jm040222y
11614 2422 None 14 Human Functional pIC50 = 5.5 5.5 -13 3
Evaluation of the functional effect on cAMP responses in RGT cells expressing human mGlu3 receptorEvaluation of the functional effect on cAMP responses in RGT cells expressing human mGlu3 receptor
ChEMBL 199 2 3 3 -0.2 C[C@@H]1C[C@@]([C@H]2[C@@H]1[C@@H]2C(=O)O)(N)C(=O)O 10.1021/jm040222y
CHEMBL192051 2422 None 14 Human Functional pIC50 = 5.5 5.5 -13 3
Evaluation of the functional effect on cAMP responses in RGT cells expressing human mGlu3 receptorEvaluation of the functional effect on cAMP responses in RGT cells expressing human mGlu3 receptor
ChEMBL 199 2 3 3 -0.2 C[C@@H]1C[C@@]([C@H]2[C@@H]1[C@@H]2C(=O)O)(N)C(=O)O 10.1021/jm040222y
122190331 123527 None 0 Rat Functional pIC50 = 5.5 5.5 - 1
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 420 4 0 5 4.2 C[C@@H]1CN(c2ccc(F)cc2)C(=O)c2cc(COc3ncccc3C(F)(F)F)nn21 10.1021/acs.jmedchem.5b01005
CHEMBL3617515 123527 None 0 Rat Functional pIC50 = 5.5 5.5 - 1
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 420 4 0 5 4.2 C[C@@H]1CN(c2ccc(F)cc2)C(=O)c2cc(COc3ncccc3C(F)(F)F)nn21 10.1021/acs.jmedchem.5b01005
122190432 123398 None 0 Rat Functional pIC50 = 6.5 6.5 - 1
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 387 4 0 6 3.3 C[C@@H]1CN(c2cccc(F)n2)C(=O)c2cc(COc3ccc(Cl)cn3)nn21 10.1021/acs.jmedchem.5b01005
CHEMBL3616489 123398 None 0 Rat Functional pIC50 = 6.5 6.5 - 1
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 387 4 0 6 3.3 C[C@@H]1CN(c2cccc(F)n2)C(=O)c2cc(COc3ccc(Cl)cn3)nn21 10.1021/acs.jmedchem.5b01005
122455994 162393 None 0 Rat Functional pIC50 = 6.5 6.5 4 2
Negative allosteric modulation of rat mGlu3 receptor expressed in TREX cells coexpressing Galpha15 assessed as inhibition of glutamate induced-calcium mobilization preincubated for 2.3 mins followed by glutamate addition measured for 2.6 mins by Fluo-4 AM dye based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor expressed in TREX cells coexpressing Galpha15 assessed as inhibition of glutamate induced-calcium mobilization preincubated for 2.3 mins followed by glutamate addition measured for 2.6 mins by Fluo-4 AM dye based fluorescence assay
ChEMBL 326 6 0 5 2.8 O=c1nc(OCCOc2ccccc2)ccn1-c1ccc(F)cc1 10.1021/acsmedchemlett.7b00249
CHEMBL4164285 162393 None 0 Rat Functional pIC50 = 6.5 6.5 4 2
Negative allosteric modulation of rat mGlu3 receptor expressed in TREX cells coexpressing Galpha15 assessed as inhibition of glutamate induced-calcium mobilization preincubated for 2.3 mins followed by glutamate addition measured for 2.6 mins by Fluo-4 AM dye based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor expressed in TREX cells coexpressing Galpha15 assessed as inhibition of glutamate induced-calcium mobilization preincubated for 2.3 mins followed by glutamate addition measured for 2.6 mins by Fluo-4 AM dye based fluorescence assay
ChEMBL 326 6 0 5 2.8 O=c1nc(OCCOc2ccccc2)ccn1-c1ccc(F)cc1 10.1021/acsmedchemlett.7b00249
122190331 123527 None 0 Rat Functional pIC50 = 5.5 5.5 - 1
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 420 4 0 5 4.2 C[C@@H]1CN(c2ccc(F)cc2)C(=O)c2cc(COc3ncccc3C(F)(F)F)nn21 10.1021/acs.jmedchem.5b01005
CHEMBL3617515 123527 None 0 Rat Functional pIC50 = 5.5 5.5 - 1
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 420 4 0 5 4.2 C[C@@H]1CN(c2ccc(F)cc2)C(=O)c2cc(COc3ncccc3C(F)(F)F)nn21 10.1021/acs.jmedchem.5b01005
11442010 56325 None 0 Rat Functional pIC50 = 8.5 8.5 2 3
Antagonist activity at rat mGluR3 receptor expressed in CHO cells assessed as inhibition of GIRK currentAntagonist activity at rat mGluR3 receptor expressed in CHO cells assessed as inhibition of GIRK current
ChEMBL 439 4 1 4 5.9 CCOc1cc2c(cc1C(F)(F)F)NC(=O)CC(c1cccc(-c3ccnc(C)c3)c1)=N2 10.1016/j.bmcl.2010.09.125
CHEMBL1629866 56325 None 0 Rat Functional pIC50 = 8.5 8.5 2 3
Antagonist activity at rat mGluR3 receptor expressed in CHO cells assessed as inhibition of GIRK currentAntagonist activity at rat mGluR3 receptor expressed in CHO cells assessed as inhibition of GIRK current
ChEMBL 439 4 1 4 5.9 CCOc1cc2c(cc1C(F)(F)F)NC(=O)CC(c1cccc(-c3ccnc(C)c3)c1)=N2 10.1016/j.bmcl.2010.09.125
11304010 56323 None 0 Rat Functional pIC50 = 7.5 7.5 -10 3
Antagonist activity at rat mGluR3 receptor expressed in CHO cells assessed as inhibition of GIRK currentAntagonist activity at rat mGluR3 receptor expressed in CHO cells assessed as inhibition of GIRK current
ChEMBL 395 2 1 3 5.8 Cc1cc(-c2cccc(C3=Nc4cc(Cl)c(Cl)cc4NC(=O)C3)c2)ccn1 10.1016/j.bmcl.2010.09.125
CHEMBL1629864 56323 None 0 Rat Functional pIC50 = 7.5 7.5 -10 3
Antagonist activity at rat mGluR3 receptor expressed in CHO cells assessed as inhibition of GIRK currentAntagonist activity at rat mGluR3 receptor expressed in CHO cells assessed as inhibition of GIRK current
ChEMBL 395 2 1 3 5.8 Cc1cc(-c2cccc(C3=Nc4cc(Cl)c(Cl)cc4NC(=O)C3)c2)ccn1 10.1016/j.bmcl.2010.09.125
6324634 148032 None 10 Human Functional pIC50 = 4.5 4.5 -6 2
In vitro antagonist activity at recombinant human Metabotropic glutamate receptor 3 expressed in RGT cells.In vitro antagonist activity at recombinant human Metabotropic glutamate receptor 3 expressed in RGT cells.
ChEMBL 355 10 3 3 3.5 N[C@@H](C[C@H](CCCC(c1ccccc1)c1ccccc1)C(=O)O)C(=O)O 10.1016/s0960-894x(98)00352-7
CHEMBL39338 148032 None 10 Human Functional pIC50 = 4.5 4.5 -6 2
In vitro antagonist activity at recombinant human Metabotropic glutamate receptor 3 expressed in RGT cells.In vitro antagonist activity at recombinant human Metabotropic glutamate receptor 3 expressed in RGT cells.
ChEMBL 355 10 3 3 3.5 N[C@@H](C[C@H](CCCC(c1ccccc1)c1ccccc1)C(=O)O)C(=O)O 10.1016/s0960-894x(98)00352-7
6324634 148032 None 10 Human Functional pIC50 = 4.5 4.5 -6 2
Tested for agonist activity in non-neuronal cells (RGT) expressing human Metabotropic glutamate receptor 3 by measuring ACPD (3 uM) induced inhibition of forskolin (15 uM)-stimulated cAMP formationTested for agonist activity in non-neuronal cells (RGT) expressing human Metabotropic glutamate receptor 3 by measuring ACPD (3 uM) induced inhibition of forskolin (15 uM)-stimulated cAMP formation
ChEMBL 355 10 3 3 3.5 N[C@@H](C[C@H](CCCC(c1ccccc1)c1ccccc1)C(=O)O)C(=O)O 10.1016/s0960-894x(98)00091-2
CHEMBL39338 148032 None 10 Human Functional pIC50 = 4.5 4.5 -6 2
Tested for agonist activity in non-neuronal cells (RGT) expressing human Metabotropic glutamate receptor 3 by measuring ACPD (3 uM) induced inhibition of forskolin (15 uM)-stimulated cAMP formationTested for agonist activity in non-neuronal cells (RGT) expressing human Metabotropic glutamate receptor 3 by measuring ACPD (3 uM) induced inhibition of forskolin (15 uM)-stimulated cAMP formation
ChEMBL 355 10 3 3 3.5 N[C@@H](C[C@H](CCCC(c1ccccc1)c1ccccc1)C(=O)O)C(=O)O 10.1016/s0960-894x(98)00091-2
60204018 90358 None 0 Rat Functional pIC50 = 6.5 6.5 - 1
Negative allosteric modulation of rat mGlu3 receptor transfected in human TREX cells assessed as inhibition of glutamate-induced calcium mobilization after 2.5 minsNegative allosteric modulation of rat mGlu3 receptor transfected in human TREX cells assessed as inhibition of glutamate-induced calcium mobilization after 2.5 mins
ChEMBL 335 2 1 3 2.7 COc1ccc(C#Cc2ccc(C(=O)N3CCC[C@@H](O)C3)cc2)cc1 10.1021/jm400439t
CHEMBL2385878 90358 None 0 Rat Functional pIC50 = 6.5 6.5 - 1
Negative allosteric modulation of rat mGlu3 receptor transfected in human TREX cells assessed as inhibition of glutamate-induced calcium mobilization after 2.5 minsNegative allosteric modulation of rat mGlu3 receptor transfected in human TREX cells assessed as inhibition of glutamate-induced calcium mobilization after 2.5 mins
ChEMBL 335 2 1 3 2.7 COc1ccc(C#Cc2ccc(C(=O)N3CCC[C@@H](O)C3)cc2)cc1 10.1021/jm400439t
CHEMBL2385888 90358 None 0 Rat Functional pIC50 = 6.5 6.5 - 1
Negative allosteric modulation of rat mGlu3 receptor transfected in human TREX cells assessed as inhibition of glutamate-induced calcium mobilization after 2.5 minsNegative allosteric modulation of rat mGlu3 receptor transfected in human TREX cells assessed as inhibition of glutamate-induced calcium mobilization after 2.5 mins
ChEMBL 335 2 1 3 2.7 COc1ccc(C#Cc2ccc(C(=O)N3CCC[C@@H](O)C3)cc2)cc1 10.1021/jm400439t
71136653 123470 None 0 Human Functional pIC50 = 5.5 5.5 -51 2
Antagonist activity at human recombinant mGlu3 receptor expressed in AV12 cells assessed as inhibition of glutamate-stimulated Ca2+ mobilization after 1.5 hrs by FLIPR assayAntagonist activity at human recombinant mGlu3 receptor expressed in AV12 cells assessed as inhibition of glutamate-stimulated Ca2+ mobilization after 1.5 hrs by FLIPR assay
ChEMBL 284 4 4 6 -0.6 N[C@@]1(C(=O)O)C[C@H](Sc2nnc[nH]2)[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/acs.jmedchem.5b01124
CHEMBL3616854 123470 None 0 Human Functional pIC50 = 5.5 5.5 -51 2
Antagonist activity at human recombinant mGlu3 receptor expressed in AV12 cells assessed as inhibition of glutamate-stimulated Ca2+ mobilization after 1.5 hrs by FLIPR assayAntagonist activity at human recombinant mGlu3 receptor expressed in AV12 cells assessed as inhibition of glutamate-stimulated Ca2+ mobilization after 1.5 hrs by FLIPR assay
ChEMBL 284 4 4 6 -0.6 N[C@@]1(C(=O)O)C[C@H](Sc2nnc[nH]2)[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/acs.jmedchem.5b01124
122190416 123592 None 0 Rat Functional pIC50 = 6.5 6.5 16 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 398 5 0 6 3.7 COc1cccc(N2C[C@@H](C)n3nc(COc4ccc(Cl)cn4)cc3C2=O)c1 10.1021/acs.jmedchem.5b01005
CHEMBL3617639 123592 None 0 Rat Functional pIC50 = 6.5 6.5 16 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 398 5 0 6 3.7 COc1cccc(N2C[C@@H](C)n3nc(COc4ccc(Cl)cn4)cc3C2=O)c1 10.1021/acs.jmedchem.5b01005
122190426 123602 None 0 Rat Functional pIC50 = 6.5 6.5 3 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 411 4 0 6 3.7 C[C@@H]1CN(c2cc(F)cc(C#N)c2)C(=O)c2cc(COc3ccc(Cl)cn3)nn21 10.1021/acs.jmedchem.5b01005
CHEMBL3617649 123602 None 0 Rat Functional pIC50 = 6.5 6.5 3 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 411 4 0 6 3.7 C[C@@H]1CN(c2cc(F)cc(C#N)c2)C(=O)c2cc(COc3ccc(Cl)cn3)nn21 10.1021/acs.jmedchem.5b01005
90643973 112065 None 0 Rat Functional pIC50 = 5.5 5.5 1 2
Inhibition of rat mGlu3 receptor transfected in HEK293 cells coexpressing mouse Galpha15 assessed as decrease in glutamate-induced calcium signaling by fluorescence plate reader analysis in presence of glutamate at EC87 concentrationInhibition of rat mGlu3 receptor transfected in HEK293 cells coexpressing mouse Galpha15 assessed as decrease in glutamate-induced calcium signaling by fluorescence plate reader analysis in presence of glutamate at EC87 concentration
ChEMBL 382 4 1 6 3.4 O=c1c2ccc(-c3cccnc3)cc2n2nc(-c3ccccc3)cc2n1CCO 10.1016/j.bmcl.2014.04.051
CHEMBL3288674 112065 None 0 Rat Functional pIC50 = 5.5 5.5 1 2
Inhibition of rat mGlu3 receptor transfected in HEK293 cells coexpressing mouse Galpha15 assessed as decrease in glutamate-induced calcium signaling by fluorescence plate reader analysis in presence of glutamate at EC87 concentrationInhibition of rat mGlu3 receptor transfected in HEK293 cells coexpressing mouse Galpha15 assessed as decrease in glutamate-induced calcium signaling by fluorescence plate reader analysis in presence of glutamate at EC87 concentration
ChEMBL 382 4 1 6 3.4 O=c1c2ccc(-c3cccnc3)cc2n2nc(-c3ccccc3)cc2n1CCO 10.1016/j.bmcl.2014.04.051
122190416 123592 None 0 Rat Functional pIC50 = 6.5 6.5 16 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 398 5 0 6 3.7 COc1cccc(N2C[C@@H](C)n3nc(COc4ccc(Cl)cn4)cc3C2=O)c1 10.1021/acs.jmedchem.5b01005
CHEMBL3617639 123592 None 0 Rat Functional pIC50 = 6.5 6.5 16 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 398 5 0 6 3.7 COc1cccc(N2C[C@@H](C)n3nc(COc4ccc(Cl)cn4)cc3C2=O)c1 10.1021/acs.jmedchem.5b01005
122190426 123602 None 0 Rat Functional pIC50 = 6.5 6.5 3 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 411 4 0 6 3.7 C[C@@H]1CN(c2cc(F)cc(C#N)c2)C(=O)c2cc(COc3ccc(Cl)cn3)nn21 10.1021/acs.jmedchem.5b01005
CHEMBL3617649 123602 None 0 Rat Functional pIC50 = 6.5 6.5 3 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 411 4 0 6 3.7 C[C@@H]1CN(c2cc(F)cc(C#N)c2)C(=O)c2cc(COc3ccc(Cl)cn3)nn21 10.1021/acs.jmedchem.5b01005
122190399 123575 None 0 Rat Functional pIC50 = 6.5 6.5 4 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 382 5 0 6 3.2 COc1ccc(N2C[C@@H](C)n3nc(COc4ccc(F)cn4)cc3C2=O)cc1 10.1021/acs.jmedchem.5b01005
CHEMBL3617622 123575 None 0 Rat Functional pIC50 = 6.5 6.5 4 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 382 5 0 6 3.2 COc1ccc(N2C[C@@H](C)n3nc(COc4ccc(F)cn4)cc3C2=O)cc1 10.1021/acs.jmedchem.5b01005
122190399 123575 None 0 Rat Functional pIC50 = 6.5 6.5 4 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 382 5 0 6 3.2 COc1ccc(N2C[C@@H](C)n3nc(COc4ccc(F)cn4)cc3C2=O)cc1 10.1021/acs.jmedchem.5b01005
CHEMBL3617622 123575 None 0 Rat Functional pIC50 = 6.5 6.5 4 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 382 5 0 6 3.2 COc1ccc(N2C[C@@H](C)n3nc(COc4ccc(F)cn4)cc3C2=O)cc1 10.1021/acs.jmedchem.5b01005
122190409 123585 None 0 Rat Functional pIC50 = 6.5 6.5 16 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 402 4 0 5 4.4 C[C@@H]1CN(c2ccccc2Cl)C(=O)c2cc(COc3ccc(Cl)cn3)nn21 10.1021/acs.jmedchem.5b01005
CHEMBL3617632 123585 None 0 Rat Functional pIC50 = 6.5 6.5 16 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 402 4 0 5 4.4 C[C@@H]1CN(c2ccccc2Cl)C(=O)c2cc(COc3ccc(Cl)cn3)nn21 10.1021/acs.jmedchem.5b01005
122190427 123603 None 0 Rat Functional pIC50 = 6.5 6.5 - 1
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 369 4 0 6 3.1 C[C@@H]1CN(c2ccccn2)C(=O)c2cc(COc3ccc(Cl)cn3)nn21 10.1021/acs.jmedchem.5b01005
CHEMBL3617650 123603 None 0 Rat Functional pIC50 = 6.5 6.5 - 1
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 369 4 0 6 3.1 C[C@@H]1CN(c2ccccn2)C(=O)c2cc(COc3ccc(Cl)cn3)nn21 10.1021/acs.jmedchem.5b01005
22224657 96225 None 0 Rat Functional pIC50 = 7.5 7.5 -2 2
Antagonist activity at rat mGluR3 expressed in CHO cells assessed as inhibition of glutamate-induced GIRK currentAntagonist activity at rat mGluR3 expressed in CHO cells assessed as inhibition of glutamate-induced GIRK current
ChEMBL 396 3 1 4 5.1 O=C1CC(c2cccc(-n3ccnc3)c2)=Nc2ccc(-c3ccccc3F)cc2N1 10.1016/j.bmcl.2008.02.076
CHEMBL260636 96225 None 0 Rat Functional pIC50 = 7.5 7.5 -2 2
Antagonist activity at rat mGluR3 expressed in CHO cells assessed as inhibition of glutamate-induced GIRK currentAntagonist activity at rat mGluR3 expressed in CHO cells assessed as inhibition of glutamate-induced GIRK current
ChEMBL 396 3 1 4 5.1 O=C1CC(c2cccc(-n3ccnc3)c2)=Nc2ccc(-c3ccccc3F)cc2N1 10.1016/j.bmcl.2008.02.076
9952648 96361 None 0 Rat Functional pIC50 = 7.5 7.5 -1 2
Antagonist activity at rat mGluR3 receptor expressed in CHO cells assessed as inhibition of GIRK currentAntagonist activity at rat mGluR3 receptor expressed in CHO cells assessed as inhibition of GIRK current
ChEMBL 397 3 1 5 4.5 O=C1CC(c2cccc(-n3ccnn3)c2)=Nc2ccc(-c3ccccc3F)cc2N1 10.1016/j.bmcl.2010.09.125
CHEMBL261288 96361 None 0 Rat Functional pIC50 = 7.5 7.5 -1 2
Antagonist activity at rat mGluR3 receptor expressed in CHO cells assessed as inhibition of GIRK currentAntagonist activity at rat mGluR3 receptor expressed in CHO cells assessed as inhibition of GIRK current
ChEMBL 397 3 1 5 4.5 O=C1CC(c2cccc(-n3ccnn3)c2)=Nc2ccc(-c3ccccc3F)cc2N1 10.1016/j.bmcl.2010.09.125
122190409 123585 None 0 Rat Functional pIC50 = 6.5 6.5 16 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 402 4 0 5 4.4 C[C@@H]1CN(c2ccccc2Cl)C(=O)c2cc(COc3ccc(Cl)cn3)nn21 10.1021/acs.jmedchem.5b01005
CHEMBL3617632 123585 None 0 Rat Functional pIC50 = 6.5 6.5 16 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 402 4 0 5 4.4 C[C@@H]1CN(c2ccccc2Cl)C(=O)c2cc(COc3ccc(Cl)cn3)nn21 10.1021/acs.jmedchem.5b01005
122190427 123603 None 0 Rat Functional pIC50 = 6.5 6.5 - 1
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 369 4 0 6 3.1 C[C@@H]1CN(c2ccccn2)C(=O)c2cc(COc3ccc(Cl)cn3)nn21 10.1021/acs.jmedchem.5b01005
CHEMBL3617650 123603 None 0 Rat Functional pIC50 = 6.5 6.5 - 1
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 369 4 0 6 3.1 C[C@@H]1CN(c2ccccn2)C(=O)c2cc(COc3ccc(Cl)cn3)nn21 10.1021/acs.jmedchem.5b01005
71681826 90095 None 0 Human Functional pIC50 = 5.5 5.5 -1 3
Antagonist activity at human mGlu3 receptor expressed in golden Syrian hamster AV12 cells coexpressing EAAT1 assessed as inhibition of forskolin-stimulated cAMP production after 20 mins by HTRF assayAntagonist activity at human mGlu3 receptor expressed in golden Syrian hamster AV12 cells coexpressing EAAT1 assessed as inhibition of forskolin-stimulated cAMP production after 20 mins by HTRF assay
ChEMBL 293 4 3 4 1.3 N[C@@]1(C(=O)O)C[C@H](Sc2ccccc2)[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/jm4000165
CHEMBL2381651 90095 None 0 Human Functional pIC50 = 5.5 5.5 -1 3
Antagonist activity at human mGlu3 receptor expressed in golden Syrian hamster AV12 cells coexpressing EAAT1 assessed as inhibition of forskolin-stimulated cAMP production after 20 mins by HTRF assayAntagonist activity at human mGlu3 receptor expressed in golden Syrian hamster AV12 cells coexpressing EAAT1 assessed as inhibition of forskolin-stimulated cAMP production after 20 mins by HTRF assay
ChEMBL 293 4 3 4 1.3 N[C@@]1(C(=O)O)C[C@H](Sc2ccccc2)[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/jm4000165
71681826 90095 None 0 Human Functional pIC50 = 5.5 5.5 -1 3
Antagonist activity at human recombinant mGlu3 receptor expressed in AV12 cells assessed as reversal of DCG-4-inhibited, forskolin-stimulated cAMP production after 1 hr by fluorescence assayAntagonist activity at human recombinant mGlu3 receptor expressed in AV12 cells assessed as reversal of DCG-4-inhibited, forskolin-stimulated cAMP production after 1 hr by fluorescence assay
ChEMBL 293 4 3 4 1.3 N[C@@]1(C(=O)O)C[C@H](Sc2ccccc2)[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/acs.jmedchem.5b01124
CHEMBL2381651 90095 None 0 Human Functional pIC50 = 5.5 5.5 -1 3
Antagonist activity at human recombinant mGlu3 receptor expressed in AV12 cells assessed as reversal of DCG-4-inhibited, forskolin-stimulated cAMP production after 1 hr by fluorescence assayAntagonist activity at human recombinant mGlu3 receptor expressed in AV12 cells assessed as reversal of DCG-4-inhibited, forskolin-stimulated cAMP production after 1 hr by fluorescence assay
ChEMBL 293 4 3 4 1.3 N[C@@]1(C(=O)O)C[C@H](Sc2ccccc2)[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/acs.jmedchem.5b01124
122190397 123573 None 0 Rat Functional pIC50 = 6.5 6.5 -1 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 382 5 0 6 3.2 COc1ccccc1N1C[C@@H](C)n2nc(COc3ccc(F)cn3)cc2C1=O 10.1021/acs.jmedchem.5b01005
CHEMBL3617620 123573 None 0 Rat Functional pIC50 = 6.5 6.5 -1 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 382 5 0 6 3.2 COc1ccccc1N1C[C@@H](C)n2nc(COc3ccc(F)cn3)cc2C1=O 10.1021/acs.jmedchem.5b01005
140839143 162299 None 0 Rat Functional pIC50 = 6.5 6.5 18 2
Negative allosteric modulation of rat mGlu3 receptor expressed in TREX cells coexpressing Galpha15 assessed as inhibition of glutamate induced-calcium mobilization preincubated for 2.3 mins followed by glutamate addition measured for 2.6 mins by Fluo-4 AM dye based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor expressed in TREX cells coexpressing Galpha15 assessed as inhibition of glutamate induced-calcium mobilization preincubated for 2.3 mins followed by glutamate addition measured for 2.6 mins by Fluo-4 AM dye based fluorescence assay
ChEMBL 332 6 0 5 3.2 N#Cc1cccc(-n2ccc(OCCOc3ccccc3)cc2=O)c1 10.1021/acsmedchemlett.7b00249
CHEMBL4162785 162299 None 0 Rat Functional pIC50 = 6.5 6.5 18 2
Negative allosteric modulation of rat mGlu3 receptor expressed in TREX cells coexpressing Galpha15 assessed as inhibition of glutamate induced-calcium mobilization preincubated for 2.3 mins followed by glutamate addition measured for 2.6 mins by Fluo-4 AM dye based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor expressed in TREX cells coexpressing Galpha15 assessed as inhibition of glutamate induced-calcium mobilization preincubated for 2.3 mins followed by glutamate addition measured for 2.6 mins by Fluo-4 AM dye based fluorescence assay
ChEMBL 332 6 0 5 3.2 N#Cc1cccc(-n2ccc(OCCOc3ccccc3)cc2=O)c1 10.1021/acsmedchemlett.7b00249
122190397 123573 None 0 Rat Functional pIC50 = 6.5 6.5 -1 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 382 5 0 6 3.2 COc1ccccc1N1C[C@@H](C)n2nc(COc3ccc(F)cn3)cc2C1=O 10.1021/acs.jmedchem.5b01005
CHEMBL3617620 123573 None 0 Rat Functional pIC50 = 6.5 6.5 -1 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 382 5 0 6 3.2 COc1ccccc1N1C[C@@H](C)n2nc(COc3ccc(F)cn3)cc2C1=O 10.1021/acs.jmedchem.5b01005
70051296 90092 None 0 Human Functional pIC50 = 5.5 5.5 1 3
Antagonist activity at human mGlu3 receptor expressed in golden Syrian hamster AV12 cells coexpressing EAAT1 assessed as inhibition of forskolin-stimulated cAMP production after 20 mins by HTRF assayAntagonist activity at human mGlu3 receptor expressed in golden Syrian hamster AV12 cells coexpressing EAAT1 assessed as inhibition of forskolin-stimulated cAMP production after 20 mins by HTRF assay
ChEMBL 242 3 4 4 -1.4 CC(=O)N[C@@H]1C[C@@](N)(C(=O)O)[C@@H]2[C@@H](C(=O)O)[C@@H]21 10.1021/jm4000165
CHEMBL2381648 90092 None 0 Human Functional pIC50 = 5.5 5.5 1 3
Antagonist activity at human mGlu3 receptor expressed in golden Syrian hamster AV12 cells coexpressing EAAT1 assessed as inhibition of forskolin-stimulated cAMP production after 20 mins by HTRF assayAntagonist activity at human mGlu3 receptor expressed in golden Syrian hamster AV12 cells coexpressing EAAT1 assessed as inhibition of forskolin-stimulated cAMP production after 20 mins by HTRF assay
ChEMBL 242 3 4 4 -1.4 CC(=O)N[C@@H]1C[C@@](N)(C(=O)O)[C@@H]2[C@@H](C(=O)O)[C@@H]21 10.1021/jm4000165
140839143 162299 None 0 Rat Functional pIC50 = 6.5 6.5 18 2
Negative allosteric modulation of rat mGlu3 receptor expressed in TREX cells coexpressing Galpha15 assessed as inhibition of glutamate induced-calcium mobilization preincubated for 2.3 mins followed by glutamate addition measured for 2.6 mins by Fluo-4 AM dye based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor expressed in TREX cells coexpressing Galpha15 assessed as inhibition of glutamate induced-calcium mobilization preincubated for 2.3 mins followed by glutamate addition measured for 2.6 mins by Fluo-4 AM dye based fluorescence assay
ChEMBL 332 6 0 5 3.2 N#Cc1cccc(-n2ccc(OCCOc3ccccc3)cc2=O)c1 10.1021/acsmedchemlett.7b00249
CHEMBL4162785 162299 None 0 Rat Functional pIC50 = 6.5 6.5 18 2
Negative allosteric modulation of rat mGlu3 receptor expressed in TREX cells coexpressing Galpha15 assessed as inhibition of glutamate induced-calcium mobilization preincubated for 2.3 mins followed by glutamate addition measured for 2.6 mins by Fluo-4 AM dye based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor expressed in TREX cells coexpressing Galpha15 assessed as inhibition of glutamate induced-calcium mobilization preincubated for 2.3 mins followed by glutamate addition measured for 2.6 mins by Fluo-4 AM dye based fluorescence assay
ChEMBL 332 6 0 5 3.2 N#Cc1cccc(-n2ccc(OCCOc3ccccc3)cc2=O)c1 10.1021/acsmedchemlett.7b00249
11310142 2422 None 14 Human Functional pIC50 = 5.5 5.5 -13 3
Antagonist activity at human mGlu3 receptor expressed in golden Syrian hamster AV12 cells coexpressing EAAT1 assessed as inhibition of forskolin-stimulated cAMP production after 20 mins by HTRF assayAntagonist activity at human mGlu3 receptor expressed in golden Syrian hamster AV12 cells coexpressing EAAT1 assessed as inhibition of forskolin-stimulated cAMP production after 20 mins by HTRF assay
ChEMBL 199 2 3 3 -0.2 C[C@@H]1C[C@@]([C@H]2[C@@H]1[C@@H]2C(=O)O)(N)C(=O)O 10.1021/jm4000165
11614 2422 None 14 Human Functional pIC50 = 5.5 5.5 -13 3
Antagonist activity at human mGlu3 receptor expressed in golden Syrian hamster AV12 cells coexpressing EAAT1 assessed as inhibition of forskolin-stimulated cAMP production after 20 mins by HTRF assayAntagonist activity at human mGlu3 receptor expressed in golden Syrian hamster AV12 cells coexpressing EAAT1 assessed as inhibition of forskolin-stimulated cAMP production after 20 mins by HTRF assay
ChEMBL 199 2 3 3 -0.2 C[C@@H]1C[C@@]([C@H]2[C@@H]1[C@@H]2C(=O)O)(N)C(=O)O 10.1021/jm4000165
CHEMBL192051 2422 None 14 Human Functional pIC50 = 5.5 5.5 -13 3
Antagonist activity at human mGlu3 receptor expressed in golden Syrian hamster AV12 cells coexpressing EAAT1 assessed as inhibition of forskolin-stimulated cAMP production after 20 mins by HTRF assayAntagonist activity at human mGlu3 receptor expressed in golden Syrian hamster AV12 cells coexpressing EAAT1 assessed as inhibition of forskolin-stimulated cAMP production after 20 mins by HTRF assay
ChEMBL 199 2 3 3 -0.2 C[C@@H]1C[C@@]([C@H]2[C@@H]1[C@@H]2C(=O)O)(N)C(=O)O 10.1021/jm4000165
122190394 123570 None 0 Rat Functional pIC50 = 6.5 6.5 - 1
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 366 4 0 5 3.5 Cc1ccccc1N1C[C@@H](C)n2nc(COc3ccc(F)cn3)cc2C1=O 10.1021/acs.jmedchem.5b01005
CHEMBL3617617 123570 None 0 Rat Functional pIC50 = 6.5 6.5 - 1
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 366 4 0 5 3.5 Cc1ccccc1N1C[C@@H](C)n2nc(COc3ccc(F)cn3)cc2C1=O 10.1021/acs.jmedchem.5b01005
122190394 123570 None 0 Rat Functional pIC50 = 6.5 6.5 - 1
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 366 4 0 5 3.5 Cc1ccccc1N1C[C@@H](C)n2nc(COc3ccc(F)cn3)cc2C1=O 10.1021/acs.jmedchem.5b01005
CHEMBL3617617 123570 None 0 Rat Functional pIC50 = 6.5 6.5 - 1
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 366 4 0 5 3.5 Cc1ccccc1N1C[C@@H](C)n2nc(COc3ccc(F)cn3)cc2C1=O 10.1021/acs.jmedchem.5b01005
122190406 123582 None 0 Rat Functional pIC50 = 6.5 6.5 28 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 371 4 0 6 2.8 C[C@@H]1CN(c2ccc(F)cn2)C(=O)c2cc(COc3ccc(F)cn3)nn21 10.1021/acs.jmedchem.5b01005
CHEMBL3617629 123582 None 0 Rat Functional pIC50 = 6.5 6.5 28 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 371 4 0 6 2.8 C[C@@H]1CN(c2ccc(F)cn2)C(=O)c2cc(COc3ccc(F)cn3)nn21 10.1021/acs.jmedchem.5b01005
122456122 162841 None 0 Rat Functional pIC50 = 6.5 6.5 4 2
Negative allosteric modulation of rat mGlu3 receptor expressed in TREX cells coexpressing Galpha15 assessed as inhibition of glutamate induced-calcium mobilization preincubated for 2.3 mins followed by glutamate addition measured for 2.6 mins by Fluo-4 AM dye based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor expressed in TREX cells coexpressing Galpha15 assessed as inhibition of glutamate induced-calcium mobilization preincubated for 2.3 mins followed by glutamate addition measured for 2.6 mins by Fluo-4 AM dye based fluorescence assay
ChEMBL 343 6 0 4 3.6 O=c1cc(OCCOc2cccc(F)c2)ccn1-c1ccc(F)cc1 10.1021/acsmedchemlett.7b00249
CHEMBL4171435 162841 None 0 Rat Functional pIC50 = 6.5 6.5 4 2
Negative allosteric modulation of rat mGlu3 receptor expressed in TREX cells coexpressing Galpha15 assessed as inhibition of glutamate induced-calcium mobilization preincubated for 2.3 mins followed by glutamate addition measured for 2.6 mins by Fluo-4 AM dye based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor expressed in TREX cells coexpressing Galpha15 assessed as inhibition of glutamate induced-calcium mobilization preincubated for 2.3 mins followed by glutamate addition measured for 2.6 mins by Fluo-4 AM dye based fluorescence assay
ChEMBL 343 6 0 4 3.6 O=c1cc(OCCOc2cccc(F)c2)ccn1-c1ccc(F)cc1 10.1021/acsmedchemlett.7b00249
122190406 123582 None 0 Rat Functional pIC50 = 6.5 6.5 28 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 371 4 0 6 2.8 C[C@@H]1CN(c2ccc(F)cn2)C(=O)c2cc(COc3ccc(F)cn3)nn21 10.1021/acs.jmedchem.5b01005
CHEMBL3617629 123582 None 0 Rat Functional pIC50 = 6.5 6.5 28 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 371 4 0 6 2.8 C[C@@H]1CN(c2ccc(F)cn2)C(=O)c2cc(COc3ccc(F)cn3)nn21 10.1021/acs.jmedchem.5b01005
122456122 162841 None 0 Rat Functional pIC50 = 6.5 6.5 4 2
Negative allosteric modulation of rat mGlu3 receptor expressed in TREX cells coexpressing Galpha15 assessed as inhibition of glutamate induced-calcium mobilization preincubated for 2.3 mins followed by glutamate addition measured for 2.6 mins by Fluo-4 AM dye based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor expressed in TREX cells coexpressing Galpha15 assessed as inhibition of glutamate induced-calcium mobilization preincubated for 2.3 mins followed by glutamate addition measured for 2.6 mins by Fluo-4 AM dye based fluorescence assay
ChEMBL 343 6 0 4 3.6 O=c1cc(OCCOc2cccc(F)c2)ccn1-c1ccc(F)cc1 10.1021/acsmedchemlett.7b00249
CHEMBL4171435 162841 None 0 Rat Functional pIC50 = 6.5 6.5 4 2
Negative allosteric modulation of rat mGlu3 receptor expressed in TREX cells coexpressing Galpha15 assessed as inhibition of glutamate induced-calcium mobilization preincubated for 2.3 mins followed by glutamate addition measured for 2.6 mins by Fluo-4 AM dye based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor expressed in TREX cells coexpressing Galpha15 assessed as inhibition of glutamate induced-calcium mobilization preincubated for 2.3 mins followed by glutamate addition measured for 2.6 mins by Fluo-4 AM dye based fluorescence assay
ChEMBL 343 6 0 4 3.6 O=c1cc(OCCOc2cccc(F)c2)ccn1-c1ccc(F)cc1 10.1021/acsmedchemlett.7b00249
71137008 123471 None 0 Human Functional pIC50 = 5.5 5.5 -7 2
Antagonist activity at human recombinant mGlu3 receptor expressed in AV12 cells assessed as inhibition of glutamate-stimulated Ca2+ mobilization after 1.5 hrs by FLIPR assayAntagonist activity at human recombinant mGlu3 receptor expressed in AV12 cells assessed as inhibition of glutamate-stimulated Ca2+ mobilization after 1.5 hrs by FLIPR assay
ChEMBL 298 4 4 6 -0.3 Cc1nnc(S[C@H]2C[C@@](N)(C(=O)O)[C@@H]3[C@@H](C(=O)O)[C@H]23)[nH]1 10.1021/acs.jmedchem.5b01124
CHEMBL3616855 123471 None 0 Human Functional pIC50 = 5.5 5.5 -7 2
Antagonist activity at human recombinant mGlu3 receptor expressed in AV12 cells assessed as inhibition of glutamate-stimulated Ca2+ mobilization after 1.5 hrs by FLIPR assayAntagonist activity at human recombinant mGlu3 receptor expressed in AV12 cells assessed as inhibition of glutamate-stimulated Ca2+ mobilization after 1.5 hrs by FLIPR assay
ChEMBL 298 4 4 6 -0.3 Cc1nnc(S[C@H]2C[C@@](N)(C(=O)O)[C@@H]3[C@@H](C(=O)O)[C@H]23)[nH]1 10.1021/acs.jmedchem.5b01124
122190429 123605 None 0 Rat Functional pIC50 = 6.4 6.4 - 1
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 387 4 0 6 3.3 C[C@@H]1CN(c2ncccc2F)C(=O)c2cc(COc3ccc(Cl)cn3)nn21 10.1021/acs.jmedchem.5b01005
CHEMBL3617652 123605 None 0 Rat Functional pIC50 = 6.4 6.4 - 1
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 387 4 0 6 3.3 C[C@@H]1CN(c2ncccc2F)C(=O)c2cc(COc3ccc(Cl)cn3)nn21 10.1021/acs.jmedchem.5b01005
122190429 123605 None 0 Rat Functional pIC50 = 6.4 6.4 - 1
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 387 4 0 6 3.3 C[C@@H]1CN(c2ncccc2F)C(=O)c2cc(COc3ccc(Cl)cn3)nn21 10.1021/acs.jmedchem.5b01005
CHEMBL3617652 123605 None 0 Rat Functional pIC50 = 6.4 6.4 - 1
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 387 4 0 6 3.3 C[C@@H]1CN(c2ncccc2F)C(=O)c2cc(COc3ccc(Cl)cn3)nn21 10.1021/acs.jmedchem.5b01005
122190335 123531 None 0 Rat Functional pIC50 = 5.4 5.4 - 1
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 382 5 0 6 3.2 COc1ccnc(OCc2cc3n(n2)[C@H](C)CN(c2ccc(F)cc2)C3=O)c1 10.1021/acs.jmedchem.5b01005
CHEMBL3617519 123531 None 0 Rat Functional pIC50 = 5.4 5.4 - 1
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 382 5 0 6 3.2 COc1ccnc(OCc2cc3n(n2)[C@H](C)CN(c2ccc(F)cc2)C3=O)c1 10.1021/acs.jmedchem.5b01005
122190335 123531 None 0 Rat Functional pIC50 = 5.4 5.4 - 1
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 382 5 0 6 3.2 COc1ccnc(OCc2cc3n(n2)[C@H](C)CN(c2ccc(F)cc2)C3=O)c1 10.1021/acs.jmedchem.5b01005
CHEMBL3617519 123531 None 0 Rat Functional pIC50 = 5.4 5.4 - 1
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 382 5 0 6 3.2 COc1ccnc(OCc2cc3n(n2)[C@H](C)CN(c2ccc(F)cc2)C3=O)c1 10.1021/acs.jmedchem.5b01005
67705326 153337 None 0 Human Functional pIC50 = 7.4 7.4 -2 2
Antagonist activity at recombinant human mGlu3 receptor expressed in hamster AV12 cells co-expressing human EAAT1 assessed as reduction of DCG-4-inhibited forskolin-stimulated cAMP formation after 20 mins by HTRF assayAntagonist activity at recombinant human mGlu3 receptor expressed in hamster AV12 cells co-expressing human EAAT1 assessed as reduction of DCG-4-inhibited forskolin-stimulated cAMP formation after 20 mins by HTRF assay
ChEMBL 457 7 4 6 2.5 N[C@@]1(C(=O)O)[C@H](OCc2ccc(Cl)c(Cl)c2)[C@@H](Sc2ncc[nH]2)[C@H]2[C@H](C(=O)O)[C@H]21 10.1016/j.bmcl.2016.10.067
CHEMBL3977508 153337 None 0 Human Functional pIC50 = 7.4 7.4 -2 2
Antagonist activity at recombinant human mGlu3 receptor expressed in hamster AV12 cells co-expressing human EAAT1 assessed as reduction of DCG-4-inhibited forskolin-stimulated cAMP formation after 20 mins by HTRF assayAntagonist activity at recombinant human mGlu3 receptor expressed in hamster AV12 cells co-expressing human EAAT1 assessed as reduction of DCG-4-inhibited forskolin-stimulated cAMP formation after 20 mins by HTRF assay
ChEMBL 457 7 4 6 2.5 N[C@@]1(C(=O)O)[C@H](OCc2ccc(Cl)c(Cl)c2)[C@@H](Sc2ncc[nH]2)[C@H]2[C@H](C(=O)O)[C@H]21 10.1016/j.bmcl.2016.10.067
71137011 123474 None 0 Human Functional pIC50 = 5.4 5.4 -58 2
Antagonist activity at human recombinant mGlu3 receptor expressed in AV12 cells assessed as inhibition of glutamate-stimulated Ca2+ mobilization after 1.5 hrs by FLIPR assayAntagonist activity at human recombinant mGlu3 receptor expressed in AV12 cells assessed as inhibition of glutamate-stimulated Ca2+ mobilization after 1.5 hrs by FLIPR assay
ChEMBL 299 4 5 7 -1.0 Nc1nnc(S[C@H]2C[C@@](N)(C(=O)O)[C@@H]3[C@@H](C(=O)O)[C@H]23)[nH]1 10.1021/acs.jmedchem.5b01124
CHEMBL3616858 123474 None 0 Human Functional pIC50 = 5.4 5.4 -58 2
Antagonist activity at human recombinant mGlu3 receptor expressed in AV12 cells assessed as inhibition of glutamate-stimulated Ca2+ mobilization after 1.5 hrs by FLIPR assayAntagonist activity at human recombinant mGlu3 receptor expressed in AV12 cells assessed as inhibition of glutamate-stimulated Ca2+ mobilization after 1.5 hrs by FLIPR assay
ChEMBL 299 4 5 7 -1.0 Nc1nnc(S[C@H]2C[C@@](N)(C(=O)O)[C@@H]3[C@@H](C(=O)O)[C@H]23)[nH]1 10.1021/acs.jmedchem.5b01124
10237 4051 None 22 Rat Functional pIC50 = 6.4 6.4 1 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 387 4 0 6 3.3 Clc1ccc(nc1)OCc1nn2c(c1)C(=O)N(C[C@H]2C)c1cccnc1F 10.1021/acs.jmedchem.5b01005
122190433 4051 None 22 Rat Functional pIC50 = 6.4 6.4 1 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 387 4 0 6 3.3 Clc1ccc(nc1)OCc1nn2c(c1)C(=O)N(C[C@H]2C)c1cccnc1F 10.1021/acs.jmedchem.5b01005
CHEMBL3617655 4051 None 22 Rat Functional pIC50 = 6.4 6.4 1 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 387 4 0 6 3.3 Clc1ccc(nc1)OCc1nn2c(c1)C(=O)N(C[C@H]2C)c1cccnc1F 10.1021/acs.jmedchem.5b01005
122190413 123589 None 0 Rat Functional pIC50 = 6.4 6.4 9 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 382 4 0 5 4.0 Cc1cccc(N2C[C@@H](C)n3nc(COc4ccc(Cl)cn4)cc3C2=O)c1 10.1021/acs.jmedchem.5b01005
CHEMBL3617636 123589 None 0 Rat Functional pIC50 = 6.4 6.4 9 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 382 4 0 5 4.0 Cc1cccc(N2C[C@@H](C)n3nc(COc4ccc(Cl)cn4)cc3C2=O)c1 10.1021/acs.jmedchem.5b01005
122456028 162822 None 0 Rat Functional pIC50 = 6.4 6.4 5 2
Negative allosteric modulation of rat mGlu3 receptor expressed in TREX cells coexpressing Galpha15 assessed as inhibition of glutamate induced-calcium mobilization preincubated for 2.3 mins followed by glutamate addition measured for 2.6 mins by Fluo-4 AM dye based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor expressed in TREX cells coexpressing Galpha15 assessed as inhibition of glutamate induced-calcium mobilization preincubated for 2.3 mins followed by glutamate addition measured for 2.6 mins by Fluo-4 AM dye based fluorescence assay
ChEMBL 325 6 0 4 3.4 O=c1cc(OCCOc2ccccc2)ccn1-c1cccc(F)c1 10.1021/acsmedchemlett.7b00249
CHEMBL4171110 162822 None 0 Rat Functional pIC50 = 6.4 6.4 5 2
Negative allosteric modulation of rat mGlu3 receptor expressed in TREX cells coexpressing Galpha15 assessed as inhibition of glutamate induced-calcium mobilization preincubated for 2.3 mins followed by glutamate addition measured for 2.6 mins by Fluo-4 AM dye based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor expressed in TREX cells coexpressing Galpha15 assessed as inhibition of glutamate induced-calcium mobilization preincubated for 2.3 mins followed by glutamate addition measured for 2.6 mins by Fluo-4 AM dye based fluorescence assay
ChEMBL 325 6 0 4 3.4 O=c1cc(OCCOc2ccccc2)ccn1-c1cccc(F)c1 10.1021/acsmedchemlett.7b00249
122456028 162822 None 0 Rat Functional pIC50 = 6.4 6.4 5 2
Negative allosteric modulation of rat mGlu3 receptor expressed in TREX cells coexpressing Galpha15 assessed as inhibition of glutamate induced-calcium mobilization preincubated for 2.3 mins followed by glutamate addition measured for 2.6 mins by Fluo-4 AM dye based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor expressed in TREX cells coexpressing Galpha15 assessed as inhibition of glutamate induced-calcium mobilization preincubated for 2.3 mins followed by glutamate addition measured for 2.6 mins by Fluo-4 AM dye based fluorescence assay
ChEMBL 325 6 0 4 3.4 O=c1cc(OCCOc2ccccc2)ccn1-c1cccc(F)c1 10.1021/acsmedchemlett.7b00249
CHEMBL4171110 162822 None 0 Rat Functional pIC50 = 6.4 6.4 5 2
Negative allosteric modulation of rat mGlu3 receptor expressed in TREX cells coexpressing Galpha15 assessed as inhibition of glutamate induced-calcium mobilization preincubated for 2.3 mins followed by glutamate addition measured for 2.6 mins by Fluo-4 AM dye based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor expressed in TREX cells coexpressing Galpha15 assessed as inhibition of glutamate induced-calcium mobilization preincubated for 2.3 mins followed by glutamate addition measured for 2.6 mins by Fluo-4 AM dye based fluorescence assay
ChEMBL 325 6 0 4 3.4 O=c1cc(OCCOc2ccccc2)ccn1-c1cccc(F)c1 10.1021/acsmedchemlett.7b00249
10237 4051 None 22 Rat Functional pIC50 = 6.4 6.4 1 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 387 4 0 6 3.3 Clc1ccc(nc1)OCc1nn2c(c1)C(=O)N(C[C@H]2C)c1cccnc1F 10.1021/acs.jmedchem.5b01005
122190433 4051 None 22 Rat Functional pIC50 = 6.4 6.4 1 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 387 4 0 6 3.3 Clc1ccc(nc1)OCc1nn2c(c1)C(=O)N(C[C@H]2C)c1cccnc1F 10.1021/acs.jmedchem.5b01005
CHEMBL3617655 4051 None 22 Rat Functional pIC50 = 6.4 6.4 1 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 387 4 0 6 3.3 Clc1ccc(nc1)OCc1nn2c(c1)C(=O)N(C[C@H]2C)c1cccnc1F 10.1021/acs.jmedchem.5b01005
122190413 123589 None 0 Rat Functional pIC50 = 6.4 6.4 9 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 382 4 0 5 4.0 Cc1cccc(N2C[C@@H](C)n3nc(COc4ccc(Cl)cn4)cc3C2=O)c1 10.1021/acs.jmedchem.5b01005
CHEMBL3617636 123589 None 0 Rat Functional pIC50 = 6.4 6.4 9 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 382 4 0 5 4.0 Cc1cccc(N2C[C@@H](C)n3nc(COc4ccc(Cl)cn4)cc3C2=O)c1 10.1021/acs.jmedchem.5b01005
44329033 210439 None 0 Rat Functional pIC50 = 7.4 7.4 9 5
Antagonistic activity against metabotropic glutamate receptor 3 (mGluR3) was evaluatedAntagonistic activity against metabotropic glutamate receptor 3 (mGluR3) was evaluated
ChEMBL 409 7 3 4 4.1 CC(C)C[C@@H]1[C@H](C(=O)O)[C@H]1C(N)(CC1c2ccccc2Oc2ccccc21)C(=O)O 10.1016/s0960-894x(98)00510-1
CHEMBL97200 210439 None 0 Rat Functional pIC50 = 7.4 7.4 9 5
Antagonistic activity against metabotropic glutamate receptor 3 (mGluR3) was evaluatedAntagonistic activity against metabotropic glutamate receptor 3 (mGluR3) was evaluated
ChEMBL 409 7 3 4 4.1 CC(C)C[C@@H]1[C@H](C(=O)O)[C@H]1C(N)(CC1c2ccccc2Oc2ccccc21)C(=O)O 10.1016/s0960-894x(98)00510-1
44302686 203373 None 0 Human Functional pIC50 = 4.4 4.4 1 2
In vitro antagonist activity at recombinant human Metabotropic glutamate receptor 3 expressed in RGT cells.In vitro antagonist activity at recombinant human Metabotropic glutamate receptor 3 expressed in RGT cells.
ChEMBL 332 4 3 4 1.4 N[C@]1(C(=O)O)C[C@H](C(=O)O)N(Cc2c(Cl)cccc2Cl)C1 10.1016/s0960-894x(98)00352-7
CHEMBL60164 203373 None 0 Human Functional pIC50 = 4.4 4.4 1 2
In vitro antagonist activity at recombinant human Metabotropic glutamate receptor 3 expressed in RGT cells.In vitro antagonist activity at recombinant human Metabotropic glutamate receptor 3 expressed in RGT cells.
ChEMBL 332 4 3 4 1.4 N[C@]1(C(=O)O)C[C@H](C(=O)O)N(Cc2c(Cl)cccc2Cl)C1 10.1016/s0960-894x(98)00352-7
122190414 123590 None 0 Rat Functional pIC50 = 6.4 6.4 - 1
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 382 4 0 5 4.0 Cc1ccc(N2C[C@@H](C)n3nc(COc4ccc(Cl)cn4)cc3C2=O)cc1 10.1021/acs.jmedchem.5b01005
CHEMBL3617637 123590 None 0 Rat Functional pIC50 = 6.4 6.4 - 1
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 382 4 0 5 4.0 Cc1ccc(N2C[C@@H](C)n3nc(COc4ccc(Cl)cn4)cc3C2=O)cc1 10.1021/acs.jmedchem.5b01005
122190437 123611 None 0 Rat Functional pIC50 = 6.4 6.4 - 1
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 387 4 0 6 3.3 C[C@@H]1CN(c2ccc(F)nc2)C(=O)c2cc(COc3ccc(Cl)cn3)nn21 10.1021/acs.jmedchem.5b01005
CHEMBL3617659 123611 None 0 Rat Functional pIC50 = 6.4 6.4 - 1
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 387 4 0 6 3.3 C[C@@H]1CN(c2ccc(F)nc2)C(=O)c2cc(COc3ccc(Cl)cn3)nn21 10.1021/acs.jmedchem.5b01005
122190329 123525 None 0 Rat Functional pIC50 = 5.4 5.4 - 1
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 435 5 0 5 4.7 C[C@@H]1CN(c2ccc(F)cc2)C(=O)c2cc(COc3ccc(OC(F)(F)F)cc3)nn21 10.1021/acs.jmedchem.5b01005
CHEMBL3617513 123525 None 0 Rat Functional pIC50 = 5.4 5.4 - 1
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 435 5 0 5 4.7 C[C@@H]1CN(c2ccc(F)cc2)C(=O)c2cc(COc3ccc(OC(F)(F)F)cc3)nn21 10.1021/acs.jmedchem.5b01005
122190329 123525 None 0 Rat Functional pIC50 = 5.4 5.4 - 1
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 435 5 0 5 4.7 C[C@@H]1CN(c2ccc(F)cc2)C(=O)c2cc(COc3ccc(OC(F)(F)F)cc3)nn21 10.1021/acs.jmedchem.5b01005
CHEMBL3617513 123525 None 0 Rat Functional pIC50 = 5.4 5.4 - 1
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 435 5 0 5 4.7 C[C@@H]1CN(c2ccc(F)cc2)C(=O)c2cc(COc3ccc(OC(F)(F)F)cc3)nn21 10.1021/acs.jmedchem.5b01005
122190437 123611 None 0 Rat Functional pIC50 = 6.4 6.4 - 1
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 387 4 0 6 3.3 C[C@@H]1CN(c2ccc(F)nc2)C(=O)c2cc(COc3ccc(Cl)cn3)nn21 10.1021/acs.jmedchem.5b01005
CHEMBL3617659 123611 None 0 Rat Functional pIC50 = 6.4 6.4 - 1
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 387 4 0 6 3.3 C[C@@H]1CN(c2ccc(F)nc2)C(=O)c2cc(COc3ccc(Cl)cn3)nn21 10.1021/acs.jmedchem.5b01005
67637138 183724 None 0 Human Functional pIC50 = 7.4 7.4 -2 2
Antagonist activity at human recombinant mGlu3 receptor stably expressed in golden hamster AV12 cells co-expressing rat EAAT1 assessed as reduction in DCG IV-induced inhibition of forskolin-stimulated cAMP accumulation preincubated for 20 mins followed by incubation with cAMP-d2 conjugate and anti-cAMP cryptate for 1 hr by HTRF assayAntagonist activity at human recombinant mGlu3 receptor stably expressed in golden hamster AV12 cells co-expressing rat EAAT1 assessed as reduction in DCG IV-induced inhibition of forskolin-stimulated cAMP accumulation preincubated for 20 mins followed by incubation with cAMP-d2 conjugate and anti-cAMP cryptate for 1 hr by HTRF assay
ChEMBL 341 5 4 5 0.6 N[C@@]1(C(=O)O)[C@H](CSc2ccc(F)cc2)[C@@H](O)[C@@H]2[C@H]1[C@H]2C(=O)O 10.1021/acs.jmedchem.6b01119
CHEMBL4776989 183724 None 0 Human Functional pIC50 = 7.4 7.4 -2 2
Antagonist activity at human recombinant mGlu3 receptor stably expressed in golden hamster AV12 cells co-expressing rat EAAT1 assessed as reduction in DCG IV-induced inhibition of forskolin-stimulated cAMP accumulation preincubated for 20 mins followed by incubation with cAMP-d2 conjugate and anti-cAMP cryptate for 1 hr by HTRF assayAntagonist activity at human recombinant mGlu3 receptor stably expressed in golden hamster AV12 cells co-expressing rat EAAT1 assessed as reduction in DCG IV-induced inhibition of forskolin-stimulated cAMP accumulation preincubated for 20 mins followed by incubation with cAMP-d2 conjugate and anti-cAMP cryptate for 1 hr by HTRF assay
ChEMBL 341 5 4 5 0.6 N[C@@]1(C(=O)O)[C@H](CSc2ccc(F)cc2)[C@@H](O)[C@@H]2[C@H]1[C@H]2C(=O)O 10.1021/acs.jmedchem.6b01119
CHEMBL4802329 183724 None 0 Human Functional pIC50 = 7.4 7.4 -2 2
Antagonist activity at human recombinant mGlu3 receptor stably expressed in golden hamster AV12 cells co-expressing rat EAAT1 assessed as reduction in DCG IV-induced inhibition of forskolin-stimulated cAMP accumulation preincubated for 20 mins followed by incubation with cAMP-d2 conjugate and anti-cAMP cryptate for 1 hr by HTRF assayAntagonist activity at human recombinant mGlu3 receptor stably expressed in golden hamster AV12 cells co-expressing rat EAAT1 assessed as reduction in DCG IV-induced inhibition of forskolin-stimulated cAMP accumulation preincubated for 20 mins followed by incubation with cAMP-d2 conjugate and anti-cAMP cryptate for 1 hr by HTRF assay
ChEMBL 341 5 4 5 0.6 N[C@@]1(C(=O)O)[C@H](CSc2ccc(F)cc2)[C@@H](O)[C@@H]2[C@H]1[C@H]2C(=O)O 10.1021/acs.jmedchem.6b01119
122190414 123590 None 0 Rat Functional pIC50 = 6.4 6.4 - 1
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 382 4 0 5 4.0 Cc1ccc(N2C[C@@H](C)n3nc(COc4ccc(Cl)cn4)cc3C2=O)cc1 10.1021/acs.jmedchem.5b01005
CHEMBL3617637 123590 None 0 Rat Functional pIC50 = 6.4 6.4 - 1
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 382 4 0 5 4.0 Cc1ccc(N2C[C@@H](C)n3nc(COc4ccc(Cl)cn4)cc3C2=O)cc1 10.1021/acs.jmedchem.5b01005
122190315 123511 None 0 Rat Functional pIC50 = 6.4 6.4 -1 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 387 4 0 4 4.1 C[C@@H]1CN(c2ccc(F)cc2)C(=O)c2cc(COc3ccc(F)cc3F)nn21 10.1021/acs.jmedchem.5b01005
CHEMBL3617499 123511 None 0 Rat Functional pIC50 = 6.4 6.4 -1 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 387 4 0 4 4.1 C[C@@H]1CN(c2ccc(F)cc2)C(=O)c2cc(COc3ccc(F)cc3F)nn21 10.1021/acs.jmedchem.5b01005
122190424 123600 None 0 Rat Functional pIC50 = 6.4 6.4 - 1
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 404 4 0 5 4.0 C[C@@H]1CN(c2cc(F)cc(F)c2)C(=O)c2cc(COc3ccc(Cl)cn3)nn21 10.1021/acs.jmedchem.5b01005
CHEMBL3617647 123600 None 0 Rat Functional pIC50 = 6.4 6.4 - 1
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 404 4 0 5 4.0 C[C@@H]1CN(c2cc(F)cc(F)c2)C(=O)c2cc(COc3ccc(Cl)cn3)nn21 10.1021/acs.jmedchem.5b01005
122190315 123511 None 0 Rat Functional pIC50 = 6.4 6.4 -1 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 387 4 0 4 4.1 C[C@@H]1CN(c2ccc(F)cc2)C(=O)c2cc(COc3ccc(F)cc3F)nn21 10.1021/acs.jmedchem.5b01005
CHEMBL3617499 123511 None 0 Rat Functional pIC50 = 6.4 6.4 -1 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 387 4 0 4 4.1 C[C@@H]1CN(c2ccc(F)cc2)C(=O)c2cc(COc3ccc(F)cc3F)nn21 10.1021/acs.jmedchem.5b01005
9952648 96361 None 0 Rat Functional pIC50 = 7.4 7.4 -1 2
Antagonist activity at rat mGluR3 expressed in CHO cells assessed as inhibition of glutamate-induced GIRK currentAntagonist activity at rat mGluR3 expressed in CHO cells assessed as inhibition of glutamate-induced GIRK current
ChEMBL 397 3 1 5 4.5 O=C1CC(c2cccc(-n3ccnn3)c2)=Nc2ccc(-c3ccccc3F)cc2N1 10.1016/j.bmcl.2008.02.076
CHEMBL261288 96361 None 0 Rat Functional pIC50 = 7.4 7.4 -1 2
Antagonist activity at rat mGluR3 expressed in CHO cells assessed as inhibition of glutamate-induced GIRK currentAntagonist activity at rat mGluR3 expressed in CHO cells assessed as inhibition of glutamate-induced GIRK current
ChEMBL 397 3 1 5 4.5 O=C1CC(c2cccc(-n3ccnn3)c2)=Nc2ccc(-c3ccccc3F)cc2N1 10.1016/j.bmcl.2008.02.076
44348911 16573 None 0 Human Functional pIC50 = 6.4 6.4 -1 2
Effect on 1S,3R-ACPD-induced inhibition of forskolin stimulated cyclic-AMP in RGT cells expressing human Metabotropic glutamate receptor 3Effect on 1S,3R-ACPD-induced inhibition of forskolin stimulated cyclic-AMP in RGT cells expressing human Metabotropic glutamate receptor 3
ChEMBL 331 6 3 3 2.1 N[C@@](CCc1cccc(C(F)(F)F)c1)(C(=O)O)C1C[C@@H]1C(=O)O 10.1021/jm970498o
CHEMBL123847 16573 None 0 Human Functional pIC50 = 6.4 6.4 -1 2
Effect on 1S,3R-ACPD-induced inhibition of forskolin stimulated cyclic-AMP in RGT cells expressing human Metabotropic glutamate receptor 3Effect on 1S,3R-ACPD-induced inhibition of forskolin stimulated cyclic-AMP in RGT cells expressing human Metabotropic glutamate receptor 3
ChEMBL 331 6 3 3 2.1 N[C@@](CCc1cccc(C(F)(F)F)c1)(C(=O)O)C1C[C@@H]1C(=O)O 10.1021/jm970498o
122190424 123600 None 0 Rat Functional pIC50 = 6.4 6.4 - 1
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 404 4 0 5 4.0 C[C@@H]1CN(c2cc(F)cc(F)c2)C(=O)c2cc(COc3ccc(Cl)cn3)nn21 10.1021/acs.jmedchem.5b01005
CHEMBL3617647 123600 None 0 Rat Functional pIC50 = 6.4 6.4 - 1
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 404 4 0 5 4.0 C[C@@H]1CN(c2cc(F)cc(F)c2)C(=O)c2cc(COc3ccc(Cl)cn3)nn21 10.1021/acs.jmedchem.5b01005
11503055 2400 None 2 Human Functional pIC50 = 5.4 5.4 31 2
Negative allosteric modulation of human mGlu3 receptor assessed as Ca2+ flux by FLIPR assayNegative allosteric modulation of human mGlu3 receptor assessed as Ca2+ flux by FLIPR assay
ChEMBL 400 4 1 4 3.9 Clc1ccc(c(c1)Cl)CN[C@H]1CCN(C1)c1ncc(cn1)Br 10.1021/jm400439t
9694 2400 None 2 Human Functional pIC50 = 5.4 5.4 31 2
Negative allosteric modulation of human mGlu3 receptor assessed as Ca2+ flux by FLIPR assayNegative allosteric modulation of human mGlu3 receptor assessed as Ca2+ flux by FLIPR assay
ChEMBL 400 4 1 4 3.9 Clc1ccc(c(c1)Cl)CN[C@H]1CCN(C1)c1ncc(cn1)Br 10.1021/jm400439t
CHEMBL2204436 2400 None 2 Human Functional pIC50 = 5.4 5.4 31 2
Negative allosteric modulation of human mGlu3 receptor assessed as Ca2+ flux by FLIPR assayNegative allosteric modulation of human mGlu3 receptor assessed as Ca2+ flux by FLIPR assay
ChEMBL 400 4 1 4 3.9 Clc1ccc(c(c1)Cl)CN[C@H]1CCN(C1)c1ncc(cn1)Br 10.1021/jm400439t
122190418 123594 None 0 Rat Functional pIC50 = 6.4 6.4 11 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 393 4 0 6 3.6 C[C@@H]1CN(c2ccccc2C#N)C(=O)c2cc(COc3ccc(Cl)cn3)nn21 10.1021/acs.jmedchem.5b01005
CHEMBL3617641 123594 None 0 Rat Functional pIC50 = 6.4 6.4 11 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 393 4 0 6 3.6 C[C@@H]1CN(c2ccccc2C#N)C(=O)c2cc(COc3ccc(Cl)cn3)nn21 10.1021/acs.jmedchem.5b01005
71136653 123470 None 0 Human Functional pIC50 = 5.4 5.4 -51 2
Antagonist activity at human recombinant mGlu3 receptor expressed in AV12 cells assessed as reversal of DCG-4-inhibited, forskolin-stimulated cAMP production after 1 hr by fluorescence assayAntagonist activity at human recombinant mGlu3 receptor expressed in AV12 cells assessed as reversal of DCG-4-inhibited, forskolin-stimulated cAMP production after 1 hr by fluorescence assay
ChEMBL 284 4 4 6 -0.6 N[C@@]1(C(=O)O)C[C@H](Sc2nnc[nH]2)[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/acs.jmedchem.5b01124
CHEMBL3616854 123470 None 0 Human Functional pIC50 = 5.4 5.4 -51 2
Antagonist activity at human recombinant mGlu3 receptor expressed in AV12 cells assessed as reversal of DCG-4-inhibited, forskolin-stimulated cAMP production after 1 hr by fluorescence assayAntagonist activity at human recombinant mGlu3 receptor expressed in AV12 cells assessed as reversal of DCG-4-inhibited, forskolin-stimulated cAMP production after 1 hr by fluorescence assay
ChEMBL 284 4 4 6 -0.6 N[C@@]1(C(=O)O)C[C@H](Sc2nnc[nH]2)[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/acs.jmedchem.5b01124
122190418 123594 None 0 Rat Functional pIC50 = 6.4 6.4 11 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 393 4 0 6 3.6 C[C@@H]1CN(c2ccccc2C#N)C(=O)c2cc(COc3ccc(Cl)cn3)nn21 10.1021/acs.jmedchem.5b01005
CHEMBL3617641 123594 None 0 Rat Functional pIC50 = 6.4 6.4 11 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 393 4 0 6 3.6 C[C@@H]1CN(c2ccccc2C#N)C(=O)c2cc(COc3ccc(Cl)cn3)nn21 10.1021/acs.jmedchem.5b01005
122190404 123580 None 0 Rat Functional pIC50 = 6.4 6.4 - 1
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 353 4 0 6 2.6 C[C@@H]1CN(c2cccnc2)C(=O)c2cc(COc3ccc(F)cn3)nn21 10.1021/acs.jmedchem.5b01005
CHEMBL3617627 123580 None 0 Rat Functional pIC50 = 6.4 6.4 - 1
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 353 4 0 6 2.6 C[C@@H]1CN(c2cccnc2)C(=O)c2cc(COc3ccc(F)cn3)nn21 10.1021/acs.jmedchem.5b01005
122190404 123580 None 0 Rat Functional pIC50 = 6.4 6.4 - 1
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 353 4 0 6 2.6 C[C@@H]1CN(c2cccnc2)C(=O)c2cc(COc3ccc(F)cn3)nn21 10.1021/acs.jmedchem.5b01005
CHEMBL3617627 123580 None 0 Rat Functional pIC50 = 6.4 6.4 - 1
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 353 4 0 6 2.6 C[C@@H]1CN(c2cccnc2)C(=O)c2cc(COc3ccc(F)cn3)nn21 10.1021/acs.jmedchem.5b01005
122190417 123593 None 0 Rat Functional pIC50 = 6.4 6.4 10 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 398 5 0 6 3.7 COc1ccc(N2C[C@@H](C)n3nc(COc4ccc(Cl)cn4)cc3C2=O)cc1 10.1021/acs.jmedchem.5b01005
CHEMBL3617640 123593 None 0 Rat Functional pIC50 = 6.4 6.4 10 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 398 5 0 6 3.7 COc1ccc(N2C[C@@H](C)n3nc(COc4ccc(Cl)cn4)cc3C2=O)cc1 10.1021/acs.jmedchem.5b01005
122190417 123593 None 0 Rat Functional pIC50 = 6.4 6.4 10 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 398 5 0 6 3.7 COc1ccc(N2C[C@@H](C)n3nc(COc4ccc(Cl)cn4)cc3C2=O)cc1 10.1021/acs.jmedchem.5b01005
CHEMBL3617640 123593 None 0 Rat Functional pIC50 = 6.4 6.4 10 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 398 5 0 6 3.7 COc1ccc(N2C[C@@H](C)n3nc(COc4ccc(Cl)cn4)cc3C2=O)cc1 10.1021/acs.jmedchem.5b01005
122456139 162176 None 0 Rat Functional pIC50 = 6.4 6.4 17 2
Negative allosteric modulation of rat mGlu3 receptor expressed in TREX cells coexpressing Galpha15 assessed as inhibition of glutamate induced-calcium mobilization preincubated for 2.3 mins followed by glutamate addition measured for 2.6 mins by Fluo-4 AM dye based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor expressed in TREX cells coexpressing Galpha15 assessed as inhibition of glutamate induced-calcium mobilization preincubated for 2.3 mins followed by glutamate addition measured for 2.6 mins by Fluo-4 AM dye based fluorescence assay
ChEMBL 360 6 0 5 3.5 O=c1cc(OCCOc2ncccc2Cl)ccn1-c1ccc(F)cc1 10.1021/acsmedchemlett.7b00249
CHEMBL4160819 162176 None 0 Rat Functional pIC50 = 6.4 6.4 17 2
Negative allosteric modulation of rat mGlu3 receptor expressed in TREX cells coexpressing Galpha15 assessed as inhibition of glutamate induced-calcium mobilization preincubated for 2.3 mins followed by glutamate addition measured for 2.6 mins by Fluo-4 AM dye based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor expressed in TREX cells coexpressing Galpha15 assessed as inhibition of glutamate induced-calcium mobilization preincubated for 2.3 mins followed by glutamate addition measured for 2.6 mins by Fluo-4 AM dye based fluorescence assay
ChEMBL 360 6 0 5 3.5 O=c1cc(OCCOc2ncccc2Cl)ccn1-c1ccc(F)cc1 10.1021/acsmedchemlett.7b00249
122456139 162176 None 0 Rat Functional pIC50 = 6.4 6.4 17 2
Negative allosteric modulation of rat mGlu3 receptor expressed in TREX cells coexpressing Galpha15 assessed as inhibition of glutamate induced-calcium mobilization preincubated for 2.3 mins followed by glutamate addition measured for 2.6 mins by Fluo-4 AM dye based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor expressed in TREX cells coexpressing Galpha15 assessed as inhibition of glutamate induced-calcium mobilization preincubated for 2.3 mins followed by glutamate addition measured for 2.6 mins by Fluo-4 AM dye based fluorescence assay
ChEMBL 360 6 0 5 3.5 O=c1cc(OCCOc2ncccc2Cl)ccn1-c1ccc(F)cc1 10.1021/acsmedchemlett.7b00249
CHEMBL4160819 162176 None 0 Rat Functional pIC50 = 6.4 6.4 17 2
Negative allosteric modulation of rat mGlu3 receptor expressed in TREX cells coexpressing Galpha15 assessed as inhibition of glutamate induced-calcium mobilization preincubated for 2.3 mins followed by glutamate addition measured for 2.6 mins by Fluo-4 AM dye based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor expressed in TREX cells coexpressing Galpha15 assessed as inhibition of glutamate induced-calcium mobilization preincubated for 2.3 mins followed by glutamate addition measured for 2.6 mins by Fluo-4 AM dye based fluorescence assay
ChEMBL 360 6 0 5 3.5 O=c1cc(OCCOc2ncccc2Cl)ccn1-c1ccc(F)cc1 10.1021/acsmedchemlett.7b00249
60204017 2573 None 26 Rat Functional pIC50 = 6.4 6.4 - 1
Negative allosteric modulation of rat mGlu3 receptor transfected in human TREX cells assessed as inhibition of glutamate-induced calcium mobilization after 2.5 minsNegative allosteric modulation of rat mGlu3 receptor transfected in human TREX cells assessed as inhibition of glutamate-induced calcium mobilization after 2.5 mins
ChEMBL 353 2 1 3 2.8 COc1ccc(cc1)C#Cc1ccc(c(c1)F)C(=O)N1CCC[C@H](C1)O 10.1021/jm400439t
8765 2573 None 26 Rat Functional pIC50 = 6.4 6.4 - 1
Negative allosteric modulation of rat mGlu3 receptor transfected in human TREX cells assessed as inhibition of glutamate-induced calcium mobilization after 2.5 minsNegative allosteric modulation of rat mGlu3 receptor transfected in human TREX cells assessed as inhibition of glutamate-induced calcium mobilization after 2.5 mins
ChEMBL 353 2 1 3 2.8 COc1ccc(cc1)C#Cc1ccc(c(c1)F)C(=O)N1CCC[C@H](C1)O 10.1021/jm400439t
CHEMBL2385886 2573 None 26 Rat Functional pIC50 = 6.4 6.4 - 1
Negative allosteric modulation of rat mGlu3 receptor transfected in human TREX cells assessed as inhibition of glutamate-induced calcium mobilization after 2.5 minsNegative allosteric modulation of rat mGlu3 receptor transfected in human TREX cells assessed as inhibition of glutamate-induced calcium mobilization after 2.5 mins
ChEMBL 353 2 1 3 2.8 COc1ccc(cc1)C#Cc1ccc(c(c1)F)C(=O)N1CCC[C@H](C1)O 10.1021/jm400439t
90643976 112068 None 0 Rat Functional pIC50 = 5.4 5.4 - 1
Inhibition of rat mGlu3 receptor transfected in HEK293 cells coexpressing mouse Galpha15 assessed as decrease in glutamate-induced calcium signaling by fluorescence plate reader analysis in presence of glutamate at EC87 concentrationInhibition of rat mGlu3 receptor transfected in HEK293 cells coexpressing mouse Galpha15 assessed as decrease in glutamate-induced calcium signaling by fluorescence plate reader analysis in presence of glutamate at EC87 concentration
ChEMBL 402 2 0 5 5.1 Cn1c(=O)c2ccc(-c3ccc4ccncc4c3)cc2n2nc(-c3ccccc3)cc12 10.1016/j.bmcl.2014.04.051
CHEMBL3288680 112068 None 0 Rat Functional pIC50 = 5.4 5.4 - 1
Inhibition of rat mGlu3 receptor transfected in HEK293 cells coexpressing mouse Galpha15 assessed as decrease in glutamate-induced calcium signaling by fluorescence plate reader analysis in presence of glutamate at EC87 concentrationInhibition of rat mGlu3 receptor transfected in HEK293 cells coexpressing mouse Galpha15 assessed as decrease in glutamate-induced calcium signaling by fluorescence plate reader analysis in presence of glutamate at EC87 concentration
ChEMBL 402 2 0 5 5.1 Cn1c(=O)c2ccc(-c3ccc4ccncc4c3)cc2n2nc(-c3ccccc3)cc12 10.1016/j.bmcl.2014.04.051
60204016 90366 None 0 Rat Functional pIC50 = 6.3 6.3 - 1
Negative allosteric modulation of rat mGlu3 receptor transfected in human TREX cells assessed as inhibition of glutamate-induced calcium mobilization after 2.5 minsNegative allosteric modulation of rat mGlu3 receptor transfected in human TREX cells assessed as inhibition of glutamate-induced calcium mobilization after 2.5 mins
ChEMBL 353 2 1 3 2.8 COc1ccc(C#Cc2ccc(C(=O)N3CCC[C@@H](O)C3)cc2F)cc1 10.1021/jm400439t
CHEMBL2385887 90366 None 0 Rat Functional pIC50 = 6.3 6.3 - 1
Negative allosteric modulation of rat mGlu3 receptor transfected in human TREX cells assessed as inhibition of glutamate-induced calcium mobilization after 2.5 minsNegative allosteric modulation of rat mGlu3 receptor transfected in human TREX cells assessed as inhibition of glutamate-induced calcium mobilization after 2.5 mins
ChEMBL 353 2 1 3 2.8 COc1ccc(C#Cc2ccc(C(=O)N3CCC[C@@H](O)C3)cc2F)cc1 10.1021/jm400439t
162652146 180319 None 0 Human Functional pIC50 = 5.3 5.3 -1 2
Antagonist activity at human recombinant mGlu3 receptor stably expressed in golden hamster AV12 cells co-expressing rat EAAT1 assessed as reduction in DCG IV-induced inhibition of forskolin-stimulated cAMP accumulation preincubated for 20 mins followed by incubation with cAMP-d2 conjugate and anti-cAMP cryptate for 1 hr by HTRF assayAntagonist activity at human recombinant mGlu3 receptor stably expressed in golden hamster AV12 cells co-expressing rat EAAT1 assessed as reduction in DCG IV-induced inhibition of forskolin-stimulated cAMP accumulation preincubated for 20 mins followed by incubation with cAMP-d2 conjugate and anti-cAMP cryptate for 1 hr by HTRF assay
ChEMBL 289 5 4 5 -0.2 CC(C)SC[C@@H]1[C@@H](O)[C@@H]2[C@@H]([C@H]2C(=O)O)[C@]1(N)C(=O)O 10.1021/acs.jmedchem.6b01119
CHEMBL4749728 180319 None 0 Human Functional pIC50 = 5.3 5.3 -1 2
Antagonist activity at human recombinant mGlu3 receptor stably expressed in golden hamster AV12 cells co-expressing rat EAAT1 assessed as reduction in DCG IV-induced inhibition of forskolin-stimulated cAMP accumulation preincubated for 20 mins followed by incubation with cAMP-d2 conjugate and anti-cAMP cryptate for 1 hr by HTRF assayAntagonist activity at human recombinant mGlu3 receptor stably expressed in golden hamster AV12 cells co-expressing rat EAAT1 assessed as reduction in DCG IV-induced inhibition of forskolin-stimulated cAMP accumulation preincubated for 20 mins followed by incubation with cAMP-d2 conjugate and anti-cAMP cryptate for 1 hr by HTRF assay
ChEMBL 289 5 4 5 -0.2 CC(C)SC[C@@H]1[C@@H](O)[C@@H]2[C@@H]([C@H]2C(=O)O)[C@]1(N)C(=O)O 10.1021/acs.jmedchem.6b01119
122190314 123510 None 0 Rat Functional pIC50 = 6.3 6.3 -5 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 369 4 0 4 4.0 C[C@@H]1CN(c2ccc(F)cc2)C(=O)c2cc(COc3ccc(F)cc3)nn21 10.1021/acs.jmedchem.5b01005
CHEMBL3617498 123510 None 0 Rat Functional pIC50 = 6.3 6.3 -5 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 369 4 0 4 4.0 C[C@@H]1CN(c2ccc(F)cc2)C(=O)c2cc(COc3ccc(F)cc3)nn21 10.1021/acs.jmedchem.5b01005
60204016 90366 None 0 Rat Functional pIC50 = 6.3 6.3 - 1
Negative allosteric modulation of rat mGlu3 receptor transfected in human TREX cells assessed as inhibition of glutamate-induced calcium mobilization after 2.5 minsNegative allosteric modulation of rat mGlu3 receptor transfected in human TREX cells assessed as inhibition of glutamate-induced calcium mobilization after 2.5 mins
ChEMBL 353 2 1 3 2.8 COc1ccc(C#Cc2ccc(C(=O)N3CCC[C@@H](O)C3)cc2F)cc1 10.1021/jm400439t
CHEMBL2385887 90366 None 0 Rat Functional pIC50 = 6.3 6.3 - 1
Negative allosteric modulation of rat mGlu3 receptor transfected in human TREX cells assessed as inhibition of glutamate-induced calcium mobilization after 2.5 minsNegative allosteric modulation of rat mGlu3 receptor transfected in human TREX cells assessed as inhibition of glutamate-induced calcium mobilization after 2.5 mins
ChEMBL 353 2 1 3 2.8 COc1ccc(C#Cc2ccc(C(=O)N3CCC[C@@H](O)C3)cc2F)cc1 10.1021/jm400439t
71137034 123466 None 0 Human Functional pIC50 = 6.3 6.3 -7 2
Antagonist activity at human recombinant mGlu3 receptor expressed in AV12 cells assessed as reversal of DCG-4-inhibited, forskolin-stimulated cAMP production after 1 hr by fluorescence assayAntagonist activity at human recombinant mGlu3 receptor expressed in AV12 cells assessed as reversal of DCG-4-inhibited, forskolin-stimulated cAMP production after 1 hr by fluorescence assay
ChEMBL 334 5 4 6 0.3 N[C@@]1(C(=O)O)C[C@@H](Sc2nnc(C(F)F)[nH]2)[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/acs.jmedchem.5b01124
CHEMBL3616850 123466 None 0 Human Functional pIC50 = 6.3 6.3 -7 2
Antagonist activity at human recombinant mGlu3 receptor expressed in AV12 cells assessed as reversal of DCG-4-inhibited, forskolin-stimulated cAMP production after 1 hr by fluorescence assayAntagonist activity at human recombinant mGlu3 receptor expressed in AV12 cells assessed as reversal of DCG-4-inhibited, forskolin-stimulated cAMP production after 1 hr by fluorescence assay
ChEMBL 334 5 4 6 0.3 N[C@@]1(C(=O)O)C[C@@H](Sc2nnc(C(F)F)[nH]2)[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/acs.jmedchem.5b01124
57338826 149715 None 0 Human Functional pIC50 = 7.3 7.3 -1 5
Antagonist activity at recombinant human mGlu3 receptor expressed in hamster AV12 cells co-expressing human EAAT1 assessed as reduction of DCG-4-inhibited forskolin-stimulated cAMP formation after 20 mins by HTRF assayAntagonist activity at recombinant human mGlu3 receptor expressed in hamster AV12 cells co-expressing human EAAT1 assessed as reduction of DCG-4-inhibited forskolin-stimulated cAMP formation after 20 mins by HTRF assay
ChEMBL 375 5 4 5 1.0 N[C@@]1(C(=O)O)[C@H](OCc2ccc(Cl)c(Cl)c2)[C@@H](O)[C@@H]2[C@H]1[C@H]2C(=O)O 10.1016/j.bmcl.2016.10.067
CHEMBL3947221 149715 None 0 Human Functional pIC50 = 7.3 7.3 -1 5
Antagonist activity at recombinant human mGlu3 receptor expressed in hamster AV12 cells co-expressing human EAAT1 assessed as reduction of DCG-4-inhibited forskolin-stimulated cAMP formation after 20 mins by HTRF assayAntagonist activity at recombinant human mGlu3 receptor expressed in hamster AV12 cells co-expressing human EAAT1 assessed as reduction of DCG-4-inhibited forskolin-stimulated cAMP formation after 20 mins by HTRF assay
ChEMBL 375 5 4 5 1.0 N[C@@]1(C(=O)O)[C@H](OCc2ccc(Cl)c(Cl)c2)[C@@H](O)[C@@H]2[C@H]1[C@H]2C(=O)O 10.1016/j.bmcl.2016.10.067
122190314 123510 None 0 Rat Functional pIC50 = 6.3 6.3 -5 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 369 4 0 4 4.0 C[C@@H]1CN(c2ccc(F)cc2)C(=O)c2cc(COc3ccc(F)cc3)nn21 10.1021/acs.jmedchem.5b01005
CHEMBL3617498 123510 None 0 Rat Functional pIC50 = 6.3 6.3 -5 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 369 4 0 4 4.0 C[C@@H]1CN(c2ccc(F)cc2)C(=O)c2cc(COc3ccc(F)cc3)nn21 10.1021/acs.jmedchem.5b01005
10852666 78772 None 0 Human Functional pIC50 = 6.3 6.3 -1 2
Ability to block 1S,3R-ACPD-induced inhibition of forskolin stimulated cyclic-AMP in non-neuronal cell line expressing human Metabotropic glutamate receptor 3Ability to block 1S,3R-ACPD-induced inhibition of forskolin stimulated cyclic-AMP in non-neuronal cell line expressing human Metabotropic glutamate receptor 3
ChEMBL 313 6 3 3 2.3 NC(CCc1cccc2ccccc12)(C(=O)O)[C@H]1C[C@@H]1C(=O)O 10.1021/jm970497w
CHEMBL2112583 78772 None 0 Human Functional pIC50 = 6.3 6.3 -1 2
Ability to block 1S,3R-ACPD-induced inhibition of forskolin stimulated cyclic-AMP in non-neuronal cell line expressing human Metabotropic glutamate receptor 3Ability to block 1S,3R-ACPD-induced inhibition of forskolin stimulated cyclic-AMP in non-neuronal cell line expressing human Metabotropic glutamate receptor 3
ChEMBL 313 6 3 3 2.3 NC(CCc1cccc2ccccc12)(C(=O)O)[C@H]1C[C@@H]1C(=O)O 10.1021/jm970497w
122190434 123608 None 0 Rat Functional pIC50 = 6.3 6.3 - 1
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 387 4 0 6 3.3 C[C@@H]1CN(c2cnccc2F)C(=O)c2cc(COc3ccc(Cl)cn3)nn21 10.1021/acs.jmedchem.5b01005
CHEMBL3617656 123608 None 0 Rat Functional pIC50 = 6.3 6.3 - 1
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 387 4 0 6 3.3 C[C@@H]1CN(c2cnccc2F)C(=O)c2cc(COc3ccc(Cl)cn3)nn21 10.1021/acs.jmedchem.5b01005
122190435 123609 None 0 Rat Functional pIC50 = 6.3 6.3 - 1
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 387 4 0 6 3.3 C[C@@H]1CN(c2cncc(F)c2)C(=O)c2cc(COc3ccc(Cl)cn3)nn21 10.1021/acs.jmedchem.5b01005
CHEMBL3617657 123609 None 0 Rat Functional pIC50 = 6.3 6.3 - 1
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 387 4 0 6 3.3 C[C@@H]1CN(c2cncc(F)c2)C(=O)c2cc(COc3ccc(Cl)cn3)nn21 10.1021/acs.jmedchem.5b01005
122190435 123609 None 0 Rat Functional pIC50 = 6.3 6.3 - 1
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 387 4 0 6 3.3 C[C@@H]1CN(c2cncc(F)c2)C(=O)c2cc(COc3ccc(Cl)cn3)nn21 10.1021/acs.jmedchem.5b01005
CHEMBL3617657 123609 None 0 Rat Functional pIC50 = 6.3 6.3 - 1
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 387 4 0 6 3.3 C[C@@H]1CN(c2cncc(F)c2)C(=O)c2cc(COc3ccc(Cl)cn3)nn21 10.1021/acs.jmedchem.5b01005
122190434 123608 None 0 Rat Functional pIC50 = 6.3 6.3 - 1
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 387 4 0 6 3.3 C[C@@H]1CN(c2cnccc2F)C(=O)c2cc(COc3ccc(Cl)cn3)nn21 10.1021/acs.jmedchem.5b01005
CHEMBL3617656 123608 None 0 Rat Functional pIC50 = 6.3 6.3 - 1
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 387 4 0 6 3.3 C[C@@H]1CN(c2cnccc2F)C(=O)c2cc(COc3ccc(Cl)cn3)nn21 10.1021/acs.jmedchem.5b01005
90643974 112066 None 0 Rat Functional pIC50 = 6.3 6.3 3 2
Inhibition of rat mGlu3 receptor transfected in HEK293 cells coexpressing mouse Galpha15 assessed as decrease in glutamate-induced calcium signaling by fluorescence plate reader analysis in presence of glutamate at EC87 concentrationInhibition of rat mGlu3 receptor transfected in HEK293 cells coexpressing mouse Galpha15 assessed as decrease in glutamate-induced calcium signaling by fluorescence plate reader analysis in presence of glutamate at EC87 concentration
ChEMBL 352 2 0 5 3.9 Cn1c(=O)c2ccc(-c3ccncc3)cc2n2nc(-c3ccccc3)cc12 10.1016/j.bmcl.2014.04.051
CHEMBL3288675 112066 None 0 Rat Functional pIC50 = 6.3 6.3 3 2
Inhibition of rat mGlu3 receptor transfected in HEK293 cells coexpressing mouse Galpha15 assessed as decrease in glutamate-induced calcium signaling by fluorescence plate reader analysis in presence of glutamate at EC87 concentrationInhibition of rat mGlu3 receptor transfected in HEK293 cells coexpressing mouse Galpha15 assessed as decrease in glutamate-induced calcium signaling by fluorescence plate reader analysis in presence of glutamate at EC87 concentration
ChEMBL 352 2 0 5 3.9 Cn1c(=O)c2ccc(-c3ccncc3)cc2n2nc(-c3ccccc3)cc12 10.1016/j.bmcl.2014.04.051
122190312 123508 None 0 Rat Functional pIC50 = 6.3 6.3 -2 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 369 4 0 4 4.0 C[C@@H]1CN(c2ccc(F)cc2)C(=O)c2cc(COc3ccccc3F)nn21 10.1021/acs.jmedchem.5b01005
CHEMBL3617496 123508 None 0 Rat Functional pIC50 = 6.3 6.3 -2 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 369 4 0 4 4.0 C[C@@H]1CN(c2ccc(F)cc2)C(=O)c2cc(COc3ccccc3F)nn21 10.1021/acs.jmedchem.5b01005
122190425 123601 None 0 Rat Functional pIC50 = 6.3 6.3 - 1
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 411 4 0 6 3.7 C[C@@H]1CN(c2cc(F)ccc2C#N)C(=O)c2cc(COc3ccc(Cl)cn3)nn21 10.1021/acs.jmedchem.5b01005
CHEMBL3617648 123601 None 0 Rat Functional pIC50 = 6.3 6.3 - 1
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 411 4 0 6 3.7 C[C@@H]1CN(c2cc(F)ccc2C#N)C(=O)c2cc(COc3ccc(Cl)cn3)nn21 10.1021/acs.jmedchem.5b01005
71137010 123465 None 0 Human Functional pIC50 = 6.3 6.3 -5 2
Antagonist activity at human recombinant mGlu3 receptor expressed in AV12 cells assessed as reversal of DCG-4-inhibited, forskolin-stimulated cAMP production after 1 hr by fluorescence assayAntagonist activity at human recombinant mGlu3 receptor expressed in AV12 cells assessed as reversal of DCG-4-inhibited, forskolin-stimulated cAMP production after 1 hr by fluorescence assay
ChEMBL 352 4 4 6 0.4 N[C@@]1(C(=O)O)C[C@@H](Sc2nnc(C(F)(F)F)[nH]2)[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/acs.jmedchem.5b01124
CHEMBL3616849 123465 None 0 Human Functional pIC50 = 6.3 6.3 -5 2
Antagonist activity at human recombinant mGlu3 receptor expressed in AV12 cells assessed as reversal of DCG-4-inhibited, forskolin-stimulated cAMP production after 1 hr by fluorescence assayAntagonist activity at human recombinant mGlu3 receptor expressed in AV12 cells assessed as reversal of DCG-4-inhibited, forskolin-stimulated cAMP production after 1 hr by fluorescence assay
ChEMBL 352 4 4 6 0.4 N[C@@]1(C(=O)O)C[C@@H](Sc2nnc(C(F)(F)F)[nH]2)[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/acs.jmedchem.5b01124
122190425 123601 None 0 Rat Functional pIC50 = 6.3 6.3 - 1
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 411 4 0 6 3.7 C[C@@H]1CN(c2cc(F)ccc2C#N)C(=O)c2cc(COc3ccc(Cl)cn3)nn21 10.1021/acs.jmedchem.5b01005
CHEMBL3617648 123601 None 0 Rat Functional pIC50 = 6.3 6.3 - 1
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 411 4 0 6 3.7 C[C@@H]1CN(c2cc(F)ccc2C#N)C(=O)c2cc(COc3ccc(Cl)cn3)nn21 10.1021/acs.jmedchem.5b01005
90643963 112058 None 0 Rat Functional pIC50 = 6.3 6.3 3 2
Inhibition of rat mGlu3 receptor transfected in HEK293 cells coexpressing mouse Galpha15 assessed as decrease in glutamate-induced calcium signaling by fluorescence plate reader analysis in presence of glutamate at EC87 concentrationInhibition of rat mGlu3 receptor transfected in HEK293 cells coexpressing mouse Galpha15 assessed as decrease in glutamate-induced calcium signaling by fluorescence plate reader analysis in presence of glutamate at EC87 concentration
ChEMBL 366 2 0 5 4.2 Cc1cccc(-c2cc3n(C)c(=O)c4ccc(-c5cccnc5)cc4n3n2)c1 10.1016/j.bmcl.2014.04.051
CHEMBL3288653 112058 None 0 Rat Functional pIC50 = 6.3 6.3 3 2
Inhibition of rat mGlu3 receptor transfected in HEK293 cells coexpressing mouse Galpha15 assessed as decrease in glutamate-induced calcium signaling by fluorescence plate reader analysis in presence of glutamate at EC87 concentrationInhibition of rat mGlu3 receptor transfected in HEK293 cells coexpressing mouse Galpha15 assessed as decrease in glutamate-induced calcium signaling by fluorescence plate reader analysis in presence of glutamate at EC87 concentration
ChEMBL 366 2 0 5 4.2 Cc1cccc(-c2cc3n(C)c(=O)c4ccc(-c5cccnc5)cc4n3n2)c1 10.1016/j.bmcl.2014.04.051
122190312 123508 None 0 Rat Functional pIC50 = 6.3 6.3 -2 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 369 4 0 4 4.0 C[C@@H]1CN(c2ccc(F)cc2)C(=O)c2cc(COc3ccccc3F)nn21 10.1021/acs.jmedchem.5b01005
CHEMBL3617496 123508 None 0 Rat Functional pIC50 = 6.3 6.3 -2 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 369 4 0 4 4.0 C[C@@H]1CN(c2ccc(F)cc2)C(=O)c2cc(COc3ccccc3F)nn21 10.1021/acs.jmedchem.5b01005
122190319 123515 None 0 Rat Functional pIC50 = 6.3 6.3 -1 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 385 4 0 4 4.5 C[C@@H]1CN(c2ccc(F)cc2)C(=O)c2cc(COc3ccccc3Cl)nn21 10.1021/acs.jmedchem.5b01005
CHEMBL3617503 123515 None 0 Rat Functional pIC50 = 6.3 6.3 -1 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 385 4 0 4 4.5 C[C@@H]1CN(c2ccc(F)cc2)C(=O)c2cc(COc3ccccc3Cl)nn21 10.1021/acs.jmedchem.5b01005
122190319 123515 None 0 Rat Functional pIC50 = 6.3 6.3 -1 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 385 4 0 4 4.5 C[C@@H]1CN(c2ccc(F)cc2)C(=O)c2cc(COc3ccccc3Cl)nn21 10.1021/acs.jmedchem.5b01005
CHEMBL3617503 123515 None 0 Rat Functional pIC50 = 6.3 6.3 -1 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 385 4 0 4 4.5 C[C@@H]1CN(c2ccc(F)cc2)C(=O)c2cc(COc3ccccc3Cl)nn21 10.1021/acs.jmedchem.5b01005
122190336 123532 None 0 Rat Functional pIC50 = 6.3 6.3 - 1
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 370 4 0 5 3.4 C[C@@H]1CN(c2ccc(F)cc2)C(=O)c2cc(COc3ccc(F)cn3)nn21 10.1021/acs.jmedchem.5b01005
CHEMBL3617520 123532 None 0 Rat Functional pIC50 = 6.3 6.3 - 1
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 370 4 0 5 3.4 C[C@@H]1CN(c2ccc(F)cc2)C(=O)c2cc(COc3ccc(F)cn3)nn21 10.1021/acs.jmedchem.5b01005
122190420 123596 None 0 Rat Functional pIC50 = 6.3 6.3 6 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 393 4 0 6 3.6 C[C@@H]1CN(c2ccc(C#N)cc2)C(=O)c2cc(COc3ccc(Cl)cn3)nn21 10.1021/acs.jmedchem.5b01005
CHEMBL3617643 123596 None 0 Rat Functional pIC50 = 6.3 6.3 6 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 393 4 0 6 3.6 C[C@@H]1CN(c2ccc(C#N)cc2)C(=O)c2cc(COc3ccc(Cl)cn3)nn21 10.1021/acs.jmedchem.5b01005
122190336 123532 None 0 Rat Functional pIC50 = 6.3 6.3 - 1
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 370 4 0 5 3.4 C[C@@H]1CN(c2ccc(F)cc2)C(=O)c2cc(COc3ccc(F)cn3)nn21 10.1021/acs.jmedchem.5b01005
CHEMBL3617520 123532 None 0 Rat Functional pIC50 = 6.3 6.3 - 1
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 370 4 0 5 3.4 C[C@@H]1CN(c2ccc(F)cc2)C(=O)c2cc(COc3ccc(F)cn3)nn21 10.1021/acs.jmedchem.5b01005
122190420 123596 None 0 Rat Functional pIC50 = 6.3 6.3 6 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 393 4 0 6 3.6 C[C@@H]1CN(c2ccc(C#N)cc2)C(=O)c2cc(COc3ccc(Cl)cn3)nn21 10.1021/acs.jmedchem.5b01005
CHEMBL3617643 123596 None 0 Rat Functional pIC50 = 6.3 6.3 6 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 393 4 0 6 3.6 C[C@@H]1CN(c2ccc(C#N)cc2)C(=O)c2cc(COc3ccc(Cl)cn3)nn21 10.1021/acs.jmedchem.5b01005
134137754 148036 None 0 Human Functional pIC50 = 7.3 7.3 -1 2
Antagonist activity at recombinant human mGlu3 receptor expressed in hamster AV12 cells co-expressing human EAAT1 assessed as reduction of DCG-4-inhibited forskolin-stimulated cAMP formation after 20 mins by HTRF assayAntagonist activity at recombinant human mGlu3 receptor expressed in hamster AV12 cells co-expressing human EAAT1 assessed as reduction of DCG-4-inhibited forskolin-stimulated cAMP formation after 20 mins by HTRF assay
ChEMBL 400 6 3 5 2.3 [N-]=[N+]=N[C@H]1[C@H]2[C@H](C(=O)O)[C@H]2[C@](N)(C(=O)O)[C@@H]1OCc1ccc(Cl)c(Cl)c1 10.1016/j.bmcl.2016.10.067
CHEMBL3933829 148036 None 0 Human Functional pIC50 = 7.3 7.3 -1 2
Antagonist activity at recombinant human mGlu3 receptor expressed in hamster AV12 cells co-expressing human EAAT1 assessed as reduction of DCG-4-inhibited forskolin-stimulated cAMP formation after 20 mins by HTRF assayAntagonist activity at recombinant human mGlu3 receptor expressed in hamster AV12 cells co-expressing human EAAT1 assessed as reduction of DCG-4-inhibited forskolin-stimulated cAMP formation after 20 mins by HTRF assay
ChEMBL 400 6 3 5 2.3 [N-]=[N+]=N[C@H]1[C@H]2[C@H](C(=O)O)[C@H]2[C@](N)(C(=O)O)[C@@H]1OCc1ccc(Cl)c(Cl)c1 10.1016/j.bmcl.2016.10.067
162665071 183834 None 0 Human Functional pIC50 = 6.3 6.3 -1 2
Antagonist activity at human recombinant mGlu3 receptor stably expressed in golden hamster AV12 cells co-expressing rat EAAT1 assessed as reduction in DCG IV-induced inhibition of forskolin-stimulated cAMP accumulation preincubated for 20 mins followed by incubation with cAMP-d2 conjugate and anti-cAMP cryptate for 1 hr by HTRF assayAntagonist activity at human recombinant mGlu3 receptor stably expressed in golden hamster AV12 cells co-expressing rat EAAT1 assessed as reduction in DCG IV-induced inhibition of forskolin-stimulated cAMP accumulation preincubated for 20 mins followed by incubation with cAMP-d2 conjugate and anti-cAMP cryptate for 1 hr by HTRF assay
ChEMBL 323 5 4 5 0.5 N[C@@]1(C(=O)O)[C@H](CSc2ccccc2)[C@H](O)[C@@H]2[C@H]1[C@H]2C(=O)O 10.1021/acs.jmedchem.6b01119
CHEMBL4781638 183834 None 0 Human Functional pIC50 = 6.3 6.3 -1 2
Antagonist activity at human recombinant mGlu3 receptor stably expressed in golden hamster AV12 cells co-expressing rat EAAT1 assessed as reduction in DCG IV-induced inhibition of forskolin-stimulated cAMP accumulation preincubated for 20 mins followed by incubation with cAMP-d2 conjugate and anti-cAMP cryptate for 1 hr by HTRF assayAntagonist activity at human recombinant mGlu3 receptor stably expressed in golden hamster AV12 cells co-expressing rat EAAT1 assessed as reduction in DCG IV-induced inhibition of forskolin-stimulated cAMP accumulation preincubated for 20 mins followed by incubation with cAMP-d2 conjugate and anti-cAMP cryptate for 1 hr by HTRF assay
ChEMBL 323 5 4 5 0.5 N[C@@]1(C(=O)O)[C@H](CSc2ccccc2)[C@H](O)[C@@H]2[C@H]1[C@H]2C(=O)O 10.1021/acs.jmedchem.6b01119
CHEMBL4803454 183834 None 0 Human Functional pIC50 = 6.3 6.3 -1 2
Antagonist activity at human recombinant mGlu3 receptor stably expressed in golden hamster AV12 cells co-expressing rat EAAT1 assessed as reduction in DCG IV-induced inhibition of forskolin-stimulated cAMP accumulation preincubated for 20 mins followed by incubation with cAMP-d2 conjugate and anti-cAMP cryptate for 1 hr by HTRF assayAntagonist activity at human recombinant mGlu3 receptor stably expressed in golden hamster AV12 cells co-expressing rat EAAT1 assessed as reduction in DCG IV-induced inhibition of forskolin-stimulated cAMP accumulation preincubated for 20 mins followed by incubation with cAMP-d2 conjugate and anti-cAMP cryptate for 1 hr by HTRF assay
ChEMBL 323 5 4 5 0.5 N[C@@]1(C(=O)O)[C@H](CSc2ccccc2)[C@H](O)[C@@H]2[C@H]1[C@H]2C(=O)O 10.1021/acs.jmedchem.6b01119
60210800 90356 None 0 Rat Functional pIC50 = 5.3 5.3 - 1
Negative allosteric modulation of rat mGlu3 receptor transfected in human TREX cells assessed as inhibition of glutamate-induced calcium mobilization after 2.5 minsNegative allosteric modulation of rat mGlu3 receptor transfected in human TREX cells assessed as inhibition of glutamate-induced calcium mobilization after 2.5 mins
ChEMBL 349 3 0 3 3.3 COc1ccc(C#Cc2ccc(C(=O)N3CCCC(OC)C3)cc2)cc1 10.1021/jm400439t
CHEMBL2385876 90356 None 0 Rat Functional pIC50 = 5.3 5.3 - 1
Negative allosteric modulation of rat mGlu3 receptor transfected in human TREX cells assessed as inhibition of glutamate-induced calcium mobilization after 2.5 minsNegative allosteric modulation of rat mGlu3 receptor transfected in human TREX cells assessed as inhibition of glutamate-induced calcium mobilization after 2.5 mins
ChEMBL 349 3 0 3 3.3 COc1ccc(C#Cc2ccc(C(=O)N3CCCC(OC)C3)cc2)cc1 10.1021/jm400439t
60210782 90365 None 0 Rat Functional pIC50 = 5.3 5.3 - 1
Negative allosteric modulation of rat mGlu3 receptor transfected in human TREX cells assessed as inhibition of glutamate-induced calcium mobilization after 2.5 minsNegative allosteric modulation of rat mGlu3 receptor transfected in human TREX cells assessed as inhibition of glutamate-induced calcium mobilization after 2.5 mins
ChEMBL 361 2 1 3 2.9 COc1ccc(C#Cc2ccc(C(=O)N3CC4CCC(O)C4C3)cc2)cc1 10.1021/jm400439t
CHEMBL2385885 90365 None 0 Rat Functional pIC50 = 5.3 5.3 - 1
Negative allosteric modulation of rat mGlu3 receptor transfected in human TREX cells assessed as inhibition of glutamate-induced calcium mobilization after 2.5 minsNegative allosteric modulation of rat mGlu3 receptor transfected in human TREX cells assessed as inhibition of glutamate-induced calcium mobilization after 2.5 mins
ChEMBL 361 2 1 3 2.9 COc1ccc(C#Cc2ccc(C(=O)N3CC4CCC(O)C4C3)cc2)cc1 10.1021/jm400439t
10826383 78773 None 0 Human Functional pIC50 = 6.3 6.3 1 2
Ability to block 1S,3R-ACPD-induced inhibition of forskolin stimulated cyclic-AMP in non-neuronal cell line expressing human Metabotropic glutamate receptor 3Ability to block 1S,3R-ACPD-induced inhibition of forskolin stimulated cyclic-AMP in non-neuronal cell line expressing human Metabotropic glutamate receptor 3
ChEMBL 277 7 3 3 1.5 NC(CCCc1ccccc1)(C(=O)O)[C@H]1C[C@@H]1C(=O)O 10.1021/jm970497w
CHEMBL2112584 78773 None 0 Human Functional pIC50 = 6.3 6.3 1 2
Ability to block 1S,3R-ACPD-induced inhibition of forskolin stimulated cyclic-AMP in non-neuronal cell line expressing human Metabotropic glutamate receptor 3Ability to block 1S,3R-ACPD-induced inhibition of forskolin stimulated cyclic-AMP in non-neuronal cell line expressing human Metabotropic glutamate receptor 3
ChEMBL 277 7 3 3 1.5 NC(CCCc1ccccc1)(C(=O)O)[C@H]1C[C@@H]1C(=O)O 10.1021/jm970497w
71136640 123469 None 0 Human Functional pIC50 = 5.3 5.3 -60 2
Antagonist activity at human recombinant mGlu3 receptor expressed in AV12 cells assessed as inhibition of glutamate-stimulated Ca2+ mobilization after 1.5 hrs by FLIPR assayAntagonist activity at human recombinant mGlu3 receptor expressed in AV12 cells assessed as inhibition of glutamate-stimulated Ca2+ mobilization after 1.5 hrs by FLIPR assay
ChEMBL 284 4 4 6 -0.6 N[C@@]1(C(=O)O)C[C@@H](Sc2c[nH]nn2)[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/acs.jmedchem.5b01124
CHEMBL3616853 123469 None 0 Human Functional pIC50 = 5.3 5.3 -60 2
Antagonist activity at human recombinant mGlu3 receptor expressed in AV12 cells assessed as inhibition of glutamate-stimulated Ca2+ mobilization after 1.5 hrs by FLIPR assayAntagonist activity at human recombinant mGlu3 receptor expressed in AV12 cells assessed as inhibition of glutamate-stimulated Ca2+ mobilization after 1.5 hrs by FLIPR assay
ChEMBL 284 4 4 6 -0.6 N[C@@]1(C(=O)O)C[C@@H](Sc2c[nH]nn2)[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/acs.jmedchem.5b01124
122190410 123586 None 0 Rat Functional pIC50 = 6.3 6.3 5 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 402 4 0 5 4.4 C[C@@H]1CN(c2cccc(Cl)c2)C(=O)c2cc(COc3ccc(Cl)cn3)nn21 10.1021/acs.jmedchem.5b01005
CHEMBL3617633 123586 None 0 Rat Functional pIC50 = 6.3 6.3 5 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 402 4 0 5 4.4 C[C@@H]1CN(c2cccc(Cl)c2)C(=O)c2cc(COc3ccc(Cl)cn3)nn21 10.1021/acs.jmedchem.5b01005
67633284 183753 None 0 Human Functional pIC50 = 7.3 7.3 -5 2
Antagonist activity at human recombinant mGlu3 receptor stably expressed in golden hamster AV12 cells co-expressing rat EAAT1 assessed as reduction in DCG IV-induced inhibition of forskolin-stimulated cAMP accumulation preincubated for 20 mins followed by incubation with cAMP-d2 conjugate and anti-cAMP cryptate for 1 hr by HTRF assayAntagonist activity at human recombinant mGlu3 receptor stably expressed in golden hamster AV12 cells co-expressing rat EAAT1 assessed as reduction in DCG IV-induced inhibition of forskolin-stimulated cAMP accumulation preincubated for 20 mins followed by incubation with cAMP-d2 conjugate and anti-cAMP cryptate for 1 hr by HTRF assay
ChEMBL 391 5 4 5 1.8 N[C@@]1(C(=O)O)[C@H](CSc2ccc(Cl)c(Cl)c2)[C@@H](O)[C@@H]2[C@H]1[C@H]2C(=O)O 10.1021/acs.jmedchem.6b01119
CHEMBL4748699 183753 None 0 Human Functional pIC50 = 7.3 7.3 -5 2
Antagonist activity at human recombinant mGlu3 receptor stably expressed in golden hamster AV12 cells co-expressing rat EAAT1 assessed as reduction in DCG IV-induced inhibition of forskolin-stimulated cAMP accumulation preincubated for 20 mins followed by incubation with cAMP-d2 conjugate and anti-cAMP cryptate for 1 hr by HTRF assayAntagonist activity at human recombinant mGlu3 receptor stably expressed in golden hamster AV12 cells co-expressing rat EAAT1 assessed as reduction in DCG IV-induced inhibition of forskolin-stimulated cAMP accumulation preincubated for 20 mins followed by incubation with cAMP-d2 conjugate and anti-cAMP cryptate for 1 hr by HTRF assay
ChEMBL 391 5 4 5 1.8 N[C@@]1(C(=O)O)[C@H](CSc2ccc(Cl)c(Cl)c2)[C@@H](O)[C@@H]2[C@H]1[C@H]2C(=O)O 10.1021/acs.jmedchem.6b01119
CHEMBL4802655 183753 None 0 Human Functional pIC50 = 7.3 7.3 -5 2
Antagonist activity at human recombinant mGlu3 receptor stably expressed in golden hamster AV12 cells co-expressing rat EAAT1 assessed as reduction in DCG IV-induced inhibition of forskolin-stimulated cAMP accumulation preincubated for 20 mins followed by incubation with cAMP-d2 conjugate and anti-cAMP cryptate for 1 hr by HTRF assayAntagonist activity at human recombinant mGlu3 receptor stably expressed in golden hamster AV12 cells co-expressing rat EAAT1 assessed as reduction in DCG IV-induced inhibition of forskolin-stimulated cAMP accumulation preincubated for 20 mins followed by incubation with cAMP-d2 conjugate and anti-cAMP cryptate for 1 hr by HTRF assay
ChEMBL 391 5 4 5 1.8 N[C@@]1(C(=O)O)[C@H](CSc2ccc(Cl)c(Cl)c2)[C@@H](O)[C@@H]2[C@H]1[C@H]2C(=O)O 10.1021/acs.jmedchem.6b01119
122190410 123586 None 0 Rat Functional pIC50 = 6.3 6.3 5 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 402 4 0 5 4.4 C[C@@H]1CN(c2cccc(Cl)c2)C(=O)c2cc(COc3ccc(Cl)cn3)nn21 10.1021/acs.jmedchem.5b01005
CHEMBL3617633 123586 None 0 Rat Functional pIC50 = 6.3 6.3 5 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 402 4 0 5 4.4 C[C@@H]1CN(c2cccc(Cl)c2)C(=O)c2cc(COc3ccc(Cl)cn3)nn21 10.1021/acs.jmedchem.5b01005
10778385 78770 None 0 Human Functional pIC50 = 6.2 6.2 1 2
Ability to block 1S,3R-ACPD-induced inhibition of forskolin stimulated cyclic-AMP in non-neuronal cell line expressing human Metabotropic glutamate receptor 3Ability to block 1S,3R-ACPD-induced inhibition of forskolin stimulated cyclic-AMP in non-neuronal cell line expressing human Metabotropic glutamate receptor 3
ChEMBL 269 6 3 4 1.2 NC(CCc1ccsc1)(C(=O)O)[C@H]1C[C@@H]1C(=O)O 10.1021/jm970497w
CHEMBL2112581 78770 None 0 Human Functional pIC50 = 6.2 6.2 1 2
Ability to block 1S,3R-ACPD-induced inhibition of forskolin stimulated cyclic-AMP in non-neuronal cell line expressing human Metabotropic glutamate receptor 3Ability to block 1S,3R-ACPD-induced inhibition of forskolin stimulated cyclic-AMP in non-neuronal cell line expressing human Metabotropic glutamate receptor 3
ChEMBL 269 6 3 4 1.2 NC(CCc1ccsc1)(C(=O)O)[C@H]1C[C@@H]1C(=O)O 10.1021/jm970497w
122190412 123588 None 0 Rat Functional pIC50 = 6.2 6.2 3 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 382 4 0 5 4.0 Cc1ccccc1N1C[C@@H](C)n2nc(COc3ccc(Cl)cn3)cc2C1=O 10.1021/acs.jmedchem.5b01005
CHEMBL3617635 123588 None 0 Rat Functional pIC50 = 6.2 6.2 3 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 382 4 0 5 4.0 Cc1ccccc1N1C[C@@H](C)n2nc(COc3ccc(Cl)cn3)cc2C1=O 10.1021/acs.jmedchem.5b01005
122190412 123588 None 0 Rat Functional pIC50 = 6.2 6.2 3 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 382 4 0 5 4.0 Cc1ccccc1N1C[C@@H](C)n2nc(COc3ccc(Cl)cn3)cc2C1=O 10.1021/acs.jmedchem.5b01005
CHEMBL3617635 123588 None 0 Rat Functional pIC50 = 6.2 6.2 3 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 382 4 0 5 4.0 Cc1ccccc1N1C[C@@H](C)n2nc(COc3ccc(Cl)cn3)cc2C1=O 10.1021/acs.jmedchem.5b01005
60204017 2573 None 26 Rat Functional pIC50 = 6.2 6.2 - 1
Negative allosteric modulation of rat mGlu3 receptor transfected in human TREX cells assessed as inhibition of glutamate-induced calcium mobilization after 2.5 minsNegative allosteric modulation of rat mGlu3 receptor transfected in human TREX cells assessed as inhibition of glutamate-induced calcium mobilization after 2.5 mins
ChEMBL 353 2 1 3 2.8 COc1ccc(cc1)C#Cc1ccc(c(c1)F)C(=O)N1CCC[C@H](C1)O 10.1021/jm400439t
8765 2573 None 26 Rat Functional pIC50 = 6.2 6.2 - 1
Negative allosteric modulation of rat mGlu3 receptor transfected in human TREX cells assessed as inhibition of glutamate-induced calcium mobilization after 2.5 minsNegative allosteric modulation of rat mGlu3 receptor transfected in human TREX cells assessed as inhibition of glutamate-induced calcium mobilization after 2.5 mins
ChEMBL 353 2 1 3 2.8 COc1ccc(cc1)C#Cc1ccc(c(c1)F)C(=O)N1CCC[C@H](C1)O 10.1021/jm400439t
CHEMBL2385886 2573 None 26 Rat Functional pIC50 = 6.2 6.2 - 1
Negative allosteric modulation of rat mGlu3 receptor transfected in human TREX cells assessed as inhibition of glutamate-induced calcium mobilization after 2.5 minsNegative allosteric modulation of rat mGlu3 receptor transfected in human TREX cells assessed as inhibition of glutamate-induced calcium mobilization after 2.5 mins
ChEMBL 353 2 1 3 2.8 COc1ccc(cc1)C#Cc1ccc(c(c1)F)C(=O)N1CCC[C@H](C1)O 10.1021/jm400439t
11235624 56321 None 0 Rat Functional pIC50 = 8.2 8.2 1 3
Antagonist activity at rat mGluR3 receptor expressed in CHO cells assessed as inhibition of GIRK currentAntagonist activity at rat mGluR3 receptor expressed in CHO cells assessed as inhibition of GIRK current
ChEMBL 425 4 1 4 5.6 CCOc1cc2c(cc1C(F)(F)F)NC(=O)CC(c1cccc(-c3ccncc3)c1)=N2 10.1016/j.bmcl.2010.09.125
CHEMBL1629862 56321 None 0 Rat Functional pIC50 = 8.2 8.2 1 3
Antagonist activity at rat mGluR3 receptor expressed in CHO cells assessed as inhibition of GIRK currentAntagonist activity at rat mGluR3 receptor expressed in CHO cells assessed as inhibition of GIRK current
ChEMBL 425 4 1 4 5.6 CCOc1cc2c(cc1C(F)(F)F)NC(=O)CC(c1cccc(-c3ccncc3)c1)=N2 10.1016/j.bmcl.2010.09.125
69669747 183759 None 14 Human Functional pIC50 = 8.2 8.2 2 4
Antagonist activity at human recombinant mGlu3 receptor stably expressed in golden hamster AV12 cells co-expressing rat EAAT1 assessed as reduction in DCG IV-induced inhibition of forskolin-stimulated cAMP accumulation preincubated for 20 mins followed by incubation with cAMP-d2 conjugate and anti-cAMP cryptate for 1 hr by HTRF assayAntagonist activity at human recombinant mGlu3 receptor stably expressed in golden hamster AV12 cells co-expressing rat EAAT1 assessed as reduction in DCG IV-induced inhibition of forskolin-stimulated cAMP accumulation preincubated for 20 mins followed by incubation with cAMP-d2 conjugate and anti-cAMP cryptate for 1 hr by HTRF assay
ChEMBL 359 5 4 5 0.8 N[C@@]1(C(=O)O)[C@H](CSc2ccc(F)c(F)c2)[C@@H](O)[C@@H]2[C@H]1[C@H]2C(=O)O 10.1021/acs.jmedchem.6b01119
CHEMBL4751065 183759 None 14 Human Functional pIC50 = 8.2 8.2 2 4
Antagonist activity at human recombinant mGlu3 receptor stably expressed in golden hamster AV12 cells co-expressing rat EAAT1 assessed as reduction in DCG IV-induced inhibition of forskolin-stimulated cAMP accumulation preincubated for 20 mins followed by incubation with cAMP-d2 conjugate and anti-cAMP cryptate for 1 hr by HTRF assayAntagonist activity at human recombinant mGlu3 receptor stably expressed in golden hamster AV12 cells co-expressing rat EAAT1 assessed as reduction in DCG IV-induced inhibition of forskolin-stimulated cAMP accumulation preincubated for 20 mins followed by incubation with cAMP-d2 conjugate and anti-cAMP cryptate for 1 hr by HTRF assay
ChEMBL 359 5 4 5 0.8 N[C@@]1(C(=O)O)[C@H](CSc2ccc(F)c(F)c2)[C@@H](O)[C@@H]2[C@H]1[C@H]2C(=O)O 10.1021/acs.jmedchem.6b01119
CHEMBL4802733 183759 None 14 Human Functional pIC50 = 8.2 8.2 2 4
Antagonist activity at human recombinant mGlu3 receptor stably expressed in golden hamster AV12 cells co-expressing rat EAAT1 assessed as reduction in DCG IV-induced inhibition of forskolin-stimulated cAMP accumulation preincubated for 20 mins followed by incubation with cAMP-d2 conjugate and anti-cAMP cryptate for 1 hr by HTRF assayAntagonist activity at human recombinant mGlu3 receptor stably expressed in golden hamster AV12 cells co-expressing rat EAAT1 assessed as reduction in DCG IV-induced inhibition of forskolin-stimulated cAMP accumulation preincubated for 20 mins followed by incubation with cAMP-d2 conjugate and anti-cAMP cryptate for 1 hr by HTRF assay
ChEMBL 359 5 4 5 0.8 N[C@@]1(C(=O)O)[C@H](CSc2ccc(F)c(F)c2)[C@@H](O)[C@@H]2[C@H]1[C@H]2C(=O)O 10.1021/acs.jmedchem.6b01119
122190337 123533 None 0 Rat Functional pIC50 = 6.2 6.2 4 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 386 4 0 5 3.9 C[C@@H]1CN(c2ccc(F)cc2)C(=O)c2cc(COc3ccc(Cl)cn3)nn21 10.1021/acs.jmedchem.5b01005
CHEMBL3617521 123533 None 0 Rat Functional pIC50 = 6.2 6.2 4 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 386 4 0 5 3.9 C[C@@H]1CN(c2ccc(F)cc2)C(=O)c2cc(COc3ccc(Cl)cn3)nn21 10.1021/acs.jmedchem.5b01005
122190428 123604 None 0 Rat Functional pIC50 = 6.2 6.2 - 1
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 369 4 0 6 3.1 C[C@@H]1CN(c2cccnc2)C(=O)c2cc(COc3ccc(Cl)cn3)nn21 10.1021/acs.jmedchem.5b01005
CHEMBL3617651 123604 None 0 Rat Functional pIC50 = 6.2 6.2 - 1
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 369 4 0 6 3.1 C[C@@H]1CN(c2cccnc2)C(=O)c2cc(COc3ccc(Cl)cn3)nn21 10.1021/acs.jmedchem.5b01005
122190436 123610 None 0 Rat Functional pIC50 = 6.2 6.2 - 1
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 394 4 0 7 3.0 C[C@@H]1CN(c2cncc(C#N)c2)C(=O)c2cc(COc3ccc(Cl)cn3)nn21 10.1021/acs.jmedchem.5b01005
CHEMBL3617658 123610 None 0 Rat Functional pIC50 = 6.2 6.2 - 1
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 394 4 0 7 3.0 C[C@@H]1CN(c2cncc(C#N)c2)C(=O)c2cc(COc3ccc(Cl)cn3)nn21 10.1021/acs.jmedchem.5b01005
60204017 2573 None 26 Rat Functional pIC50 = 6.2 6.2 - 1
Negative allosteric modulation of rat mGlu3 receptor transfected in human TREX cells assessed as inhibition of glutamate-induced calcium mobilization after 2.5 minsNegative allosteric modulation of rat mGlu3 receptor transfected in human TREX cells assessed as inhibition of glutamate-induced calcium mobilization after 2.5 mins
ChEMBL 353 2 1 3 2.8 COc1ccc(cc1)C#Cc1ccc(c(c1)F)C(=O)N1CCC[C@H](C1)O 10.1021/jm400439t
8765 2573 None 26 Rat Functional pIC50 = 6.2 6.2 - 1
Negative allosteric modulation of rat mGlu3 receptor transfected in human TREX cells assessed as inhibition of glutamate-induced calcium mobilization after 2.5 minsNegative allosteric modulation of rat mGlu3 receptor transfected in human TREX cells assessed as inhibition of glutamate-induced calcium mobilization after 2.5 mins
ChEMBL 353 2 1 3 2.8 COc1ccc(cc1)C#Cc1ccc(c(c1)F)C(=O)N1CCC[C@H](C1)O 10.1021/jm400439t
CHEMBL2385886 2573 None 26 Rat Functional pIC50 = 6.2 6.2 - 1
Negative allosteric modulation of rat mGlu3 receptor transfected in human TREX cells assessed as inhibition of glutamate-induced calcium mobilization after 2.5 minsNegative allosteric modulation of rat mGlu3 receptor transfected in human TREX cells assessed as inhibition of glutamate-induced calcium mobilization after 2.5 mins
ChEMBL 353 2 1 3 2.8 COc1ccc(cc1)C#Cc1ccc(c(c1)F)C(=O)N1CCC[C@H](C1)O 10.1021/jm400439t
122190337 123533 None 0 Rat Functional pIC50 = 6.2 6.2 4 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 386 4 0 5 3.9 C[C@@H]1CN(c2ccc(F)cc2)C(=O)c2cc(COc3ccc(Cl)cn3)nn21 10.1021/acs.jmedchem.5b01005
CHEMBL3617521 123533 None 0 Rat Functional pIC50 = 6.2 6.2 4 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 386 4 0 5 3.9 C[C@@H]1CN(c2ccc(F)cc2)C(=O)c2cc(COc3ccc(Cl)cn3)nn21 10.1021/acs.jmedchem.5b01005
122190436 123610 None 0 Rat Functional pIC50 = 6.2 6.2 - 1
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 394 4 0 7 3.0 C[C@@H]1CN(c2cncc(C#N)c2)C(=O)c2cc(COc3ccc(Cl)cn3)nn21 10.1021/acs.jmedchem.5b01005
CHEMBL3617658 123610 None 0 Rat Functional pIC50 = 6.2 6.2 - 1
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 394 4 0 7 3.0 C[C@@H]1CN(c2cncc(C#N)c2)C(=O)c2cc(COc3ccc(Cl)cn3)nn21 10.1021/acs.jmedchem.5b01005
122190428 123604 None 0 Rat Functional pIC50 = 6.2 6.2 - 1
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 369 4 0 6 3.1 C[C@@H]1CN(c2cccnc2)C(=O)c2cc(COc3ccc(Cl)cn3)nn21 10.1021/acs.jmedchem.5b01005
CHEMBL3617651 123604 None 0 Rat Functional pIC50 = 6.2 6.2 - 1
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 369 4 0 6 3.1 C[C@@H]1CN(c2cccnc2)C(=O)c2cc(COc3ccc(Cl)cn3)nn21 10.1021/acs.jmedchem.5b01005
69669646 183785 None 0 Human Functional pIC50 = 7.2 7.2 -2 2
Antagonist activity at human recombinant mGlu3 receptor stably expressed in golden hamster AV12 cells co-expressing rat EAAT1 assessed as reduction in DCG IV-induced inhibition of forskolin-stimulated cAMP accumulation preincubated for 20 mins followed by incubation with cAMP-d2 conjugate and anti-cAMP cryptate for 1 hr by HTRF assayAntagonist activity at human recombinant mGlu3 receptor stably expressed in golden hamster AV12 cells co-expressing rat EAAT1 assessed as reduction in DCG IV-induced inhibition of forskolin-stimulated cAMP accumulation preincubated for 20 mins followed by incubation with cAMP-d2 conjugate and anti-cAMP cryptate for 1 hr by HTRF assay
ChEMBL 351 5 4 5 1.1 Cc1ccc(SC[C@@H]2[C@@H](O)[C@@H]3[C@@H]([C@H]3C(=O)O)[C@]2(N)C(=O)O)cc1C 10.1021/acs.jmedchem.6b01119
CHEMBL4757159 183785 None 0 Human Functional pIC50 = 7.2 7.2 -2 2
Antagonist activity at human recombinant mGlu3 receptor stably expressed in golden hamster AV12 cells co-expressing rat EAAT1 assessed as reduction in DCG IV-induced inhibition of forskolin-stimulated cAMP accumulation preincubated for 20 mins followed by incubation with cAMP-d2 conjugate and anti-cAMP cryptate for 1 hr by HTRF assayAntagonist activity at human recombinant mGlu3 receptor stably expressed in golden hamster AV12 cells co-expressing rat EAAT1 assessed as reduction in DCG IV-induced inhibition of forskolin-stimulated cAMP accumulation preincubated for 20 mins followed by incubation with cAMP-d2 conjugate and anti-cAMP cryptate for 1 hr by HTRF assay
ChEMBL 351 5 4 5 1.1 Cc1ccc(SC[C@@H]2[C@@H](O)[C@@H]3[C@@H]([C@H]3C(=O)O)[C@]2(N)C(=O)O)cc1C 10.1021/acs.jmedchem.6b01119
CHEMBL4802990 183785 None 0 Human Functional pIC50 = 7.2 7.2 -2 2
Antagonist activity at human recombinant mGlu3 receptor stably expressed in golden hamster AV12 cells co-expressing rat EAAT1 assessed as reduction in DCG IV-induced inhibition of forskolin-stimulated cAMP accumulation preincubated for 20 mins followed by incubation with cAMP-d2 conjugate and anti-cAMP cryptate for 1 hr by HTRF assayAntagonist activity at human recombinant mGlu3 receptor stably expressed in golden hamster AV12 cells co-expressing rat EAAT1 assessed as reduction in DCG IV-induced inhibition of forskolin-stimulated cAMP accumulation preincubated for 20 mins followed by incubation with cAMP-d2 conjugate and anti-cAMP cryptate for 1 hr by HTRF assay
ChEMBL 351 5 4 5 1.1 Cc1ccc(SC[C@@H]2[C@@H](O)[C@@H]3[C@@H]([C@H]3C(=O)O)[C@]2(N)C(=O)O)cc1C 10.1021/acs.jmedchem.6b01119
10359073 155064 None 0 Human Functional pIC50 = 5.2 5.2 1 2
Tested for agonist activity in non-neuronal cells (RGT) expressing human Metabotropic glutamate receptor 3 by measuring ACPD (3 uM) induced inhibition of forskolin (15 uM)-stimulated cAMP formationTested for agonist activity in non-neuronal cells (RGT) expressing human Metabotropic glutamate receptor 3 by measuring ACPD (3 uM) induced inhibition of forskolin (15 uM)-stimulated cAMP formation
ChEMBL 327 8 3 3 2.7 N[C@@H](C[C@H](CC(c1ccccc1)c1ccccc1)C(=O)O)C(=O)O 10.1016/s0960-894x(98)00091-2
CHEMBL40123 155064 None 0 Human Functional pIC50 = 5.2 5.2 1 2
Tested for agonist activity in non-neuronal cells (RGT) expressing human Metabotropic glutamate receptor 3 by measuring ACPD (3 uM) induced inhibition of forskolin (15 uM)-stimulated cAMP formationTested for agonist activity in non-neuronal cells (RGT) expressing human Metabotropic glutamate receptor 3 by measuring ACPD (3 uM) induced inhibition of forskolin (15 uM)-stimulated cAMP formation
ChEMBL 327 8 3 3 2.7 N[C@@H](C[C@H](CC(c1ccccc1)c1ccccc1)C(=O)O)C(=O)O 10.1016/s0960-894x(98)00091-2
162658340 183792 None 0 Human Functional pIC50 = 7.2 7.2 -1 2
Antagonist activity at human recombinant mGlu3 receptor stably expressed in golden hamster AV12 cells co-expressing rat EAAT1 assessed as reduction in DCG IV-induced inhibition of forskolin-stimulated cAMP accumulation preincubated for 20 mins followed by incubation with cAMP-d2 conjugate and anti-cAMP cryptate for 1 hr by HTRF assayAntagonist activity at human recombinant mGlu3 receptor stably expressed in golden hamster AV12 cells co-expressing rat EAAT1 assessed as reduction in DCG IV-induced inhibition of forskolin-stimulated cAMP accumulation preincubated for 20 mins followed by incubation with cAMP-d2 conjugate and anti-cAMP cryptate for 1 hr by HTRF assay
ChEMBL 405 6 4 5 1.9 N[C@@]1(C(=O)O)[C@H](CSCc2ccc(Cl)c(Cl)c2)[C@@H](O)[C@@H]2[C@H]1[C@H]2C(=O)O 10.1021/acs.jmedchem.6b01119
CHEMBL4760856 183792 None 0 Human Functional pIC50 = 7.2 7.2 -1 2
Antagonist activity at human recombinant mGlu3 receptor stably expressed in golden hamster AV12 cells co-expressing rat EAAT1 assessed as reduction in DCG IV-induced inhibition of forskolin-stimulated cAMP accumulation preincubated for 20 mins followed by incubation with cAMP-d2 conjugate and anti-cAMP cryptate for 1 hr by HTRF assayAntagonist activity at human recombinant mGlu3 receptor stably expressed in golden hamster AV12 cells co-expressing rat EAAT1 assessed as reduction in DCG IV-induced inhibition of forskolin-stimulated cAMP accumulation preincubated for 20 mins followed by incubation with cAMP-d2 conjugate and anti-cAMP cryptate for 1 hr by HTRF assay
ChEMBL 405 6 4 5 1.9 N[C@@]1(C(=O)O)[C@H](CSCc2ccc(Cl)c(Cl)c2)[C@@H](O)[C@@H]2[C@H]1[C@H]2C(=O)O 10.1021/acs.jmedchem.6b01119
CHEMBL4803084 183792 None 0 Human Functional pIC50 = 7.2 7.2 -1 2
Antagonist activity at human recombinant mGlu3 receptor stably expressed in golden hamster AV12 cells co-expressing rat EAAT1 assessed as reduction in DCG IV-induced inhibition of forskolin-stimulated cAMP accumulation preincubated for 20 mins followed by incubation with cAMP-d2 conjugate and anti-cAMP cryptate for 1 hr by HTRF assayAntagonist activity at human recombinant mGlu3 receptor stably expressed in golden hamster AV12 cells co-expressing rat EAAT1 assessed as reduction in DCG IV-induced inhibition of forskolin-stimulated cAMP accumulation preincubated for 20 mins followed by incubation with cAMP-d2 conjugate and anti-cAMP cryptate for 1 hr by HTRF assay
ChEMBL 405 6 4 5 1.9 N[C@@]1(C(=O)O)[C@H](CSCc2ccc(Cl)c(Cl)c2)[C@@H](O)[C@@H]2[C@H]1[C@H]2C(=O)O 10.1021/acs.jmedchem.6b01119
90098428 123472 None 0 Human Functional pIC50 = 6.2 6.2 -60 2
Antagonist activity at human recombinant mGlu3 receptor expressed in AV12 cells assessed as inhibition of glutamate-stimulated Ca2+ mobilization after 1.5 hrs by FLIPR assayAntagonist activity at human recombinant mGlu3 receptor expressed in AV12 cells assessed as inhibition of glutamate-stimulated Ca2+ mobilization after 1.5 hrs by FLIPR assay
ChEMBL 352 4 4 6 0.4 N[C@@]1(C(=O)O)C[C@H](Sc2nnc(C(F)(F)F)[nH]2)[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/acs.jmedchem.5b01124
CHEMBL3616856 123472 None 0 Human Functional pIC50 = 6.2 6.2 -60 2
Antagonist activity at human recombinant mGlu3 receptor expressed in AV12 cells assessed as inhibition of glutamate-stimulated Ca2+ mobilization after 1.5 hrs by FLIPR assayAntagonist activity at human recombinant mGlu3 receptor expressed in AV12 cells assessed as inhibition of glutamate-stimulated Ca2+ mobilization after 1.5 hrs by FLIPR assay
ChEMBL 352 4 4 6 0.4 N[C@@]1(C(=O)O)C[C@H](Sc2nnc(C(F)(F)F)[nH]2)[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/acs.jmedchem.5b01124
44302856 102786 None 0 Human Functional pIC50 = 4.2 4.2 -1 2
In vitro antagonist activity at recombinant human Metabotropic glutamate receptor 3 expressed in RGT cells.In vitro antagonist activity at recombinant human Metabotropic glutamate receptor 3 expressed in RGT cells.
ChEMBL 354 6 3 4 1.8 N[C@]1(C(=O)O)C[C@H](C(=O)O)N(CC(c2ccccc2)c2ccccc2)C1 10.1016/s0960-894x(98)00352-7
CHEMBL304919 102786 None 0 Human Functional pIC50 = 4.2 4.2 -1 2
In vitro antagonist activity at recombinant human Metabotropic glutamate receptor 3 expressed in RGT cells.In vitro antagonist activity at recombinant human Metabotropic glutamate receptor 3 expressed in RGT cells.
ChEMBL 354 6 3 4 1.8 N[C@]1(C(=O)O)C[C@H](C(=O)O)N(CC(c2ccccc2)c2ccccc2)C1 10.1016/s0960-894x(98)00352-7
90643971 112064 None 0 Rat Functional pIC50 = 6.2 6.2 1 2
Inhibition of rat mGlu3 receptor transfected in HEK293 cells coexpressing mouse Galpha15 assessed as decrease in glutamate-induced calcium signaling by fluorescence plate reader analysis in presence of glutamate at EC87 concentrationInhibition of rat mGlu3 receptor transfected in HEK293 cells coexpressing mouse Galpha15 assessed as decrease in glutamate-induced calcium signaling by fluorescence plate reader analysis in presence of glutamate at EC87 concentration
ChEMBL 386 2 0 5 4.6 Cn1c(=O)c2ccc(-c3cccnc3)cc2n2nc(-c3ccc(Cl)cc3)cc12 10.1016/j.bmcl.2014.04.051
CHEMBL3288667 112064 None 0 Rat Functional pIC50 = 6.2 6.2 1 2
Inhibition of rat mGlu3 receptor transfected in HEK293 cells coexpressing mouse Galpha15 assessed as decrease in glutamate-induced calcium signaling by fluorescence plate reader analysis in presence of glutamate at EC87 concentrationInhibition of rat mGlu3 receptor transfected in HEK293 cells coexpressing mouse Galpha15 assessed as decrease in glutamate-induced calcium signaling by fluorescence plate reader analysis in presence of glutamate at EC87 concentration
ChEMBL 386 2 0 5 4.6 Cn1c(=O)c2ccc(-c3cccnc3)cc2n2nc(-c3ccc(Cl)cc3)cc12 10.1016/j.bmcl.2014.04.051
10587622 78771 None 0 Human Functional pIC50 = 6.2 6.2 1 2
Ability to block 1S,3R-ACPD-induced inhibition of forskolin stimulated cyclic-AMP in non-neuronal cell line expressing human Metabotropic glutamate receptor 3Ability to block 1S,3R-ACPD-induced inhibition of forskolin stimulated cyclic-AMP in non-neuronal cell line expressing human Metabotropic glutamate receptor 3
ChEMBL 263 6 3 3 1.1 NC(CCc1ccccc1)(C(=O)O)[C@H]1C[C@@H]1C(=O)O 10.1021/jm970497w
CHEMBL2112582 78771 None 0 Human Functional pIC50 = 6.2 6.2 1 2
Ability to block 1S,3R-ACPD-induced inhibition of forskolin stimulated cyclic-AMP in non-neuronal cell line expressing human Metabotropic glutamate receptor 3Ability to block 1S,3R-ACPD-induced inhibition of forskolin stimulated cyclic-AMP in non-neuronal cell line expressing human Metabotropic glutamate receptor 3
ChEMBL 263 6 3 3 1.1 NC(CCc1ccccc1)(C(=O)O)[C@H]1C[C@@H]1C(=O)O 10.1021/jm970497w
10587622 78771 None 0 Human Functional pIC50 = 6.2 6.2 1 2
Effect on 1S,3R-ACPD-induced inhibition of forskolin stimulated cyclic-AMP in RGT cells expressing human Metabotropic glutamate receptor 3Effect on 1S,3R-ACPD-induced inhibition of forskolin stimulated cyclic-AMP in RGT cells expressing human Metabotropic glutamate receptor 3
ChEMBL 263 6 3 3 1.1 NC(CCc1ccccc1)(C(=O)O)[C@H]1C[C@@H]1C(=O)O 10.1021/jm970498o
CHEMBL2112582 78771 None 0 Human Functional pIC50 = 6.2 6.2 1 2
Effect on 1S,3R-ACPD-induced inhibition of forskolin stimulated cyclic-AMP in RGT cells expressing human Metabotropic glutamate receptor 3Effect on 1S,3R-ACPD-induced inhibition of forskolin stimulated cyclic-AMP in RGT cells expressing human Metabotropic glutamate receptor 3
ChEMBL 263 6 3 3 1.1 NC(CCc1ccccc1)(C(=O)O)[C@H]1C[C@@H]1C(=O)O 10.1021/jm970498o
60204018 90358 None 0 Rat Functional pIC50 = 6.2 6.2 - 1
Negative allosteric modulation of rat mGlu3 receptor transfected in human TREX cells assessed as inhibition of glutamate-induced calcium mobilization after 2.5 minsNegative allosteric modulation of rat mGlu3 receptor transfected in human TREX cells assessed as inhibition of glutamate-induced calcium mobilization after 2.5 mins
ChEMBL 335 2 1 3 2.7 COc1ccc(C#Cc2ccc(C(=O)N3CCC[C@@H](O)C3)cc2)cc1 10.1021/jm400439t
CHEMBL2385878 90358 None 0 Rat Functional pIC50 = 6.2 6.2 - 1
Negative allosteric modulation of rat mGlu3 receptor transfected in human TREX cells assessed as inhibition of glutamate-induced calcium mobilization after 2.5 minsNegative allosteric modulation of rat mGlu3 receptor transfected in human TREX cells assessed as inhibition of glutamate-induced calcium mobilization after 2.5 mins
ChEMBL 335 2 1 3 2.7 COc1ccc(C#Cc2ccc(C(=O)N3CCC[C@@H](O)C3)cc2)cc1 10.1021/jm400439t
CHEMBL2385888 90358 None 0 Rat Functional pIC50 = 6.2 6.2 - 1
Negative allosteric modulation of rat mGlu3 receptor transfected in human TREX cells assessed as inhibition of glutamate-induced calcium mobilization after 2.5 minsNegative allosteric modulation of rat mGlu3 receptor transfected in human TREX cells assessed as inhibition of glutamate-induced calcium mobilization after 2.5 mins
ChEMBL 335 2 1 3 2.7 COc1ccc(C#Cc2ccc(C(=O)N3CCC[C@@H](O)C3)cc2)cc1 10.1021/jm400439t
56587994 4045 None 29 Human Functional pIC50 = 6.2 6.2 -1 2
Negative allosteric modulation of mGlu3 assessed as inhibition of glutamate-induced calcium mobilization in presence of Galpha15 by cell based assayNegative allosteric modulation of mGlu3 assessed as inhibition of glutamate-induced calcium mobilization in presence of Galpha15 by cell based assay
ChEMBL 349 3 1 3 2.9 OC[C@@H]1CCCN(C1)C(=O)c1ccc(cc1)C#Cc1ccc(cc1)OC 10.1016/j.bmcl.2012.04.112
6225 4045 None 29 Human Functional pIC50 = 6.2 6.2 -1 2
Negative allosteric modulation of mGlu3 assessed as inhibition of glutamate-induced calcium mobilization in presence of Galpha15 by cell based assayNegative allosteric modulation of mGlu3 assessed as inhibition of glutamate-induced calcium mobilization in presence of Galpha15 by cell based assay
ChEMBL 349 3 1 3 2.9 OC[C@@H]1CCCN(C1)C(=O)c1ccc(cc1)C#Cc1ccc(cc1)OC 10.1016/j.bmcl.2012.04.112
CHEMBL2204445 4045 None 29 Human Functional pIC50 = 6.2 6.2 -1 2
Negative allosteric modulation of mGlu3 assessed as inhibition of glutamate-induced calcium mobilization in presence of Galpha15 by cell based assayNegative allosteric modulation of mGlu3 assessed as inhibition of glutamate-induced calcium mobilization in presence of Galpha15 by cell based assay
ChEMBL 349 3 1 3 2.9 OC[C@@H]1CCCN(C1)C(=O)c1ccc(cc1)C#Cc1ccc(cc1)OC 10.1016/j.bmcl.2012.04.112
60204018 90358 None 0 Rat Functional pIC50 = 6.2 6.2 - 1
Negative allosteric modulation of rat mGlu3 receptor transfected in human TREX cells assessed as inhibition of glutamate-induced calcium mobilization after 2.5 minsNegative allosteric modulation of rat mGlu3 receptor transfected in human TREX cells assessed as inhibition of glutamate-induced calcium mobilization after 2.5 mins
ChEMBL 335 2 1 3 2.7 COc1ccc(C#Cc2ccc(C(=O)N3CCC[C@@H](O)C3)cc2)cc1 10.1021/jm400439t
CHEMBL2385878 90358 None 0 Rat Functional pIC50 = 6.2 6.2 - 1
Negative allosteric modulation of rat mGlu3 receptor transfected in human TREX cells assessed as inhibition of glutamate-induced calcium mobilization after 2.5 minsNegative allosteric modulation of rat mGlu3 receptor transfected in human TREX cells assessed as inhibition of glutamate-induced calcium mobilization after 2.5 mins
ChEMBL 335 2 1 3 2.7 COc1ccc(C#Cc2ccc(C(=O)N3CCC[C@@H](O)C3)cc2)cc1 10.1021/jm400439t
CHEMBL2385888 90358 None 0 Rat Functional pIC50 = 6.2 6.2 - 1
Negative allosteric modulation of rat mGlu3 receptor transfected in human TREX cells assessed as inhibition of glutamate-induced calcium mobilization after 2.5 minsNegative allosteric modulation of rat mGlu3 receptor transfected in human TREX cells assessed as inhibition of glutamate-induced calcium mobilization after 2.5 mins
ChEMBL 335 2 1 3 2.7 COc1ccc(C#Cc2ccc(C(=O)N3CCC[C@@H](O)C3)cc2)cc1 10.1021/jm400439t
90643968 112062 None 0 Rat Functional pIC50 = 7.2 7.2 6 2
Inhibition of rat mGlu3 receptor transfected in HEK293 cells coexpressing mouse Galpha15 assessed as decrease in glutamate-induced calcium signaling by fluorescence plate reader analysis in presence of glutamate at EC87 concentrationInhibition of rat mGlu3 receptor transfected in HEK293 cells coexpressing mouse Galpha15 assessed as decrease in glutamate-induced calcium signaling by fluorescence plate reader analysis in presence of glutamate at EC87 concentration
ChEMBL 370 2 0 5 4.1 Cn1c(=O)c2ccc(-c3cccnc3)cc2n2nc(-c3ccc(F)cc3)cc12 10.1016/j.bmcl.2014.04.051
CHEMBL3288662 112062 None 0 Rat Functional pIC50 = 7.2 7.2 6 2
Inhibition of rat mGlu3 receptor transfected in HEK293 cells coexpressing mouse Galpha15 assessed as decrease in glutamate-induced calcium signaling by fluorescence plate reader analysis in presence of glutamate at EC87 concentrationInhibition of rat mGlu3 receptor transfected in HEK293 cells coexpressing mouse Galpha15 assessed as decrease in glutamate-induced calcium signaling by fluorescence plate reader analysis in presence of glutamate at EC87 concentration
ChEMBL 370 2 0 5 4.1 Cn1c(=O)c2ccc(-c3cccnc3)cc2n2nc(-c3ccc(F)cc3)cc12 10.1016/j.bmcl.2014.04.051
122190430 123606 None 0 Rat Functional pIC50 = 6.2 6.2 - 1
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 394 4 0 7 3.0 C[C@@H]1CN(c2ncccc2C#N)C(=O)c2cc(COc3ccc(Cl)cn3)nn21 10.1021/acs.jmedchem.5b01005
CHEMBL3617653 123606 None 0 Rat Functional pIC50 = 6.2 6.2 - 1
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 394 4 0 7 3.0 C[C@@H]1CN(c2ncccc2C#N)C(=O)c2cc(COc3ccc(Cl)cn3)nn21 10.1021/acs.jmedchem.5b01005
122190332 123528 None 0 Rat Functional pIC50 = 5.2 5.2 - 1
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 382 5 0 6 3.2 COc1cccnc1OCc1cc2n(n1)[C@H](C)CN(c1ccc(F)cc1)C2=O 10.1021/acs.jmedchem.5b01005
CHEMBL3617516 123528 None 0 Rat Functional pIC50 = 5.2 5.2 - 1
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 382 5 0 6 3.2 COc1cccnc1OCc1cc2n(n1)[C@H](C)CN(c1ccc(F)cc1)C2=O 10.1021/acs.jmedchem.5b01005
122190332 123528 None 0 Rat Functional pIC50 = 5.2 5.2 - 1
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 382 5 0 6 3.2 COc1cccnc1OCc1cc2n(n1)[C@H](C)CN(c1ccc(F)cc1)C2=O 10.1021/acs.jmedchem.5b01005
CHEMBL3617516 123528 None 0 Rat Functional pIC50 = 5.2 5.2 - 1
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 382 5 0 6 3.2 COc1cccnc1OCc1cc2n(n1)[C@H](C)CN(c1ccc(F)cc1)C2=O 10.1021/acs.jmedchem.5b01005
122190430 123606 None 0 Rat Functional pIC50 = 6.2 6.2 - 1
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 394 4 0 7 3.0 C[C@@H]1CN(c2ncccc2C#N)C(=O)c2cc(COc3ccc(Cl)cn3)nn21 10.1021/acs.jmedchem.5b01005
CHEMBL3617653 123606 None 0 Rat Functional pIC50 = 6.2 6.2 - 1
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 394 4 0 7 3.0 C[C@@H]1CN(c2ncccc2C#N)C(=O)c2cc(COc3ccc(Cl)cn3)nn21 10.1021/acs.jmedchem.5b01005
19702198 161416 None 11 Rat Functional pIC50 = 4.2 4.2 -1 2
Inhibitory concentration required for antagonistic activity at Metabotropic glutamate receptor 3Inhibitory concentration required for antagonistic activity at Metabotropic glutamate receptor 3
ChEMBL 173 3 3 3 -0.5 CC(N)(C(=O)O)C1CC1C(=O)O 10.1016/s0960-894x(01)00329-8
CHEMBL412445 161416 None 11 Rat Functional pIC50 = 4.2 4.2 -1 2
Inhibitory concentration required for antagonistic activity at Metabotropic glutamate receptor 3Inhibitory concentration required for antagonistic activity at Metabotropic glutamate receptor 3
ChEMBL 173 3 3 3 -0.5 CC(N)(C(=O)O)C1CC1C(=O)O 10.1016/s0960-894x(01)00329-8
122190415 123591 None 0 Rat Functional pIC50 = 6.2 6.2 - 1
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 398 5 0 6 3.7 COc1ccccc1N1C[C@@H](C)n2nc(COc3ccc(Cl)cn3)cc2C1=O 10.1021/acs.jmedchem.5b01005
CHEMBL3617638 123591 None 0 Rat Functional pIC50 = 6.2 6.2 - 1
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 398 5 0 6 3.7 COc1ccccc1N1C[C@@H](C)n2nc(COc3ccc(Cl)cn3)cc2C1=O 10.1021/acs.jmedchem.5b01005
122190415 123591 None 0 Rat Functional pIC50 = 6.2 6.2 - 1
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 398 5 0 6 3.7 COc1ccccc1N1C[C@@H](C)n2nc(COc3ccc(Cl)cn3)cc2C1=O 10.1021/acs.jmedchem.5b01005
CHEMBL3617638 123591 None 0 Rat Functional pIC50 = 6.2 6.2 - 1
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 398 5 0 6 3.7 COc1ccccc1N1C[C@@H](C)n2nc(COc3ccc(Cl)cn3)cc2C1=O 10.1021/acs.jmedchem.5b01005
90643959 112056 None 0 Rat Functional pIC50 = 6.2 6.2 1 2
Inhibition of rat mGlu3 receptor transfected in HEK293 cells coexpressing mouse Galpha15 assessed as decrease in glutamate-induced calcium signaling by fluorescence plate reader analysis in presence of glutamate at EC87 concentrationInhibition of rat mGlu3 receptor transfected in HEK293 cells coexpressing mouse Galpha15 assessed as decrease in glutamate-induced calcium signaling by fluorescence plate reader analysis in presence of glutamate at EC87 concentration
ChEMBL 460 4 1 7 3.2 COc1cccc(-c2cc3n(C)c(=O)c4ccc(-c5cccc(S(N)(=O)=O)c5)cc4n3n2)c1 10.1016/j.bmcl.2014.04.051
CHEMBL3288646 112056 None 0 Rat Functional pIC50 = 6.2 6.2 1 2
Inhibition of rat mGlu3 receptor transfected in HEK293 cells coexpressing mouse Galpha15 assessed as decrease in glutamate-induced calcium signaling by fluorescence plate reader analysis in presence of glutamate at EC87 concentrationInhibition of rat mGlu3 receptor transfected in HEK293 cells coexpressing mouse Galpha15 assessed as decrease in glutamate-induced calcium signaling by fluorescence plate reader analysis in presence of glutamate at EC87 concentration
ChEMBL 460 4 1 7 3.2 COc1cccc(-c2cc3n(C)c(=O)c4ccc(-c5cccc(S(N)(=O)=O)c5)cc4n3n2)c1 10.1016/j.bmcl.2014.04.051
1378 2417 None 39 Human Functional pIC50 = 8.1 8.1 2 14
Antagonist activity at human recombinant mGlu3 receptor stably expressed in golden hamster AV12 cells co-expressing rat EAAT1 assessed as reduction in DCG IV-induced inhibition of forskolin-stimulated cAMP accumulation preincubated for 20 mins followed by incubation with cAMP-d2 conjugate and anti-cAMP cryptate for 1 hr by HTRF assayAntagonist activity at human recombinant mGlu3 receptor stably expressed in golden hamster AV12 cells co-expressing rat EAAT1 assessed as reduction in DCG IV-induced inhibition of forskolin-stimulated cAMP accumulation preincubated for 20 mins followed by incubation with cAMP-d2 conjugate and anti-cAMP cryptate for 1 hr by HTRF assay
ChEMBL 353 5 3 4 2.8 OC(=O)[C@H]1C[C@@H]1[C@](C(=O)O)(CC1c2ccccc2Oc2c1cccc2)N 10.1021/acs.jmedchem.6b01119
1399 2417 None 39 Human Functional pIC50 = 8.1 8.1 2 14
Antagonist activity at human recombinant mGlu3 receptor stably expressed in golden hamster AV12 cells co-expressing rat EAAT1 assessed as reduction in DCG IV-induced inhibition of forskolin-stimulated cAMP accumulation preincubated for 20 mins followed by incubation with cAMP-d2 conjugate and anti-cAMP cryptate for 1 hr by HTRF assayAntagonist activity at human recombinant mGlu3 receptor stably expressed in golden hamster AV12 cells co-expressing rat EAAT1 assessed as reduction in DCG IV-induced inhibition of forskolin-stimulated cAMP accumulation preincubated for 20 mins followed by incubation with cAMP-d2 conjugate and anti-cAMP cryptate for 1 hr by HTRF assay
ChEMBL 353 5 3 4 2.8 OC(=O)[C@H]1C[C@@H]1[C@](C(=O)O)(CC1c2ccccc2Oc2c1cccc2)N 10.1021/acs.jmedchem.6b01119
9819927 2417 None 39 Human Functional pIC50 = 8.1 8.1 2 14
Antagonist activity at human recombinant mGlu3 receptor stably expressed in golden hamster AV12 cells co-expressing rat EAAT1 assessed as reduction in DCG IV-induced inhibition of forskolin-stimulated cAMP accumulation preincubated for 20 mins followed by incubation with cAMP-d2 conjugate and anti-cAMP cryptate for 1 hr by HTRF assayAntagonist activity at human recombinant mGlu3 receptor stably expressed in golden hamster AV12 cells co-expressing rat EAAT1 assessed as reduction in DCG IV-induced inhibition of forskolin-stimulated cAMP accumulation preincubated for 20 mins followed by incubation with cAMP-d2 conjugate and anti-cAMP cryptate for 1 hr by HTRF assay
ChEMBL 353 5 3 4 2.8 OC(=O)[C@H]1C[C@@H]1[C@](C(=O)O)(CC1c2ccccc2Oc2c1cccc2)N 10.1021/acs.jmedchem.6b01119
CHEMBL432038 2417 None 39 Human Functional pIC50 = 8.1 8.1 2 14
Antagonist activity at human recombinant mGlu3 receptor stably expressed in golden hamster AV12 cells co-expressing rat EAAT1 assessed as reduction in DCG IV-induced inhibition of forskolin-stimulated cAMP accumulation preincubated for 20 mins followed by incubation with cAMP-d2 conjugate and anti-cAMP cryptate for 1 hr by HTRF assayAntagonist activity at human recombinant mGlu3 receptor stably expressed in golden hamster AV12 cells co-expressing rat EAAT1 assessed as reduction in DCG IV-induced inhibition of forskolin-stimulated cAMP accumulation preincubated for 20 mins followed by incubation with cAMP-d2 conjugate and anti-cAMP cryptate for 1 hr by HTRF assay
ChEMBL 353 5 3 4 2.8 OC(=O)[C@H]1C[C@@H]1[C@](C(=O)O)(CC1c2ccccc2Oc2c1cccc2)N 10.1021/acs.jmedchem.6b01119
134155683 151450 None 0 Human Functional pIC50 = 7.2 7.2 -1 2
Antagonist activity at recombinant human mGlu3 receptor expressed in hamster AV12 cells co-expressing human EAAT1 assessed as reduction of DCG-4-inhibited forskolin-stimulated cAMP formation after 20 mins by HTRF assayAntagonist activity at recombinant human mGlu3 receptor expressed in hamster AV12 cells co-expressing human EAAT1 assessed as reduction of DCG-4-inhibited forskolin-stimulated cAMP formation after 20 mins by HTRF assay
ChEMBL 377 5 3 4 2.0 N[C@@]1(C(=O)O)[C@H](OCc2ccc(Cl)c(Cl)c2)[C@@H](F)[C@H]2[C@H](C(=O)O)[C@H]21 10.1016/j.bmcl.2016.10.067
CHEMBL3961306 151450 None 0 Human Functional pIC50 = 7.2 7.2 -1 2
Antagonist activity at recombinant human mGlu3 receptor expressed in hamster AV12 cells co-expressing human EAAT1 assessed as reduction of DCG-4-inhibited forskolin-stimulated cAMP formation after 20 mins by HTRF assayAntagonist activity at recombinant human mGlu3 receptor expressed in hamster AV12 cells co-expressing human EAAT1 assessed as reduction of DCG-4-inhibited forskolin-stimulated cAMP formation after 20 mins by HTRF assay
ChEMBL 377 5 3 4 2.0 N[C@@]1(C(=O)O)[C@H](OCc2ccc(Cl)c(Cl)c2)[C@@H](F)[C@H]2[C@H](C(=O)O)[C@H]21 10.1016/j.bmcl.2016.10.067
60204019 90363 None 0 Rat Functional pIC50 = 6.2 6.2 - 1
Negative allosteric modulation of rat mGlu3 receptor transfected in human TREX cells assessed as inhibition of glutamate-induced calcium mobilization after 2.5 minsNegative allosteric modulation of rat mGlu3 receptor transfected in human TREX cells assessed as inhibition of glutamate-induced calcium mobilization after 2.5 mins
ChEMBL 349 2 1 3 3.1 COc1ccc(C#Cc2ccc(C(=O)N3CCCC(C)(O)C3)cc2)cc1 10.1021/jm400439t
CHEMBL2385883 90363 None 0 Rat Functional pIC50 = 6.2 6.2 - 1
Negative allosteric modulation of rat mGlu3 receptor transfected in human TREX cells assessed as inhibition of glutamate-induced calcium mobilization after 2.5 minsNegative allosteric modulation of rat mGlu3 receptor transfected in human TREX cells assessed as inhibition of glutamate-induced calcium mobilization after 2.5 mins
ChEMBL 349 2 1 3 3.1 COc1ccc(C#Cc2ccc(C(=O)N3CCCC(C)(O)C3)cc2)cc1 10.1021/jm400439t
122190316 123512 None 0 Rat Functional pIC50 = 6.1 6.1 2 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 365 4 0 4 4.1 Cc1ccccc1OCc1cc2n(n1)[C@H](C)CN(c1ccc(F)cc1)C2=O 10.1021/acs.jmedchem.5b01005
CHEMBL3617500 123512 None 0 Rat Functional pIC50 = 6.1 6.1 2 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 365 4 0 4 4.1 Cc1ccccc1OCc1cc2n(n1)[C@H](C)CN(c1ccc(F)cc1)C2=O 10.1021/acs.jmedchem.5b01005
122190316 123512 None 0 Rat Functional pIC50 = 6.1 6.1 2 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 365 4 0 4 4.1 Cc1ccccc1OCc1cc2n(n1)[C@H](C)CN(c1ccc(F)cc1)C2=O 10.1021/acs.jmedchem.5b01005
CHEMBL3617500 123512 None 0 Rat Functional pIC50 = 6.1 6.1 2 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 365 4 0 4 4.1 Cc1ccccc1OCc1cc2n(n1)[C@H](C)CN(c1ccc(F)cc1)C2=O 10.1021/acs.jmedchem.5b01005
60210806 90359 None 0 Rat Functional pIC50 = 5.1 5.1 - 1
Negative allosteric modulation of rat mGlu3 receptor transfected in human TREX cells assessed as inhibition of glutamate-induced calcium mobilization after 2.5 minsNegative allosteric modulation of rat mGlu3 receptor transfected in human TREX cells assessed as inhibition of glutamate-induced calcium mobilization after 2.5 mins
ChEMBL 309 4 2 3 2.2 COc1ccc(C#Cc2ccc(C(=O)NC(C)CO)cc2)cc1 10.1021/jm400439t
CHEMBL2385879 90359 None 0 Rat Functional pIC50 = 5.1 5.1 - 1
Negative allosteric modulation of rat mGlu3 receptor transfected in human TREX cells assessed as inhibition of glutamate-induced calcium mobilization after 2.5 minsNegative allosteric modulation of rat mGlu3 receptor transfected in human TREX cells assessed as inhibition of glutamate-induced calcium mobilization after 2.5 mins
ChEMBL 309 4 2 3 2.2 COc1ccc(C#Cc2ccc(C(=O)NC(C)CO)cc2)cc1 10.1021/jm400439t
56587989 90362 None 0 Rat Functional pIC50 = 5.1 5.1 - 1
Negative allosteric modulation of rat mGlu3 receptor transfected in human TREX cells assessed as inhibition of glutamate-induced calcium mobilization after 2.5 minsNegative allosteric modulation of rat mGlu3 receptor transfected in human TREX cells assessed as inhibition of glutamate-induced calcium mobilization after 2.5 mins
ChEMBL 335 3 1 3 2.5 COc1ccc(C#Cc2ccc(C(=O)N3CCC(CO)C3)cc2)cc1 10.1021/jm400439t
CHEMBL2385882 90362 None 0 Rat Functional pIC50 = 5.1 5.1 - 1
Negative allosteric modulation of rat mGlu3 receptor transfected in human TREX cells assessed as inhibition of glutamate-induced calcium mobilization after 2.5 minsNegative allosteric modulation of rat mGlu3 receptor transfected in human TREX cells assessed as inhibition of glutamate-induced calcium mobilization after 2.5 mins
ChEMBL 335 3 1 3 2.5 COc1ccc(C#Cc2ccc(C(=O)N3CCC(CO)C3)cc2)cc1 10.1021/jm400439t
44329042 169186 None 0 Rat Functional pIC50 = 7.1 7.1 33 5
Antagonistic activity against metabotropic glutamate receptor 3 (mGluR3) was evaluatedAntagonistic activity against metabotropic glutamate receptor 3 (mGluR3) was evaluated
ChEMBL 381 6 3 4 3.5 CC[C@@H]1[C@H](C(=O)O)[C@H]1C(N)(CC1c2ccccc2Oc2ccccc21)C(=O)O 10.1016/s0960-894x(98)00510-1
CHEMBL439775 169186 None 0 Rat Functional pIC50 = 7.1 7.1 33 5
Antagonistic activity against metabotropic glutamate receptor 3 (mGluR3) was evaluatedAntagonistic activity against metabotropic glutamate receptor 3 (mGluR3) was evaluated
ChEMBL 381 6 3 4 3.5 CC[C@@H]1[C@H](C(=O)O)[C@H]1C(N)(CC1c2ccccc2Oc2ccccc21)C(=O)O 10.1016/s0960-894x(98)00510-1
21309795 150912 None 0 Human Functional pIC50 = 7.1 7.1 3 2
Antagonist activity at recombinant human mGlu3 receptor expressed in hamster AV12 cells co-expressing human EAAT1 assessed as reduction of DCG-4-inhibited forskolin-stimulated cAMP formation after 20 mins by HTRF assayAntagonist activity at recombinant human mGlu3 receptor expressed in hamster AV12 cells co-expressing human EAAT1 assessed as reduction of DCG-4-inhibited forskolin-stimulated cAMP formation after 20 mins by HTRF assay
ChEMBL 327 4 3 3 1.8 N[C@@]1(C(=O)O)[C@H](Cc2ccc(F)c(Cl)c2)C[C@H]2[C@H](C(=O)O)[C@H]21 10.1016/j.bmcl.2016.10.067
CHEMBL3956934 150912 None 0 Human Functional pIC50 = 7.1 7.1 3 2
Antagonist activity at recombinant human mGlu3 receptor expressed in hamster AV12 cells co-expressing human EAAT1 assessed as reduction of DCG-4-inhibited forskolin-stimulated cAMP formation after 20 mins by HTRF assayAntagonist activity at recombinant human mGlu3 receptor expressed in hamster AV12 cells co-expressing human EAAT1 assessed as reduction of DCG-4-inhibited forskolin-stimulated cAMP formation after 20 mins by HTRF assay
ChEMBL 327 4 3 3 1.8 N[C@@]1(C(=O)O)[C@H](Cc2ccc(F)c(Cl)c2)C[C@H]2[C@H](C(=O)O)[C@H]21 10.1016/j.bmcl.2016.10.067
10567792 78775 None 0 Human Functional pIC50 = 6.1 6.1 -3 2
Ability to block 1S,3R-ACPD-induced inhibition of forskolin stimulated cyclic-AMP in non-neuronal cell line expressing human Metabotropic glutamate receptor 3Ability to block 1S,3R-ACPD-induced inhibition of forskolin stimulated cyclic-AMP in non-neuronal cell line expressing human Metabotropic glutamate receptor 3
ChEMBL 321 6 3 3 2.5 NC(CCC12CC3CC(CC(C3)C1)C2)(C(=O)O)[C@H]1C[C@@H]1C(=O)O 10.1021/jm970497w
CHEMBL2112586 78775 None 0 Human Functional pIC50 = 6.1 6.1 -3 2
Ability to block 1S,3R-ACPD-induced inhibition of forskolin stimulated cyclic-AMP in non-neuronal cell line expressing human Metabotropic glutamate receptor 3Ability to block 1S,3R-ACPD-induced inhibition of forskolin stimulated cyclic-AMP in non-neuronal cell line expressing human Metabotropic glutamate receptor 3
ChEMBL 321 6 3 3 2.5 NC(CCC12CC3CC(CC(C3)C1)C2)(C(=O)O)[C@H]1C[C@@H]1C(=O)O 10.1021/jm970497w
53393854 83635 None 0 Rat Functional pIC50 = 6.1 6.1 2 2
Negative allosteric modulation of rat mGlu3 receptor transfected in human TREX cells assessed as inhibition of glutamate-induced calcium mobilization after 2.5 minsNegative allosteric modulation of rat mGlu3 receptor transfected in human TREX cells assessed as inhibition of glutamate-induced calcium mobilization after 2.5 mins
ChEMBL 335 2 1 3 2.7 COc1ccc(C#Cc2ccc(C(=O)N3CCCC(O)C3)cc2)cc1 10.1021/jm400439t
CHEMBL2204439 83635 None 0 Rat Functional pIC50 = 6.1 6.1 2 2
Negative allosteric modulation of rat mGlu3 receptor transfected in human TREX cells assessed as inhibition of glutamate-induced calcium mobilization after 2.5 minsNegative allosteric modulation of rat mGlu3 receptor transfected in human TREX cells assessed as inhibition of glutamate-induced calcium mobilization after 2.5 mins
ChEMBL 335 2 1 3 2.7 COc1ccc(C#Cc2ccc(C(=O)N3CCCC(O)C3)cc2)cc1 10.1021/jm400439t
10979251 90094 None 0 Human Functional pIC50 = 5.1 5.1 -1 3
Antagonist activity at human recombinant mGlu3 receptor expressed in AV12 cells assessed as inhibition of glutamate-stimulated Ca2+ mobilization after 1.5 hrs by FLIPR assayAntagonist activity at human recombinant mGlu3 receptor expressed in AV12 cells assessed as inhibition of glutamate-stimulated Ca2+ mobilization after 1.5 hrs by FLIPR assay
ChEMBL 293 4 3 4 1.3 N[C@@]1(C(=O)O)C[C@@H](Sc2ccccc2)[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/acs.jmedchem.5b01124
CHEMBL2381650 90094 None 0 Human Functional pIC50 = 5.1 5.1 -1 3
Antagonist activity at human recombinant mGlu3 receptor expressed in AV12 cells assessed as inhibition of glutamate-stimulated Ca2+ mobilization after 1.5 hrs by FLIPR assayAntagonist activity at human recombinant mGlu3 receptor expressed in AV12 cells assessed as inhibition of glutamate-stimulated Ca2+ mobilization after 1.5 hrs by FLIPR assay
ChEMBL 293 4 3 4 1.3 N[C@@]1(C(=O)O)C[C@@H](Sc2ccccc2)[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/acs.jmedchem.5b01124
86298614 112067 None 0 Rat Functional pIC50 = 7.1 7.1 3 2
Inhibition of rat mGlu3 receptor transfected in HEK293 cells coexpressing mouse Galpha15 assessed as decrease in glutamate-induced calcium signaling by fluorescence plate reader analysis in presence of glutamate at EC87 concentrationInhibition of rat mGlu3 receptor transfected in HEK293 cells coexpressing mouse Galpha15 assessed as decrease in glutamate-induced calcium signaling by fluorescence plate reader analysis in presence of glutamate at EC87 concentration
ChEMBL 353 2 0 6 3.3 Cn1c(=O)c2ccc(-c3cncnc3)cc2n2nc(-c3ccccc3)cc12 10.1016/j.bmcl.2014.04.051
CHEMBL3288676 112067 None 0 Rat Functional pIC50 = 7.1 7.1 3 2
Inhibition of rat mGlu3 receptor transfected in HEK293 cells coexpressing mouse Galpha15 assessed as decrease in glutamate-induced calcium signaling by fluorescence plate reader analysis in presence of glutamate at EC87 concentrationInhibition of rat mGlu3 receptor transfected in HEK293 cells coexpressing mouse Galpha15 assessed as decrease in glutamate-induced calcium signaling by fluorescence plate reader analysis in presence of glutamate at EC87 concentration
ChEMBL 353 2 0 6 3.3 Cn1c(=O)c2ccc(-c3cncnc3)cc2n2nc(-c3ccccc3)cc12 10.1016/j.bmcl.2014.04.051
44300389 13664 None 0 Rat Functional pIC50 = 4.1 4.1 1 2
Inhibitory concentration required for antagonistic activity at Metabotropic glutamate receptor 3Inhibitory concentration required for antagonistic activity at Metabotropic glutamate receptor 3
ChEMBL 342 4 3 4 0.9 N[C@]1(C(=O)O)C[C@H](C(=O)O)N(Cc2ccccc2Br)C1 10.1016/s0960-894x(01)00329-8
CHEMBL1194613 13664 None 0 Rat Functional pIC50 = 4.1 4.1 1 2
Inhibitory concentration required for antagonistic activity at Metabotropic glutamate receptor 3Inhibitory concentration required for antagonistic activity at Metabotropic glutamate receptor 3
ChEMBL 342 4 3 4 0.9 N[C@]1(C(=O)O)C[C@H](C(=O)O)N(Cc2ccccc2Br)C1 10.1016/s0960-894x(01)00329-8
CHEMBL552984 13664 None 0 Rat Functional pIC50 = 4.1 4.1 1 2
Inhibitory concentration required for antagonistic activity at Metabotropic glutamate receptor 3Inhibitory concentration required for antagonistic activity at Metabotropic glutamate receptor 3
ChEMBL 342 4 3 4 0.9 N[C@]1(C(=O)O)C[C@H](C(=O)O)N(Cc2ccccc2Br)C1 10.1016/s0960-894x(01)00329-8
122190313 123509 None 0 Rat Functional pIC50 = 6.1 6.1 -10 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 369 4 0 4 4.0 C[C@@H]1CN(c2ccc(F)cc2)C(=O)c2cc(COc3cccc(F)c3)nn21 10.1021/acs.jmedchem.5b01005
CHEMBL3617497 123509 None 0 Rat Functional pIC50 = 6.1 6.1 -10 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 369 4 0 4 4.0 C[C@@H]1CN(c2ccc(F)cc2)C(=O)c2cc(COc3cccc(F)c3)nn21 10.1021/acs.jmedchem.5b01005
122190313 123509 None 0 Rat Functional pIC50 = 6.1 6.1 -10 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 369 4 0 4 4.0 C[C@@H]1CN(c2ccc(F)cc2)C(=O)c2cc(COc3cccc(F)c3)nn21 10.1021/acs.jmedchem.5b01005
CHEMBL3617497 123509 None 0 Rat Functional pIC50 = 6.1 6.1 -10 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 369 4 0 4 4.0 C[C@@H]1CN(c2ccc(F)cc2)C(=O)c2cc(COc3cccc(F)c3)nn21 10.1021/acs.jmedchem.5b01005
122190327 123523 None 0 Rat Functional pIC50 = 6.1 6.1 2 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 376 4 0 5 3.7 C[C@@H]1CN(c2ccc(F)cc2)C(=O)c2cc(COc3ccc(C#N)cc3)nn21 10.1021/acs.jmedchem.5b01005
CHEMBL3617511 123523 None 0 Rat Functional pIC50 = 6.1 6.1 2 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 376 4 0 5 3.7 C[C@@H]1CN(c2ccc(F)cc2)C(=O)c2cc(COc3ccc(C#N)cc3)nn21 10.1021/acs.jmedchem.5b01005
86298614 112067 None 0 Rat Functional pIC50 = 7.1 7.1 3 2
Inhibition of rat mGlu3 receptor transfected in HEK293 cells coexpressing mouse Galpha15 assessed as decrease in glutamate-induced calcium signaling by fluorescence plate reader analysis in presence of glutamate at EC87 concentrationInhibition of rat mGlu3 receptor transfected in HEK293 cells coexpressing mouse Galpha15 assessed as decrease in glutamate-induced calcium signaling by fluorescence plate reader analysis in presence of glutamate at EC87 concentration
ChEMBL 353 2 0 6 3.3 Cn1c(=O)c2ccc(-c3cncnc3)cc2n2nc(-c3ccccc3)cc12 10.1016/j.bmcl.2014.04.051
CHEMBL3288676 112067 None 0 Rat Functional pIC50 = 7.1 7.1 3 2
Inhibition of rat mGlu3 receptor transfected in HEK293 cells coexpressing mouse Galpha15 assessed as decrease in glutamate-induced calcium signaling by fluorescence plate reader analysis in presence of glutamate at EC87 concentrationInhibition of rat mGlu3 receptor transfected in HEK293 cells coexpressing mouse Galpha15 assessed as decrease in glutamate-induced calcium signaling by fluorescence plate reader analysis in presence of glutamate at EC87 concentration
ChEMBL 353 2 0 6 3.3 Cn1c(=O)c2ccc(-c3cncnc3)cc2n2nc(-c3ccccc3)cc12 10.1016/j.bmcl.2014.04.051
89554734 160255 None 0 Human Functional pIC50 = 5.1 5.1 -676 2
Negative allosteric modulation at mGluR3 receptor (unknown origin) assessed as effect on intracellular calcium flux measured after 5 min by Fluo-4AM dye based FLIPR analysisNegative allosteric modulation at mGluR3 receptor (unknown origin) assessed as effect on intracellular calcium flux measured after 5 min by Fluo-4AM dye based FLIPR analysis
ChEMBL 419 4 1 6 2.5 Cn1cc(-c2cc(C(N)=O)nc3cc(CN4CCO[C@@H](C(F)(F)F)C4)ccc23)cn1 10.1021/acsmedchemlett.3c00210
CHEMBL4109210 160255 None 0 Human Functional pIC50 = 5.1 5.1 -676 2
Negative allosteric modulation at mGluR3 receptor (unknown origin) assessed as effect on intracellular calcium flux measured after 5 min by Fluo-4AM dye based FLIPR analysisNegative allosteric modulation at mGluR3 receptor (unknown origin) assessed as effect on intracellular calcium flux measured after 5 min by Fluo-4AM dye based FLIPR analysis
ChEMBL 419 4 1 6 2.5 Cn1cc(-c2cc(C(N)=O)nc3cc(CN4CCO[C@@H](C(F)(F)F)C4)ccc23)cn1 10.1021/acsmedchemlett.3c00210
122190327 123523 None 0 Rat Functional pIC50 = 6.1 6.1 2 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 376 4 0 5 3.7 C[C@@H]1CN(c2ccc(F)cc2)C(=O)c2cc(COc3ccc(C#N)cc3)nn21 10.1021/acs.jmedchem.5b01005
CHEMBL3617511 123523 None 0 Rat Functional pIC50 = 6.1 6.1 2 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 376 4 0 5 3.7 C[C@@H]1CN(c2ccc(F)cc2)C(=O)c2cc(COc3ccc(C#N)cc3)nn21 10.1021/acs.jmedchem.5b01005
10492773 16792 None 0 Human Functional pIC50 = 7.1 7.1 2 2
Effect on 1S,3R-ACPD-induced inhibition of forskolin stimulated cyclic-AMP in RGT cells expressing human Metabotropic glutamate receptor 3Effect on 1S,3R-ACPD-induced inhibition of forskolin stimulated cyclic-AMP in RGT cells expressing human Metabotropic glutamate receptor 3
ChEMBL 277 6 3 3 1.4 Cc1cccc(CC[C@](N)(C(=O)O)[C@H]2C[C@@H]2C(=O)O)c1 10.1021/jm970498o
CHEMBL124501 16792 None 0 Human Functional pIC50 = 7.1 7.1 2 2
Effect on 1S,3R-ACPD-induced inhibition of forskolin stimulated cyclic-AMP in RGT cells expressing human Metabotropic glutamate receptor 3Effect on 1S,3R-ACPD-induced inhibition of forskolin stimulated cyclic-AMP in RGT cells expressing human Metabotropic glutamate receptor 3
ChEMBL 277 6 3 3 1.4 Cc1cccc(CC[C@](N)(C(=O)O)[C@H]2C[C@@H]2C(=O)O)c1 10.1021/jm970498o
10828532 78796 None 0 Human Functional pIC50 = 7.1 7.1 22 2
Effect on 1S,3R-ACPD-induced inhibition of forskolin stimulated cyclic-AMP in RGT cells expressing human Metabotropic glutamate receptor 3Effect on 1S,3R-ACPD-induced inhibition of forskolin stimulated cyclic-AMP in RGT cells expressing human Metabotropic glutamate receptor 3
ChEMBL 307 7 4 4 0.8 NC(CCc1cccc(C(=O)O)c1)(C(=O)O)[C@H]1C[C@@H]1C(=O)O 10.1021/jm970498o
CHEMBL2112634 78796 None 0 Human Functional pIC50 = 7.1 7.1 22 2
Effect on 1S,3R-ACPD-induced inhibition of forskolin stimulated cyclic-AMP in RGT cells expressing human Metabotropic glutamate receptor 3Effect on 1S,3R-ACPD-induced inhibition of forskolin stimulated cyclic-AMP in RGT cells expressing human Metabotropic glutamate receptor 3
ChEMBL 307 7 4 4 0.8 NC(CCc1cccc(C(=O)O)c1)(C(=O)O)[C@H]1C[C@@H]1C(=O)O 10.1021/jm970498o
122190419 123595 None 0 Rat Functional pIC50 = 6.1 6.1 - 1
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 393 4 0 6 3.6 C[C@@H]1CN(c2cccc(C#N)c2)C(=O)c2cc(COc3ccc(Cl)cn3)nn21 10.1021/acs.jmedchem.5b01005
CHEMBL3617642 123595 None 0 Rat Functional pIC50 = 6.1 6.1 - 1
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 393 4 0 6 3.6 C[C@@H]1CN(c2cccc(C#N)c2)C(=O)c2cc(COc3ccc(Cl)cn3)nn21 10.1021/acs.jmedchem.5b01005
134139744 146047 None 0 Human Functional pIC50 = 7.1 7.1 1 2
Antagonist activity at recombinant human mGlu3 receptor expressed in hamster AV12 cells co-expressing human EAAT1 assessed as reduction of DCG-4-inhibited forskolin-stimulated cAMP formation after 20 mins by HTRF assayAntagonist activity at recombinant human mGlu3 receptor expressed in hamster AV12 cells co-expressing human EAAT1 assessed as reduction of DCG-4-inhibited forskolin-stimulated cAMP formation after 20 mins by HTRF assay
ChEMBL 375 5 4 5 1.0 N[C@@]1(C(=O)O)[C@H](OCc2cccc(Cl)c2Cl)[C@H](O)[C@@H]2[C@H]1[C@H]2C(=O)O 10.1016/j.bmcl.2016.10.067
CHEMBL3918170 146047 None 0 Human Functional pIC50 = 7.1 7.1 1 2
Antagonist activity at recombinant human mGlu3 receptor expressed in hamster AV12 cells co-expressing human EAAT1 assessed as reduction of DCG-4-inhibited forskolin-stimulated cAMP formation after 20 mins by HTRF assayAntagonist activity at recombinant human mGlu3 receptor expressed in hamster AV12 cells co-expressing human EAAT1 assessed as reduction of DCG-4-inhibited forskolin-stimulated cAMP formation after 20 mins by HTRF assay
ChEMBL 375 5 4 5 1.0 N[C@@]1(C(=O)O)[C@H](OCc2cccc(Cl)c2Cl)[C@H](O)[C@@H]2[C@H]1[C@H]2C(=O)O 10.1016/j.bmcl.2016.10.067
122190326 123522 None 0 Rat Functional pIC50 = 6.1 6.1 3 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 379 5 0 4 4.4 CCc1ccc(OCc2cc3n(n2)[C@H](C)CN(c2ccc(F)cc2)C3=O)cc1 10.1021/acs.jmedchem.5b01005
CHEMBL3617510 123522 None 0 Rat Functional pIC50 = 6.1 6.1 3 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 379 5 0 4 4.4 CCc1ccc(OCc2cc3n(n2)[C@H](C)CN(c2ccc(F)cc2)C3=O)cc1 10.1021/acs.jmedchem.5b01005
122190326 123522 None 0 Rat Functional pIC50 = 6.1 6.1 3 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 379 5 0 4 4.4 CCc1ccc(OCc2cc3n(n2)[C@H](C)CN(c2ccc(F)cc2)C3=O)cc1 10.1021/acs.jmedchem.5b01005
CHEMBL3617510 123522 None 0 Rat Functional pIC50 = 6.1 6.1 3 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 379 5 0 4 4.4 CCc1ccc(OCc2cc3n(n2)[C@H](C)CN(c2ccc(F)cc2)C3=O)cc1 10.1021/acs.jmedchem.5b01005
122190419 123595 None 0 Rat Functional pIC50 = 6.1 6.1 - 1
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 393 4 0 6 3.6 C[C@@H]1CN(c2cccc(C#N)c2)C(=O)c2cc(COc3ccc(Cl)cn3)nn21 10.1021/acs.jmedchem.5b01005
CHEMBL3617642 123595 None 0 Rat Functional pIC50 = 6.1 6.1 - 1
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 393 4 0 6 3.6 C[C@@H]1CN(c2cccc(C#N)c2)C(=O)c2cc(COc3ccc(Cl)cn3)nn21 10.1021/acs.jmedchem.5b01005
134141510 147156 None 0 Human Functional pIC50 = 7.1 7.1 2 2
Antagonist activity at recombinant human mGlu3 receptor expressed in hamster AV12 cells co-expressing human EAAT1 assessed as reduction of DCG-4-inhibited forskolin-stimulated cAMP formation after 20 mins by HTRF assayAntagonist activity at recombinant human mGlu3 receptor expressed in hamster AV12 cells co-expressing human EAAT1 assessed as reduction of DCG-4-inhibited forskolin-stimulated cAMP formation after 20 mins by HTRF assay
ChEMBL 339 5 4 5 0.1 Cc1cc(CO[C@@H]2[C@H](O)[C@@H]3[C@@H]([C@H]3C(=O)O)[C@]2(N)C(=O)O)ccc1F 10.1016/j.bmcl.2016.10.067
CHEMBL3927108 147156 None 0 Human Functional pIC50 = 7.1 7.1 2 2
Antagonist activity at recombinant human mGlu3 receptor expressed in hamster AV12 cells co-expressing human EAAT1 assessed as reduction of DCG-4-inhibited forskolin-stimulated cAMP formation after 20 mins by HTRF assayAntagonist activity at recombinant human mGlu3 receptor expressed in hamster AV12 cells co-expressing human EAAT1 assessed as reduction of DCG-4-inhibited forskolin-stimulated cAMP formation after 20 mins by HTRF assay
ChEMBL 339 5 4 5 0.1 Cc1cc(CO[C@@H]2[C@H](O)[C@@H]3[C@@H]([C@H]3C(=O)O)[C@]2(N)C(=O)O)ccc1F 10.1016/j.bmcl.2016.10.067
122190421 123597 None 0 Rat Functional pIC50 = 6.1 6.1 7 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 404 4 0 5 4.0 C[C@@H]1CN(c2cccc(F)c2F)C(=O)c2cc(COc3ccc(Cl)cn3)nn21 10.1021/acs.jmedchem.5b01005
CHEMBL3617644 123597 None 0 Rat Functional pIC50 = 6.1 6.1 7 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 404 4 0 5 4.0 C[C@@H]1CN(c2cccc(F)c2F)C(=O)c2cc(COc3ccc(Cl)cn3)nn21 10.1021/acs.jmedchem.5b01005
122190421 123597 None 0 Rat Functional pIC50 = 6.1 6.1 7 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 404 4 0 5 4.0 C[C@@H]1CN(c2cccc(F)c2F)C(=O)c2cc(COc3ccc(Cl)cn3)nn21 10.1021/acs.jmedchem.5b01005
CHEMBL3617644 123597 None 0 Rat Functional pIC50 = 6.1 6.1 7 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 404 4 0 5 4.0 C[C@@H]1CN(c2cccc(F)c2F)C(=O)c2cc(COc3ccc(Cl)cn3)nn21 10.1021/acs.jmedchem.5b01005
10358265 102181 None 0 Human Functional pIC50 = 5.1 5.1 2 2
In vitro antagonist activity at recombinant human Metabotropic glutamate receptor 3 expressed in RGT cells.In vitro antagonist activity at recombinant human Metabotropic glutamate receptor 3 expressed in RGT cells.
ChEMBL 314 4 3 4 1.3 N[C@]1(C(=O)O)C[C@H](C(=O)O)N(Cc2cccc3ccccc23)C1 10.1016/s0960-894x(98)00352-7
CHEMBL302411 102181 None 0 Human Functional pIC50 = 5.1 5.1 2 2
In vitro antagonist activity at recombinant human Metabotropic glutamate receptor 3 expressed in RGT cells.In vitro antagonist activity at recombinant human Metabotropic glutamate receptor 3 expressed in RGT cells.
ChEMBL 314 4 3 4 1.3 N[C@]1(C(=O)O)C[C@H](C(=O)O)N(Cc2cccc3ccccc23)C1 10.1016/s0960-894x(98)00352-7
71136655 123468 None 0 Human Functional pIC50 = 6.1 6.1 -12 2
Antagonist activity at human recombinant mGlu3 receptor expressed in AV12 cells assessed as reversal of DCG-4-inhibited, forskolin-stimulated cAMP production after 1 hr by fluorescence assayAntagonist activity at human recombinant mGlu3 receptor expressed in AV12 cells assessed as reversal of DCG-4-inhibited, forskolin-stimulated cAMP production after 1 hr by fluorescence assay
ChEMBL 326 5 4 6 0.5 CC(C)c1nnc(S[C@@H]2C[C@@](N)(C(=O)O)[C@@H]3[C@@H](C(=O)O)[C@H]23)[nH]1 10.1021/acs.jmedchem.5b01124
CHEMBL3616852 123468 None 0 Human Functional pIC50 = 6.1 6.1 -12 2
Antagonist activity at human recombinant mGlu3 receptor expressed in AV12 cells assessed as reversal of DCG-4-inhibited, forskolin-stimulated cAMP production after 1 hr by fluorescence assayAntagonist activity at human recombinant mGlu3 receptor expressed in AV12 cells assessed as reversal of DCG-4-inhibited, forskolin-stimulated cAMP production after 1 hr by fluorescence assay
ChEMBL 326 5 4 6 0.5 CC(C)c1nnc(S[C@@H]2C[C@@](N)(C(=O)O)[C@@H]3[C@@H](C(=O)O)[C@H]23)[nH]1 10.1021/acs.jmedchem.5b01124
122190405 123581 None 0 Rat Functional pIC50 = 6.1 6.1 - 1
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 353 4 0 6 2.6 C[C@@H]1CN(c2ccncc2)C(=O)c2cc(COc3ccc(F)cn3)nn21 10.1021/acs.jmedchem.5b01005
CHEMBL3617628 123581 None 0 Rat Functional pIC50 = 6.1 6.1 - 1
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 353 4 0 6 2.6 C[C@@H]1CN(c2ccncc2)C(=O)c2cc(COc3ccc(F)cn3)nn21 10.1021/acs.jmedchem.5b01005
90643954 112053 None 0 Rat Functional pIC50 = 6.1 6.1 2 2
Inhibition of rat mGlu3 receptor transfected in HEK293 cells coexpressing mouse Galpha15 assessed as decrease in glutamate-induced calcium signaling by fluorescence plate reader analysis in presence of glutamate at EC87 concentrationInhibition of rat mGlu3 receptor transfected in HEK293 cells coexpressing mouse Galpha15 assessed as decrease in glutamate-induced calcium signaling by fluorescence plate reader analysis in presence of glutamate at EC87 concentration
ChEMBL 430 3 1 6 3.2 Cn1c(=O)c2ccc(-c3cccc(S(N)(=O)=O)c3)cc2n2nc(-c3ccccc3)cc12 10.1016/j.bmcl.2014.04.051
CHEMBL3288636 112053 None 0 Rat Functional pIC50 = 6.1 6.1 2 2
Inhibition of rat mGlu3 receptor transfected in HEK293 cells coexpressing mouse Galpha15 assessed as decrease in glutamate-induced calcium signaling by fluorescence plate reader analysis in presence of glutamate at EC87 concentrationInhibition of rat mGlu3 receptor transfected in HEK293 cells coexpressing mouse Galpha15 assessed as decrease in glutamate-induced calcium signaling by fluorescence plate reader analysis in presence of glutamate at EC87 concentration
ChEMBL 430 3 1 6 3.2 Cn1c(=O)c2ccc(-c3cccc(S(N)(=O)=O)c3)cc2n2nc(-c3ccccc3)cc12 10.1016/j.bmcl.2014.04.051
122190405 123581 None 0 Rat Functional pIC50 = 6.1 6.1 - 1
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 353 4 0 6 2.6 C[C@@H]1CN(c2ccncc2)C(=O)c2cc(COc3ccc(F)cn3)nn21 10.1021/acs.jmedchem.5b01005
CHEMBL3617628 123581 None 0 Rat Functional pIC50 = 6.1 6.1 - 1
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 353 4 0 6 2.6 C[C@@H]1CN(c2ccncc2)C(=O)c2cc(COc3ccc(F)cn3)nn21 10.1021/acs.jmedchem.5b01005
10979251 90094 None 0 Human Functional pIC50 = 6.1 6.1 -1 3
Antagonist activity at human mGlu3 receptor expressed in golden Syrian hamster AV12 cells coexpressing EAAT1 assessed as inhibition of forskolin-stimulated cAMP production after 20 mins by HTRF assayAntagonist activity at human mGlu3 receptor expressed in golden Syrian hamster AV12 cells coexpressing EAAT1 assessed as inhibition of forskolin-stimulated cAMP production after 20 mins by HTRF assay
ChEMBL 293 4 3 4 1.3 N[C@@]1(C(=O)O)C[C@@H](Sc2ccccc2)[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/jm4000165
CHEMBL2381650 90094 None 0 Human Functional pIC50 = 6.1 6.1 -1 3
Antagonist activity at human mGlu3 receptor expressed in golden Syrian hamster AV12 cells coexpressing EAAT1 assessed as inhibition of forskolin-stimulated cAMP production after 20 mins by HTRF assayAntagonist activity at human mGlu3 receptor expressed in golden Syrian hamster AV12 cells coexpressing EAAT1 assessed as inhibition of forskolin-stimulated cAMP production after 20 mins by HTRF assay
ChEMBL 293 4 3 4 1.3 N[C@@]1(C(=O)O)C[C@@H](Sc2ccccc2)[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/jm4000165
122190403 123579 None 0 Rat Functional pIC50 = 6.0 6.0 3 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 353 4 0 6 2.6 C[C@@H]1CN(c2ccccn2)C(=O)c2cc(COc3ccc(F)cn3)nn21 10.1021/acs.jmedchem.5b01005
CHEMBL3617626 123579 None 0 Rat Functional pIC50 = 6.0 6.0 3 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 353 4 0 6 2.6 C[C@@H]1CN(c2ccccn2)C(=O)c2cc(COc3ccc(F)cn3)nn21 10.1021/acs.jmedchem.5b01005
122190403 123579 None 0 Rat Functional pIC50 = 6.0 6.0 3 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 353 4 0 6 2.6 C[C@@H]1CN(c2ccccn2)C(=O)c2cc(COc3ccc(F)cn3)nn21 10.1021/acs.jmedchem.5b01005
CHEMBL3617626 123579 None 0 Rat Functional pIC50 = 6.0 6.0 3 2
Negative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor assessed as calcium mobilization by cell based fluorescence assay
ChEMBL 353 4 0 6 2.6 C[C@@H]1CN(c2ccccn2)C(=O)c2cc(COc3ccc(F)cn3)nn21 10.1021/acs.jmedchem.5b01005
122456062 162544 None 0 Rat Functional pIC50 = 6.0 6.0 -1 2
Negative allosteric modulation of rat mGlu3 receptor expressed in TREX cells coexpressing Galpha15 assessed as inhibition of glutamate induced-calcium mobilization preincubated for 2.3 mins followed by glutamate addition measured for 2.6 mins by Fluo-4 AM dye based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor expressed in TREX cells coexpressing Galpha15 assessed as inhibition of glutamate induced-calcium mobilization preincubated for 2.3 mins followed by glutamate addition measured for 2.6 mins by Fluo-4 AM dye based fluorescence assay
ChEMBL 325 6 0 4 3.4 O=c1cc(OCCOc2ccccc2)ccn1-c1ccc(F)cc1 10.1021/acsmedchemlett.7b00249
CHEMBL4166631 162544 None 0 Rat Functional pIC50 = 6.0 6.0 -1 2
Negative allosteric modulation of rat mGlu3 receptor expressed in TREX cells coexpressing Galpha15 assessed as inhibition of glutamate induced-calcium mobilization preincubated for 2.3 mins followed by glutamate addition measured for 2.6 mins by Fluo-4 AM dye based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor expressed in TREX cells coexpressing Galpha15 assessed as inhibition of glutamate induced-calcium mobilization preincubated for 2.3 mins followed by glutamate addition measured for 2.6 mins by Fluo-4 AM dye based fluorescence assay
ChEMBL 325 6 0 4 3.4 O=c1cc(OCCOc2ccccc2)ccn1-c1ccc(F)cc1 10.1021/acsmedchemlett.7b00249
10385210 13037 None 0 Rat Functional pIC50 = 4.0 4.0 -2 3
Inhibitory concentration required for antagonistic activity at Metabotropic glutamate receptor 3Inhibitory concentration required for antagonistic activity at Metabotropic glutamate receptor 3
ChEMBL 309 5 3 6 0.0 N[C@]1(C(=O)O)C[C@H](C(=O)O)N(Cc2cccc([N+](=O)[O-])c2)C1 10.1016/s0960-894x(01)00329-8
CHEMBL1189910 13037 None 0 Rat Functional pIC50 = 4.0 4.0 -2 3
Inhibitory concentration required for antagonistic activity at Metabotropic glutamate receptor 3Inhibitory concentration required for antagonistic activity at Metabotropic glutamate receptor 3
ChEMBL 309 5 3 6 0.0 N[C@]1(C(=O)O)C[C@H](C(=O)O)N(Cc2cccc([N+](=O)[O-])c2)C1 10.1016/s0960-894x(01)00329-8
CHEMBL539760 13037 None 0 Rat Functional pIC50 = 4.0 4.0 -2 3
Inhibitory concentration required for antagonistic activity at Metabotropic glutamate receptor 3Inhibitory concentration required for antagonistic activity at Metabotropic glutamate receptor 3
ChEMBL 309 5 3 6 0.0 N[C@]1(C(=O)O)C[C@H](C(=O)O)N(Cc2cccc([N+](=O)[O-])c2)C1 10.1016/s0960-894x(01)00329-8
122456062 162544 None 0 Rat Functional pIC50 = 6.0 6.0 -1 2
Negative allosteric modulation of rat mGlu3 receptor expressed in TREX cells coexpressing Galpha15 assessed as inhibition of glutamate induced-calcium mobilization preincubated for 2.3 mins followed by glutamate addition measured for 2.6 mins by Fluo-4 AM dye based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor expressed in TREX cells coexpressing Galpha15 assessed as inhibition of glutamate induced-calcium mobilization preincubated for 2.3 mins followed by glutamate addition measured for 2.6 mins by Fluo-4 AM dye based fluorescence assay
ChEMBL 325 6 0 4 3.4 O=c1cc(OCCOc2ccccc2)ccn1-c1ccc(F)cc1 10.1021/acsmedchemlett.7b00249
CHEMBL4166631 162544 None 0 Rat Functional pIC50 = 6.0 6.0 -1 2
Negative allosteric modulation of rat mGlu3 receptor expressed in TREX cells coexpressing Galpha15 assessed as inhibition of glutamate induced-calcium mobilization preincubated for 2.3 mins followed by glutamate addition measured for 2.6 mins by Fluo-4 AM dye based fluorescence assayNegative allosteric modulation of rat mGlu3 receptor expressed in TREX cells coexpressing Galpha15 assessed as inhibition of glutamate induced-calcium mobilization preincubated for 2.3 mins followed by glutamate addition measured for 2.6 mins by Fluo-4 AM dye based fluorescence assay
ChEMBL 325 6 0 4 3.4 O=c1cc(OCCOc2ccccc2)ccn1-c1ccc(F)cc1 10.1021/acsmedchemlett.7b00249
71137012 123467 None 0 Human Functional pIC50 = 7.0 7.0 -11 2
Antagonist activity at human recombinant mGlu3 receptor expressed in AV12 cells assessed as inhibition of glutamate-stimulated Ca2+ mobilization after 1.5 hrs by FLIPR assayAntagonist activity at human recombinant mGlu3 receptor expressed in AV12 cells assessed as inhibition of glutamate-stimulated Ca2+ mobilization after 1.5 hrs by FLIPR assay
ChEMBL 299 4 5 7 -1.0 Nc1nnc(S[C@@H]2C[C@@](N)(C(=O)O)[C@@H]3[C@@H](C(=O)O)[C@H]23)[nH]1 10.1021/acs.jmedchem.5b01124
CHEMBL3616851 123467 None 0 Human Functional pIC50 = 7.0 7.0 -11 2
Antagonist activity at human recombinant mGlu3 receptor expressed in AV12 cells assessed as inhibition of glutamate-stimulated Ca2+ mobilization after 1.5 hrs by FLIPR assayAntagonist activity at human recombinant mGlu3 receptor expressed in AV12 cells assessed as inhibition of glutamate-stimulated Ca2+ mobilization after 1.5 hrs by FLIPR assay
ChEMBL 299 4 5 7 -1.0 Nc1nnc(S[C@@H]2C[C@@](N)(C(=O)O)[C@@H]3[C@@H](C(=O)O)[C@H]23)[nH]1 10.1021/acs.jmedchem.5b01124
162654849 183776 None 0 Human Functional pIC50 = 6.0 6.0 1 2
Antagonist activity at human recombinant mGlu3 receptor stably expressed in golden hamster AV12 cells co-expressing rat EAAT1 assessed as reduction in DCG IV-induced inhibition of forskolin-stimulated cAMP accumulation preincubated for 20 mins followed by incubation with cAMP-d2 conjugate and anti-cAMP cryptate for 1 hr by HTRF assayAntagonist activity at human recombinant mGlu3 receptor stably expressed in golden hamster AV12 cells co-expressing rat EAAT1 assessed as reduction in DCG IV-induced inhibition of forskolin-stimulated cAMP accumulation preincubated for 20 mins followed by incubation with cAMP-d2 conjugate and anti-cAMP cryptate for 1 hr by HTRF assay
ChEMBL 341 5 4 5 0.6 N[C@@]1(C(=O)O)[C@H](CSc2ccccc2F)[C@@H](O)[C@@H]2[C@H]1[C@H]2C(=O)O 10.1021/acs.jmedchem.6b01119
CHEMBL4755204 183776 None 0 Human Functional pIC50 = 6.0 6.0 1 2
Antagonist activity at human recombinant mGlu3 receptor stably expressed in golden hamster AV12 cells co-expressing rat EAAT1 assessed as reduction in DCG IV-induced inhibition of forskolin-stimulated cAMP accumulation preincubated for 20 mins followed by incubation with cAMP-d2 conjugate and anti-cAMP cryptate for 1 hr by HTRF assayAntagonist activity at human recombinant mGlu3 receptor stably expressed in golden hamster AV12 cells co-expressing rat EAAT1 assessed as reduction in DCG IV-induced inhibition of forskolin-stimulated cAMP accumulation preincubated for 20 mins followed by incubation with cAMP-d2 conjugate and anti-cAMP cryptate for 1 hr by HTRF assay
ChEMBL 341 5 4 5 0.6 N[C@@]1(C(=O)O)[C@H](CSc2ccccc2F)[C@@H](O)[C@@H]2[C@H]1[C@H]2C(=O)O 10.1021/acs.jmedchem.6b01119
CHEMBL4802906 183776 None 0 Human Functional pIC50 = 6.0 6.0 1 2
Antagonist activity at human recombinant mGlu3 receptor stably expressed in golden hamster AV12 cells co-expressing rat EAAT1 assessed as reduction in DCG IV-induced inhibition of forskolin-stimulated cAMP accumulation preincubated for 20 mins followed by incubation with cAMP-d2 conjugate and anti-cAMP cryptate for 1 hr by HTRF assayAntagonist activity at human recombinant mGlu3 receptor stably expressed in golden hamster AV12 cells co-expressing rat EAAT1 assessed as reduction in DCG IV-induced inhibition of forskolin-stimulated cAMP accumulation preincubated for 20 mins followed by incubation with cAMP-d2 conjugate and anti-cAMP cryptate for 1 hr by HTRF assay
ChEMBL 341 5 4 5 0.6 N[C@@]1(C(=O)O)[C@H](CSc2ccccc2F)[C@@H](O)[C@@H]2[C@H]1[C@H]2C(=O)O 10.1021/acs.jmedchem.6b01119
11298568 69397 None 1 Human Functional pIC50 = 5.0 5.0 -5 2
Evaluation of the functional effect on cAMP responses in RGT cells expressing human mGlu3 receptorEvaluation of the functional effect on cAMP responses in RGT cells expressing human mGlu3 receptor
ChEMBL 199 2 3 3 -0.2 C[C@@H]1C[C@H]2[C@H](C(=O)O)[C@H]2[C@]1(N)C(=O)O 10.1021/jm040222y
CHEMBL192977 69397 None 1 Human Functional pIC50 = 5.0 5.0 -5 2
Evaluation of the functional effect on cAMP responses in RGT cells expressing human mGlu3 receptorEvaluation of the functional effect on cAMP responses in RGT cells expressing human mGlu3 receptor
ChEMBL 199 2 3 3 -0.2 C[C@@H]1C[C@H]2[C@H](C(=O)O)[C@H]2[C@]1(N)C(=O)O 10.1021/jm040222y
137635882 155984 None 0 Human Functional pIC50 = 5 5.0 -1 2
Antagonist activity at human mGlu3 receptor expressed in HEK cells assessed as reversal of DCG-4 inhibited forskolin-stimulated cAMP formation after 20 mins by HTRF assayAntagonist activity at human mGlu3 receptor expressed in HEK cells assessed as reversal of DCG-4 inhibited forskolin-stimulated cAMP formation after 20 mins by HTRF assay
ChEMBL 310 4 4 4 0.2 N[C@@]1(C(=O)O)C[C@H](NC(=O)C2CCCCC2)[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/acs.jmedchem.7b01481
CHEMBL4060567 155984 None 0 Human Functional pIC50 = 5 5.0 -1 2
Antagonist activity at human mGlu3 receptor expressed in HEK cells assessed as reversal of DCG-4 inhibited forskolin-stimulated cAMP formation after 20 mins by HTRF assayAntagonist activity at human mGlu3 receptor expressed in HEK cells assessed as reversal of DCG-4 inhibited forskolin-stimulated cAMP formation after 20 mins by HTRF assay
ChEMBL 310 4 4 4 0.2 N[C@@]1(C(=O)O)C[C@H](NC(=O)C2CCCCC2)[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/acs.jmedchem.7b01481
44322840 112634 None 0 Human Functional pKi = 7 7.0 - 0
Agonist potency against cloned Metabotropic glutamate receptor 3 (mGluR-3).Agonist potency against cloned Metabotropic glutamate receptor 3 (mGluR-3).
ChEMBL 201 2 4 4 -1.5 N[C@]1(C(=O)O)C2C(C[C@H]1O)[C@@H]2C(=O)O 10.1021/jm000007r
CHEMBL330097 112634 None 0 Human Functional pKi = 7 7.0 - 0
Agonist potency against cloned Metabotropic glutamate receptor 3 (mGluR-3).Agonist potency against cloned Metabotropic glutamate receptor 3 (mGluR-3).
ChEMBL 201 2 4 4 -1.5 N[C@]1(C(=O)O)C2C(C[C@H]1O)[C@@H]2C(=O)O 10.1021/jm000007r
1378 2417 None 39 Human Functional pKi = 7.9 7.9 2 14
Agonist potency against cloned Metabotropic glutamate receptor 3 (mGluR-3).Agonist potency against cloned Metabotropic glutamate receptor 3 (mGluR-3).
ChEMBL 353 5 3 4 2.8 OC(=O)[C@H]1C[C@@H]1[C@](C(=O)O)(CC1c2ccccc2Oc2c1cccc2)N 10.1021/jm000007r
1399 2417 None 39 Human Functional pKi = 7.9 7.9 2 14
Agonist potency against cloned Metabotropic glutamate receptor 3 (mGluR-3).Agonist potency against cloned Metabotropic glutamate receptor 3 (mGluR-3).
ChEMBL 353 5 3 4 2.8 OC(=O)[C@H]1C[C@@H]1[C@](C(=O)O)(CC1c2ccccc2Oc2c1cccc2)N 10.1021/jm000007r
9819927 2417 None 39 Human Functional pKi = 7.9 7.9 2 14
Agonist potency against cloned Metabotropic glutamate receptor 3 (mGluR-3).Agonist potency against cloned Metabotropic glutamate receptor 3 (mGluR-3).
ChEMBL 353 5 3 4 2.8 OC(=O)[C@H]1C[C@@H]1[C@](C(=O)O)(CC1c2ccccc2Oc2c1cccc2)N 10.1021/jm000007r
CHEMBL432038 2417 None 39 Human Functional pKi = 7.9 7.9 2 14
Agonist potency against cloned Metabotropic glutamate receptor 3 (mGluR-3).Agonist potency against cloned Metabotropic glutamate receptor 3 (mGluR-3).
ChEMBL 353 5 3 4 2.8 OC(=O)[C@H]1C[C@@H]1[C@](C(=O)O)(CC1c2ccccc2Oc2c1cccc2)N 10.1021/jm000007r
44322529 209324 None 1 Human Functional pKi = 6.7 6.7 - 0
Agonist potency against cloned Metabotropic glutamate receptor 3 (mGluR-3).Agonist potency against cloned Metabotropic glutamate receptor 3 (mGluR-3).
ChEMBL 367 6 3 4 3.1 N[C@H](C(=O)O)[C@@H]1[C@@H](C(=O)O)[C@@H]1CCC1c2ccccc2Oc2ccccc21 10.1021/jm000007r
CHEMBL90675 209324 None 1 Human Functional pKi = 6.7 6.7 - 0
Agonist potency against cloned Metabotropic glutamate receptor 3 (mGluR-3).Agonist potency against cloned Metabotropic glutamate receptor 3 (mGluR-3).
ChEMBL 367 6 3 4 3.1 N[C@H](C(=O)O)[C@@H]1[C@@H](C(=O)O)[C@@H]1CCC1c2ccccc2Oc2ccccc21 10.1021/jm000007r
44322921 209295 None 1 Human Functional pKi = 5.7 5.7 - 0
Agonist potency against cloned Metabotropic glutamate receptor 3 (mGluR-3).Agonist potency against cloned Metabotropic glutamate receptor 3 (mGluR-3).
ChEMBL 185 2 3 3 -0.5 N[C@@]1(C(=O)O)CC2CC1[C@H]2C(=O)O 10.1021/jm000007r
CHEMBL90501 209295 None 1 Human Functional pKi = 5.7 5.7 - 0
Agonist potency against cloned Metabotropic glutamate receptor 3 (mGluR-3).Agonist potency against cloned Metabotropic glutamate receptor 3 (mGluR-3).
ChEMBL 185 2 3 3 -0.5 N[C@@]1(C(=O)O)CC2CC1[C@H]2C(=O)O 10.1021/jm000007r
6324634 148032 None 10 Human Functional pKi = 4.5 4.5 -6 2
Agonist potency against cloned Metabotropic glutamate receptor 3 (mGluR-3).Agonist potency against cloned Metabotropic glutamate receptor 3 (mGluR-3).
ChEMBL 355 10 3 3 3.5 N[C@@H](C[C@H](CCCC(c1ccccc1)c1ccccc1)C(=O)O)C(=O)O 10.1021/jm000007r
CHEMBL39338 148032 None 10 Human Functional pKi = 4.5 4.5 -6 2
Agonist potency against cloned Metabotropic glutamate receptor 3 (mGluR-3).Agonist potency against cloned Metabotropic glutamate receptor 3 (mGluR-3).
ChEMBL 355 10 3 3 3.5 N[C@@H](C[C@H](CCCC(c1ccccc1)c1ccccc1)C(=O)O)C(=O)O 10.1021/jm000007r
1393 1539 None 42 Human Functional pKi = 7.4 7.4 -4 6
Agonist potency against cloned Metabotropic glutamate receptor 3 (mGluR-3).Agonist potency against cloned Metabotropic glutamate receptor 3 (mGluR-3).
ChEMBL 185 2 3 3 -0.5 OC(=O)[C@H]1[C@H]2[C@@H]1[C@](CC2)(N)C(=O)O 10.1021/jm000007r
1396 1539 None 42 Human Functional pKi = 7.4 7.4 -4 6
Agonist potency against cloned Metabotropic glutamate receptor 3 (mGluR-3).Agonist potency against cloned Metabotropic glutamate receptor 3 (mGluR-3).
ChEMBL 185 2 3 3 -0.5 OC(=O)[C@H]1[C@H]2[C@@H]1[C@](CC2)(N)C(=O)O 10.1021/jm000007r
213056 1539 None 42 Human Functional pKi = 7.4 7.4 -4 6
Agonist potency against cloned Metabotropic glutamate receptor 3 (mGluR-3).Agonist potency against cloned Metabotropic glutamate receptor 3 (mGluR-3).
ChEMBL 185 2 3 3 -0.5 OC(=O)[C@H]1[C@H]2[C@@H]1[C@](CC2)(N)C(=O)O 10.1021/jm000007r
CHEMBL8759 1539 None 42 Human Functional pKi = 7.4 7.4 -4 6
Agonist potency against cloned Metabotropic glutamate receptor 3 (mGluR-3).Agonist potency against cloned Metabotropic glutamate receptor 3 (mGluR-3).
ChEMBL 185 2 3 3 -0.5 OC(=O)[C@H]1[C@H]2[C@@H]1[C@](CC2)(N)C(=O)O 10.1021/jm000007r
10197984 2421 None 36 Human Functional pKi = 8.3 8.3 -1 5
Agonist potency against cloned Metabotropic glutamate receptor 3 (mGluR-3).Agonist potency against cloned Metabotropic glutamate receptor 3 (mGluR-3).
ChEMBL 187 2 3 4 -1.5 OC(=O)[C@H]1[C@H]2[C@@H]1[C@](CO2)(N)C(=O)O 10.1021/jm000007r
1394 2421 None 36 Human Functional pKi = 8.3 8.3 -1 5
Agonist potency against cloned Metabotropic glutamate receptor 3 (mGluR-3).Agonist potency against cloned Metabotropic glutamate receptor 3 (mGluR-3).
ChEMBL 187 2 3 4 -1.5 OC(=O)[C@H]1[C@H]2[C@@H]1[C@](CO2)(N)C(=O)O 10.1021/jm000007r
CHEMBL275079 2421 None 36 Human Functional pKi = 8.3 8.3 -1 5
Agonist potency against cloned Metabotropic glutamate receptor 3 (mGluR-3).Agonist potency against cloned Metabotropic glutamate receptor 3 (mGluR-3).
ChEMBL 187 2 3 4 -1.5 OC(=O)[C@H]1[C@H]2[C@@H]1[C@](CO2)(N)C(=O)O 10.1021/jm000007r
1370 3263 None 42 Human Functional pKi = 4.4 4.4 - 6
Agonist potency against cloned Metabotropic glutamate receptor 3 (mGluR-3).Agonist potency against cloned Metabotropic glutamate receptor 3 (mGluR-3).
ChEMBL 189 3 3 6 -2.5 OC(=O)[C@H](Cn1oc(=O)[nH]c1=O)N 10.1021/jm000007r
1372 3263 None 42 Human Functional pKi = 4.4 4.4 - 6
Agonist potency against cloned Metabotropic glutamate receptor 3 (mGluR-3).Agonist potency against cloned Metabotropic glutamate receptor 3 (mGluR-3).
ChEMBL 189 3 3 6 -2.5 OC(=O)[C@H](Cn1oc(=O)[nH]c1=O)N 10.1021/jm000007r
40539 3263 None 42 Human Functional pKi = 4.4 4.4 - 6
Agonist potency against cloned Metabotropic glutamate receptor 3 (mGluR-3).Agonist potency against cloned Metabotropic glutamate receptor 3 (mGluR-3).
ChEMBL 189 3 3 6 -2.5 OC(=O)[C@H](Cn1oc(=O)[nH]c1=O)N 10.1021/jm000007r
6971145 3263 None 42 Human Functional pKi = 4.4 4.4 - 6
Agonist potency against cloned Metabotropic glutamate receptor 3 (mGluR-3).Agonist potency against cloned Metabotropic glutamate receptor 3 (mGluR-3).
ChEMBL 189 3 3 6 -2.5 OC(=O)[C@H](Cn1oc(=O)[nH]c1=O)N 10.1021/jm000007r
CHEMBL279956 3263 None 42 Human Functional pKi = 4.4 4.4 - 6
Agonist potency against cloned Metabotropic glutamate receptor 3 (mGluR-3).Agonist potency against cloned Metabotropic glutamate receptor 3 (mGluR-3).
ChEMBL 189 3 3 6 -2.5 OC(=O)[C@H](Cn1oc(=O)[nH]c1=O)N 10.1021/jm000007r
DB02999 3263 None 42 Human Functional pKi = 4.4 4.4 - 6
Agonist potency against cloned Metabotropic glutamate receptor 3 (mGluR-3).Agonist potency against cloned Metabotropic glutamate receptor 3 (mGluR-3).
ChEMBL 189 3 3 6 -2.5 OC(=O)[C@H](Cn1oc(=O)[nH]c1=O)N 10.1021/jm000007r
1392 73 None 32 Human Functional pKi = 6.4 6.4 -9 4
Agonist potency against cloned Metabotropic glutamate receptor 3 (mGluR-3).Agonist potency against cloned Metabotropic glutamate receptor 3 (mGluR-3).
ChEMBL 174 2 4 4 -1.8 OC(=O)[C@@H]1NC[C@@](C1)(N)C(=O)O 10.1021/jm000007r
5310984 73 None 32 Human Functional pKi = 6.4 6.4 -9 4
Agonist potency against cloned Metabotropic glutamate receptor 3 (mGluR-3).Agonist potency against cloned Metabotropic glutamate receptor 3 (mGluR-3).
ChEMBL 174 2 4 4 -1.8 OC(=O)[C@@H]1NC[C@@](C1)(N)C(=O)O 10.1021/jm000007r
CHEMBL40086 73 None 32 Human Functional pKi = 6.4 6.4 -9 4
Agonist potency against cloned Metabotropic glutamate receptor 3 (mGluR-3).Agonist potency against cloned Metabotropic glutamate receptor 3 (mGluR-3).
ChEMBL 174 2 4 4 -1.8 OC(=O)[C@@H]1NC[C@@](C1)(N)C(=O)O 10.1021/jm000007r
1368 2290 None 30 Human Functional pKi = 6.4 6.4 - 11
Agonist potency against cloned Metabotropic glutamate receptor 3 (mGluR-3).Agonist potency against cloned Metabotropic glutamate receptor 3 (mGluR-3).
ChEMBL 159 3 3 3 -0.9 N[C@@H]([C@H]1C[C@@H]1C(=O)O)C(=O)O 10.1021/jm000007r
5310956 2290 None 30 Human Functional pKi = 6.4 6.4 - 11
Agonist potency against cloned Metabotropic glutamate receptor 3 (mGluR-3).Agonist potency against cloned Metabotropic glutamate receptor 3 (mGluR-3).
ChEMBL 159 3 3 3 -0.9 N[C@@H]([C@H]1C[C@@H]1C(=O)O)C(=O)O 10.1021/jm000007r
CHEMBL280563 2290 None 30 Human Functional pKi = 6.4 6.4 - 11
Agonist potency against cloned Metabotropic glutamate receptor 3 (mGluR-3).Agonist potency against cloned Metabotropic glutamate receptor 3 (mGluR-3).
ChEMBL 159 3 3 3 -0.9 N[C@@H]([C@H]1C[C@@H]1C(=O)O)C(=O)O 10.1021/jm000007r
10330132 101437 None 1 Human Functional pKi = 4.3 4.3 -10 2
Agonist potency against cloned Metabotropic glutamate receptor 3 (mGluR-3).Agonist potency against cloned Metabotropic glutamate receptor 3 (mGluR-3).
ChEMBL 189 2 4 5 -2.2 NN1C[C@@](N)(C(=O)O)C[C@@H]1C(=O)O 10.1021/jm000007r
CHEMBL297150 101437 None 1 Human Functional pKi = 4.3 4.3 -10 2
Agonist potency against cloned Metabotropic glutamate receptor 3 (mGluR-3).Agonist potency against cloned Metabotropic glutamate receptor 3 (mGluR-3).
ChEMBL 189 2 4 5 -2.2 NN1C[C@@](N)(C(=O)O)C[C@@H]1C(=O)O 10.1021/jm000007r
10359073 155064 None 0 Human Functional pKi = 5.2 5.2 1 2
Agonist potency against cloned Metabotropic glutamate receptor 3 (mGluR-3).Agonist potency against cloned Metabotropic glutamate receptor 3 (mGluR-3).
ChEMBL 327 8 3 3 2.7 N[C@@H](C[C@H](CC(c1ccccc1)c1ccccc1)C(=O)O)C(=O)O 10.1021/jm000007r
CHEMBL40123 155064 None 0 Human Functional pKi = 5.2 5.2 1 2
Agonist potency against cloned Metabotropic glutamate receptor 3 (mGluR-3).Agonist potency against cloned Metabotropic glutamate receptor 3 (mGluR-3).
ChEMBL 327 8 3 3 2.7 N[C@@H](C[C@H](CC(c1ccccc1)c1ccccc1)C(=O)O)C(=O)O 10.1021/jm000007r
10058694 209061 None 1 Human Functional pKi = 8.1 8.1 - 0
Agonist potency against cloned Metabotropic glutamate receptor 3 (mGluR-3).Agonist potency against cloned Metabotropic glutamate receptor 3 (mGluR-3).
ChEMBL 203 2 3 4 -0.8 N[C@@]1(C(=O)O)CSC2C1[C@H]2C(=O)O 10.1021/jm000007r
CHEMBL88999 209061 None 1 Human Functional pKi = 8.1 8.1 - 0
Agonist potency against cloned Metabotropic glutamate receptor 3 (mGluR-3).Agonist potency against cloned Metabotropic glutamate receptor 3 (mGluR-3).
ChEMBL 203 2 3 4 -0.8 N[C@@]1(C(=O)O)CSC2C1[C@H]2C(=O)O 10.1021/jm000007r
1310 2315 None 61 Human Functional pKi = 5.1 5.1 -251 17
Agonist potency against cloned Metabotropic glutamate receptor 3 (mGluR-3).Agonist potency against cloned Metabotropic glutamate receptor 3 (mGluR-3).
ChEMBL 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N 10.1021/jm000007r
1369 2315 None 61 Human Functional pKi = 5.1 5.1 -251 17
Agonist potency against cloned Metabotropic glutamate receptor 3 (mGluR-3).Agonist potency against cloned Metabotropic glutamate receptor 3 (mGluR-3).
ChEMBL 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N 10.1021/jm000007r
33032 2315 None 61 Human Functional pKi = 5.1 5.1 -251 17
Agonist potency against cloned Metabotropic glutamate receptor 3 (mGluR-3).Agonist potency against cloned Metabotropic glutamate receptor 3 (mGluR-3).
ChEMBL 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N 10.1021/jm000007r
44272391 2315 None 61 Human Functional pKi = 5.1 5.1 -251 17
Agonist potency against cloned Metabotropic glutamate receptor 3 (mGluR-3).Agonist potency against cloned Metabotropic glutamate receptor 3 (mGluR-3).
ChEMBL 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N 10.1021/jm000007r
88747398 2315 None 61 Human Functional pKi = 5.1 5.1 -251 17
Agonist potency against cloned Metabotropic glutamate receptor 3 (mGluR-3).Agonist potency against cloned Metabotropic glutamate receptor 3 (mGluR-3).
ChEMBL 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N 10.1021/jm000007r
CHEMBL575060 2315 None 61 Human Functional pKi = 5.1 5.1 -251 17
Agonist potency against cloned Metabotropic glutamate receptor 3 (mGluR-3).Agonist potency against cloned Metabotropic glutamate receptor 3 (mGluR-3).
ChEMBL 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N 10.1021/jm000007r
DB00142 2315 None 61 Human Functional pKi = 5.1 5.1 -251 17
Agonist potency against cloned Metabotropic glutamate receptor 3 (mGluR-3).Agonist potency against cloned Metabotropic glutamate receptor 3 (mGluR-3).
ChEMBL 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N 10.1021/jm000007r
1310 2315 None 61 Rat Functional pEC50 = 8.3 8.3 -29 17
NoneNone
Drug Central 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N None
1369 2315 None 61 Rat Functional pEC50 = 8.3 8.3 -29 17
NoneNone
Drug Central 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N None
33032 2315 None 61 Rat Functional pEC50 = 8.3 8.3 -29 17
NoneNone
Drug Central 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N None
44272391 2315 None 61 Rat Functional pEC50 = 8.3 8.3 -29 17
NoneNone
Drug Central 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N None
88747398 2315 None 61 Rat Functional pEC50 = 8.3 8.3 -29 17
NoneNone
Drug Central 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N None
CHEMBL575060 2315 None 61 Rat Functional pEC50 = 8.3 8.3 -29 17
NoneNone
Drug Central 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N None
DB00142 2315 None 61 Rat Functional pEC50 = 8.3 8.3 -29 17
NoneNone
Drug Central 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N None
49836087 1061 None 0 Human Functional pEC50 = 4.9 4.9 -16 2
UnclassifiedUnclassified
Guide to Pharmacology 328 2 2 4 3.3 O/N=C\1/c2ccccc2OC2(C1C2)C(=O)Nc1ccc(cc1)Cl 21105727
6222 1061 None 0 Human Functional pEC50 = 4.9 4.9 -16 2
UnclassifiedUnclassified
Guide to Pharmacology 328 2 2 4 3.3 O/N=C\1/c2ccccc2OC2(C1C2)C(=O)Nc1ccc(cc1)Cl 21105727
CHEMBL1630805 1061 None 0 Human Functional pEC50 = 4.9 4.9 -16 2
UnclassifiedUnclassified
Guide to Pharmacology 328 2 2 4 3.3 O/N=C\1/c2ccccc2OC2(C1C2)C(=O)Nc1ccc(cc1)Cl 21105727
49858118 1110 None 0 Human Functional pEC50 = 5.0 5.0 -10 2
UnclassifiedUnclassified
Guide to Pharmacology 324 3 2 5 2.7 O/N=C\1/c2ccccc2OC2(C1C2)C(=O)Nc1ccc(cc1)OC 21105727
6224 1110 None 0 Human Functional pEC50 = 5.0 5.0 -10 2
UnclassifiedUnclassified
Guide to Pharmacology 324 3 2 5 2.7 O/N=C\1/c2ccccc2OC2(C1C2)C(=O)Nc1ccc(cc1)OC 21105727
CHEMBL1630807 1110 None 0 Human Functional pEC50 = 5.0 5.0 -10 2
UnclassifiedUnclassified
Guide to Pharmacology 324 3 2 5 2.7 O/N=C\1/c2ccccc2OC2(C1C2)C(=O)Nc1ccc(cc1)OC 21105727
49858117 1089 None 4 Human Functional pEC50 = 5.1 5.1 -5 2
UnclassifiedUnclassified
Guide to Pharmacology 308 2 2 4 3.0 O/N=C\1/c2ccccc2OC2(C1C2)C(=O)Nc1ccc(cc1)C 21105727
6223 1089 None 4 Human Functional pEC50 = 5.1 5.1 -5 2
UnclassifiedUnclassified
Guide to Pharmacology 308 2 2 4 3.0 O/N=C\1/c2ccccc2OC2(C1C2)C(=O)Nc1ccc(cc1)C 21105727
CHEMBL1630806 1089 None 4 Human Functional pEC50 = 5.1 5.1 -5 2
UnclassifiedUnclassified
Guide to Pharmacology 308 2 2 4 3.0 O/N=C\1/c2ccccc2OC2(C1C2)C(=O)Nc1ccc(cc1)C 21105727
1310 2315 None 61 Human Functional pEC50 = 5.4 5.4 -251 17
UnclassifiedUnclassified
Guide to Pharmacology 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N 10443583
1369 2315 None 61 Human Functional pEC50 = 5.4 5.4 -251 17
UnclassifiedUnclassified
Guide to Pharmacology 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N 10443583
33032 2315 None 61 Human Functional pEC50 = 5.4 5.4 -251 17
UnclassifiedUnclassified
Guide to Pharmacology 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N 10443583
44272391 2315 None 61 Human Functional pEC50 = 5.4 5.4 -251 17
UnclassifiedUnclassified
Guide to Pharmacology 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N 10443583
88747398 2315 None 61 Human Functional pEC50 = 5.4 5.4 -251 17
UnclassifiedUnclassified
Guide to Pharmacology 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N 10443583
CHEMBL575060 2315 None 61 Human Functional pEC50 = 5.4 5.4 -251 17
UnclassifiedUnclassified
Guide to Pharmacology 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N 10443583
DB00142 2315 None 61 Human Functional pEC50 = 5.4 5.4 -251 17
UnclassifiedUnclassified
Guide to Pharmacology 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N 10443583
6219 2585 None 0 Rat Functional pEC50 = 7.5 7.5 -1 3
UnclassifiedUnclassified
Guide to Pharmacology 401 1 1 3 4.0 N#Cc1cccc(c1)C1=Nc2ccc(cc2NC(=O)CC1)I 17416742
73755191 2585 None 0 Rat Functional pEC50 = 7.5 7.5 -1 3
UnclassifiedUnclassified
Guide to Pharmacology 401 1 1 3 4.0 N#Cc1cccc(c1)C1=Nc2ccc(cc2NC(=O)CC1)I 17416742
11158623 3351 None 11 Rat Functional pIC50 < 8 8.0 -1 4
UnclassifiedUnclassified
Guide to Pharmacology 423 2 1 3 6.2 O=C1CC(=Nc2c(N1)cc(c(c2)C)C(F)(F)F)c1cccc(c1)c1cc(C)nc(c1)C 20971004
6226 3351 None 11 Rat Functional pIC50 < 8 8.0 -1 4
UnclassifiedUnclassified
Guide to Pharmacology 423 2 1 3 6.2 O=C1CC(=Nc2c(N1)cc(c(c2)C)C(F)(F)F)c1cccc(c1)c1cc(C)nc(c1)C 20971004
CHEMBL1629855 3351 None 11 Rat Functional pIC50 < 8 8.0 -1 4
UnclassifiedUnclassified
Guide to Pharmacology 423 2 1 3 6.2 O=C1CC(=Nc2c(N1)cc(c(c2)C)C(F)(F)F)c1cccc(c1)c1cc(C)nc(c1)C 20971004
11503055 2400 None 2 Human Functional pIC50 = 6.7 6.7 31 2
Assessed in AV-12 cells expressing the human mGlu3, activated by glutamate as agonist.Assessed in AV-12 cells expressing the human mGlu3, activated by glutamate as agonist.
Guide to Pharmacology 400 4 1 4 3.9 Clc1ccc(c(c1)Cl)CN[C@H]1CCN(C1)c1ncc(cn1)Br 22607673
9694 2400 None 2 Human Functional pIC50 = 6.7 6.7 31 2
Assessed in AV-12 cells expressing the human mGlu3, activated by glutamate as agonist.Assessed in AV-12 cells expressing the human mGlu3, activated by glutamate as agonist.
Guide to Pharmacology 400 4 1 4 3.9 Clc1ccc(c(c1)Cl)CN[C@H]1CCN(C1)c1ncc(cn1)Br 22607673
CHEMBL2204436 2400 None 2 Human Functional pIC50 = 6.7 6.7 31 2
Assessed in AV-12 cells expressing the human mGlu3, activated by glutamate as agonist.Assessed in AV-12 cells expressing the human mGlu3, activated by glutamate as agonist.
Guide to Pharmacology 400 4 1 4 3.9 Clc1ccc(c(c1)Cl)CN[C@H]1CCN(C1)c1ncc(cn1)Br 22607673
56587994 4045 None 29 Rat Functional pIC50 = 6 6.0 1 2
UnclassifiedUnclassified
Guide to Pharmacology 349 3 1 3 2.9 OC[C@@H]1CCCN(C1)C(=O)c1ccc(cc1)C#Cc1ccc(cc1)OC 22607673
6225 4045 None 29 Rat Functional pIC50 = 6 6.0 1 2
UnclassifiedUnclassified
Guide to Pharmacology 349 3 1 3 2.9 OC[C@@H]1CCCN(C1)C(=O)c1ccc(cc1)C#Cc1ccc(cc1)OC 22607673
CHEMBL2204445 4045 None 29 Rat Functional pIC50 = 6 6.0 1 2
UnclassifiedUnclassified
Guide to Pharmacology 349 3 1 3 2.9 OC[C@@H]1CCCN(C1)C(=O)c1ccc(cc1)C#Cc1ccc(cc1)OC 22607673
60204017 2573 None 26 Rat Functional pIC50 = 6.2 6.2 - 1
UnclassifiedUnclassified
Guide to Pharmacology 353 2 1 3 2.8 COc1ccc(cc1)C#Cc1ccc(c(c1)F)C(=O)N1CCC[C@H](C1)O 23718281
8765 2573 None 26 Rat Functional pIC50 = 6.2 6.2 - 1
UnclassifiedUnclassified
Guide to Pharmacology 353 2 1 3 2.8 COc1ccc(cc1)C#Cc1ccc(c(c1)F)C(=O)N1CCC[C@H](C1)O 23718281
CHEMBL2385886 2573 None 26 Rat Functional pIC50 = 6.2 6.2 - 1
UnclassifiedUnclassified
Guide to Pharmacology 353 2 1 3 2.8 COc1ccc(cc1)C#Cc1ccc(c(c1)F)C(=O)N1CCC[C@H](C1)O 23718281
10237 4051 None 22 Human Functional pIC50 = 6.4 6.4 -1 2
UnclassifiedUnclassified
Guide to Pharmacology 387 4 0 6 3.3 Clc1ccc(nc1)OCc1nn2c(c1)C(=O)N(C[C@H]2C)c1cccnc1F 26335039
122190433 4051 None 22 Human Functional pIC50 = 6.4 6.4 -1 2
UnclassifiedUnclassified
Guide to Pharmacology 387 4 0 6 3.3 Clc1ccc(nc1)OCc1nn2c(c1)C(=O)N(C[C@H]2C)c1cccnc1F 26335039
CHEMBL3617655 4051 None 22 Human Functional pIC50 = 6.4 6.4 -1 2
UnclassifiedUnclassified
Guide to Pharmacology 387 4 0 6 3.3 Clc1ccc(nc1)OCc1nn2c(c1)C(=O)N(C[C@H]2C)c1cccnc1F 26335039
11158623 3351 None 11 Human Functional pIC50 = 6.6 6.6 -50 4
UnclassifiedUnclassified
Guide to Pharmacology 423 2 1 3 6.2 O=C1CC(=Nc2c(N1)cc(c(c2)C)C(F)(F)F)c1cccc(c1)c1cc(C)nc(c1)C 22091727
6226 3351 None 11 Human Functional pIC50 = 6.6 6.6 -50 4
UnclassifiedUnclassified
Guide to Pharmacology 423 2 1 3 6.2 O=C1CC(=Nc2c(N1)cc(c(c2)C)C(F)(F)F)c1cccc(c1)c1cc(C)nc(c1)C 22091727
CHEMBL1629855 3351 None 11 Human Functional pIC50 = 6.6 6.6 -50 4
UnclassifiedUnclassified
Guide to Pharmacology 423 2 1 3 6.2 O=C1CC(=Nc2c(N1)cc(c(c2)C)C(F)(F)F)c1cccc(c1)c1cc(C)nc(c1)C 22091727
6220 2586 None 0 Rat Functional pIC50 = 7.7 7.7 -1 3
UnclassifiedUnclassified
Guide to Pharmacology 405 2 1 3 5.4 O=C1CCC(=Nc2c(N1)ccc(c2)Br)c1cccc(c1)c1ccncc1 17416742
73755192 2586 None 0 Rat Functional pIC50 = 7.7 7.7 -1 3
UnclassifiedUnclassified
Guide to Pharmacology 405 2 1 3 5.4 O=C1CCC(=Nc2c(N1)ccc(c2)Br)c1cccc(c1)c1ccncc1 17416742
6221 2587 None 0 Rat Functional pIC50 = 7.7 7.7 -1 3
UnclassifiedUnclassified
Guide to Pharmacology 354 1 1 4 3.6 N#Cc1nccc(c1)C1=Nc2ccc(cc2NC(=O)CC1)Br 17416742
73755193 2587 None 0 Rat Functional pIC50 = 7.7 7.7 -1 3
UnclassifiedUnclassified
Guide to Pharmacology 354 1 1 4 3.6 N#Cc1nccc(c1)C1=Nc2ccc(cc2NC(=O)CC1)Br 17416742




Ligands (move mouse cursor over ligand name to see structure) Receptor Activity Chemical information
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DOI

9794208 90084 None 2 Human Binding pEC50 = 10.0 10.0 - 0
Agonist activity at human mGlu3 receptor expressed in golden Syrian hamster AV12 cells coexpressing EAAT1 after 20 mins by HTRF assayAgonist activity at human mGlu3 receptor expressed in golden Syrian hamster AV12 cells coexpressing EAAT1 after 20 mins by HTRF assay
ChEMBL 199 2 3 4 -1.3 N[C@@]1(C(=O)O)CC(=O)[C@@H]2[C@H]1[C@H]2C(=O)O 10.1021/jm4000165
CHEMBL2381640 90084 None 2 Human Binding pEC50 = 10.0 10.0 - 0
Agonist activity at human mGlu3 receptor expressed in golden Syrian hamster AV12 cells coexpressing EAAT1 after 20 mins by HTRF assayAgonist activity at human mGlu3 receptor expressed in golden Syrian hamster AV12 cells coexpressing EAAT1 after 20 mins by HTRF assay
ChEMBL 199 2 3 4 -1.3 N[C@@]1(C(=O)O)CC(=O)[C@@H]2[C@H]1[C@H]2C(=O)O 10.1021/jm4000165
139119037 90096 None 0 Human Binding pEC50 = 9.6 9.6 - 0
Agonist activity at human mGlu3 receptor expressed in golden Syrian hamster AV12 cells coexpressing EAAT1 after 20 mins by HTRF assayAgonist activity at human mGlu3 receptor expressed in golden Syrian hamster AV12 cells coexpressing EAAT1 after 20 mins by HTRF assay
ChEMBL 203 2 3 3 -0.5 N[C@@]1(C(=O)O)C[C@@H](F)[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/jm4000165
15479143 90096 None 0 Human Binding pEC50 = 9.6 9.6 - 0
Agonist activity at human mGlu3 receptor expressed in golden Syrian hamster AV12 cells coexpressing EAAT1 after 20 mins by HTRF assayAgonist activity at human mGlu3 receptor expressed in golden Syrian hamster AV12 cells coexpressing EAAT1 after 20 mins by HTRF assay
ChEMBL 203 2 3 3 -0.5 N[C@@]1(C(=O)O)C[C@@H](F)[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/jm4000165
CHEMBL2381652 90096 None 0 Human Binding pEC50 = 9.6 9.6 - 0
Agonist activity at human mGlu3 receptor expressed in golden Syrian hamster AV12 cells coexpressing EAAT1 after 20 mins by HTRF assayAgonist activity at human mGlu3 receptor expressed in golden Syrian hamster AV12 cells coexpressing EAAT1 after 20 mins by HTRF assay
ChEMBL 203 2 3 3 -0.5 N[C@@]1(C(=O)O)C[C@@H](F)[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/jm4000165
6603885 102256 None 18 Rat Binding pEC50 = 5 5.0 - 0
Concentration for half maximal activation of metabotropic glutamate mGluR3 in ratConcentration for half maximal activation of metabotropic glutamate mGluR3 in rat
ChEMBL 158 2 3 5 -0.5 N[C@H](C(=O)O)c1cc(O)no1 10.1021/jm00009a001
6971208 102256 None 18 Rat Binding pEC50 = 5 5.0 - 0
Concentration for half maximal activation of metabotropic glutamate mGluR3 in ratConcentration for half maximal activation of metabotropic glutamate mGluR3 in rat
ChEMBL 158 2 3 5 -0.5 N[C@H](C(=O)O)c1cc(O)no1 10.1021/jm00009a001
CHEMBL30285 102256 None 18 Rat Binding pEC50 = 5 5.0 - 0
Concentration for half maximal activation of metabotropic glutamate mGluR3 in ratConcentration for half maximal activation of metabotropic glutamate mGluR3 in rat
ChEMBL 158 2 3 5 -0.5 N[C@H](C(=O)O)c1cc(O)no1 10.1021/jm00009a001
90643879 111936 None 0 Rat Binding pEC50 = 6.0 6.0 - 0
Positive allosteric modulation of rat mGluR3 receptor expressed in HEK293 cells assessed as potentiation of glutamate-induced thallium flux incubated for 2.5 mins prior to glutamate addition measured after 2.5 mins by GIRK assayPositive allosteric modulation of rat mGluR3 receptor expressed in HEK293 cells assessed as potentiation of glutamate-induced thallium flux incubated for 2.5 mins prior to glutamate addition measured after 2.5 mins by GIRK assay
ChEMBL 456 12 2 6 5.4 COc1ccc(C(=O)O)cc1OCCCCOc1ccc(C(=O)CC2CCCC2)c(O)c1C 10.1021/jm5000563
CHEMBL3287702 111936 None 0 Rat Binding pEC50 = 6.0 6.0 - 0
Positive allosteric modulation of rat mGluR3 receptor expressed in HEK293 cells assessed as potentiation of glutamate-induced thallium flux incubated for 2.5 mins prior to glutamate addition measured after 2.5 mins by GIRK assayPositive allosteric modulation of rat mGluR3 receptor expressed in HEK293 cells assessed as potentiation of glutamate-induced thallium flux incubated for 2.5 mins prior to glutamate addition measured after 2.5 mins by GIRK assay
ChEMBL 456 12 2 6 5.4 COc1ccc(C(=O)O)cc1OCCCCOc1ccc(C(=O)CC2CCCC2)c(O)c1C 10.1021/jm5000563
164609979 184681 None 0 Rat Binding pEC50 = 6.0 6.0 - 0
Positive allosteric modulator activity at rat mGlu3 receptor transfected in GIRK channel overexpressing cells assessed as potentiation of glutamate-induced response by thallium mobilization assayPositive allosteric modulator activity at rat mGlu3 receptor transfected in GIRK channel overexpressing cells assessed as potentiation of glutamate-induced response by thallium mobilization assay
ChEMBL 444 10 2 6 5.1 COc1ccc(C(=O)O)cc1OC[C@@H](C)COc1ccc(C(=O)CC(C)(C)C)c(O)c1C 10.1016/j.bmcl.2021.128342
CHEMBL4848547 184681 None 0 Rat Binding pEC50 = 6.0 6.0 - 0
Positive allosteric modulator activity at rat mGlu3 receptor transfected in GIRK channel overexpressing cells assessed as potentiation of glutamate-induced response by thallium mobilization assayPositive allosteric modulator activity at rat mGlu3 receptor transfected in GIRK channel overexpressing cells assessed as potentiation of glutamate-induced response by thallium mobilization assay
ChEMBL 444 10 2 6 5.1 COc1ccc(C(=O)O)cc1OC[C@@H](C)COc1ccc(C(=O)CC(C)(C)C)c(O)c1C 10.1016/j.bmcl.2021.128342
164619502 186306 None 0 Rat Binding pEC50 = 6.0 6.0 - 0
Positive allosteric modulator activity at rat mGlu3 receptor transfected in GIRK channel overexpressing cells assessed as potentiation of glutamate-induced response by thallium mobilization assayPositive allosteric modulator activity at rat mGlu3 receptor transfected in GIRK channel overexpressing cells assessed as potentiation of glutamate-induced response by thallium mobilization assay
ChEMBL 432 9 2 5 5.3 Cc1c(OC[C@@H](C)COc2ccc(C(=O)O)c(F)c2)ccc(C(=O)CC(C)(C)C)c1O 10.1016/j.bmcl.2021.128342
CHEMBL4872955 186306 None 0 Rat Binding pEC50 = 6.0 6.0 - 0
Positive allosteric modulator activity at rat mGlu3 receptor transfected in GIRK channel overexpressing cells assessed as potentiation of glutamate-induced response by thallium mobilization assayPositive allosteric modulator activity at rat mGlu3 receptor transfected in GIRK channel overexpressing cells assessed as potentiation of glutamate-induced response by thallium mobilization assay
ChEMBL 432 9 2 5 5.3 Cc1c(OC[C@@H](C)COc2ccc(C(=O)O)c(F)c2)ccc(C(=O)CC(C)(C)C)c1O 10.1016/j.bmcl.2021.128342
164621278 185638 None 0 Rat Binding pEC50 = 6.0 6.0 - 0
Positive allosteric modulator activity at rat mGlu3 receptor transfected in GIRK channel overexpressing cells assessed as potentiation of glutamate-induced response by thallium mobilization assayPositive allosteric modulator activity at rat mGlu3 receptor transfected in GIRK channel overexpressing cells assessed as potentiation of glutamate-induced response by thallium mobilization assay
ChEMBL 418 8 2 5 5.0 Cc1c(OC[C@H](C)Oc2ccc(F)c(C(=O)O)c2)ccc(C(=O)CC(C)(C)C)c1O 10.1016/j.bmcl.2021.128342
CHEMBL4862801 185638 None 0 Rat Binding pEC50 = 6.0 6.0 - 0
Positive allosteric modulator activity at rat mGlu3 receptor transfected in GIRK channel overexpressing cells assessed as potentiation of glutamate-induced response by thallium mobilization assayPositive allosteric modulator activity at rat mGlu3 receptor transfected in GIRK channel overexpressing cells assessed as potentiation of glutamate-induced response by thallium mobilization assay
ChEMBL 418 8 2 5 5.0 Cc1c(OC[C@H](C)Oc2ccc(F)c(C(=O)O)c2)ccc(C(=O)CC(C)(C)C)c1O 10.1016/j.bmcl.2021.128342
164620998 185979 None 0 Rat Binding pEC50 = 6.0 6.0 - 0
Positive allosteric modulator activity at rat mGlu3 receptor transfected in GIRK channel overexpressing cells assessed as potentiation of glutamate-induced response by thallium mobilization assayPositive allosteric modulator activity at rat mGlu3 receptor transfected in GIRK channel overexpressing cells assessed as potentiation of glutamate-induced response by thallium mobilization assay
ChEMBL 432 10 2 5 5.4 Cc1c(OCCCCOc2ccc(C(=O)O)c(F)c2)ccc(C(=O)CC(C)(C)C)c1O 10.1016/j.bmcl.2021.128342
CHEMBL4868114 185979 None 0 Rat Binding pEC50 = 6.0 6.0 - 0
Positive allosteric modulator activity at rat mGlu3 receptor transfected in GIRK channel overexpressing cells assessed as potentiation of glutamate-induced response by thallium mobilization assayPositive allosteric modulator activity at rat mGlu3 receptor transfected in GIRK channel overexpressing cells assessed as potentiation of glutamate-induced response by thallium mobilization assay
ChEMBL 432 10 2 5 5.4 Cc1c(OCCCCOc2ccc(C(=O)O)c(F)c2)ccc(C(=O)CC(C)(C)C)c1O 10.1016/j.bmcl.2021.128342
164619969 185635 None 0 Rat Binding pEC50 = 6.0 6.0 - 0
Positive allosteric modulator activity at rat mGlu3 receptor transfected in GIRK channel overexpressing cells assessed as potentiation of glutamate-induced response by thallium mobilization assayPositive allosteric modulator activity at rat mGlu3 receptor transfected in GIRK channel overexpressing cells assessed as potentiation of glutamate-induced response by thallium mobilization assay
ChEMBL 418 8 2 5 5.0 Cc1c(O[C@@H](C)COc2ccc(F)c(C(=O)O)c2)ccc(C(=O)CC(C)(C)C)c1O 10.1016/j.bmcl.2021.128342
CHEMBL4862778 185635 None 0 Rat Binding pEC50 = 6.0 6.0 - 0
Positive allosteric modulator activity at rat mGlu3 receptor transfected in GIRK channel overexpressing cells assessed as potentiation of glutamate-induced response by thallium mobilization assayPositive allosteric modulator activity at rat mGlu3 receptor transfected in GIRK channel overexpressing cells assessed as potentiation of glutamate-induced response by thallium mobilization assay
ChEMBL 418 8 2 5 5.0 Cc1c(O[C@@H](C)COc2ccc(F)c(C(=O)O)c2)ccc(C(=O)CC(C)(C)C)c1O 10.1016/j.bmcl.2021.128342
90643874 111931 None 0 Rat Binding pEC50 = 5.9 5.9 - 0
Positive allosteric modulation of rat mGluR3 receptor expressed in HEK293 cells assessed as potentiation of glutamate-induced thallium flux incubated for 2.5 mins prior to glutamate addition measured after 2.5 mins by GIRK assayPositive allosteric modulation of rat mGluR3 receptor expressed in HEK293 cells assessed as potentiation of glutamate-induced thallium flux incubated for 2.5 mins prior to glutamate addition measured after 2.5 mins by GIRK assay
ChEMBL 434 11 2 5 5.5 Cc1c(OCCCCOc2ccc(C(=O)O)cc2Cl)ccc(C(=O)CC(C)C)c1O 10.1021/jm5000563
CHEMBL3287697 111931 None 0 Rat Binding pEC50 = 5.9 5.9 - 0
Positive allosteric modulation of rat mGluR3 receptor expressed in HEK293 cells assessed as potentiation of glutamate-induced thallium flux incubated for 2.5 mins prior to glutamate addition measured after 2.5 mins by GIRK assayPositive allosteric modulation of rat mGluR3 receptor expressed in HEK293 cells assessed as potentiation of glutamate-induced thallium flux incubated for 2.5 mins prior to glutamate addition measured after 2.5 mins by GIRK assay
ChEMBL 434 11 2 5 5.5 Cc1c(OCCCCOc2ccc(C(=O)O)cc2Cl)ccc(C(=O)CC(C)C)c1O 10.1021/jm5000563
164610619 184860 None 0 Rat Binding pEC50 = 5.9 5.9 - 0
Positive allosteric modulator activity at rat mGlu3 receptor transfected in GIRK channel overexpressing cells assessed as potentiation of glutamate-induced response by thallium mobilization assayPositive allosteric modulator activity at rat mGlu3 receptor transfected in GIRK channel overexpressing cells assessed as potentiation of glutamate-induced response by thallium mobilization assay
ChEMBL 432 9 2 5 5.3 Cc1c(OC[C@@H](C)COc2ccc(F)c(C(=O)O)c2)ccc(C(=O)CC(C)(C)C)c1O 10.1016/j.bmcl.2021.128342
CHEMBL4850952 184860 None 0 Rat Binding pEC50 = 5.9 5.9 - 0
Positive allosteric modulator activity at rat mGlu3 receptor transfected in GIRK channel overexpressing cells assessed as potentiation of glutamate-induced response by thallium mobilization assayPositive allosteric modulator activity at rat mGlu3 receptor transfected in GIRK channel overexpressing cells assessed as potentiation of glutamate-induced response by thallium mobilization assay
ChEMBL 432 9 2 5 5.3 Cc1c(OC[C@@H](C)COc2ccc(F)c(C(=O)O)c2)ccc(C(=O)CC(C)(C)C)c1O 10.1016/j.bmcl.2021.128342
71681823 90088 None 0 Human Binding pEC50 = 7.9 7.9 - 0
Agonist activity at human mGlu3 receptor expressed in golden Syrian hamster AV12 cells coexpressing EAAT1 after 20 mins by HTRF assayAgonist activity at human mGlu3 receptor expressed in golden Syrian hamster AV12 cells coexpressing EAAT1 after 20 mins by HTRF assay
ChEMBL 226 3 3 4 -0.2 [N-]=[N+]=N[C@@H]1C[C@@](N)(C(=O)O)[C@@H]2[C@@H](C(=O)O)[C@@H]21 10.1021/jm4000165
CHEMBL2381644 90088 None 0 Human Binding pEC50 = 7.9 7.9 - 0
Agonist activity at human mGlu3 receptor expressed in golden Syrian hamster AV12 cells coexpressing EAAT1 after 20 mins by HTRF assayAgonist activity at human mGlu3 receptor expressed in golden Syrian hamster AV12 cells coexpressing EAAT1 after 20 mins by HTRF assay
ChEMBL 226 3 3 4 -0.2 [N-]=[N+]=N[C@@H]1C[C@@](N)(C(=O)O)[C@@H]2[C@@H](C(=O)O)[C@@H]21 10.1021/jm4000165
164627219 186487 None 0 Rat Binding pEC50 = 5.9 5.9 - 0
Positive allosteric modulator activity at rat mGlu3 receptor transfected in GIRK channel overexpressing cells assessed as potentiation of glutamate-induced response by thallium mobilization assayPositive allosteric modulator activity at rat mGlu3 receptor transfected in GIRK channel overexpressing cells assessed as potentiation of glutamate-induced response by thallium mobilization assay
ChEMBL 418 8 2 5 5.0 Cc1c(OC[C@@H](C)Oc2ccc(F)c(C(=O)O)c2)ccc(C(=O)CC(C)(C)C)c1O 10.1016/j.bmcl.2021.128342
CHEMBL4875653 186487 None 0 Rat Binding pEC50 = 5.9 5.9 - 0
Positive allosteric modulator activity at rat mGlu3 receptor transfected in GIRK channel overexpressing cells assessed as potentiation of glutamate-induced response by thallium mobilization assayPositive allosteric modulator activity at rat mGlu3 receptor transfected in GIRK channel overexpressing cells assessed as potentiation of glutamate-induced response by thallium mobilization assay
ChEMBL 418 8 2 5 5.0 Cc1c(OC[C@@H](C)Oc2ccc(F)c(C(=O)O)c2)ccc(C(=O)CC(C)(C)C)c1O 10.1016/j.bmcl.2021.128342
164614107 185236 None 0 Rat Binding pEC50 = 5.9 5.9 - 0
Positive allosteric modulator activity at rat mGlu3 receptor transfected in GIRK channel overexpressing cells assessed as potentiation of glutamate-induced response by thallium mobilization assayPositive allosteric modulator activity at rat mGlu3 receptor transfected in GIRK channel overexpressing cells assessed as potentiation of glutamate-induced response by thallium mobilization assay
ChEMBL 432 10 2 5 5.4 Cc1c(OCCCCOc2ccc(C(=O)O)cc2F)ccc(C(=O)CC(C)(C)C)c1O 10.1016/j.bmcl.2021.128342
CHEMBL4856556 185236 None 0 Rat Binding pEC50 = 5.9 5.9 - 0
Positive allosteric modulator activity at rat mGlu3 receptor transfected in GIRK channel overexpressing cells assessed as potentiation of glutamate-induced response by thallium mobilization assayPositive allosteric modulator activity at rat mGlu3 receptor transfected in GIRK channel overexpressing cells assessed as potentiation of glutamate-induced response by thallium mobilization assay
ChEMBL 432 10 2 5 5.4 Cc1c(OCCCCOc2ccc(C(=O)O)cc2F)ccc(C(=O)CC(C)(C)C)c1O 10.1016/j.bmcl.2021.128342
164609025 184547 None 0 Rat Binding pEC50 = 6.9 6.9 - 0
Positive allosteric modulator activity at rat mGlu3 receptor transfected in GIRK channel overexpressing cells assessed as potentiation of glutamate-induced response by thallium mobilization assayPositive allosteric modulator activity at rat mGlu3 receptor transfected in GIRK channel overexpressing cells assessed as potentiation of glutamate-induced response by thallium mobilization assay
ChEMBL 448 10 2 5 5.9 Cc1c(OCCCCOc2ccc(Cl)c(C(=O)O)c2)ccc(C(=O)CC(C)(C)C)c1O 10.1016/j.bmcl.2021.128342
CHEMBL4846460 184547 None 0 Rat Binding pEC50 = 6.9 6.9 - 0
Positive allosteric modulator activity at rat mGlu3 receptor transfected in GIRK channel overexpressing cells assessed as potentiation of glutamate-induced response by thallium mobilization assayPositive allosteric modulator activity at rat mGlu3 receptor transfected in GIRK channel overexpressing cells assessed as potentiation of glutamate-induced response by thallium mobilization assay
ChEMBL 448 10 2 5 5.9 Cc1c(OCCCCOc2ccc(Cl)c(C(=O)O)c2)ccc(C(=O)CC(C)(C)C)c1O 10.1016/j.bmcl.2021.128342
164611059 184685 None 0 Rat Binding pEC50 = 5.9 5.9 - 0
Positive allosteric modulator activity at rat mGlu3 receptor transfected in GIRK channel overexpressing cells assessed as potentiation of glutamate-induced response by thallium mobilization assayPositive allosteric modulator activity at rat mGlu3 receptor transfected in GIRK channel overexpressing cells assessed as potentiation of glutamate-induced response by thallium mobilization assay
ChEMBL 432 9 2 5 5.3 Cc1c(OC[C@@H](C)COc2ccc(C(=O)O)cc2F)ccc(C(=O)CC(C)(C)C)c1O 10.1016/j.bmcl.2021.128342
CHEMBL4848600 184685 None 0 Rat Binding pEC50 = 5.9 5.9 - 0
Positive allosteric modulator activity at rat mGlu3 receptor transfected in GIRK channel overexpressing cells assessed as potentiation of glutamate-induced response by thallium mobilization assayPositive allosteric modulator activity at rat mGlu3 receptor transfected in GIRK channel overexpressing cells assessed as potentiation of glutamate-induced response by thallium mobilization assay
ChEMBL 432 9 2 5 5.3 Cc1c(OC[C@@H](C)COc2ccc(C(=O)O)cc2F)ccc(C(=O)CC(C)(C)C)c1O 10.1016/j.bmcl.2021.128342
164611874 185220 None 0 Rat Binding pEC50 = 5.9 5.9 - 0
Positive allosteric modulator activity at rat mGlu3 receptor transfected in GIRK channel overexpressing cells assessed as potentiation of glutamate-induced response by thallium mobilization assayPositive allosteric modulator activity at rat mGlu3 receptor transfected in GIRK channel overexpressing cells assessed as potentiation of glutamate-induced response by thallium mobilization assay
ChEMBL 428 9 2 5 5.4 Cc1cc(OC[C@H](C)COc2ccc(C(=O)CC(C)(C)C)c(O)c2C)ccc1C(=O)O 10.1016/j.bmcl.2021.128342
CHEMBL4856242 185220 None 0 Rat Binding pEC50 = 5.9 5.9 - 0
Positive allosteric modulator activity at rat mGlu3 receptor transfected in GIRK channel overexpressing cells assessed as potentiation of glutamate-induced response by thallium mobilization assayPositive allosteric modulator activity at rat mGlu3 receptor transfected in GIRK channel overexpressing cells assessed as potentiation of glutamate-induced response by thallium mobilization assay
ChEMBL 428 9 2 5 5.4 Cc1cc(OC[C@H](C)COc2ccc(C(=O)CC(C)(C)C)c(O)c2C)ccc1C(=O)O 10.1016/j.bmcl.2021.128342
70052526 90086 None 1 Human Binding pEC50 = 7.9 7.9 - 1
Agonist activity at human mGlu3 receptor expressed in golden Syrian hamster AV12 cells coexpressing EAAT1 after 20 mins by HTRF assayAgonist activity at human mGlu3 receptor expressed in golden Syrian hamster AV12 cells coexpressing EAAT1 after 20 mins by HTRF assay
ChEMBL 201 2 4 4 -1.5 N[C@@]1(C(=O)O)C[C@@H](O)[C@@H]2[C@H]1[C@H]2C(=O)O 10.1021/jm4000165
CHEMBL2381642 90086 None 1 Human Binding pEC50 = 7.9 7.9 - 1
Agonist activity at human mGlu3 receptor expressed in golden Syrian hamster AV12 cells coexpressing EAAT1 after 20 mins by HTRF assayAgonist activity at human mGlu3 receptor expressed in golden Syrian hamster AV12 cells coexpressing EAAT1 after 20 mins by HTRF assay
ChEMBL 201 2 4 4 -1.5 N[C@@]1(C(=O)O)C[C@@H](O)[C@@H]2[C@H]1[C@H]2C(=O)O 10.1021/jm4000165
90643871 111927 None 0 Rat Binding pEC50 = 5.9 5.9 - 0
Positive allosteric modulation of rat mGluR3 receptor expressed in HEK293 cells assessed as potentiation of glutamate-induced thallium flux incubated for 2.5 mins prior to glutamate addition measured after 2.5 mins by GIRK assayPositive allosteric modulation of rat mGluR3 receptor expressed in HEK293 cells assessed as potentiation of glutamate-induced thallium flux incubated for 2.5 mins prior to glutamate addition measured after 2.5 mins by GIRK assay
ChEMBL 418 11 2 5 5.0 Cc1c(OCCCCOc2ccc(C(=O)O)cc2F)ccc(C(=O)CC(C)C)c1O 10.1021/jm5000563
CHEMBL3287693 111927 None 0 Rat Binding pEC50 = 5.9 5.9 - 0
Positive allosteric modulation of rat mGluR3 receptor expressed in HEK293 cells assessed as potentiation of glutamate-induced thallium flux incubated for 2.5 mins prior to glutamate addition measured after 2.5 mins by GIRK assayPositive allosteric modulation of rat mGluR3 receptor expressed in HEK293 cells assessed as potentiation of glutamate-induced thallium flux incubated for 2.5 mins prior to glutamate addition measured after 2.5 mins by GIRK assay
ChEMBL 418 11 2 5 5.0 Cc1c(OCCCCOc2ccc(C(=O)O)cc2F)ccc(C(=O)CC(C)C)c1O 10.1021/jm5000563
90643860 111912 None 0 Rat Binding pEC50 = 5.8 5.8 - 0
Positive allosteric modulation of rat mGluR3 receptor expressed in HEK293 cells assessed as potentiation of glutamate-induced thallium flux incubated for 2.5 mins prior to glutamate addition measured after 2.5 mins by GIRK assayPositive allosteric modulation of rat mGluR3 receptor expressed in HEK293 cells assessed as potentiation of glutamate-induced thallium flux incubated for 2.5 mins prior to glutamate addition measured after 2.5 mins by GIRK assay
ChEMBL 400 11 2 5 4.9 Cc1c(OCCCCOc2cccc(C(=O)O)c2)ccc(C(=O)CC(C)C)c1O 10.1021/jm5000563
CHEMBL3287675 111912 None 0 Rat Binding pEC50 = 5.8 5.8 - 0
Positive allosteric modulation of rat mGluR3 receptor expressed in HEK293 cells assessed as potentiation of glutamate-induced thallium flux incubated for 2.5 mins prior to glutamate addition measured after 2.5 mins by GIRK assayPositive allosteric modulation of rat mGluR3 receptor expressed in HEK293 cells assessed as potentiation of glutamate-induced thallium flux incubated for 2.5 mins prior to glutamate addition measured after 2.5 mins by GIRK assay
ChEMBL 400 11 2 5 4.9 Cc1c(OCCCCOc2cccc(C(=O)O)c2)ccc(C(=O)CC(C)C)c1O 10.1021/jm5000563
164611067 184722 None 0 Rat Binding pEC50 = 5.8 5.8 - 0
Positive allosteric modulator activity at rat mGlu3 receptor transfected in GIRK channel overexpressing cells assessed as potentiation of glutamate-induced response by thallium mobilization assayPositive allosteric modulator activity at rat mGlu3 receptor transfected in GIRK channel overexpressing cells assessed as potentiation of glutamate-induced response by thallium mobilization assay
ChEMBL 444 10 2 6 5.1 COc1cc(OC[C@H](C)COc2ccc(C(=O)CC(C)(C)C)c(O)c2C)ccc1C(=O)O 10.1016/j.bmcl.2021.128342
CHEMBL4849142 184722 None 0 Rat Binding pEC50 = 5.8 5.8 - 0
Positive allosteric modulator activity at rat mGlu3 receptor transfected in GIRK channel overexpressing cells assessed as potentiation of glutamate-induced response by thallium mobilization assayPositive allosteric modulator activity at rat mGlu3 receptor transfected in GIRK channel overexpressing cells assessed as potentiation of glutamate-induced response by thallium mobilization assay
ChEMBL 444 10 2 6 5.1 COc1cc(OC[C@H](C)COc2ccc(C(=O)CC(C)(C)C)c(O)c2C)ccc1C(=O)O 10.1016/j.bmcl.2021.128342
70051926 90085 None 1 Human Binding pEC50 = 7.8 7.8 - 0
Agonist activity at human mGlu3 receptor expressed in golden Syrian hamster AV12 cells coexpressing EAAT1 after 20 mins by HTRF assayAgonist activity at human mGlu3 receptor expressed in golden Syrian hamster AV12 cells coexpressing EAAT1 after 20 mins by HTRF assay
ChEMBL 197 2 3 3 -0.3 C=C1C[C@@](N)(C(=O)O)[C@@H]2[C@@H](C(=O)O)[C@H]12 10.1021/jm4000165
CHEMBL2381641 90085 None 1 Human Binding pEC50 = 7.8 7.8 - 0
Agonist activity at human mGlu3 receptor expressed in golden Syrian hamster AV12 cells coexpressing EAAT1 after 20 mins by HTRF assayAgonist activity at human mGlu3 receptor expressed in golden Syrian hamster AV12 cells coexpressing EAAT1 after 20 mins by HTRF assay
ChEMBL 197 2 3 3 -0.3 C=C1C[C@@](N)(C(=O)O)[C@@H]2[C@@H](C(=O)O)[C@H]12 10.1021/jm4000165
90643887 111957 None 0 Rat Binding pEC50 = 6.8 6.8 - 0
Positive allosteric modulation of rat mGluR3 receptor expressed in HEK293 cells assessed as potentiation of glutamate-induced thallium flux incubated for 2.5 mins prior to glutamate addition measured after 2.5 mins by GIRK assayPositive allosteric modulation of rat mGluR3 receptor expressed in HEK293 cells assessed as potentiation of glutamate-induced thallium flux incubated for 2.5 mins prior to glutamate addition measured after 2.5 mins by GIRK assay
ChEMBL 444 11 2 6 5.3 COc1ccc(C(=O)O)cc1OCCCCOc1ccc(C(=O)CC(C)(C)C)c(O)c1C 10.1021/jm5000563
CHEMBL3287723 111957 None 0 Rat Binding pEC50 = 6.8 6.8 - 0
Positive allosteric modulation of rat mGluR3 receptor expressed in HEK293 cells assessed as potentiation of glutamate-induced thallium flux incubated for 2.5 mins prior to glutamate addition measured after 2.5 mins by GIRK assayPositive allosteric modulation of rat mGluR3 receptor expressed in HEK293 cells assessed as potentiation of glutamate-induced thallium flux incubated for 2.5 mins prior to glutamate addition measured after 2.5 mins by GIRK assay
ChEMBL 444 11 2 6 5.3 COc1ccc(C(=O)O)cc1OCCCCOc1ccc(C(=O)CC(C)(C)C)c(O)c1C 10.1021/jm5000563
164615875 185550 None 0 Rat Binding pEC50 = 5.8 5.8 - 0
Positive allosteric modulator activity at rat mGlu3 receptor transfected in GIRK channel overexpressing cells assessed as potentiation of glutamate-induced response by thallium mobilization assayPositive allosteric modulator activity at rat mGlu3 receptor transfected in GIRK channel overexpressing cells assessed as potentiation of glutamate-induced response by thallium mobilization assay
ChEMBL 428 9 2 5 5.4 Cc1cc(C(=O)O)ccc1OC[C@H](C)COc1ccc(C(=O)CC(C)(C)C)c(O)c1C 10.1016/j.bmcl.2021.128342
CHEMBL4861618 185550 None 0 Rat Binding pEC50 = 5.8 5.8 - 0
Positive allosteric modulator activity at rat mGlu3 receptor transfected in GIRK channel overexpressing cells assessed as potentiation of glutamate-induced response by thallium mobilization assayPositive allosteric modulator activity at rat mGlu3 receptor transfected in GIRK channel overexpressing cells assessed as potentiation of glutamate-induced response by thallium mobilization assay
ChEMBL 428 9 2 5 5.4 Cc1cc(C(=O)O)ccc1OC[C@H](C)COc1ccc(C(=O)CC(C)(C)C)c(O)c1C 10.1016/j.bmcl.2021.128342
164623088 185591 None 0 Rat Binding pEC50 = 5.8 5.8 - 0
Positive allosteric modulator activity at rat mGlu3 receptor transfected in GIRK channel overexpressing cells assessed as potentiation of glutamate-induced response by thallium mobilization assayPositive allosteric modulator activity at rat mGlu3 receptor transfected in GIRK channel overexpressing cells assessed as potentiation of glutamate-induced response by thallium mobilization assay
ChEMBL 448 9 2 5 5.8 Cc1c(OC[C@@H](C)COc2ccc(C(=O)O)cc2Cl)ccc(C(=O)CC(C)(C)C)c1O 10.1016/j.bmcl.2021.128342
CHEMBL4862244 185591 None 0 Rat Binding pEC50 = 5.8 5.8 - 0
Positive allosteric modulator activity at rat mGlu3 receptor transfected in GIRK channel overexpressing cells assessed as potentiation of glutamate-induced response by thallium mobilization assayPositive allosteric modulator activity at rat mGlu3 receptor transfected in GIRK channel overexpressing cells assessed as potentiation of glutamate-induced response by thallium mobilization assay
ChEMBL 448 9 2 5 5.8 Cc1c(OC[C@@H](C)COc2ccc(C(=O)O)cc2Cl)ccc(C(=O)CC(C)(C)C)c1O 10.1016/j.bmcl.2021.128342
11344646 126844 None 0 Human Binding pEC50 = 6.8 6.8 1 2
Agonist activity at human mGlu3 receptor expressed in golden Syrian hamster AV12 cells coexpressing EAAT1 after 20 mins by HTRF assayAgonist activity at human mGlu3 receptor expressed in golden Syrian hamster AV12 cells coexpressing EAAT1 after 20 mins by HTRF assay
ChEMBL 199 2 3 3 -0.2 C[C@H]1C[C@@](N)(C(=O)O)[C@@H]2[C@@H](C(=O)O)[C@H]12 10.1021/jm4000165
CHEMBL365368 126844 None 0 Human Binding pEC50 = 6.8 6.8 1 2
Agonist activity at human mGlu3 receptor expressed in golden Syrian hamster AV12 cells coexpressing EAAT1 after 20 mins by HTRF assayAgonist activity at human mGlu3 receptor expressed in golden Syrian hamster AV12 cells coexpressing EAAT1 after 20 mins by HTRF assay
ChEMBL 199 2 3 3 -0.2 C[C@H]1C[C@@](N)(C(=O)O)[C@@H]2[C@@H](C(=O)O)[C@H]12 10.1021/jm4000165
164610947 185357 None 0 Rat Binding pEC50 = 6.8 6.8 - 0
Positive allosteric modulator activity at rat mGlu3 receptor transfected in GIRK channel overexpressing cells assessed as potentiation of glutamate-induced response by thallium mobilization assayPositive allosteric modulator activity at rat mGlu3 receptor transfected in GIRK channel overexpressing cells assessed as potentiation of glutamate-induced response by thallium mobilization assay
ChEMBL 415 10 2 6 4.7 Cc1c(OCCCCOc2cncc(C(=O)O)c2)ccc(C(=O)CC(C)(C)C)c1O 10.1016/j.bmcl.2021.128342
CHEMBL4858387 185357 None 0 Rat Binding pEC50 = 6.8 6.8 - 0
Positive allosteric modulator activity at rat mGlu3 receptor transfected in GIRK channel overexpressing cells assessed as potentiation of glutamate-induced response by thallium mobilization assayPositive allosteric modulator activity at rat mGlu3 receptor transfected in GIRK channel overexpressing cells assessed as potentiation of glutamate-induced response by thallium mobilization assay
ChEMBL 415 10 2 6 4.7 Cc1c(OCCCCOc2cncc(C(=O)O)c2)ccc(C(=O)CC(C)(C)C)c1O 10.1016/j.bmcl.2021.128342
90643883 111952 None 0 Rat Binding pEC50 = 5.7 5.7 - 0
Positive allosteric modulation of rat mGluR3 receptor expressed in HEK293 cells assessed as potentiation of glutamate-induced thallium flux incubated for 2.5 mins prior to glutamate addition measured after 2.5 mins by GIRK assayPositive allosteric modulation of rat mGluR3 receptor expressed in HEK293 cells assessed as potentiation of glutamate-induced thallium flux incubated for 2.5 mins prior to glutamate addition measured after 2.5 mins by GIRK assay
ChEMBL 416 12 2 6 4.6 CCCC(=O)c1ccc(OCCCCOc2c(OC)cccc2C(=O)O)c(C)c1O 10.1021/jm5000563
CHEMBL3287718 111952 None 0 Rat Binding pEC50 = 5.7 5.7 - 0
Positive allosteric modulation of rat mGluR3 receptor expressed in HEK293 cells assessed as potentiation of glutamate-induced thallium flux incubated for 2.5 mins prior to glutamate addition measured after 2.5 mins by GIRK assayPositive allosteric modulation of rat mGluR3 receptor expressed in HEK293 cells assessed as potentiation of glutamate-induced thallium flux incubated for 2.5 mins prior to glutamate addition measured after 2.5 mins by GIRK assay
ChEMBL 416 12 2 6 4.6 CCCC(=O)c1ccc(OCCCCOc2c(OC)cccc2C(=O)O)c(C)c1O 10.1021/jm5000563
164609925 185373 None 0 Rat Binding pEC50 = 5.7 5.7 - 0
Positive allosteric modulator activity at rat mGlu3 receptor transfected in GIRK channel overexpressing cells assessed as potentiation of glutamate-induced response by thallium mobilization assayPositive allosteric modulator activity at rat mGlu3 receptor transfected in GIRK channel overexpressing cells assessed as potentiation of glutamate-induced response by thallium mobilization assay
ChEMBL 430 9 2 6 4.9 COc1ccc(C(=O)O)cc1O[C@H](C)COc1ccc(C(=O)CC(C)(C)C)c(O)c1C 10.1016/j.bmcl.2021.128342
CHEMBL4858717 185373 None 0 Rat Binding pEC50 = 5.7 5.7 - 0
Positive allosteric modulator activity at rat mGlu3 receptor transfected in GIRK channel overexpressing cells assessed as potentiation of glutamate-induced response by thallium mobilization assayPositive allosteric modulator activity at rat mGlu3 receptor transfected in GIRK channel overexpressing cells assessed as potentiation of glutamate-induced response by thallium mobilization assay
ChEMBL 430 9 2 6 4.9 COc1ccc(C(=O)O)cc1O[C@H](C)COc1ccc(C(=O)CC(C)(C)C)c(O)c1C 10.1016/j.bmcl.2021.128342
90643869 111925 None 0 Rat Binding pEC50 = 5.7 5.7 - 0
Positive allosteric modulation of rat mGluR3 receptor expressed in HEK293 cells assessed as potentiation of glutamate-induced thallium flux incubated for 2.5 mins prior to glutamate addition measured after 2.5 mins by GIRK assayPositive allosteric modulation of rat mGluR3 receptor expressed in HEK293 cells assessed as potentiation of glutamate-induced thallium flux incubated for 2.5 mins prior to glutamate addition measured after 2.5 mins by GIRK assay
ChEMBL 414 11 2 5 5.2 Cc1cc(C(=O)O)ccc1OCCCCOc1ccc(C(=O)CC(C)C)c(O)c1C 10.1021/jm5000563
CHEMBL3287691 111925 None 0 Rat Binding pEC50 = 5.7 5.7 - 0
Positive allosteric modulation of rat mGluR3 receptor expressed in HEK293 cells assessed as potentiation of glutamate-induced thallium flux incubated for 2.5 mins prior to glutamate addition measured after 2.5 mins by GIRK assayPositive allosteric modulation of rat mGluR3 receptor expressed in HEK293 cells assessed as potentiation of glutamate-induced thallium flux incubated for 2.5 mins prior to glutamate addition measured after 2.5 mins by GIRK assay
ChEMBL 414 11 2 5 5.2 Cc1cc(C(=O)O)ccc1OCCCCOc1ccc(C(=O)CC(C)C)c(O)c1C 10.1021/jm5000563
90643873 111930 None 0 Rat Binding pEC50 = 5.7 5.7 - 0
Positive allosteric modulation of rat mGluR3 receptor expressed in HEK293 cells assessed as potentiation of glutamate-induced thallium flux incubated for 2.5 mins prior to glutamate addition measured after 2.5 mins by GIRK assayPositive allosteric modulation of rat mGluR3 receptor expressed in HEK293 cells assessed as potentiation of glutamate-induced thallium flux incubated for 2.5 mins prior to glutamate addition measured after 2.5 mins by GIRK assay
ChEMBL 456 13 2 6 5.4 Cc1c(OCCCCOCOc2ccc(C(=O)O)cc2)ccc(C(=O)CC2CCCC2)c1O 10.1021/jm5000563
CHEMBL3287696 111930 None 0 Rat Binding pEC50 = 5.7 5.7 - 0
Positive allosteric modulation of rat mGluR3 receptor expressed in HEK293 cells assessed as potentiation of glutamate-induced thallium flux incubated for 2.5 mins prior to glutamate addition measured after 2.5 mins by GIRK assayPositive allosteric modulation of rat mGluR3 receptor expressed in HEK293 cells assessed as potentiation of glutamate-induced thallium flux incubated for 2.5 mins prior to glutamate addition measured after 2.5 mins by GIRK assay
ChEMBL 456 13 2 6 5.4 Cc1c(OCCCCOCOc2ccc(C(=O)O)cc2)ccc(C(=O)CC2CCCC2)c1O 10.1021/jm5000563
60096211 90093 None 0 Human Binding pEC50 = 6.7 6.7 5 2
Agonist activity at human mGlu3 receptor expressed in golden Syrian hamster AV12 cells coexpressing EAAT1 after 20 mins by HTRF assayAgonist activity at human mGlu3 receptor expressed in golden Syrian hamster AV12 cells coexpressing EAAT1 after 20 mins by HTRF assay
ChEMBL 242 3 4 4 -1.4 CC(=O)N[C@H]1C[C@@](N)(C(=O)O)[C@@H]2[C@@H](C(=O)O)[C@H]12 10.1021/jm4000165
CHEMBL2381649 90093 None 0 Human Binding pEC50 = 6.7 6.7 5 2
Agonist activity at human mGlu3 receptor expressed in golden Syrian hamster AV12 cells coexpressing EAAT1 after 20 mins by HTRF assayAgonist activity at human mGlu3 receptor expressed in golden Syrian hamster AV12 cells coexpressing EAAT1 after 20 mins by HTRF assay
ChEMBL 242 3 4 4 -1.4 CC(=O)N[C@H]1C[C@@](N)(C(=O)O)[C@@H]2[C@@H](C(=O)O)[C@H]12 10.1021/jm4000165
90643863 111919 None 0 Rat Binding pEC50 = 5.7 5.7 - 0
Positive allosteric modulation of rat mGluR3 receptor expressed in HEK293 cells assessed as potentiation of glutamate-induced thallium flux incubated for 2.5 mins prior to glutamate addition measured after 2.5 mins by GIRK assayPositive allosteric modulation of rat mGluR3 receptor expressed in HEK293 cells assessed as potentiation of glutamate-induced thallium flux incubated for 2.5 mins prior to glutamate addition measured after 2.5 mins by GIRK assay
ChEMBL 434 11 2 5 5.5 Cc1c(OCCCCOc2ccc(C(=O)O)c(Cl)c2)ccc(C(=O)CC(C)C)c1O 10.1021/jm5000563
CHEMBL3287683 111919 None 0 Rat Binding pEC50 = 5.7 5.7 - 0
Positive allosteric modulation of rat mGluR3 receptor expressed in HEK293 cells assessed as potentiation of glutamate-induced thallium flux incubated for 2.5 mins prior to glutamate addition measured after 2.5 mins by GIRK assayPositive allosteric modulation of rat mGluR3 receptor expressed in HEK293 cells assessed as potentiation of glutamate-induced thallium flux incubated for 2.5 mins prior to glutamate addition measured after 2.5 mins by GIRK assay
ChEMBL 434 11 2 5 5.5 Cc1c(OCCCCOc2ccc(C(=O)O)c(Cl)c2)ccc(C(=O)CC(C)C)c1O 10.1021/jm5000563
164624284 186135 None 0 Rat Binding pEC50 = 5.7 5.7 - 0
Positive allosteric modulator activity at rat mGlu3 receptor transfected in GIRK channel overexpressing cells assessed as potentiation of glutamate-induced response by thallium mobilization assayPositive allosteric modulator activity at rat mGlu3 receptor transfected in GIRK channel overexpressing cells assessed as potentiation of glutamate-induced response by thallium mobilization assay
ChEMBL 448 9 2 5 5.8 Cc1c(OC[C@@H](C)COc2ccc(Cl)c(C(=O)O)c2)ccc(C(=O)CC(C)(C)C)c1O 10.1016/j.bmcl.2021.128342
CHEMBL4870631 186135 None 0 Rat Binding pEC50 = 5.7 5.7 - 0
Positive allosteric modulator activity at rat mGlu3 receptor transfected in GIRK channel overexpressing cells assessed as potentiation of glutamate-induced response by thallium mobilization assayPositive allosteric modulator activity at rat mGlu3 receptor transfected in GIRK channel overexpressing cells assessed as potentiation of glutamate-induced response by thallium mobilization assay
ChEMBL 448 9 2 5 5.8 Cc1c(OC[C@@H](C)COc2ccc(Cl)c(C(=O)O)c2)ccc(C(=O)CC(C)(C)C)c1O 10.1016/j.bmcl.2021.128342
164613604 185290 None 0 Rat Binding pEC50 = 5.7 5.7 - 0
Positive allosteric modulator activity at rat mGlu3 receptor transfected in GIRK channel overexpressing cells assessed as potentiation of glutamate-induced response by thallium mobilization assayPositive allosteric modulator activity at rat mGlu3 receptor transfected in GIRK channel overexpressing cells assessed as potentiation of glutamate-induced response by thallium mobilization assay
ChEMBL 430 9 2 6 4.9 COc1ccc(C(=O)O)cc1O[C@@H](C)COc1ccc(C(=O)CC(C)(C)C)c(O)c1C 10.1016/j.bmcl.2021.128342
CHEMBL4857426 185290 None 0 Rat Binding pEC50 = 5.7 5.7 - 0
Positive allosteric modulator activity at rat mGlu3 receptor transfected in GIRK channel overexpressing cells assessed as potentiation of glutamate-induced response by thallium mobilization assayPositive allosteric modulator activity at rat mGlu3 receptor transfected in GIRK channel overexpressing cells assessed as potentiation of glutamate-induced response by thallium mobilization assay
ChEMBL 430 9 2 6 4.9 COc1ccc(C(=O)O)cc1O[C@@H](C)COc1ccc(C(=O)CC(C)(C)C)c(O)c1C 10.1016/j.bmcl.2021.128342
90643864 111920 None 0 Rat Binding pEC50 = 5.7 5.7 - 0
Positive allosteric modulation of rat mGluR3 receptor expressed in HEK293 cells assessed as potentiation of glutamate-induced thallium flux incubated for 2.5 mins prior to glutamate addition measured after 2.5 mins by GIRK assayPositive allosteric modulation of rat mGluR3 receptor expressed in HEK293 cells assessed as potentiation of glutamate-induced thallium flux incubated for 2.5 mins prior to glutamate addition measured after 2.5 mins by GIRK assay
ChEMBL 460 11 2 5 6.1 Cc1c(OCCCCOc2ccc(C(=O)O)c(Cl)c2)ccc(C(=O)CC2CCCC2)c1O 10.1021/jm5000563
CHEMBL3287684 111920 None 0 Rat Binding pEC50 = 5.7 5.7 - 0
Positive allosteric modulation of rat mGluR3 receptor expressed in HEK293 cells assessed as potentiation of glutamate-induced thallium flux incubated for 2.5 mins prior to glutamate addition measured after 2.5 mins by GIRK assayPositive allosteric modulation of rat mGluR3 receptor expressed in HEK293 cells assessed as potentiation of glutamate-induced thallium flux incubated for 2.5 mins prior to glutamate addition measured after 2.5 mins by GIRK assay
ChEMBL 460 11 2 5 6.1 Cc1c(OCCCCOc2ccc(C(=O)O)c(Cl)c2)ccc(C(=O)CC2CCCC2)c1O 10.1021/jm5000563
71681825 90089 None 0 Human Binding pEC50 = 7.6 7.6 - 0
Agonist activity at human mGlu3 receptor expressed in golden Syrian hamster AV12 cells coexpressing EAAT1 after 20 mins by HTRF assayAgonist activity at human mGlu3 receptor expressed in golden Syrian hamster AV12 cells coexpressing EAAT1 after 20 mins by HTRF assay
ChEMBL 226 3 3 4 -0.2 [N-]=[N+]=N[C@H]1C[C@@](N)(C(=O)O)[C@@H]2[C@@H](C(=O)O)[C@H]12 10.1021/jm4000165
CHEMBL2381645 90089 None 0 Human Binding pEC50 = 7.6 7.6 - 0
Agonist activity at human mGlu3 receptor expressed in golden Syrian hamster AV12 cells coexpressing EAAT1 after 20 mins by HTRF assayAgonist activity at human mGlu3 receptor expressed in golden Syrian hamster AV12 cells coexpressing EAAT1 after 20 mins by HTRF assay
ChEMBL 226 3 3 4 -0.2 [N-]=[N+]=N[C@H]1C[C@@](N)(C(=O)O)[C@@H]2[C@@H](C(=O)O)[C@H]12 10.1021/jm4000165
11275666 90091 None 1 Human Binding pEC50 = 7.6 7.6 15 2
Agonist activity at human mGlu3 receptor expressed in golden Syrian hamster AV12 cells coexpressing EAAT1 after 20 mins by HTRF assayAgonist activity at human mGlu3 receptor expressed in golden Syrian hamster AV12 cells coexpressing EAAT1 after 20 mins by HTRF assay
ChEMBL 200 2 4 4 -1.6 N[C@H]1C[C@@](N)(C(=O)O)[C@@H]2[C@@H](C(=O)O)[C@H]12 10.1021/jm4000165
CHEMBL2381647 90091 None 1 Human Binding pEC50 = 7.6 7.6 15 2
Agonist activity at human mGlu3 receptor expressed in golden Syrian hamster AV12 cells coexpressing EAAT1 after 20 mins by HTRF assayAgonist activity at human mGlu3 receptor expressed in golden Syrian hamster AV12 cells coexpressing EAAT1 after 20 mins by HTRF assay
ChEMBL 200 2 4 4 -1.6 N[C@H]1C[C@@](N)(C(=O)O)[C@@H]2[C@@H](C(=O)O)[C@H]12 10.1021/jm4000165
164612248 184996 None 0 Rat Binding pEC50 = 5.6 5.6 - 0
Positive allosteric modulator activity at rat mGlu3 receptor transfected in GIRK channel overexpressing cells assessed as potentiation of glutamate-induced response by thallium mobilization assayPositive allosteric modulator activity at rat mGlu3 receptor transfected in GIRK channel overexpressing cells assessed as potentiation of glutamate-induced response by thallium mobilization assay
ChEMBL 418 8 2 5 5.0 Cc1c(O[C@H](C)COc2ccc(F)c(C(=O)O)c2)ccc(C(=O)CC(C)(C)C)c1O 10.1016/j.bmcl.2021.128342
CHEMBL4852903 184996 None 0 Rat Binding pEC50 = 5.6 5.6 - 0
Positive allosteric modulator activity at rat mGlu3 receptor transfected in GIRK channel overexpressing cells assessed as potentiation of glutamate-induced response by thallium mobilization assayPositive allosteric modulator activity at rat mGlu3 receptor transfected in GIRK channel overexpressing cells assessed as potentiation of glutamate-induced response by thallium mobilization assay
ChEMBL 418 8 2 5 5.0 Cc1c(O[C@H](C)COc2ccc(F)c(C(=O)O)c2)ccc(C(=O)CC(C)(C)C)c1O 10.1016/j.bmcl.2021.128342
90643866 111922 None 0 Rat Binding pEC50 = 5.6 5.6 - 0
Positive allosteric modulation of rat mGluR3 receptor expressed in HEK293 cells assessed as potentiation of glutamate-induced thallium flux incubated for 2.5 mins prior to glutamate addition measured after 2.5 mins by GIRK assayPositive allosteric modulation of rat mGluR3 receptor expressed in HEK293 cells assessed as potentiation of glutamate-induced thallium flux incubated for 2.5 mins prior to glutamate addition measured after 2.5 mins by GIRK assay
ChEMBL 444 11 2 5 5.5 Cc1c(OCCCCOc2ccc(F)c(C(=O)O)c2)ccc(C(=O)CC2CCCC2)c1O 10.1021/jm5000563
CHEMBL3287688 111922 None 0 Rat Binding pEC50 = 5.6 5.6 - 0
Positive allosteric modulation of rat mGluR3 receptor expressed in HEK293 cells assessed as potentiation of glutamate-induced thallium flux incubated for 2.5 mins prior to glutamate addition measured after 2.5 mins by GIRK assayPositive allosteric modulation of rat mGluR3 receptor expressed in HEK293 cells assessed as potentiation of glutamate-induced thallium flux incubated for 2.5 mins prior to glutamate addition measured after 2.5 mins by GIRK assay
ChEMBL 444 11 2 5 5.5 Cc1c(OCCCCOc2ccc(F)c(C(=O)O)c2)ccc(C(=O)CC2CCCC2)c1O 10.1021/jm5000563
90643889 111960 None 0 Rat Binding pEC50 = 6.6 6.6 - 0
Positive allosteric modulation of rat mGluR3 receptor expressed in HEK293 cells assessed as potentiation of glutamate-induced thallium flux incubated for 2.5 mins prior to glutamate addition measured after 2.5 mins by GIRK assayPositive allosteric modulation of rat mGluR3 receptor expressed in HEK293 cells assessed as potentiation of glutamate-induced thallium flux incubated for 2.5 mins prior to glutamate addition measured after 2.5 mins by GIRK assay
ChEMBL 432 10 2 5 5.4 Cc1c(OCCCCOc2ccc(F)c(C(=O)O)c2)ccc(C(=O)CC(C)(C)C)c1O 10.1021/jm5000563
CHEMBL3287726 111960 None 0 Rat Binding pEC50 = 6.6 6.6 - 0
Positive allosteric modulation of rat mGluR3 receptor expressed in HEK293 cells assessed as potentiation of glutamate-induced thallium flux incubated for 2.5 mins prior to glutamate addition measured after 2.5 mins by GIRK assayPositive allosteric modulation of rat mGluR3 receptor expressed in HEK293 cells assessed as potentiation of glutamate-induced thallium flux incubated for 2.5 mins prior to glutamate addition measured after 2.5 mins by GIRK assay
ChEMBL 432 10 2 5 5.4 Cc1c(OCCCCOc2ccc(F)c(C(=O)O)c2)ccc(C(=O)CC(C)(C)C)c1O 10.1021/jm5000563
1393 1539 None 42 Human Binding pEC50 = 7.6 7.6 -1 6
Agonist activity at human mGlu3 receptor expressed in golden Syrian hamster AV12 cells coexpressing EAAT1 after 20 mins by HTRF assayAgonist activity at human mGlu3 receptor expressed in golden Syrian hamster AV12 cells coexpressing EAAT1 after 20 mins by HTRF assay
ChEMBL 185 2 3 3 -0.5 OC(=O)[C@H]1[C@H]2[C@@H]1[C@](CC2)(N)C(=O)O 10.1021/jm4000165
1396 1539 None 42 Human Binding pEC50 = 7.6 7.6 -1 6
Agonist activity at human mGlu3 receptor expressed in golden Syrian hamster AV12 cells coexpressing EAAT1 after 20 mins by HTRF assayAgonist activity at human mGlu3 receptor expressed in golden Syrian hamster AV12 cells coexpressing EAAT1 after 20 mins by HTRF assay
ChEMBL 185 2 3 3 -0.5 OC(=O)[C@H]1[C@H]2[C@@H]1[C@](CC2)(N)C(=O)O 10.1021/jm4000165
213056 1539 None 42 Human Binding pEC50 = 7.6 7.6 -1 6
Agonist activity at human mGlu3 receptor expressed in golden Syrian hamster AV12 cells coexpressing EAAT1 after 20 mins by HTRF assayAgonist activity at human mGlu3 receptor expressed in golden Syrian hamster AV12 cells coexpressing EAAT1 after 20 mins by HTRF assay
ChEMBL 185 2 3 3 -0.5 OC(=O)[C@H]1[C@H]2[C@@H]1[C@](CC2)(N)C(=O)O 10.1021/jm4000165
CHEMBL8759 1539 None 42 Human Binding pEC50 = 7.6 7.6 -1 6
Agonist activity at human mGlu3 receptor expressed in golden Syrian hamster AV12 cells coexpressing EAAT1 after 20 mins by HTRF assayAgonist activity at human mGlu3 receptor expressed in golden Syrian hamster AV12 cells coexpressing EAAT1 after 20 mins by HTRF assay
ChEMBL 185 2 3 3 -0.5 OC(=O)[C@H]1[C@H]2[C@@H]1[C@](CC2)(N)C(=O)O 10.1021/jm4000165
56929215 111910 None 0 Rat Binding pEC50 = 5.6 5.6 - 0
Positive allosteric modulation of rat mGluR3 receptor expressed in HEK293 cells assessed as potentiation of glutamate-induced thallium flux incubated for 2.5 mins prior to glutamate addition measured after 2.5 mins by GIRK assayPositive allosteric modulation of rat mGluR3 receptor expressed in HEK293 cells assessed as potentiation of glutamate-induced thallium flux incubated for 2.5 mins prior to glutamate addition measured after 2.5 mins by GIRK assay
ChEMBL 400 11 2 5 4.9 Cc1c(OCCCCOc2ccc(C(=O)O)cc2)ccc(C(=O)CC(C)C)c1O 10.1021/jm5000563
CHEMBL3287671 111910 None 0 Rat Binding pEC50 = 5.6 5.6 - 0
Positive allosteric modulation of rat mGluR3 receptor expressed in HEK293 cells assessed as potentiation of glutamate-induced thallium flux incubated for 2.5 mins prior to glutamate addition measured after 2.5 mins by GIRK assayPositive allosteric modulation of rat mGluR3 receptor expressed in HEK293 cells assessed as potentiation of glutamate-induced thallium flux incubated for 2.5 mins prior to glutamate addition measured after 2.5 mins by GIRK assay
ChEMBL 400 11 2 5 4.9 Cc1c(OCCCCOc2ccc(C(=O)O)cc2)ccc(C(=O)CC(C)C)c1O 10.1021/jm5000563
1377 1340 None 23 Rat Binding pEC50 = 6.5 6.5 -2 6
Concentration for half maximal activation of metabotropic glutamate mGluR3 in ratConcentration for half maximal activation of metabotropic glutamate mGluR3 in rat
ChEMBL 203 4 4 4 -1.6 N[C@@H](C1[C@H]([C@@H]1C(=O)O)C(=O)O)C(=O)O 10.1021/jm00009a001
5310979 1340 None 23 Rat Binding pEC50 = 6.5 6.5 -2 6
Concentration for half maximal activation of metabotropic glutamate mGluR3 in ratConcentration for half maximal activation of metabotropic glutamate mGluR3 in rat
ChEMBL 203 4 4 4 -1.6 N[C@@H](C1[C@H]([C@@H]1C(=O)O)C(=O)O)C(=O)O 10.1021/jm00009a001
CHEMBL284193 1340 None 23 Rat Binding pEC50 = 6.5 6.5 -2 6
Concentration for half maximal activation of metabotropic glutamate mGluR3 in ratConcentration for half maximal activation of metabotropic glutamate mGluR3 in rat
ChEMBL 203 4 4 4 -1.6 N[C@@H](C1[C@H]([C@@H]1C(=O)O)C(=O)O)C(=O)O 10.1021/jm00009a001
86765132 111959 None 0 Rat Binding pEC50 = 6.5 6.5 - 0
Positive allosteric modulation of rat mGluR3 receptor expressed in HEK293 cells assessed as potentiation of glutamate-induced thallium flux incubated for 2.5 mins prior to glutamate addition measured after 2.5 mins by GIRK assayPositive allosteric modulation of rat mGluR3 receptor expressed in HEK293 cells assessed as potentiation of glutamate-induced thallium flux incubated for 2.5 mins prior to glutamate addition measured after 2.5 mins by GIRK assay
ChEMBL 428 10 2 5 5.6 Cc1c(OCCCCOc2ccc(C(=O)CC(C)(C)C)c(O)c2C)cccc1C(=O)O 10.1021/jm5000563
CHEMBL3287725 111959 None 0 Rat Binding pEC50 = 6.5 6.5 - 0
Positive allosteric modulation of rat mGluR3 receptor expressed in HEK293 cells assessed as potentiation of glutamate-induced thallium flux incubated for 2.5 mins prior to glutamate addition measured after 2.5 mins by GIRK assayPositive allosteric modulation of rat mGluR3 receptor expressed in HEK293 cells assessed as potentiation of glutamate-induced thallium flux incubated for 2.5 mins prior to glutamate addition measured after 2.5 mins by GIRK assay
ChEMBL 428 10 2 5 5.6 Cc1c(OCCCCOc2ccc(C(=O)CC(C)(C)C)c(O)c2C)cccc1C(=O)O 10.1021/jm5000563
1310 2315 None 61 Rat Binding pEC50 = 5.5 5.5 -1 18
Concentration for half maximal activation of metabotropic glutamate mGluR3 in ratConcentration for half maximal activation of metabotropic glutamate mGluR3 in rat
ChEMBL 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N 10.1021/jm00009a001
1369 2315 None 61 Rat Binding pEC50 = 5.5 5.5 -1 18
Concentration for half maximal activation of metabotropic glutamate mGluR3 in ratConcentration for half maximal activation of metabotropic glutamate mGluR3 in rat
ChEMBL 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N 10.1021/jm00009a001
33032 2315 None 61 Rat Binding pEC50 = 5.5 5.5 -1 18
Concentration for half maximal activation of metabotropic glutamate mGluR3 in ratConcentration for half maximal activation of metabotropic glutamate mGluR3 in rat
ChEMBL 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N 10.1021/jm00009a001
44272391 2315 None 61 Rat Binding pEC50 = 5.5 5.5 -1 18
Concentration for half maximal activation of metabotropic glutamate mGluR3 in ratConcentration for half maximal activation of metabotropic glutamate mGluR3 in rat
ChEMBL 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N 10.1021/jm00009a001
88747398 2315 None 61 Rat Binding pEC50 = 5.5 5.5 -1 18
Concentration for half maximal activation of metabotropic glutamate mGluR3 in ratConcentration for half maximal activation of metabotropic glutamate mGluR3 in rat
ChEMBL 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N 10.1021/jm00009a001
CHEMBL575060 2315 None 61 Rat Binding pEC50 = 5.5 5.5 -1 18
Concentration for half maximal activation of metabotropic glutamate mGluR3 in ratConcentration for half maximal activation of metabotropic glutamate mGluR3 in rat
ChEMBL 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N 10.1021/jm00009a001
DB00142 2315 None 61 Rat Binding pEC50 = 5.5 5.5 -1 18
Concentration for half maximal activation of metabotropic glutamate mGluR3 in ratConcentration for half maximal activation of metabotropic glutamate mGluR3 in rat
ChEMBL 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N 10.1021/jm00009a001
6604704 101455 None 23 Human Binding pEC50 = 4.5 4.5 - 0
Compound was tested for the inhibition of Metabotropic glutamate receptor 3 (mGluR3)Compound was tested for the inhibition of Metabotropic glutamate receptor 3 (mGluR3)
ChEMBL 173 2 3 3 -0.3 N[C@@]1(C(=O)O)CC[C@H](C(=O)O)C1 10.1021/jm970719q
CHEMBL29726 101455 None 23 Human Binding pEC50 = 4.5 4.5 - 0
Compound was tested for the inhibition of Metabotropic glutamate receptor 3 (mGluR3)Compound was tested for the inhibition of Metabotropic glutamate receptor 3 (mGluR3)
ChEMBL 173 2 3 3 -0.3 N[C@@]1(C(=O)O)CC[C@H](C(=O)O)C1 10.1021/jm970719q
164627946 186490 None 0 Rat Binding pEC50 = 6.5 6.5 - 0
Positive allosteric modulator activity at rat mGlu3 receptor transfected in GIRK channel overexpressing cells assessed as potentiation of glutamate-induced response by thallium mobilization assayPositive allosteric modulator activity at rat mGlu3 receptor transfected in GIRK channel overexpressing cells assessed as potentiation of glutamate-induced response by thallium mobilization assay
ChEMBL 428 10 2 5 5.6 Cc1ccc(OCCCCOc2ccc(C(=O)CC(C)(C)C)c(O)c2C)cc1C(=O)O 10.1016/j.bmcl.2021.128342
CHEMBL4875695 186490 None 0 Rat Binding pEC50 = 6.5 6.5 - 0
Positive allosteric modulator activity at rat mGlu3 receptor transfected in GIRK channel overexpressing cells assessed as potentiation of glutamate-induced response by thallium mobilization assayPositive allosteric modulator activity at rat mGlu3 receptor transfected in GIRK channel overexpressing cells assessed as potentiation of glutamate-induced response by thallium mobilization assay
ChEMBL 428 10 2 5 5.6 Cc1ccc(OCCCCOc2ccc(C(=O)CC(C)(C)C)c(O)c2C)cc1C(=O)O 10.1016/j.bmcl.2021.128342
90643888 111958 None 0 Rat Binding pEC50 = 6.5 6.5 - 0
Positive allosteric modulation of rat mGluR3 receptor expressed in HEK293 cells assessed as potentiation of glutamate-induced thallium flux incubated for 2.5 mins prior to glutamate addition measured after 2.5 mins by GIRK assayPositive allosteric modulation of rat mGluR3 receptor expressed in HEK293 cells assessed as potentiation of glutamate-induced thallium flux incubated for 2.5 mins prior to glutamate addition measured after 2.5 mins by GIRK assay
ChEMBL 444 11 2 6 5.3 COc1cc(C(=O)O)ccc1OCCCCOc1ccc(C(=O)CC(C)(C)C)c(O)c1C 10.1021/jm5000563
CHEMBL3287724 111958 None 0 Rat Binding pEC50 = 6.5 6.5 - 0
Positive allosteric modulation of rat mGluR3 receptor expressed in HEK293 cells assessed as potentiation of glutamate-induced thallium flux incubated for 2.5 mins prior to glutamate addition measured after 2.5 mins by GIRK assayPositive allosteric modulation of rat mGluR3 receptor expressed in HEK293 cells assessed as potentiation of glutamate-induced thallium flux incubated for 2.5 mins prior to glutamate addition measured after 2.5 mins by GIRK assay
ChEMBL 444 11 2 6 5.3 COc1cc(C(=O)O)ccc1OCCCCOc1ccc(C(=O)CC(C)(C)C)c(O)c1C 10.1021/jm5000563
1310 2315 None 61 Rat Binding pEC50 = 5.5 5.5 -1 18
Agonist activity at rat mGlu3 receptor by FRET based mGlu sensor assayAgonist activity at rat mGlu3 receptor by FRET based mGlu sensor assay
ChEMBL 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N 10.1021/acs.jmedchem.5b01333
1369 2315 None 61 Rat Binding pEC50 = 5.5 5.5 -1 18
Agonist activity at rat mGlu3 receptor by FRET based mGlu sensor assayAgonist activity at rat mGlu3 receptor by FRET based mGlu sensor assay
ChEMBL 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N 10.1021/acs.jmedchem.5b01333
33032 2315 None 61 Rat Binding pEC50 = 5.5 5.5 -1 18
Agonist activity at rat mGlu3 receptor by FRET based mGlu sensor assayAgonist activity at rat mGlu3 receptor by FRET based mGlu sensor assay
ChEMBL 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N 10.1021/acs.jmedchem.5b01333
44272391 2315 None 61 Rat Binding pEC50 = 5.5 5.5 -1 18
Agonist activity at rat mGlu3 receptor by FRET based mGlu sensor assayAgonist activity at rat mGlu3 receptor by FRET based mGlu sensor assay
ChEMBL 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N 10.1021/acs.jmedchem.5b01333
88747398 2315 None 61 Rat Binding pEC50 = 5.5 5.5 -1 18
Agonist activity at rat mGlu3 receptor by FRET based mGlu sensor assayAgonist activity at rat mGlu3 receptor by FRET based mGlu sensor assay
ChEMBL 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N 10.1021/acs.jmedchem.5b01333
CHEMBL575060 2315 None 61 Rat Binding pEC50 = 5.5 5.5 -1 18
Agonist activity at rat mGlu3 receptor by FRET based mGlu sensor assayAgonist activity at rat mGlu3 receptor by FRET based mGlu sensor assay
ChEMBL 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N 10.1021/acs.jmedchem.5b01333
DB00142 2315 None 61 Rat Binding pEC50 = 5.5 5.5 -1 18
Agonist activity at rat mGlu3 receptor by FRET based mGlu sensor assayAgonist activity at rat mGlu3 receptor by FRET based mGlu sensor assay
ChEMBL 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N 10.1021/acs.jmedchem.5b01333
90643861 111913 None 0 Rat Binding pEC50 = 5.5 5.5 - 0
Positive allosteric modulation of rat mGluR3 receptor expressed in HEK293 cells assessed as potentiation of glutamate-induced thallium flux incubated for 2.5 mins prior to glutamate addition measured after 2.5 mins by GIRK assayPositive allosteric modulation of rat mGluR3 receptor expressed in HEK293 cells assessed as potentiation of glutamate-induced thallium flux incubated for 2.5 mins prior to glutamate addition measured after 2.5 mins by GIRK assay
ChEMBL 426 11 2 5 5.4 Cc1c(OCCCCOc2cccc(C(=O)O)c2)ccc(C(=O)CC2CCCC2)c1O 10.1021/jm5000563
CHEMBL3287676 111913 None 0 Rat Binding pEC50 = 5.5 5.5 - 0
Positive allosteric modulation of rat mGluR3 receptor expressed in HEK293 cells assessed as potentiation of glutamate-induced thallium flux incubated for 2.5 mins prior to glutamate addition measured after 2.5 mins by GIRK assayPositive allosteric modulation of rat mGluR3 receptor expressed in HEK293 cells assessed as potentiation of glutamate-induced thallium flux incubated for 2.5 mins prior to glutamate addition measured after 2.5 mins by GIRK assay
ChEMBL 426 11 2 5 5.4 Cc1c(OCCCCOc2cccc(C(=O)O)c2)ccc(C(=O)CC2CCCC2)c1O 10.1021/jm5000563
164623240 185826 None 0 Rat Binding pEC50 = 5.4 5.4 - 0
Positive allosteric modulator activity at rat mGlu3 receptor transfected in GIRK channel overexpressing cells assessed as potentiation of glutamate-induced response by thallium mobilization assayPositive allosteric modulator activity at rat mGlu3 receptor transfected in GIRK channel overexpressing cells assessed as potentiation of glutamate-induced response by thallium mobilization assay
ChEMBL 430 9 2 6 4.9 COc1ccc(C(=O)O)cc1OC[C@H](C)Oc1ccc(C(=O)CC(C)(C)C)c(O)c1C 10.1016/j.bmcl.2021.128342
CHEMBL4865723 185826 None 0 Rat Binding pEC50 = 5.4 5.4 - 0
Positive allosteric modulator activity at rat mGlu3 receptor transfected in GIRK channel overexpressing cells assessed as potentiation of glutamate-induced response by thallium mobilization assayPositive allosteric modulator activity at rat mGlu3 receptor transfected in GIRK channel overexpressing cells assessed as potentiation of glutamate-induced response by thallium mobilization assay
ChEMBL 430 9 2 6 4.9 COc1ccc(C(=O)O)cc1OC[C@H](C)Oc1ccc(C(=O)CC(C)(C)C)c(O)c1C 10.1016/j.bmcl.2021.128342
164616933 185171 None 0 Rat Binding pEC50 = 6.4 6.4 - 0
Positive allosteric modulator activity at rat mGlu3 receptor transfected in GIRK channel overexpressing cells assessed as potentiation of glutamate-induced response by thallium mobilization assayPositive allosteric modulator activity at rat mGlu3 receptor transfected in GIRK channel overexpressing cells assessed as potentiation of glutamate-induced response by thallium mobilization assay
ChEMBL 444 10 2 6 5.1 COc1ccc(C(=O)O)cc1OC[C@H](C)COc1ccc(C(=O)CC(C)(C)C)c(O)c1C 10.1016/j.bmcl.2021.128342
CHEMBL4855540 185171 None 0 Rat Binding pEC50 = 6.4 6.4 - 0
Positive allosteric modulator activity at rat mGlu3 receptor transfected in GIRK channel overexpressing cells assessed as potentiation of glutamate-induced response by thallium mobilization assayPositive allosteric modulator activity at rat mGlu3 receptor transfected in GIRK channel overexpressing cells assessed as potentiation of glutamate-induced response by thallium mobilization assay
ChEMBL 444 10 2 6 5.1 COc1ccc(C(=O)O)cc1OC[C@H](C)COc1ccc(C(=O)CC(C)(C)C)c(O)c1C 10.1016/j.bmcl.2021.128342
90643876 111933 None 0 Rat Binding pEC50 = 5.4 5.4 - 0
Positive allosteric modulation of rat mGluR3 receptor expressed in HEK293 cells assessed as potentiation of glutamate-induced thallium flux incubated for 2.5 mins prior to glutamate addition measured after 2.5 mins by GIRK assayPositive allosteric modulation of rat mGluR3 receptor expressed in HEK293 cells assessed as potentiation of glutamate-induced thallium flux incubated for 2.5 mins prior to glutamate addition measured after 2.5 mins by GIRK assay
ChEMBL 414 11 2 5 5.2 Cc1cc(OCCCCOc2ccc(C(=O)CC(C)C)c(O)c2C)ccc1C(=O)O 10.1021/jm5000563
CHEMBL3287699 111933 None 0 Rat Binding pEC50 = 5.4 5.4 - 0
Positive allosteric modulation of rat mGluR3 receptor expressed in HEK293 cells assessed as potentiation of glutamate-induced thallium flux incubated for 2.5 mins prior to glutamate addition measured after 2.5 mins by GIRK assayPositive allosteric modulation of rat mGluR3 receptor expressed in HEK293 cells assessed as potentiation of glutamate-induced thallium flux incubated for 2.5 mins prior to glutamate addition measured after 2.5 mins by GIRK assay
ChEMBL 414 11 2 5 5.2 Cc1cc(OCCCCOc2ccc(C(=O)CC(C)C)c(O)c2C)ccc1C(=O)O 10.1021/jm5000563
164624303 186163 None 0 Rat Binding pEC50 = 5.4 5.4 - 0
Positive allosteric modulator activity at rat mGlu3 receptor transfected in GIRK channel overexpressing cells assessed as potentiation of glutamate-induced response by thallium mobilization assayPositive allosteric modulator activity at rat mGlu3 receptor transfected in GIRK channel overexpressing cells assessed as potentiation of glutamate-induced response by thallium mobilization assay
ChEMBL 432 9 2 5 5.3 Cc1c(OC[C@@H](C)COc2cc(C(=O)O)ccc2F)ccc(C(=O)CC(C)(C)C)c1O 10.1016/j.bmcl.2021.128342
CHEMBL4871013 186163 None 0 Rat Binding pEC50 = 5.4 5.4 - 0
Positive allosteric modulator activity at rat mGlu3 receptor transfected in GIRK channel overexpressing cells assessed as potentiation of glutamate-induced response by thallium mobilization assayPositive allosteric modulator activity at rat mGlu3 receptor transfected in GIRK channel overexpressing cells assessed as potentiation of glutamate-induced response by thallium mobilization assay
ChEMBL 432 9 2 5 5.3 Cc1c(OC[C@@H](C)COc2cc(C(=O)O)ccc2F)ccc(C(=O)CC(C)(C)C)c1O 10.1016/j.bmcl.2021.128342
1370 3263 None 42 Rat Binding pEC50 = 4.4 4.4 - 8
Concentration for half maximal activation of metabotropic glutamate mGluR3 in ratConcentration for half maximal activation of metabotropic glutamate mGluR3 in rat
ChEMBL 189 3 3 6 -2.5 OC(=O)[C@H](Cn1oc(=O)[nH]c1=O)N 10.1021/jm00009a001
1372 3263 None 42 Rat Binding pEC50 = 4.4 4.4 - 8
Concentration for half maximal activation of metabotropic glutamate mGluR3 in ratConcentration for half maximal activation of metabotropic glutamate mGluR3 in rat
ChEMBL 189 3 3 6 -2.5 OC(=O)[C@H](Cn1oc(=O)[nH]c1=O)N 10.1021/jm00009a001
40539 3263 None 42 Rat Binding pEC50 = 4.4 4.4 - 8
Concentration for half maximal activation of metabotropic glutamate mGluR3 in ratConcentration for half maximal activation of metabotropic glutamate mGluR3 in rat
ChEMBL 189 3 3 6 -2.5 OC(=O)[C@H](Cn1oc(=O)[nH]c1=O)N 10.1021/jm00009a001
6971145 3263 None 42 Rat Binding pEC50 = 4.4 4.4 - 8
Concentration for half maximal activation of metabotropic glutamate mGluR3 in ratConcentration for half maximal activation of metabotropic glutamate mGluR3 in rat
ChEMBL 189 3 3 6 -2.5 OC(=O)[C@H](Cn1oc(=O)[nH]c1=O)N 10.1021/jm00009a001
CHEMBL279956 3263 None 42 Rat Binding pEC50 = 4.4 4.4 - 8
Concentration for half maximal activation of metabotropic glutamate mGluR3 in ratConcentration for half maximal activation of metabotropic glutamate mGluR3 in rat
ChEMBL 189 3 3 6 -2.5 OC(=O)[C@H](Cn1oc(=O)[nH]c1=O)N 10.1021/jm00009a001
DB02999 3263 None 42 Rat Binding pEC50 = 4.4 4.4 - 8
Concentration for half maximal activation of metabotropic glutamate mGluR3 in ratConcentration for half maximal activation of metabotropic glutamate mGluR3 in rat
ChEMBL 189 3 3 6 -2.5 OC(=O)[C@H](Cn1oc(=O)[nH]c1=O)N 10.1021/jm00009a001
90643886 111955 None 0 Rat Binding pEC50 = 6.4 6.4 - 0
Positive allosteric modulation of rat mGluR3 receptor expressed in HEK293 cells assessed as potentiation of glutamate-induced thallium flux incubated for 2.5 mins prior to glutamate addition measured after 2.5 mins by GIRK assayPositive allosteric modulation of rat mGluR3 receptor expressed in HEK293 cells assessed as potentiation of glutamate-induced thallium flux incubated for 2.5 mins prior to glutamate addition measured after 2.5 mins by GIRK assay
ChEMBL 404 11 2 5 4.8 CCCC(=O)c1ccc(OCCCCOc2ccc(F)c(C(=O)O)c2)c(C)c1O 10.1021/jm5000563
CHEMBL3287721 111955 None 0 Rat Binding pEC50 = 6.4 6.4 - 0
Positive allosteric modulation of rat mGluR3 receptor expressed in HEK293 cells assessed as potentiation of glutamate-induced thallium flux incubated for 2.5 mins prior to glutamate addition measured after 2.5 mins by GIRK assayPositive allosteric modulation of rat mGluR3 receptor expressed in HEK293 cells assessed as potentiation of glutamate-induced thallium flux incubated for 2.5 mins prior to glutamate addition measured after 2.5 mins by GIRK assay
ChEMBL 404 11 2 5 4.8 CCCC(=O)c1ccc(OCCCCOc2ccc(F)c(C(=O)O)c2)c(C)c1O 10.1021/jm5000563
164616255 185054 None 0 Rat Binding pEC50 = 6.3 6.3 - 0
Positive allosteric modulator activity at rat mGlu3 receptor transfected in GIRK channel overexpressing cells assessed as potentiation of glutamate-induced response by thallium mobilization assayPositive allosteric modulator activity at rat mGlu3 receptor transfected in GIRK channel overexpressing cells assessed as potentiation of glutamate-induced response by thallium mobilization assay
ChEMBL 445 10 2 5 5.1 CNC(=O)c1cc(OCCCCOc2ccc(C(=O)CC(C)(C)C)c(O)c2C)ccc1F 10.1016/j.bmcl.2021.128342
CHEMBL4853748 185054 None 0 Rat Binding pEC50 = 6.3 6.3 - 0
Positive allosteric modulator activity at rat mGlu3 receptor transfected in GIRK channel overexpressing cells assessed as potentiation of glutamate-induced response by thallium mobilization assayPositive allosteric modulator activity at rat mGlu3 receptor transfected in GIRK channel overexpressing cells assessed as potentiation of glutamate-induced response by thallium mobilization assay
ChEMBL 445 10 2 5 5.1 CNC(=O)c1cc(OCCCCOc2ccc(C(=O)CC(C)(C)C)c(O)c2C)ccc1F 10.1016/j.bmcl.2021.128342
164608826 184573 None 0 Rat Binding pEC50 = 6.3 6.3 - 0
Positive allosteric modulator activity at rat mGlu3 receptor transfected in GIRK channel overexpressing cells assessed as potentiation of glutamate-induced response by thallium mobilization assayPositive allosteric modulator activity at rat mGlu3 receptor transfected in GIRK channel overexpressing cells assessed as potentiation of glutamate-induced response by thallium mobilization assay
ChEMBL 444 11 2 6 5.3 COc1ccc(OCCCCOc2ccc(C(=O)CC(C)(C)C)c(O)c2C)cc1C(=O)O 10.1016/j.bmcl.2021.128342
CHEMBL4846872 184573 None 0 Rat Binding pEC50 = 6.3 6.3 - 0
Positive allosteric modulator activity at rat mGlu3 receptor transfected in GIRK channel overexpressing cells assessed as potentiation of glutamate-induced response by thallium mobilization assayPositive allosteric modulator activity at rat mGlu3 receptor transfected in GIRK channel overexpressing cells assessed as potentiation of glutamate-induced response by thallium mobilization assay
ChEMBL 444 11 2 6 5.3 COc1ccc(OCCCCOc2ccc(C(=O)CC(C)(C)C)c(O)c2C)cc1C(=O)O 10.1016/j.bmcl.2021.128342
90643884 111953 None 0 Rat Binding pEC50 = 6.3 6.3 - 0
Positive allosteric modulation of rat mGluR3 receptor expressed in HEK293 cells assessed as potentiation of glutamate-induced thallium flux incubated for 2.5 mins prior to glutamate addition measured after 2.5 mins by GIRK assayPositive allosteric modulation of rat mGluR3 receptor expressed in HEK293 cells assessed as potentiation of glutamate-induced thallium flux incubated for 2.5 mins prior to glutamate addition measured after 2.5 mins by GIRK assay
ChEMBL 416 12 2 6 4.6 CCCC(=O)c1ccc(OCCCCOc2cc(C(=O)O)ccc2OC)c(C)c1O 10.1021/jm5000563
CHEMBL3287719 111953 None 0 Rat Binding pEC50 = 6.3 6.3 - 0
Positive allosteric modulation of rat mGluR3 receptor expressed in HEK293 cells assessed as potentiation of glutamate-induced thallium flux incubated for 2.5 mins prior to glutamate addition measured after 2.5 mins by GIRK assayPositive allosteric modulation of rat mGluR3 receptor expressed in HEK293 cells assessed as potentiation of glutamate-induced thallium flux incubated for 2.5 mins prior to glutamate addition measured after 2.5 mins by GIRK assay
ChEMBL 416 12 2 6 4.6 CCCC(=O)c1ccc(OCCCCOc2cc(C(=O)O)ccc2OC)c(C)c1O 10.1021/jm5000563
164611777 185031 None 0 Rat Binding pEC50 = 6.3 6.3 - 0
Positive allosteric modulator activity at rat mGlu3 receptor transfected in GIRK channel overexpressing cells assessed as potentiation of glutamate-induced response by thallium mobilization assayPositive allosteric modulator activity at rat mGlu3 receptor transfected in GIRK channel overexpressing cells assessed as potentiation of glutamate-induced response by thallium mobilization assay
ChEMBL 444 10 2 6 5.1 COc1cc(C(=O)O)ccc1OC[C@H](C)COc1ccc(C(=O)CC(C)(C)C)c(O)c1C 10.1016/j.bmcl.2021.128342
CHEMBL4853369 185031 None 0 Rat Binding pEC50 = 6.3 6.3 - 0
Positive allosteric modulator activity at rat mGlu3 receptor transfected in GIRK channel overexpressing cells assessed as potentiation of glutamate-induced response by thallium mobilization assayPositive allosteric modulator activity at rat mGlu3 receptor transfected in GIRK channel overexpressing cells assessed as potentiation of glutamate-induced response by thallium mobilization assay
ChEMBL 444 10 2 6 5.1 COc1cc(C(=O)O)ccc1OC[C@H](C)COc1ccc(C(=O)CC(C)(C)C)c(O)c1C 10.1016/j.bmcl.2021.128342
71681824 90090 None 0 Human Binding pEC50 = 7.2 7.2 - 0
Agonist activity at human mGlu3 receptor expressed in golden Syrian hamster AV12 cells coexpressing EAAT1 after 20 mins by HTRF assayAgonist activity at human mGlu3 receptor expressed in golden Syrian hamster AV12 cells coexpressing EAAT1 after 20 mins by HTRF assay
ChEMBL 200 2 4 4 -1.6 N[C@@H]1C[C@@](N)(C(=O)O)[C@@H]2[C@@H](C(=O)O)[C@@H]21 10.1021/jm4000165
CHEMBL2381646 90090 None 0 Human Binding pEC50 = 7.2 7.2 - 0
Agonist activity at human mGlu3 receptor expressed in golden Syrian hamster AV12 cells coexpressing EAAT1 after 20 mins by HTRF assayAgonist activity at human mGlu3 receptor expressed in golden Syrian hamster AV12 cells coexpressing EAAT1 after 20 mins by HTRF assay
ChEMBL 200 2 4 4 -1.6 N[C@@H]1C[C@@](N)(C(=O)O)[C@@H]2[C@@H](C(=O)O)[C@@H]21 10.1021/jm4000165
1310 2315 None 61 Rat Binding pEC50 = 7.2 7.2 -1 18
Agonist activity at rat mGlu3 receptor expressed in HEK293 cells by [35S]GTP-gamma binding assayAgonist activity at rat mGlu3 receptor expressed in HEK293 cells by [35S]GTP-gamma binding assay
ChEMBL 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N 10.1021/acs.jmedchem.5b01333
1369 2315 None 61 Rat Binding pEC50 = 7.2 7.2 -1 18
Agonist activity at rat mGlu3 receptor expressed in HEK293 cells by [35S]GTP-gamma binding assayAgonist activity at rat mGlu3 receptor expressed in HEK293 cells by [35S]GTP-gamma binding assay
ChEMBL 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N 10.1021/acs.jmedchem.5b01333
33032 2315 None 61 Rat Binding pEC50 = 7.2 7.2 -1 18
Agonist activity at rat mGlu3 receptor expressed in HEK293 cells by [35S]GTP-gamma binding assayAgonist activity at rat mGlu3 receptor expressed in HEK293 cells by [35S]GTP-gamma binding assay
ChEMBL 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N 10.1021/acs.jmedchem.5b01333
44272391 2315 None 61 Rat Binding pEC50 = 7.2 7.2 -1 18
Agonist activity at rat mGlu3 receptor expressed in HEK293 cells by [35S]GTP-gamma binding assayAgonist activity at rat mGlu3 receptor expressed in HEK293 cells by [35S]GTP-gamma binding assay
ChEMBL 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N 10.1021/acs.jmedchem.5b01333
88747398 2315 None 61 Rat Binding pEC50 = 7.2 7.2 -1 18
Agonist activity at rat mGlu3 receptor expressed in HEK293 cells by [35S]GTP-gamma binding assayAgonist activity at rat mGlu3 receptor expressed in HEK293 cells by [35S]GTP-gamma binding assay
ChEMBL 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N 10.1021/acs.jmedchem.5b01333
CHEMBL575060 2315 None 61 Rat Binding pEC50 = 7.2 7.2 -1 18
Agonist activity at rat mGlu3 receptor expressed in HEK293 cells by [35S]GTP-gamma binding assayAgonist activity at rat mGlu3 receptor expressed in HEK293 cells by [35S]GTP-gamma binding assay
ChEMBL 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N 10.1021/acs.jmedchem.5b01333
DB00142 2315 None 61 Rat Binding pEC50 = 7.2 7.2 -1 18
Agonist activity at rat mGlu3 receptor expressed in HEK293 cells by [35S]GTP-gamma binding assayAgonist activity at rat mGlu3 receptor expressed in HEK293 cells by [35S]GTP-gamma binding assay
ChEMBL 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N 10.1021/acs.jmedchem.5b01333
90643881 111948 None 0 Rat Binding pEC50 = 6.2 6.2 - 0
Positive allosteric modulation of rat mGluR3 receptor expressed in HEK293 cells assessed as potentiation of glutamate-induced thallium flux incubated for 2.5 mins prior to glutamate addition measured after 2.5 mins by GIRK assayPositive allosteric modulation of rat mGluR3 receptor expressed in HEK293 cells assessed as potentiation of glutamate-induced thallium flux incubated for 2.5 mins prior to glutamate addition measured after 2.5 mins by GIRK assay
ChEMBL 416 11 2 6 4.5 COc1ccc(C(=O)O)cc1OCCCCOc1ccc(C(=O)C(C)C)c(O)c1C 10.1021/jm5000563
CHEMBL3287714 111948 None 0 Rat Binding pEC50 = 6.2 6.2 - 0
Positive allosteric modulation of rat mGluR3 receptor expressed in HEK293 cells assessed as potentiation of glutamate-induced thallium flux incubated for 2.5 mins prior to glutamate addition measured after 2.5 mins by GIRK assayPositive allosteric modulation of rat mGluR3 receptor expressed in HEK293 cells assessed as potentiation of glutamate-induced thallium flux incubated for 2.5 mins prior to glutamate addition measured after 2.5 mins by GIRK assay
ChEMBL 416 11 2 6 4.5 COc1ccc(C(=O)O)cc1OCCCCOc1ccc(C(=O)C(C)C)c(O)c1C 10.1021/jm5000563
11084869 90087 None 1 Human Binding pEC50 = 8.2 8.2 - 1
Agonist activity at human mGlu3 receptor expressed in golden Syrian hamster AV12 cells coexpressing EAAT1 after 20 mins by HTRF assayAgonist activity at human mGlu3 receptor expressed in golden Syrian hamster AV12 cells coexpressing EAAT1 after 20 mins by HTRF assay
ChEMBL 201 2 4 4 -1.5 N[C@@]1(C(=O)O)C[C@H](O)[C@@H]2[C@H]1[C@H]2C(=O)O 10.1021/jm4000165
CHEMBL2381643 90087 None 1 Human Binding pEC50 = 8.2 8.2 - 1
Agonist activity at human mGlu3 receptor expressed in golden Syrian hamster AV12 cells coexpressing EAAT1 after 20 mins by HTRF assayAgonist activity at human mGlu3 receptor expressed in golden Syrian hamster AV12 cells coexpressing EAAT1 after 20 mins by HTRF assay
ChEMBL 201 2 4 4 -1.5 N[C@@]1(C(=O)O)C[C@H](O)[C@@H]2[C@H]1[C@H]2C(=O)O 10.1021/jm4000165
1310 2315 None 61 Human Binding pEC50 = 7.2 7.2 1 18
Agonist activity at human mGluR3 receptor expressed in HEK cellsAgonist activity at human mGluR3 receptor expressed in HEK cells
ChEMBL 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N 10.1039/C1MD00186H
1369 2315 None 61 Human Binding pEC50 = 7.2 7.2 1 18
Agonist activity at human mGluR3 receptor expressed in HEK cellsAgonist activity at human mGluR3 receptor expressed in HEK cells
ChEMBL 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N 10.1039/C1MD00186H
33032 2315 None 61 Human Binding pEC50 = 7.2 7.2 1 18
Agonist activity at human mGluR3 receptor expressed in HEK cellsAgonist activity at human mGluR3 receptor expressed in HEK cells
ChEMBL 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N 10.1039/C1MD00186H
44272391 2315 None 61 Human Binding pEC50 = 7.2 7.2 1 18
Agonist activity at human mGluR3 receptor expressed in HEK cellsAgonist activity at human mGluR3 receptor expressed in HEK cells
ChEMBL 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N 10.1039/C1MD00186H
88747398 2315 None 61 Human Binding pEC50 = 7.2 7.2 1 18
Agonist activity at human mGluR3 receptor expressed in HEK cellsAgonist activity at human mGluR3 receptor expressed in HEK cells
ChEMBL 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N 10.1039/C1MD00186H
CHEMBL575060 2315 None 61 Human Binding pEC50 = 7.2 7.2 1 18
Agonist activity at human mGluR3 receptor expressed in HEK cellsAgonist activity at human mGluR3 receptor expressed in HEK cells
ChEMBL 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N 10.1039/C1MD00186H
DB00142 2315 None 61 Human Binding pEC50 = 7.2 7.2 1 18
Agonist activity at human mGluR3 receptor expressed in HEK cellsAgonist activity at human mGluR3 receptor expressed in HEK cells
ChEMBL 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N 10.1039/C1MD00186H
1310 2315 None 61 Rat Binding pEC50 = 7.2 7.2 -1 18
Agonist activity at rat mGlu3 receptor expressed in HEK293 cells by [35S]GTP-gamma binding assayAgonist activity at rat mGlu3 receptor expressed in HEK293 cells by [35S]GTP-gamma binding assay
ChEMBL 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N 10.1021/acs.jmedchem.5b01333
1369 2315 None 61 Rat Binding pEC50 = 7.2 7.2 -1 18
Agonist activity at rat mGlu3 receptor expressed in HEK293 cells by [35S]GTP-gamma binding assayAgonist activity at rat mGlu3 receptor expressed in HEK293 cells by [35S]GTP-gamma binding assay
ChEMBL 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N 10.1021/acs.jmedchem.5b01333
33032 2315 None 61 Rat Binding pEC50 = 7.2 7.2 -1 18
Agonist activity at rat mGlu3 receptor expressed in HEK293 cells by [35S]GTP-gamma binding assayAgonist activity at rat mGlu3 receptor expressed in HEK293 cells by [35S]GTP-gamma binding assay
ChEMBL 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N 10.1021/acs.jmedchem.5b01333
44272391 2315 None 61 Rat Binding pEC50 = 7.2 7.2 -1 18
Agonist activity at rat mGlu3 receptor expressed in HEK293 cells by [35S]GTP-gamma binding assayAgonist activity at rat mGlu3 receptor expressed in HEK293 cells by [35S]GTP-gamma binding assay
ChEMBL 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N 10.1021/acs.jmedchem.5b01333
88747398 2315 None 61 Rat Binding pEC50 = 7.2 7.2 -1 18
Agonist activity at rat mGlu3 receptor expressed in HEK293 cells by [35S]GTP-gamma binding assayAgonist activity at rat mGlu3 receptor expressed in HEK293 cells by [35S]GTP-gamma binding assay
ChEMBL 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N 10.1021/acs.jmedchem.5b01333
CHEMBL575060 2315 None 61 Rat Binding pEC50 = 7.2 7.2 -1 18
Agonist activity at rat mGlu3 receptor expressed in HEK293 cells by [35S]GTP-gamma binding assayAgonist activity at rat mGlu3 receptor expressed in HEK293 cells by [35S]GTP-gamma binding assay
ChEMBL 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N 10.1021/acs.jmedchem.5b01333
DB00142 2315 None 61 Rat Binding pEC50 = 7.2 7.2 -1 18
Agonist activity at rat mGlu3 receptor expressed in HEK293 cells by [35S]GTP-gamma binding assayAgonist activity at rat mGlu3 receptor expressed in HEK293 cells by [35S]GTP-gamma binding assay
ChEMBL 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N 10.1021/acs.jmedchem.5b01333
90643858 111929 None 0 Rat Binding pEC50 = 6.2 6.2 - 0
Positive allosteric modulation of rat mGluR3 receptor expressed in HEK293 cells assessed as potentiation of glutamate-induced thallium flux incubated for 2.5 mins prior to glutamate addition measured after 2.5 mins by GIRK assayPositive allosteric modulation of rat mGluR3 receptor expressed in HEK293 cells assessed as potentiation of glutamate-induced thallium flux incubated for 2.5 mins prior to glutamate addition measured after 2.5 mins by GIRK assay
ChEMBL 430 12 2 6 4.9 COc1cc(C(=O)O)ccc1OCCCCOc1ccc(C(=O)CC(C)C)c(O)c1C 10.1021/jm5000563
CHEMBL3287695 111929 None 0 Rat Binding pEC50 = 6.2 6.2 - 0
Positive allosteric modulation of rat mGluR3 receptor expressed in HEK293 cells assessed as potentiation of glutamate-induced thallium flux incubated for 2.5 mins prior to glutamate addition measured after 2.5 mins by GIRK assayPositive allosteric modulation of rat mGluR3 receptor expressed in HEK293 cells assessed as potentiation of glutamate-induced thallium flux incubated for 2.5 mins prior to glutamate addition measured after 2.5 mins by GIRK assay
ChEMBL 430 12 2 6 4.9 COc1cc(C(=O)O)ccc1OCCCCOc1ccc(C(=O)CC(C)C)c(O)c1C 10.1021/jm5000563
90643880 111943 None 0 Rat Binding pEC50 = 5.2 5.2 - 0
Positive allosteric modulation of rat mGluR3 receptor expressed in HEK293 cells assessed as potentiation of glutamate-induced thallium flux incubated for 2.5 mins prior to glutamate addition measured after 2.5 mins by GIRK assayPositive allosteric modulation of rat mGluR3 receptor expressed in HEK293 cells assessed as potentiation of glutamate-induced thallium flux incubated for 2.5 mins prior to glutamate addition measured after 2.5 mins by GIRK assay
ChEMBL 402 11 2 6 4.2 CCC(=O)c1ccc(OCCCCOc2cc(C(=O)O)ccc2OC)c(C)c1O 10.1021/jm5000563
CHEMBL3287709 111943 None 0 Rat Binding pEC50 = 5.2 5.2 - 0
Positive allosteric modulation of rat mGluR3 receptor expressed in HEK293 cells assessed as potentiation of glutamate-induced thallium flux incubated for 2.5 mins prior to glutamate addition measured after 2.5 mins by GIRK assayPositive allosteric modulation of rat mGluR3 receptor expressed in HEK293 cells assessed as potentiation of glutamate-induced thallium flux incubated for 2.5 mins prior to glutamate addition measured after 2.5 mins by GIRK assay
ChEMBL 402 11 2 6 4.2 CCC(=O)c1ccc(OCCCCOc2cc(C(=O)O)ccc2OC)c(C)c1O 10.1021/jm5000563
164624801 186317 None 0 Rat Binding pEC50 = 6.2 6.2 - 0
Positive allosteric modulator activity at rat mGlu3 receptor transfected in GIRK channel overexpressing cells assessed as potentiation of glutamate-induced response by thallium mobilization assayPositive allosteric modulator activity at rat mGlu3 receptor transfected in GIRK channel overexpressing cells assessed as potentiation of glutamate-induced response by thallium mobilization assay
ChEMBL 432 9 2 5 5.3 Cc1c(OC[C@H](C)COc2ccc(F)c(C(=O)O)c2)ccc(C(=O)CC(C)(C)C)c1O 10.1016/j.bmcl.2021.128342
CHEMBL4873125 186317 None 0 Rat Binding pEC50 = 6.2 6.2 - 0
Positive allosteric modulator activity at rat mGlu3 receptor transfected in GIRK channel overexpressing cells assessed as potentiation of glutamate-induced response by thallium mobilization assayPositive allosteric modulator activity at rat mGlu3 receptor transfected in GIRK channel overexpressing cells assessed as potentiation of glutamate-induced response by thallium mobilization assay
ChEMBL 432 9 2 5 5.3 Cc1c(OC[C@H](C)COc2ccc(F)c(C(=O)O)c2)ccc(C(=O)CC(C)(C)C)c1O 10.1016/j.bmcl.2021.128342
164617451 185058 None 0 Rat Binding pEC50 = 6.2 6.2 - 0
Positive allosteric modulator activity at rat mGlu3 receptor transfected in GIRK channel overexpressing cells assessed as potentiation of glutamate-induced response by thallium mobilization assayPositive allosteric modulator activity at rat mGlu3 receptor transfected in GIRK channel overexpressing cells assessed as potentiation of glutamate-induced response by thallium mobilization assay
ChEMBL 444 11 2 6 5.3 COc1cc(OCCCCOc2ccc(C(=O)CC(C)(C)C)c(O)c2C)cc(C(=O)O)c1 10.1016/j.bmcl.2021.128342
CHEMBL4853794 185058 None 0 Rat Binding pEC50 = 6.2 6.2 - 0
Positive allosteric modulator activity at rat mGlu3 receptor transfected in GIRK channel overexpressing cells assessed as potentiation of glutamate-induced response by thallium mobilization assayPositive allosteric modulator activity at rat mGlu3 receptor transfected in GIRK channel overexpressing cells assessed as potentiation of glutamate-induced response by thallium mobilization assay
ChEMBL 444 11 2 6 5.3 COc1cc(OCCCCOc2ccc(C(=O)CC(C)(C)C)c(O)c2C)cc(C(=O)O)c1 10.1016/j.bmcl.2021.128342
90643878 111935 None 0 Rat Binding pEC50 = 6.1 6.1 - 0
Positive allosteric modulation of rat mGluR3 receptor expressed in HEK293 cells assessed as potentiation of glutamate-induced thallium flux incubated for 2.5 mins prior to glutamate addition measured after 2.5 mins by GIRK assayPositive allosteric modulation of rat mGluR3 receptor expressed in HEK293 cells assessed as potentiation of glutamate-induced thallium flux incubated for 2.5 mins prior to glutamate addition measured after 2.5 mins by GIRK assay
ChEMBL 430 12 2 6 4.9 COc1ccc(C(=O)O)cc1OCCCCOc1ccc(C(=O)CC(C)C)c(O)c1C 10.1021/jm5000563
CHEMBL3287701 111935 None 0 Rat Binding pEC50 = 6.1 6.1 - 0
Positive allosteric modulation of rat mGluR3 receptor expressed in HEK293 cells assessed as potentiation of glutamate-induced thallium flux incubated for 2.5 mins prior to glutamate addition measured after 2.5 mins by GIRK assayPositive allosteric modulation of rat mGluR3 receptor expressed in HEK293 cells assessed as potentiation of glutamate-induced thallium flux incubated for 2.5 mins prior to glutamate addition measured after 2.5 mins by GIRK assay
ChEMBL 430 12 2 6 4.9 COc1ccc(C(=O)O)cc1OCCCCOc1ccc(C(=O)CC(C)C)c(O)c1C 10.1021/jm5000563
164621310 185671 None 0 Rat Binding pEC50 = 7.1 7.1 - 0
Positive allosteric modulator activity at rat mGlu3 receptor transfected in GIRK channel overexpressing cells assessed as potentiation of glutamate-induced response by thallium mobilization assayPositive allosteric modulator activity at rat mGlu3 receptor transfected in GIRK channel overexpressing cells assessed as potentiation of glutamate-induced response by thallium mobilization assay
ChEMBL 429 10 2 6 5.0 Cc1ncc(OCCCCOc2ccc(C(=O)CC(C)(C)C)c(O)c2C)cc1C(=O)O 10.1016/j.bmcl.2021.128342
CHEMBL4863303 185671 None 0 Rat Binding pEC50 = 7.1 7.1 - 0
Positive allosteric modulator activity at rat mGlu3 receptor transfected in GIRK channel overexpressing cells assessed as potentiation of glutamate-induced response by thallium mobilization assayPositive allosteric modulator activity at rat mGlu3 receptor transfected in GIRK channel overexpressing cells assessed as potentiation of glutamate-induced response by thallium mobilization assay
ChEMBL 429 10 2 6 5.0 Cc1ncc(OCCCCOc2ccc(C(=O)CC(C)(C)C)c(O)c2C)cc1C(=O)O 10.1016/j.bmcl.2021.128342
1377 1340 None 23 Rat Binding pEC50 = 7.1 7.1 -2 6
Agonist activity at rat mGlu3 receptor by FRET based mGlu sensor assayAgonist activity at rat mGlu3 receptor by FRET based mGlu sensor assay
ChEMBL 203 4 4 4 -1.6 N[C@@H](C1[C@H]([C@@H]1C(=O)O)C(=O)O)C(=O)O 10.1021/acs.jmedchem.5b01333
5310979 1340 None 23 Rat Binding pEC50 = 7.1 7.1 -2 6
Agonist activity at rat mGlu3 receptor by FRET based mGlu sensor assayAgonist activity at rat mGlu3 receptor by FRET based mGlu sensor assay
ChEMBL 203 4 4 4 -1.6 N[C@@H](C1[C@H]([C@@H]1C(=O)O)C(=O)O)C(=O)O 10.1021/acs.jmedchem.5b01333
CHEMBL284193 1340 None 23 Rat Binding pEC50 = 7.1 7.1 -2 6
Agonist activity at rat mGlu3 receptor by FRET based mGlu sensor assayAgonist activity at rat mGlu3 receptor by FRET based mGlu sensor assay
ChEMBL 203 4 4 4 -1.6 N[C@@H](C1[C@H]([C@@H]1C(=O)O)C(=O)O)C(=O)O 10.1021/acs.jmedchem.5b01333
104766 33 None 30 Rat Binding pEC50 = 5.1 5.1 -10 11
Concentration for half maximal activation of metabotropic glutamate mGluR3 in ratConcentration for half maximal activation of metabotropic glutamate mGluR3 in rat
ChEMBL 173 2 3 3 -0.3 OC(=O)[C@@H]1CC[C@@](C1)(N)C(=O)O 10.1021/jm00009a001
1365 33 None 30 Rat Binding pEC50 = 5.1 5.1 -10 11
Concentration for half maximal activation of metabotropic glutamate mGluR3 in ratConcentration for half maximal activation of metabotropic glutamate mGluR3 in rat
ChEMBL 173 2 3 3 -0.3 OC(=O)[C@@H]1CC[C@@](C1)(N)C(=O)O 10.1021/jm00009a001
CHEMBL34453 33 None 30 Rat Binding pEC50 = 5.1 5.1 -10 11
Concentration for half maximal activation of metabotropic glutamate mGluR3 in ratConcentration for half maximal activation of metabotropic glutamate mGluR3 in rat
ChEMBL 173 2 3 3 -0.3 OC(=O)[C@@H]1CC[C@@](C1)(N)C(=O)O 10.1021/jm00009a001
164616491 185497 None 0 Rat Binding pEC50 = 6.1 6.1 - 0
Positive allosteric modulator activity at rat mGlu3 receptor transfected in GIRK channel overexpressing cells assessed as potentiation of glutamate-induced response by thallium mobilization assayPositive allosteric modulator activity at rat mGlu3 receptor transfected in GIRK channel overexpressing cells assessed as potentiation of glutamate-induced response by thallium mobilization assay
ChEMBL 430 9 2 6 4.9 COc1ccc(C(=O)O)cc1OC[C@@H](C)Oc1ccc(C(=O)CC(C)(C)C)c(O)c1C 10.1016/j.bmcl.2021.128342
CHEMBL4860693 185497 None 0 Rat Binding pEC50 = 6.1 6.1 - 0
Positive allosteric modulator activity at rat mGlu3 receptor transfected in GIRK channel overexpressing cells assessed as potentiation of glutamate-induced response by thallium mobilization assayPositive allosteric modulator activity at rat mGlu3 receptor transfected in GIRK channel overexpressing cells assessed as potentiation of glutamate-induced response by thallium mobilization assay
ChEMBL 430 9 2 6 4.9 COc1ccc(C(=O)O)cc1OC[C@@H](C)Oc1ccc(C(=O)CC(C)(C)C)c(O)c1C 10.1016/j.bmcl.2021.128342
164620553 185875 None 0 Rat Binding pEC50 = 6.1 6.1 - 0
Positive allosteric modulator activity at rat mGlu3 receptor transfected in GIRK channel overexpressing cells assessed as potentiation of glutamate-induced response by thallium mobilization assayPositive allosteric modulator activity at rat mGlu3 receptor transfected in GIRK channel overexpressing cells assessed as potentiation of glutamate-induced response by thallium mobilization assay
ChEMBL 448 9 2 5 5.8 Cc1c(OC[C@@H](C)COc2ccc(C(=O)O)c(Cl)c2)ccc(C(=O)CC(C)(C)C)c1O 10.1016/j.bmcl.2021.128342
CHEMBL4866466 185875 None 0 Rat Binding pEC50 = 6.1 6.1 - 0
Positive allosteric modulator activity at rat mGlu3 receptor transfected in GIRK channel overexpressing cells assessed as potentiation of glutamate-induced response by thallium mobilization assayPositive allosteric modulator activity at rat mGlu3 receptor transfected in GIRK channel overexpressing cells assessed as potentiation of glutamate-induced response by thallium mobilization assay
ChEMBL 448 9 2 5 5.8 Cc1c(OC[C@@H](C)COc2ccc(C(=O)O)c(Cl)c2)ccc(C(=O)CC(C)(C)C)c1O 10.1016/j.bmcl.2021.128342
164625596 185848 None 0 Rat Binding pEC50 = 6.1 6.1 - 0
Positive allosteric modulator activity at rat mGlu3 receptor transfected in GIRK channel overexpressing cells assessed as potentiation of glutamate-induced response by thallium mobilization assayPositive allosteric modulator activity at rat mGlu3 receptor transfected in GIRK channel overexpressing cells assessed as potentiation of glutamate-induced response by thallium mobilization assay
ChEMBL 428 10 2 5 5.6 Cc1ccc(C(=O)O)cc1OCCCCOc1ccc(C(=O)CC(C)(C)C)c(O)c1C 10.1016/j.bmcl.2021.128342
CHEMBL4866163 185848 None 0 Rat Binding pEC50 = 6.1 6.1 - 0
Positive allosteric modulator activity at rat mGlu3 receptor transfected in GIRK channel overexpressing cells assessed as potentiation of glutamate-induced response by thallium mobilization assayPositive allosteric modulator activity at rat mGlu3 receptor transfected in GIRK channel overexpressing cells assessed as potentiation of glutamate-induced response by thallium mobilization assay
ChEMBL 428 10 2 5 5.6 Cc1ccc(C(=O)O)cc1OCCCCOc1ccc(C(=O)CC(C)(C)C)c(O)c1C 10.1016/j.bmcl.2021.128342
139054390 207381 None 56 Rat Binding pEC50 = 5.1 5.1 - 5
Effect on Metabotropic glutamate receptor 3Effect on Metabotropic glutamate receptor 3
ChEMBL 147 4 3 3 -0.7 N[C@H](CCC(=O)O)C(=O)O 10.1021/jm9703597
23327 207381 None 56 Rat Binding pEC50 = 5.1 5.1 - 5
Effect on Metabotropic glutamate receptor 3Effect on Metabotropic glutamate receptor 3
ChEMBL 147 4 3 3 -0.7 N[C@H](CCC(=O)O)C(=O)O 10.1021/jm9703597
CHEMBL76232 207381 None 56 Rat Binding pEC50 = 5.1 5.1 - 5
Effect on Metabotropic glutamate receptor 3Effect on Metabotropic glutamate receptor 3
ChEMBL 147 4 3 3 -0.7 N[C@H](CCC(=O)O)C(=O)O 10.1021/jm9703597
90643865 111921 None 0 Rat Binding pEC50 = 6.0 6.0 - 0
Positive allosteric modulation of rat mGluR3 receptor expressed in HEK293 cells assessed as potentiation of glutamate-induced thallium flux incubated for 2.5 mins prior to glutamate addition measured after 2.5 mins by GIRK assayPositive allosteric modulation of rat mGluR3 receptor expressed in HEK293 cells assessed as potentiation of glutamate-induced thallium flux incubated for 2.5 mins prior to glutamate addition measured after 2.5 mins by GIRK assay
ChEMBL 418 11 2 5 5.0 Cc1c(OCCCCOc2ccc(F)c(C(=O)O)c2)ccc(C(=O)CC(C)C)c1O 10.1021/jm5000563
CHEMBL3287687 111921 None 0 Rat Binding pEC50 = 6.0 6.0 - 0
Positive allosteric modulation of rat mGluR3 receptor expressed in HEK293 cells assessed as potentiation of glutamate-induced thallium flux incubated for 2.5 mins prior to glutamate addition measured after 2.5 mins by GIRK assayPositive allosteric modulation of rat mGluR3 receptor expressed in HEK293 cells assessed as potentiation of glutamate-induced thallium flux incubated for 2.5 mins prior to glutamate addition measured after 2.5 mins by GIRK assay
ChEMBL 418 11 2 5 5.0 Cc1c(OCCCCOc2ccc(F)c(C(=O)O)c2)ccc(C(=O)CC(C)C)c1O 10.1021/jm5000563
70052526 90086 None 1 Human Binding pIC50 = 8.0 8.0 - 1
Agonist activity at mGlu3 (unknown origin)Agonist activity at mGlu3 (unknown origin)
ChEMBL 201 2 4 4 -1.5 N[C@@]1(C(=O)O)C[C@@H](O)[C@@H]2[C@H]1[C@H]2C(=O)O 10.1021/acs.jmedchem.6b01119
CHEMBL2381642 90086 None 1 Human Binding pIC50 = 8.0 8.0 - 1
Agonist activity at mGlu3 (unknown origin)Agonist activity at mGlu3 (unknown origin)
ChEMBL 201 2 4 4 -1.5 N[C@@]1(C(=O)O)C[C@@H](O)[C@@H]2[C@H]1[C@H]2C(=O)O 10.1021/acs.jmedchem.6b01119
145949267 162912 None 11 Rat Binding pIC50 = 5.9 5.9 - 0
Negative allosteric modulation of rat mGlu3R expressed in HEK cells harboring GIRK assessed as reduction in glutamate-induced thallium flux preincubated for 5 mins followed by glutamate addition and measured after 2 mins by BTC-AM-dye based fluorescence assayNegative allosteric modulation of rat mGlu3R expressed in HEK cells harboring GIRK assessed as reduction in glutamate-induced thallium flux preincubated for 5 mins followed by glutamate addition and measured after 2 mins by BTC-AM-dye based fluorescence assay
ChEMBL 339 6 0 4 3.8 C[C@@H](COc1ccn(-c2ccc(F)cc2)c(=O)c1)Oc1ccccc1 10.1016/j.bmcl.2019.07.030
CHEMBL4172540 162912 None 11 Rat Binding pIC50 = 5.9 5.9 - 0
Negative allosteric modulation of rat mGlu3R expressed in HEK cells harboring GIRK assessed as reduction in glutamate-induced thallium flux preincubated for 5 mins followed by glutamate addition and measured after 2 mins by BTC-AM-dye based fluorescence assayNegative allosteric modulation of rat mGlu3R expressed in HEK cells harboring GIRK assessed as reduction in glutamate-induced thallium flux preincubated for 5 mins followed by glutamate addition and measured after 2 mins by BTC-AM-dye based fluorescence assay
ChEMBL 339 6 0 4 3.8 C[C@@H](COc1ccn(-c2ccc(F)cc2)c(=O)c1)Oc1ccccc1 10.1016/j.bmcl.2019.07.030
10089411 7529 None 0 Rat Binding pIC50 = 5.9 5.9 - 1
Compound was evaluated for the inhibition of binding of [3H]glutamate against rat recombinant Metabotropic glutamate receptor 3 expressed in HEK293 cellsCompound was evaluated for the inhibition of binding of [3H]glutamate against rat recombinant Metabotropic glutamate receptor 3 expressed in HEK293 cells
ChEMBL 353 5 3 4 2.7 NC(C(=O)O)[C@@H]1[C@@H](C(=O)O)[C@@H]1CC1c2ccccc2Oc2ccccc21 10.1016/s0960-894x(01)00656-4
CHEMBL108735 7529 None 0 Rat Binding pIC50 = 5.9 5.9 - 1
Compound was evaluated for the inhibition of binding of [3H]glutamate against rat recombinant Metabotropic glutamate receptor 3 expressed in HEK293 cellsCompound was evaluated for the inhibition of binding of [3H]glutamate against rat recombinant Metabotropic glutamate receptor 3 expressed in HEK293 cells
ChEMBL 353 5 3 4 2.7 NC(C(=O)O)[C@@H]1[C@@H](C(=O)O)[C@@H]1CC1c2ccccc2Oc2ccccc21 10.1016/s0960-894x(01)00656-4
155533264 171927 None 0 Rat Binding pIC50 = 5.9 5.9 - 0
Negative allosteric modulation of rat mGlu3R expressed in HEK cells harboring GIRK assessed as reduction in glutamate-induced thallium fluxNegative allosteric modulation of rat mGlu3R expressed in HEK cells harboring GIRK assessed as reduction in glutamate-induced thallium flux
ChEMBL 335 6 0 4 4.0 Cc1cccc(-n2ccc(OC[C@H](C)Oc3ccccc3)cc2=O)c1 10.1016/j.bmcl.2019.07.030
CHEMBL4468538 171927 None 0 Rat Binding pIC50 = 5.9 5.9 - 0
Negative allosteric modulation of rat mGlu3R expressed in HEK cells harboring GIRK assessed as reduction in glutamate-induced thallium fluxNegative allosteric modulation of rat mGlu3R expressed in HEK cells harboring GIRK assessed as reduction in glutamate-induced thallium flux
ChEMBL 335 6 0 4 4.0 Cc1cccc(-n2ccc(OC[C@H](C)Oc3ccccc3)cc2=O)c1 10.1016/j.bmcl.2019.07.030
155556417 174603 None 0 Rat Binding pIC50 = 5.9 5.9 - 0
Negative allosteric modulation of rat mGlu3R expressed in HEK cells harboring GIRK assessed as reduction in glutamate-induced thallium fluxNegative allosteric modulation of rat mGlu3R expressed in HEK cells harboring GIRK assessed as reduction in glutamate-induced thallium flux
ChEMBL 349 7 0 4 4.2 Cc1cccc(-n2ccc(OC[C@H](C)COc3ccccc3)cc2=O)c1 10.1016/j.bmcl.2019.07.030
CHEMBL4554871 174603 None 0 Rat Binding pIC50 = 5.9 5.9 - 0
Negative allosteric modulation of rat mGlu3R expressed in HEK cells harboring GIRK assessed as reduction in glutamate-induced thallium fluxNegative allosteric modulation of rat mGlu3R expressed in HEK cells harboring GIRK assessed as reduction in glutamate-induced thallium flux
ChEMBL 349 7 0 4 4.2 Cc1cccc(-n2ccc(OC[C@H](C)COc3ccccc3)cc2=O)c1 10.1016/j.bmcl.2019.07.030
1378 2417 None 39 Rat Binding pIC50 = 7.9 7.9 -5 10
Concentration required to inhibit metabotropic glutamate receptor 3 activity of rat expressed in CHO cellsConcentration required to inhibit metabotropic glutamate receptor 3 activity of rat expressed in CHO cells
ChEMBL 353 5 3 4 2.8 OC(=O)[C@H]1C[C@@H]1[C@](C(=O)O)(CC1c2ccccc2Oc2c1cccc2)N 10.1021/jm0400294
1399 2417 None 39 Rat Binding pIC50 = 7.9 7.9 -5 10
Concentration required to inhibit metabotropic glutamate receptor 3 activity of rat expressed in CHO cellsConcentration required to inhibit metabotropic glutamate receptor 3 activity of rat expressed in CHO cells
ChEMBL 353 5 3 4 2.8 OC(=O)[C@H]1C[C@@H]1[C@](C(=O)O)(CC1c2ccccc2Oc2c1cccc2)N 10.1021/jm0400294
9819927 2417 None 39 Rat Binding pIC50 = 7.9 7.9 -5 10
Concentration required to inhibit metabotropic glutamate receptor 3 activity of rat expressed in CHO cellsConcentration required to inhibit metabotropic glutamate receptor 3 activity of rat expressed in CHO cells
ChEMBL 353 5 3 4 2.8 OC(=O)[C@H]1C[C@@H]1[C@](C(=O)O)(CC1c2ccccc2Oc2c1cccc2)N 10.1021/jm0400294
CHEMBL432038 2417 None 39 Rat Binding pIC50 = 7.9 7.9 -5 10
Concentration required to inhibit metabotropic glutamate receptor 3 activity of rat expressed in CHO cellsConcentration required to inhibit metabotropic glutamate receptor 3 activity of rat expressed in CHO cells
ChEMBL 353 5 3 4 2.8 OC(=O)[C@H]1C[C@@H]1[C@](C(=O)O)(CC1c2ccccc2Oc2c1cccc2)N 10.1021/jm0400294
155542406 173229 None 0 Rat Binding pIC50 = 5.9 5.9 - 0
Negative allosteric modulation of rat mGlu3R expressed in HEK cells harboring GIRK assessed as reduction in glutamate-induced thallium fluxNegative allosteric modulation of rat mGlu3R expressed in HEK cells harboring GIRK assessed as reduction in glutamate-induced thallium flux
ChEMBL 369 7 0 4 4.6 C[C@H](COc1ccccc1)COc1ccn(-c2cccc(Cl)c2)c(=O)c1 10.1016/j.bmcl.2019.07.030
CHEMBL4520808 173229 None 0 Rat Binding pIC50 = 5.9 5.9 - 0
Negative allosteric modulation of rat mGlu3R expressed in HEK cells harboring GIRK assessed as reduction in glutamate-induced thallium fluxNegative allosteric modulation of rat mGlu3R expressed in HEK cells harboring GIRK assessed as reduction in glutamate-induced thallium flux
ChEMBL 369 7 0 4 4.6 C[C@H](COc1ccccc1)COc1ccn(-c2cccc(Cl)c2)c(=O)c1 10.1016/j.bmcl.2019.07.030
56587994 4045 None 29 Human Binding pIC50 = 5.8 5.8 - 0
Negative allosteric modulation of mGlu3 assessed as thallium flux through GIRK channels by cell-based assayNegative allosteric modulation of mGlu3 assessed as thallium flux through GIRK channels by cell-based assay
ChEMBL 349 3 1 3 2.9 OC[C@@H]1CCCN(C1)C(=O)c1ccc(cc1)C#Cc1ccc(cc1)OC 10.1016/j.bmcl.2012.04.112
6225 4045 None 29 Human Binding pIC50 = 5.8 5.8 - 0
Negative allosteric modulation of mGlu3 assessed as thallium flux through GIRK channels by cell-based assayNegative allosteric modulation of mGlu3 assessed as thallium flux through GIRK channels by cell-based assay
ChEMBL 349 3 1 3 2.9 OC[C@@H]1CCCN(C1)C(=O)c1ccc(cc1)C#Cc1ccc(cc1)OC 10.1016/j.bmcl.2012.04.112
CHEMBL2204445 4045 None 29 Human Binding pIC50 = 5.8 5.8 - 0
Negative allosteric modulation of mGlu3 assessed as thallium flux through GIRK channels by cell-based assayNegative allosteric modulation of mGlu3 assessed as thallium flux through GIRK channels by cell-based assay
ChEMBL 349 3 1 3 2.9 OC[C@@H]1CCCN(C1)C(=O)c1ccc(cc1)C#Cc1ccc(cc1)OC 10.1016/j.bmcl.2012.04.112
56587994 4045 None 29 Human Binding pIC50 = 5.8 5.8 - 0
Negative allosteric modulation of mGlu3 assessed as thallium flux through GIRK channels by cell-based assayNegative allosteric modulation of mGlu3 assessed as thallium flux through GIRK channels by cell-based assay
ChEMBL 349 3 1 3 2.9 OC[C@@H]1CCCN(C1)C(=O)c1ccc(cc1)C#Cc1ccc(cc1)OC 10.1016/j.bmcl.2012.04.112
6225 4045 None 29 Human Binding pIC50 = 5.8 5.8 - 0
Negative allosteric modulation of mGlu3 assessed as thallium flux through GIRK channels by cell-based assayNegative allosteric modulation of mGlu3 assessed as thallium flux through GIRK channels by cell-based assay
ChEMBL 349 3 1 3 2.9 OC[C@@H]1CCCN(C1)C(=O)c1ccc(cc1)C#Cc1ccc(cc1)OC 10.1016/j.bmcl.2012.04.112
CHEMBL2204445 4045 None 29 Human Binding pIC50 = 5.8 5.8 - 0
Negative allosteric modulation of mGlu3 assessed as thallium flux through GIRK channels by cell-based assayNegative allosteric modulation of mGlu3 assessed as thallium flux through GIRK channels by cell-based assay
ChEMBL 349 3 1 3 2.9 OC[C@@H]1CCCN(C1)C(=O)c1ccc(cc1)C#Cc1ccc(cc1)OC 10.1016/j.bmcl.2012.04.112
155563014 175393 None 0 Rat Binding pIC50 = 5.8 5.8 - 0
Negative allosteric modulation of rat mGlu3R expressed in HEK cells harboring GIRK assessed as reduction in glutamate-induced thallium fluxNegative allosteric modulation of rat mGlu3R expressed in HEK cells harboring GIRK assessed as reduction in glutamate-induced thallium flux
ChEMBL 335 6 0 4 4.0 Cc1cccc(-n2ccc(O[C@H](C)COc3ccccc3)cc2=O)c1 10.1016/j.bmcl.2019.07.030
CHEMBL4572957 175393 None 0 Rat Binding pIC50 = 5.8 5.8 - 0
Negative allosteric modulation of rat mGlu3R expressed in HEK cells harboring GIRK assessed as reduction in glutamate-induced thallium fluxNegative allosteric modulation of rat mGlu3R expressed in HEK cells harboring GIRK assessed as reduction in glutamate-induced thallium flux
ChEMBL 335 6 0 4 4.0 Cc1cccc(-n2ccc(O[C@H](C)COc3ccccc3)cc2=O)c1 10.1016/j.bmcl.2019.07.030
1378 2417 None 39 Rat Binding pIC50 = 7.8 7.8 -5 10
Compound was evaluated for the inhibition of binding of [3H]glutamate against rat recombinant mGluR3 receptors expressed in HEK293 cellsCompound was evaluated for the inhibition of binding of [3H]glutamate against rat recombinant mGluR3 receptors expressed in HEK293 cells
ChEMBL 353 5 3 4 2.8 OC(=O)[C@H]1C[C@@H]1[C@](C(=O)O)(CC1c2ccccc2Oc2c1cccc2)N 10.1016/s0960-894x(01)00656-4
1399 2417 None 39 Rat Binding pIC50 = 7.8 7.8 -5 10
Compound was evaluated for the inhibition of binding of [3H]glutamate against rat recombinant mGluR3 receptors expressed in HEK293 cellsCompound was evaluated for the inhibition of binding of [3H]glutamate against rat recombinant mGluR3 receptors expressed in HEK293 cells
ChEMBL 353 5 3 4 2.8 OC(=O)[C@H]1C[C@@H]1[C@](C(=O)O)(CC1c2ccccc2Oc2c1cccc2)N 10.1016/s0960-894x(01)00656-4
9819927 2417 None 39 Rat Binding pIC50 = 7.8 7.8 -5 10
Compound was evaluated for the inhibition of binding of [3H]glutamate against rat recombinant mGluR3 receptors expressed in HEK293 cellsCompound was evaluated for the inhibition of binding of [3H]glutamate against rat recombinant mGluR3 receptors expressed in HEK293 cells
ChEMBL 353 5 3 4 2.8 OC(=O)[C@H]1C[C@@H]1[C@](C(=O)O)(CC1c2ccccc2Oc2c1cccc2)N 10.1016/s0960-894x(01)00656-4
CHEMBL432038 2417 None 39 Rat Binding pIC50 = 7.8 7.8 -5 10
Compound was evaluated for the inhibition of binding of [3H]glutamate against rat recombinant mGluR3 receptors expressed in HEK293 cellsCompound was evaluated for the inhibition of binding of [3H]glutamate against rat recombinant mGluR3 receptors expressed in HEK293 cells
ChEMBL 353 5 3 4 2.8 OC(=O)[C@H]1C[C@@H]1[C@](C(=O)O)(CC1c2ccccc2Oc2c1cccc2)N 10.1016/s0960-894x(01)00656-4
11503055 2400 None 2 Human Binding pIC50 = 6.7 6.7 - 0
Negative allosteric modulation of human mGlu3 expressed in AV-12 cells in presence of glutamate EC90 concentration by FLIPR assayNegative allosteric modulation of human mGlu3 expressed in AV-12 cells in presence of glutamate EC90 concentration by FLIPR assay
ChEMBL 400 4 1 4 3.9 Clc1ccc(c(c1)Cl)CN[C@H]1CCN(C1)c1ncc(cn1)Br 10.1016/j.bmcl.2012.04.112
9694 2400 None 2 Human Binding pIC50 = 6.7 6.7 - 0
Negative allosteric modulation of human mGlu3 expressed in AV-12 cells in presence of glutamate EC90 concentration by FLIPR assayNegative allosteric modulation of human mGlu3 expressed in AV-12 cells in presence of glutamate EC90 concentration by FLIPR assay
ChEMBL 400 4 1 4 3.9 Clc1ccc(c(c1)Cl)CN[C@H]1CCN(C1)c1ncc(cn1)Br 10.1016/j.bmcl.2012.04.112
CHEMBL2204436 2400 None 2 Human Binding pIC50 = 6.7 6.7 - 0
Negative allosteric modulation of human mGlu3 expressed in AV-12 cells in presence of glutamate EC90 concentration by FLIPR assayNegative allosteric modulation of human mGlu3 expressed in AV-12 cells in presence of glutamate EC90 concentration by FLIPR assay
ChEMBL 400 4 1 4 3.9 Clc1ccc(c(c1)Cl)CN[C@H]1CCN(C1)c1ncc(cn1)Br 10.1016/j.bmcl.2012.04.112
89554892 150689 None 0 Human Binding pIC50 = 4.7 4.7 - 1
Binding affinity to mGluR3 (unknown origin) by FLIPR assayBinding affinity to mGluR3 (unknown origin) by FLIPR assay
ChEMBL 416 6 1 5 4.0 COc1ccc(-c2cc(C(N)=O)nc3cc(CCc4cnc(C)nc4)ccc23)c(F)c1 10.1021/acsmedchemlett.3c00175
CHEMBL3955188 150689 None 0 Human Binding pIC50 = 4.7 4.7 - 1
Binding affinity to mGluR3 (unknown origin) by FLIPR assayBinding affinity to mGluR3 (unknown origin) by FLIPR assay
ChEMBL 416 6 1 5 4.0 COc1ccc(-c2cc(C(N)=O)nc3cc(CCc4cnc(C)nc4)ccc23)c(F)c1 10.1021/acsmedchemlett.3c00175
53393868 83637 None 6 Human Binding pIC50 = 5.7 5.7 - 0
Negative allosteric modulation of mGlu3 assessed as thallium flux through GIRK channels by cell-based assayNegative allosteric modulation of mGlu3 assessed as thallium flux through GIRK channels by cell-based assay
ChEMBL 349 3 1 3 2.9 COc1ccc(C#Cc2ccc(C(=O)N3CCCC(CO)C3)cc2)cc1 10.1016/j.bmcl.2012.04.112
CHEMBL2204442 83637 None 6 Human Binding pIC50 = 5.7 5.7 - 0
Negative allosteric modulation of mGlu3 assessed as thallium flux through GIRK channels by cell-based assayNegative allosteric modulation of mGlu3 assessed as thallium flux through GIRK channels by cell-based assay
ChEMBL 349 3 1 3 2.9 COc1ccc(C#Cc2ccc(C(=O)N3CCCC(CO)C3)cc2)cc1 10.1016/j.bmcl.2012.04.112
53393868 83637 None 6 Human Binding pIC50 = 5.7 5.7 - 0
Negative allosteric modulation of mGlu3 assessed as thallium flux through GIRK channels by cell-based assayNegative allosteric modulation of mGlu3 assessed as thallium flux through GIRK channels by cell-based assay
ChEMBL 349 3 1 3 2.9 COc1ccc(C#Cc2ccc(C(=O)N3CCCC(CO)C3)cc2)cc1 10.1016/j.bmcl.2012.04.112
CHEMBL2204442 83637 None 6 Human Binding pIC50 = 5.7 5.7 - 0
Negative allosteric modulation of mGlu3 assessed as thallium flux through GIRK channels by cell-based assayNegative allosteric modulation of mGlu3 assessed as thallium flux through GIRK channels by cell-based assay
ChEMBL 349 3 1 3 2.9 COc1ccc(C#Cc2ccc(C(=O)N3CCCC(CO)C3)cc2)cc1 10.1016/j.bmcl.2012.04.112
1397 2529 None 15 Rat Binding pIC50 = 7.6 7.6 -2 5
Concentration required to inhibit metabotropic glutamate receptor 3 activity of rat expressed in CHO cellsConcentration required to inhibit metabotropic glutamate receptor 3 activity of rat expressed in CHO cells
ChEMBL 377 5 3 4 2.1 OC(=O)[C@]1(N)[C@H](OCc2ccc(c(c2)Cl)Cl)C[C@@H]2[C@H]1[C@@]2(F)C(=O)O 10.1021/jm0400294
9886034 2529 None 15 Rat Binding pIC50 = 7.6 7.6 -2 5
Concentration required to inhibit metabotropic glutamate receptor 3 activity of rat expressed in CHO cellsConcentration required to inhibit metabotropic glutamate receptor 3 activity of rat expressed in CHO cells
ChEMBL 377 5 3 4 2.1 OC(=O)[C@]1(N)[C@H](OCc2ccc(c(c2)Cl)Cl)C[C@@H]2[C@H]1[C@@]2(F)C(=O)O 10.1021/jm0400294
CHEMBL186453 2529 None 15 Rat Binding pIC50 = 7.6 7.6 -2 5
Concentration required to inhibit metabotropic glutamate receptor 3 activity of rat expressed in CHO cellsConcentration required to inhibit metabotropic glutamate receptor 3 activity of rat expressed in CHO cells
ChEMBL 377 5 3 4 2.1 OC(=O)[C@]1(N)[C@H](OCc2ccc(c(c2)Cl)Cl)C[C@@H]2[C@H]1[C@@]2(F)C(=O)O 10.1021/jm0400294
53393854 83635 None 0 Human Binding pIC50 = 5.6 5.6 - 0
Negative allosteric modulation of mGlu3 assessed as thallium flux through GIRK channels by cell-based assayNegative allosteric modulation of mGlu3 assessed as thallium flux through GIRK channels by cell-based assay
ChEMBL 335 2 1 3 2.7 COc1ccc(C#Cc2ccc(C(=O)N3CCCC(O)C3)cc2)cc1 10.1016/j.bmcl.2012.04.112
CHEMBL2204439 83635 None 0 Human Binding pIC50 = 5.6 5.6 - 0
Negative allosteric modulation of mGlu3 assessed as thallium flux through GIRK channels by cell-based assayNegative allosteric modulation of mGlu3 assessed as thallium flux through GIRK channels by cell-based assay
ChEMBL 335 2 1 3 2.7 COc1ccc(C#Cc2ccc(C(=O)N3CCCC(O)C3)cc2)cc1 10.1016/j.bmcl.2012.04.112
53393854 83635 None 0 Human Binding pIC50 = 5.6 5.6 - 0
Negative allosteric modulation of mGlu3 assessed as thallium flux through GIRK channels by cell-based assayNegative allosteric modulation of mGlu3 assessed as thallium flux through GIRK channels by cell-based assay
ChEMBL 335 2 1 3 2.7 COc1ccc(C#Cc2ccc(C(=O)N3CCCC(O)C3)cc2)cc1 10.1016/j.bmcl.2012.04.112
CHEMBL2204439 83635 None 0 Human Binding pIC50 = 5.6 5.6 - 0
Negative allosteric modulation of mGlu3 assessed as thallium flux through GIRK channels by cell-based assayNegative allosteric modulation of mGlu3 assessed as thallium flux through GIRK channels by cell-based assay
ChEMBL 335 2 1 3 2.7 COc1ccc(C#Cc2ccc(C(=O)N3CCCC(O)C3)cc2)cc1 10.1016/j.bmcl.2012.04.112
1393 1539 None 42 Human Binding pIC50 = 7.6 7.6 -1 6
Agonist activity at mGlu3 (unknown origin)Agonist activity at mGlu3 (unknown origin)
ChEMBL 185 2 3 3 -0.5 OC(=O)[C@H]1[C@H]2[C@@H]1[C@](CC2)(N)C(=O)O 10.1021/acs.jmedchem.6b01119
1396 1539 None 42 Human Binding pIC50 = 7.6 7.6 -1 6
Agonist activity at mGlu3 (unknown origin)Agonist activity at mGlu3 (unknown origin)
ChEMBL 185 2 3 3 -0.5 OC(=O)[C@H]1[C@H]2[C@@H]1[C@](CC2)(N)C(=O)O 10.1021/acs.jmedchem.6b01119
213056 1539 None 42 Human Binding pIC50 = 7.6 7.6 -1 6
Agonist activity at mGlu3 (unknown origin)Agonist activity at mGlu3 (unknown origin)
ChEMBL 185 2 3 3 -0.5 OC(=O)[C@H]1[C@H]2[C@@H]1[C@](CC2)(N)C(=O)O 10.1021/acs.jmedchem.6b01119
CHEMBL8759 1539 None 42 Human Binding pIC50 = 7.6 7.6 -1 6
Agonist activity at mGlu3 (unknown origin)Agonist activity at mGlu3 (unknown origin)
ChEMBL 185 2 3 3 -0.5 OC(=O)[C@H]1[C@H]2[C@@H]1[C@](CC2)(N)C(=O)O 10.1021/acs.jmedchem.6b01119
11158623 3351 None 11 Human Binding pIC50 = 6.6 6.6 - 2
Negative allosteric modulation of mGlu3 by cell-based assayNegative allosteric modulation of mGlu3 by cell-based assay
ChEMBL 423 2 1 3 6.2 O=C1CC(=Nc2c(N1)cc(c(c2)C)C(F)(F)F)c1cccc(c1)c1cc(C)nc(c1)C 10.1016/j.bmcl.2012.04.112
6226 3351 None 11 Human Binding pIC50 = 6.6 6.6 - 2
Negative allosteric modulation of mGlu3 by cell-based assayNegative allosteric modulation of mGlu3 by cell-based assay
ChEMBL 423 2 1 3 6.2 O=C1CC(=Nc2c(N1)cc(c(c2)C)C(F)(F)F)c1cccc(c1)c1cc(C)nc(c1)C 10.1016/j.bmcl.2012.04.112
CHEMBL1629855 3351 None 11 Human Binding pIC50 = 6.6 6.6 - 2
Negative allosteric modulation of mGlu3 by cell-based assayNegative allosteric modulation of mGlu3 by cell-based assay
ChEMBL 423 2 1 3 6.2 O=C1CC(=Nc2c(N1)cc(c(c2)C)C(F)(F)F)c1cccc(c1)c1cc(C)nc(c1)C 10.1016/j.bmcl.2012.04.112
11158623 3351 None 11 Human Binding pIC50 = 6.6 6.6 - 2
Negative allosteric modulation of mGlu3 receptor (unknown origin)Negative allosteric modulation of mGlu3 receptor (unknown origin)
ChEMBL 423 2 1 3 6.2 O=C1CC(=Nc2c(N1)cc(c(c2)C)C(F)(F)F)c1cccc(c1)c1cc(C)nc(c1)C 10.1021/jm400439t
6226 3351 None 11 Human Binding pIC50 = 6.6 6.6 - 2
Negative allosteric modulation of mGlu3 receptor (unknown origin)Negative allosteric modulation of mGlu3 receptor (unknown origin)
ChEMBL 423 2 1 3 6.2 O=C1CC(=Nc2c(N1)cc(c(c2)C)C(F)(F)F)c1cccc(c1)c1cc(C)nc(c1)C 10.1021/jm400439t
CHEMBL1629855 3351 None 11 Human Binding pIC50 = 6.6 6.6 - 2
Negative allosteric modulation of mGlu3 receptor (unknown origin)Negative allosteric modulation of mGlu3 receptor (unknown origin)
ChEMBL 423 2 1 3 6.2 O=C1CC(=Nc2c(N1)cc(c(c2)C)C(F)(F)F)c1cccc(c1)c1cc(C)nc(c1)C 10.1021/jm400439t
155544343 173483 None 0 Rat Binding pIC50 = 5.6 5.6 - 0
Negative allosteric modulation of rat mGlu3R expressed in HEK cells harboring GIRK assessed as reduction in glutamate-induced thallium fluxNegative allosteric modulation of rat mGlu3R expressed in HEK cells harboring GIRK assessed as reduction in glutamate-induced thallium flux
ChEMBL 355 6 0 4 4.3 C[C@H](COc1ccccc1)Oc1ccn(-c2ccc(Cl)cc2)c(=O)c1 10.1016/j.bmcl.2019.07.030
CHEMBL4527797 173483 None 0 Rat Binding pIC50 = 5.6 5.6 - 0
Negative allosteric modulation of rat mGlu3R expressed in HEK cells harboring GIRK assessed as reduction in glutamate-induced thallium fluxNegative allosteric modulation of rat mGlu3R expressed in HEK cells harboring GIRK assessed as reduction in glutamate-induced thallium flux
ChEMBL 355 6 0 4 4.3 C[C@H](COc1ccccc1)Oc1ccn(-c2ccc(Cl)cc2)c(=O)c1 10.1016/j.bmcl.2019.07.030
68290289 117718 None 0 Human Binding pIC50 = 6.5 6.5 - 0
Negative allosteric modulation at mGluR3 (unknown origin)Negative allosteric modulation at mGluR3 (unknown origin)
ChEMBL 337 4 0 4 3.6 O=C1N(c2ccc(F)cc2)CCc2nc(COc3ccccc3)cn21 10.1016/j.bmcl.2015.01.038
CHEMBL3401195 117718 None 0 Human Binding pIC50 = 6.5 6.5 - 0
Negative allosteric modulation at mGluR3 (unknown origin)Negative allosteric modulation at mGluR3 (unknown origin)
ChEMBL 337 4 0 4 3.6 O=C1N(c2ccc(F)cc2)CCc2nc(COc3ccccc3)cn21 10.1016/j.bmcl.2015.01.038
155538767 173365 None 0 Rat Binding pIC50 = 5.5 5.5 - 0
Negative allosteric modulation of rat mGlu3R expressed in HEK cells harboring GIRK assessed as reduction in glutamate-induced thallium fluxNegative allosteric modulation of rat mGlu3R expressed in HEK cells harboring GIRK assessed as reduction in glutamate-induced thallium flux
ChEMBL 339 6 0 4 3.8 C[C@H](COc1ccccc1)Oc1ccn(-c2ccc(F)cc2)c(=O)c1 10.1016/j.bmcl.2019.07.030
CHEMBL4524912 173365 None 0 Rat Binding pIC50 = 5.5 5.5 - 0
Negative allosteric modulation of rat mGlu3R expressed in HEK cells harboring GIRK assessed as reduction in glutamate-induced thallium fluxNegative allosteric modulation of rat mGlu3R expressed in HEK cells harboring GIRK assessed as reduction in glutamate-induced thallium flux
ChEMBL 339 6 0 4 3.8 C[C@H](COc1ccccc1)Oc1ccn(-c2ccc(F)cc2)c(=O)c1 10.1016/j.bmcl.2019.07.030
155541818 173171 None 0 Rat Binding pIC50 = 5.5 5.5 - 0
Negative allosteric modulation of rat mGlu3R expressed in HEK cells harboring GIRK assessed as reduction in glutamate-induced thallium fluxNegative allosteric modulation of rat mGlu3R expressed in HEK cells harboring GIRK assessed as reduction in glutamate-induced thallium flux
ChEMBL 349 7 0 4 4.2 Cc1cccc(-n2ccc(OC[C@@H](C)COc3ccccc3)cc2=O)c1 10.1016/j.bmcl.2019.07.030
CHEMBL4519557 173171 None 0 Rat Binding pIC50 = 5.5 5.5 - 0
Negative allosteric modulation of rat mGlu3R expressed in HEK cells harboring GIRK assessed as reduction in glutamate-induced thallium fluxNegative allosteric modulation of rat mGlu3R expressed in HEK cells harboring GIRK assessed as reduction in glutamate-induced thallium flux
ChEMBL 349 7 0 4 4.2 Cc1cccc(-n2ccc(OC[C@@H](C)COc3ccccc3)cc2=O)c1 10.1016/j.bmcl.2019.07.030
155518189 170371 None 0 Rat Binding pIC50 = 5.5 5.5 - 0
Negative allosteric modulation of rat mGlu3R expressed in HEK cells harboring GIRK assessed as reduction in glutamate-induced thallium fluxNegative allosteric modulation of rat mGlu3R expressed in HEK cells harboring GIRK assessed as reduction in glutamate-induced thallium flux
ChEMBL 353 7 0 4 4.1 CC(COc1ccccc1)COc1ccn(-c2ccc(F)cc2)c(=O)c1 10.1016/j.bmcl.2019.07.030
CHEMBL4446121 170371 None 0 Rat Binding pIC50 = 5.5 5.5 - 0
Negative allosteric modulation of rat mGlu3R expressed in HEK cells harboring GIRK assessed as reduction in glutamate-induced thallium fluxNegative allosteric modulation of rat mGlu3R expressed in HEK cells harboring GIRK assessed as reduction in glutamate-induced thallium flux
ChEMBL 353 7 0 4 4.1 CC(COc1ccccc1)COc1ccn(-c2ccc(F)cc2)c(=O)c1 10.1016/j.bmcl.2019.07.030
155567480 176004 None 0 Rat Binding pIC50 = 5.5 5.5 - 0
Negative allosteric modulation of rat mGlu3R expressed in HEK cells harboring GIRK assessed as reduction in glutamate-induced thallium fluxNegative allosteric modulation of rat mGlu3R expressed in HEK cells harboring GIRK assessed as reduction in glutamate-induced thallium flux
ChEMBL 349 7 0 4 4.2 Cc1cccc(-n2ccc(OCC(C)COc3ccccc3)cc2=O)c1 10.1016/j.bmcl.2019.07.030
CHEMBL4586828 176004 None 0 Rat Binding pIC50 = 5.5 5.5 - 0
Negative allosteric modulation of rat mGlu3R expressed in HEK cells harboring GIRK assessed as reduction in glutamate-induced thallium fluxNegative allosteric modulation of rat mGlu3R expressed in HEK cells harboring GIRK assessed as reduction in glutamate-induced thallium flux
ChEMBL 349 7 0 4 4.2 Cc1cccc(-n2ccc(OCC(C)COc3ccccc3)cc2=O)c1 10.1016/j.bmcl.2019.07.030
56587985 83638 None 0 Human Binding pIC50 = 5.5 5.5 - 0
Negative allosteric modulation of mGlu3 assessed as thallium flux through GIRK channels by cell-based assayNegative allosteric modulation of mGlu3 assessed as thallium flux through GIRK channels by cell-based assay
ChEMBL 349 3 1 3 2.9 COc1ccc(C#Cc2ccc(C(=O)N3CCC[C@H](CO)C3)cc2)cc1 10.1016/j.bmcl.2012.04.112
CHEMBL2204446 83638 None 0 Human Binding pIC50 = 5.5 5.5 - 0
Negative allosteric modulation of mGlu3 assessed as thallium flux through GIRK channels by cell-based assayNegative allosteric modulation of mGlu3 assessed as thallium flux through GIRK channels by cell-based assay
ChEMBL 349 3 1 3 2.9 COc1ccc(C#Cc2ccc(C(=O)N3CCC[C@H](CO)C3)cc2)cc1 10.1016/j.bmcl.2012.04.112
53338952 83633 None 0 Human Binding pIC50 = 5.4 5.4 - 0
Negative allosteric modulation of mGlu3 assessed as thallium flux through GIRK channels by cell-based assayNegative allosteric modulation of mGlu3 assessed as thallium flux through GIRK channels by cell-based assay
ChEMBL 335 2 1 3 2.7 COc1ccc(C#Cc2ccc(C(=O)N3CCC(O)CC3)cc2)cc1 10.1016/j.bmcl.2012.04.112
CHEMBL2204437 83633 None 0 Human Binding pIC50 = 5.4 5.4 - 0
Negative allosteric modulation of mGlu3 assessed as thallium flux through GIRK channels by cell-based assayNegative allosteric modulation of mGlu3 assessed as thallium flux through GIRK channels by cell-based assay
ChEMBL 335 2 1 3 2.7 COc1ccc(C#Cc2ccc(C(=O)N3CCC(O)CC3)cc2)cc1 10.1016/j.bmcl.2012.04.112
53338952 83633 None 0 Human Binding pIC50 = 5.4 5.4 - 0
Negative allosteric modulation of mGlu3 assessed as thallium flux through GIRK channels by cell-based assayNegative allosteric modulation of mGlu3 assessed as thallium flux through GIRK channels by cell-based assay
ChEMBL 335 2 1 3 2.7 COc1ccc(C#Cc2ccc(C(=O)N3CCC(O)CC3)cc2)cc1 10.1016/j.bmcl.2012.04.112
CHEMBL2204437 83633 None 0 Human Binding pIC50 = 5.4 5.4 - 0
Negative allosteric modulation of mGlu3 assessed as thallium flux through GIRK channels by cell-based assayNegative allosteric modulation of mGlu3 assessed as thallium flux through GIRK channels by cell-based assay
ChEMBL 335 2 1 3 2.7 COc1ccc(C#Cc2ccc(C(=O)N3CCC(O)CC3)cc2)cc1 10.1016/j.bmcl.2012.04.112
155512594 169765 None 0 Rat Binding pIC50 = 5.4 5.4 - 0
Negative allosteric modulation of rat mGlu3R expressed in HEK cells harboring GIRK assessed as reduction in glutamate-induced thallium fluxNegative allosteric modulation of rat mGlu3R expressed in HEK cells harboring GIRK assessed as reduction in glutamate-induced thallium flux
ChEMBL 347 4 0 4 3.9 Cc1cccc(-n2ccc(OCC3CCc4ccccc4O3)cc2=O)c1 10.1016/j.bmcl.2019.07.030
CHEMBL4437442 169765 None 0 Rat Binding pIC50 = 5.4 5.4 - 0
Negative allosteric modulation of rat mGlu3R expressed in HEK cells harboring GIRK assessed as reduction in glutamate-induced thallium fluxNegative allosteric modulation of rat mGlu3R expressed in HEK cells harboring GIRK assessed as reduction in glutamate-induced thallium flux
ChEMBL 347 4 0 4 3.9 Cc1cccc(-n2ccc(OCC3CCc4ccccc4O3)cc2=O)c1 10.1016/j.bmcl.2019.07.030
11503055 2400 None 2 Human Binding pIC50 = 5.4 5.4 - 0
Negative allosteric modulation of mGlu3 assessed as thallium flux through GIRK channels by cell-based assayNegative allosteric modulation of mGlu3 assessed as thallium flux through GIRK channels by cell-based assay
ChEMBL 400 4 1 4 3.9 Clc1ccc(c(c1)Cl)CN[C@H]1CCN(C1)c1ncc(cn1)Br 10.1016/j.bmcl.2012.04.112
9694 2400 None 2 Human Binding pIC50 = 5.4 5.4 - 0
Negative allosteric modulation of mGlu3 assessed as thallium flux through GIRK channels by cell-based assayNegative allosteric modulation of mGlu3 assessed as thallium flux through GIRK channels by cell-based assay
ChEMBL 400 4 1 4 3.9 Clc1ccc(c(c1)Cl)CN[C@H]1CCN(C1)c1ncc(cn1)Br 10.1016/j.bmcl.2012.04.112
CHEMBL2204436 2400 None 2 Human Binding pIC50 = 5.4 5.4 - 0
Negative allosteric modulation of mGlu3 assessed as thallium flux through GIRK channels by cell-based assayNegative allosteric modulation of mGlu3 assessed as thallium flux through GIRK channels by cell-based assay
ChEMBL 400 4 1 4 3.9 Clc1ccc(c(c1)Cl)CN[C@H]1CCN(C1)c1ncc(cn1)Br 10.1016/j.bmcl.2012.04.112
56587992 83634 None 0 Human Binding pIC50 = 5.3 5.3 - 0
Negative allosteric modulation of mGlu3 assessed as thallium flux through GIRK channels by cell-based assayNegative allosteric modulation of mGlu3 assessed as thallium flux through GIRK channels by cell-based assay
ChEMBL 349 2 1 3 3.1 COc1ccc(C#Cc2ccc(C(=O)N3CCC(C)(O)CC3)cc2)cc1 10.1016/j.bmcl.2012.04.112
CHEMBL2204438 83634 None 0 Human Binding pIC50 = 5.3 5.3 - 0
Negative allosteric modulation of mGlu3 assessed as thallium flux through GIRK channels by cell-based assayNegative allosteric modulation of mGlu3 assessed as thallium flux through GIRK channels by cell-based assay
ChEMBL 349 2 1 3 3.1 COc1ccc(C#Cc2ccc(C(=O)N3CCC(C)(O)CC3)cc2)cc1 10.1016/j.bmcl.2012.04.112
56587992 83634 None 0 Human Binding pIC50 = 5.3 5.3 - 0
Negative allosteric modulation of mGlu3 assessed as thallium flux through GIRK channels by cell-based assayNegative allosteric modulation of mGlu3 assessed as thallium flux through GIRK channels by cell-based assay
ChEMBL 349 2 1 3 3.1 COc1ccc(C#Cc2ccc(C(=O)N3CCC(C)(O)CC3)cc2)cc1 10.1016/j.bmcl.2012.04.112
CHEMBL2204438 83634 None 0 Human Binding pIC50 = 5.3 5.3 - 0
Negative allosteric modulation of mGlu3 assessed as thallium flux through GIRK channels by cell-based assayNegative allosteric modulation of mGlu3 assessed as thallium flux through GIRK channels by cell-based assay
ChEMBL 349 2 1 3 3.1 COc1ccc(C#Cc2ccc(C(=O)N3CCC(C)(O)CC3)cc2)cc1 10.1016/j.bmcl.2012.04.112
155522365 170764 None 0 Rat Binding pIC50 = 6.3 6.3 - 0
Negative allosteric modulation of rat mGlu3R expressed in HEK cells harboring GIRK assessed as reduction in glutamate-induced thallium fluxNegative allosteric modulation of rat mGlu3R expressed in HEK cells harboring GIRK assessed as reduction in glutamate-induced thallium flux
ChEMBL 355 6 0 4 4.3 C[C@H](COc1ccccc1)Oc1ccn(-c2cccc(Cl)c2)c(=O)c1 10.1016/j.bmcl.2019.07.030
CHEMBL4451520 170764 None 0 Rat Binding pIC50 = 6.3 6.3 - 0
Negative allosteric modulation of rat mGlu3R expressed in HEK cells harboring GIRK assessed as reduction in glutamate-induced thallium fluxNegative allosteric modulation of rat mGlu3R expressed in HEK cells harboring GIRK assessed as reduction in glutamate-induced thallium flux
ChEMBL 355 6 0 4 4.3 C[C@H](COc1ccccc1)Oc1ccn(-c2cccc(Cl)c2)c(=O)c1 10.1016/j.bmcl.2019.07.030
56587985 83638 None 0 Human Binding pIC50 = 5.3 5.3 - 0
Negative allosteric modulation of mGlu3 assessed as thallium flux through GIRK channels by cell-based assayNegative allosteric modulation of mGlu3 assessed as thallium flux through GIRK channels by cell-based assay
ChEMBL 349 3 1 3 2.9 COc1ccc(C#Cc2ccc(C(=O)N3CCC[C@H](CO)C3)cc2)cc1 10.1016/j.bmcl.2012.04.112
CHEMBL2204446 83638 None 0 Human Binding pIC50 = 5.3 5.3 - 0
Negative allosteric modulation of mGlu3 assessed as thallium flux through GIRK channels by cell-based assayNegative allosteric modulation of mGlu3 assessed as thallium flux through GIRK channels by cell-based assay
ChEMBL 349 3 1 3 2.9 COc1ccc(C#Cc2ccc(C(=O)N3CCC[C@H](CO)C3)cc2)cc1 10.1016/j.bmcl.2012.04.112
56587978 83636 None 0 Human Binding pIC50 = 5.2 5.2 - 0
Negative allosteric modulation of mGlu3 assessed as thallium flux through GIRK channels by cell-based assayNegative allosteric modulation of mGlu3 assessed as thallium flux through GIRK channels by cell-based assay
ChEMBL 363 3 1 3 3.0 COc1ccc(C#Cc2ccc(C(=O)N3CCC[C@H](C(=O)O)C3)cc2)cc1 10.1016/j.bmcl.2012.04.112
CHEMBL2204440 83636 None 0 Human Binding pIC50 = 5.2 5.2 - 0
Negative allosteric modulation of mGlu3 assessed as thallium flux through GIRK channels by cell-based assayNegative allosteric modulation of mGlu3 assessed as thallium flux through GIRK channels by cell-based assay
ChEMBL 363 3 1 3 3.0 COc1ccc(C#Cc2ccc(C(=O)N3CCC[C@H](C(=O)O)C3)cc2)cc1 10.1016/j.bmcl.2012.04.112
56587978 83636 None 0 Human Binding pIC50 = 5.2 5.2 - 0
Negative allosteric modulation of mGlu3 assessed as thallium flux through GIRK channels by cell-based assayNegative allosteric modulation of mGlu3 assessed as thallium flux through GIRK channels by cell-based assay
ChEMBL 363 3 1 3 3.0 COc1ccc(C#Cc2ccc(C(=O)N3CCC[C@H](C(=O)O)C3)cc2)cc1 10.1016/j.bmcl.2012.04.112
CHEMBL2204440 83636 None 0 Human Binding pIC50 = 5.2 5.2 - 0
Negative allosteric modulation of mGlu3 assessed as thallium flux through GIRK channels by cell-based assayNegative allosteric modulation of mGlu3 assessed as thallium flux through GIRK channels by cell-based assay
ChEMBL 363 3 1 3 3.0 COc1ccc(C#Cc2ccc(C(=O)N3CCC[C@H](C(=O)O)C3)cc2)cc1 10.1016/j.bmcl.2012.04.112
11084869 90087 None 1 Human Binding pIC50 = 8.2 8.2 - 1
Agonist activity at mGlu3 (unknown origin)Agonist activity at mGlu3 (unknown origin)
ChEMBL 201 2 4 4 -1.5 N[C@@]1(C(=O)O)C[C@H](O)[C@@H]2[C@H]1[C@H]2C(=O)O 10.1021/acs.jmedchem.6b01119
CHEMBL2381643 90087 None 1 Human Binding pIC50 = 8.2 8.2 - 1
Agonist activity at mGlu3 (unknown origin)Agonist activity at mGlu3 (unknown origin)
ChEMBL 201 2 4 4 -1.5 N[C@@]1(C(=O)O)C[C@H](O)[C@@H]2[C@H]1[C@H]2C(=O)O 10.1021/acs.jmedchem.6b01119
68290572 117701 None 0 Human Binding pIC50 = 6.2 6.2 - 0
Negative allosteric modulation at mGluR3 (unknown origin)Negative allosteric modulation at mGluR3 (unknown origin)
ChEMBL 335 4 0 5 3.2 O=c1n(-c2ccc(F)cc2)ccc2nc(COc3ccccc3)cn12 10.1016/j.bmcl.2015.01.038
CHEMBL3401177 117701 None 0 Human Binding pIC50 = 6.2 6.2 - 0
Negative allosteric modulation at mGluR3 (unknown origin)Negative allosteric modulation at mGluR3 (unknown origin)
ChEMBL 335 4 0 5 3.2 O=c1n(-c2ccc(F)cc2)ccc2nc(COc3ccccc3)cn12 10.1016/j.bmcl.2015.01.038
9885546 110601 None 0 Rat Binding pIC50 = 7.1 7.1 - 1
Compound was evaluated for the inhibition of binding of [3H]glutamate against rat recombinant Metabotropic glutamate receptor 3 expressed in HEK293 cellsCompound was evaluated for the inhibition of binding of [3H]glutamate against rat recombinant Metabotropic glutamate receptor 3 expressed in HEK293 cells
ChEMBL 367 6 3 4 3.1 NC(C(=O)O)[C@@H]1[C@@H](C(=O)O)[C@@H]1CCC1c2ccccc2Oc2ccccc21 10.1016/s0960-894x(01)00656-4
CHEMBL325140 110601 None 0 Rat Binding pIC50 = 7.1 7.1 - 1
Compound was evaluated for the inhibition of binding of [3H]glutamate against rat recombinant Metabotropic glutamate receptor 3 expressed in HEK293 cellsCompound was evaluated for the inhibition of binding of [3H]glutamate against rat recombinant Metabotropic glutamate receptor 3 expressed in HEK293 cells
ChEMBL 367 6 3 4 3.1 NC(C(=O)O)[C@@H]1[C@@H](C(=O)O)[C@@H]1CCC1c2ccccc2Oc2ccccc21 10.1016/s0960-894x(01)00656-4
155517751 170341 None 0 Rat Binding pIC50 = 5.1 5.1 - 0
Negative allosteric modulation of rat mGlu3R expressed in HEK cells harboring GIRK assessed as reduction in glutamate-induced thallium fluxNegative allosteric modulation of rat mGlu3R expressed in HEK cells harboring GIRK assessed as reduction in glutamate-induced thallium flux
ChEMBL 351 4 0 4 3.7 O=c1cc(OCC2CCc3ccccc3O2)ccn1-c1ccc(F)cc1 10.1016/j.bmcl.2019.07.030
CHEMBL4445711 170341 None 0 Rat Binding pIC50 = 5.1 5.1 - 0
Negative allosteric modulation of rat mGlu3R expressed in HEK cells harboring GIRK assessed as reduction in glutamate-induced thallium fluxNegative allosteric modulation of rat mGlu3R expressed in HEK cells harboring GIRK assessed as reduction in glutamate-induced thallium flux
ChEMBL 351 4 0 4 3.7 O=c1cc(OCC2CCc3ccccc3O2)ccn1-c1ccc(F)cc1 10.1016/j.bmcl.2019.07.030
155536972 172339 None 0 Rat Binding pIC50 = 6.0 6.0 - 0
Negative allosteric modulation of rat mGlu3R expressed in HEK cells harboring GIRK assessed as reduction in glutamate-induced thallium fluxNegative allosteric modulation of rat mGlu3R expressed in HEK cells harboring GIRK assessed as reduction in glutamate-induced thallium flux
ChEMBL 369 7 0 4 4.6 C[C@H](COc1ccccc1)COc1ccn(-c2ccc(Cl)cc2)c(=O)c1 10.1016/j.bmcl.2019.07.030
CHEMBL4474204 172339 None 0 Rat Binding pIC50 = 6.0 6.0 - 0
Negative allosteric modulation of rat mGlu3R expressed in HEK cells harboring GIRK assessed as reduction in glutamate-induced thallium fluxNegative allosteric modulation of rat mGlu3R expressed in HEK cells harboring GIRK assessed as reduction in glutamate-induced thallium flux
ChEMBL 369 7 0 4 4.6 C[C@H](COc1ccccc1)COc1ccn(-c2ccc(Cl)cc2)c(=O)c1 10.1016/j.bmcl.2019.07.030
10353365 83279 None 1 Human Binding pKi = 9.8 9.8 5 2
Displacement of [3H]LY341495 from human recombinant mGluR3 in RGT cellsDisplacement of [3H]LY341495 from human recombinant mGluR3 in RGT cells
ChEMBL 219 2 3 4 -1.8 N[C@@]1(C(=O)O)C[S+]([O-])[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/jm060917u
CHEMBL218710 83279 None 1 Human Binding pKi = 9.8 9.8 5 2
Displacement of [3H]LY341495 from human recombinant mGluR3 in RGT cellsDisplacement of [3H]LY341495 from human recombinant mGluR3 in RGT cells
ChEMBL 219 2 3 4 -1.8 N[C@@]1(C(=O)O)C[S+]([O-])[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/jm060917u
60096178 156973 None 0 Human Binding pKi = 9.3 9.3 181 2
Displacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in HEK cell membranes after 90 mins by liquid scintillation countingDisplacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in HEK cell membranes after 90 mins by liquid scintillation counting
ChEMBL 338 4 4 4 0.6 N[C@@]1(C(=O)O)C[C@H](NC(=O)c2cccc(Cl)c2)[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/acs.jmedchem.7b01481
CHEMBL4071962 156973 None 0 Human Binding pKi = 9.3 9.3 181 2
Displacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in HEK cell membranes after 90 mins by liquid scintillation countingDisplacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in HEK cell membranes after 90 mins by liquid scintillation counting
ChEMBL 338 4 4 4 0.6 N[C@@]1(C(=O)O)C[C@H](NC(=O)c2cccc(Cl)c2)[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/acs.jmedchem.7b01481
60096231 157747 None 19 Human Binding pKi = 9.0 9.0 446 2
Displacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in HEK cell membranes after 90 mins by liquid scintillation countingDisplacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in HEK cell membranes after 90 mins by liquid scintillation counting
ChEMBL 334 5 4 5 -0.1 COc1cccc(C(=O)N[C@H]2C[C@@](N)(C(=O)O)[C@@H]3[C@@H](C(=O)O)[C@H]23)c1 10.1021/acs.jmedchem.7b01481
CHEMBL4081453 157747 None 19 Human Binding pKi = 9.0 9.0 446 2
Displacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in HEK cell membranes after 90 mins by liquid scintillation countingDisplacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in HEK cell membranes after 90 mins by liquid scintillation counting
ChEMBL 334 5 4 5 -0.1 COc1cccc(C(=O)N[C@H]2C[C@@](N)(C(=O)O)[C@@H]3[C@@H](C(=O)O)[C@H]23)c1 10.1021/acs.jmedchem.7b01481
1378 2417 None 39 Human Binding pKi = 8.9 8.9 1 10
Displacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in hamster AV12 cell membranes co-expressing rat EAAT1 incubated for 90 mins by top count scintillation methodDisplacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in hamster AV12 cell membranes co-expressing rat EAAT1 incubated for 90 mins by top count scintillation method
ChEMBL 353 5 3 4 2.8 OC(=O)[C@H]1C[C@@H]1[C@](C(=O)O)(CC1c2ccccc2Oc2c1cccc2)N 10.1021/acs.jmedchem.6b01119
1399 2417 None 39 Human Binding pKi = 8.9 8.9 1 10
Displacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in hamster AV12 cell membranes co-expressing rat EAAT1 incubated for 90 mins by top count scintillation methodDisplacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in hamster AV12 cell membranes co-expressing rat EAAT1 incubated for 90 mins by top count scintillation method
ChEMBL 353 5 3 4 2.8 OC(=O)[C@H]1C[C@@H]1[C@](C(=O)O)(CC1c2ccccc2Oc2c1cccc2)N 10.1021/acs.jmedchem.6b01119
9819927 2417 None 39 Human Binding pKi = 8.9 8.9 1 10
Displacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in hamster AV12 cell membranes co-expressing rat EAAT1 incubated for 90 mins by top count scintillation methodDisplacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in hamster AV12 cell membranes co-expressing rat EAAT1 incubated for 90 mins by top count scintillation method
ChEMBL 353 5 3 4 2.8 OC(=O)[C@H]1C[C@@H]1[C@](C(=O)O)(CC1c2ccccc2Oc2c1cccc2)N 10.1021/acs.jmedchem.6b01119
CHEMBL432038 2417 None 39 Human Binding pKi = 8.9 8.9 1 10
Displacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in hamster AV12 cell membranes co-expressing rat EAAT1 incubated for 90 mins by top count scintillation methodDisplacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in hamster AV12 cell membranes co-expressing rat EAAT1 incubated for 90 mins by top count scintillation method
ChEMBL 353 5 3 4 2.8 OC(=O)[C@H]1C[C@@H]1[C@](C(=O)O)(CC1c2ccccc2Oc2c1cccc2)N 10.1021/acs.jmedchem.6b01119
60096224 156636 None 0 Human Binding pKi = 8.8 8.8 32 2
Displacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in HEK cell membranes after 90 mins by liquid scintillation countingDisplacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in HEK cell membranes after 90 mins by liquid scintillation counting
ChEMBL 320 4 5 5 -0.4 N[C@@]1(C(=O)O)C[C@H](NC(=O)c2ccccc2O)[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/acs.jmedchem.7b01481
CHEMBL4068189 156636 None 0 Human Binding pKi = 8.8 8.8 32 2
Displacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in HEK cell membranes after 90 mins by liquid scintillation countingDisplacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in HEK cell membranes after 90 mins by liquid scintillation counting
ChEMBL 320 4 5 5 -0.4 N[C@@]1(C(=O)O)C[C@H](NC(=O)c2ccccc2O)[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/acs.jmedchem.7b01481
10197984 2421 None 36 Human Binding pKi = 6.0 6.0 -2 5
Ability to displace [3H]LY-341,495 from recombinant human Metabotropic glutamate receptor 3 expressed in RGT cells.Ability to displace [3H]LY-341,495 from recombinant human Metabotropic glutamate receptor 3 expressed in RGT cells.
ChEMBL 187 2 3 4 -1.5 OC(=O)[C@H]1[C@H]2[C@@H]1[C@](CO2)(N)C(=O)O 10.1021/jm980616n
1394 2421 None 36 Human Binding pKi = 6.0 6.0 -2 5
Ability to displace [3H]LY-341,495 from recombinant human Metabotropic glutamate receptor 3 expressed in RGT cells.Ability to displace [3H]LY-341,495 from recombinant human Metabotropic glutamate receptor 3 expressed in RGT cells.
ChEMBL 187 2 3 4 -1.5 OC(=O)[C@H]1[C@H]2[C@@H]1[C@](CO2)(N)C(=O)O 10.1021/jm980616n
CHEMBL275079 2421 None 36 Human Binding pKi = 6.0 6.0 -2 5
Ability to displace [3H]LY-341,495 from recombinant human Metabotropic glutamate receptor 3 expressed in RGT cells.Ability to displace [3H]LY-341,495 from recombinant human Metabotropic glutamate receptor 3 expressed in RGT cells.
ChEMBL 187 2 3 4 -1.5 OC(=O)[C@H]1[C@H]2[C@@H]1[C@](CO2)(N)C(=O)O 10.1021/jm980616n
1393 1539 None 42 Human Binding pKi = 7.0 7.0 -1 6
Displacement of [3H]-459477 from human recombinant mGlu3 receptor expressed in AV12 cells after 90 mins by liquid scintillation countingDisplacement of [3H]-459477 from human recombinant mGlu3 receptor expressed in AV12 cells after 90 mins by liquid scintillation counting
ChEMBL 185 2 3 3 -0.5 OC(=O)[C@H]1[C@H]2[C@@H]1[C@](CC2)(N)C(=O)O 10.1021/acs.jmedchem.5b01124
1396 1539 None 42 Human Binding pKi = 7.0 7.0 -1 6
Displacement of [3H]-459477 from human recombinant mGlu3 receptor expressed in AV12 cells after 90 mins by liquid scintillation countingDisplacement of [3H]-459477 from human recombinant mGlu3 receptor expressed in AV12 cells after 90 mins by liquid scintillation counting
ChEMBL 185 2 3 3 -0.5 OC(=O)[C@H]1[C@H]2[C@@H]1[C@](CC2)(N)C(=O)O 10.1021/acs.jmedchem.5b01124
213056 1539 None 42 Human Binding pKi = 7.0 7.0 -1 6
Displacement of [3H]-459477 from human recombinant mGlu3 receptor expressed in AV12 cells after 90 mins by liquid scintillation countingDisplacement of [3H]-459477 from human recombinant mGlu3 receptor expressed in AV12 cells after 90 mins by liquid scintillation counting
ChEMBL 185 2 3 3 -0.5 OC(=O)[C@H]1[C@H]2[C@@H]1[C@](CC2)(N)C(=O)O 10.1021/acs.jmedchem.5b01124
CHEMBL8759 1539 None 42 Human Binding pKi = 7.0 7.0 -1 6
Displacement of [3H]-459477 from human recombinant mGlu3 receptor expressed in AV12 cells after 90 mins by liquid scintillation countingDisplacement of [3H]-459477 from human recombinant mGlu3 receptor expressed in AV12 cells after 90 mins by liquid scintillation counting
ChEMBL 185 2 3 3 -0.5 OC(=O)[C@H]1[C@H]2[C@@H]1[C@](CC2)(N)C(=O)O 10.1021/acs.jmedchem.5b01124
1393 1539 None 42 Human Binding pKi = 7.0 7.0 -1 6
Displacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in HEK cell membranes after 90 mins by liquid scintillation countingDisplacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in HEK cell membranes after 90 mins by liquid scintillation counting
ChEMBL 185 2 3 3 -0.5 OC(=O)[C@H]1[C@H]2[C@@H]1[C@](CC2)(N)C(=O)O 10.1021/acs.jmedchem.7b01481
1396 1539 None 42 Human Binding pKi = 7.0 7.0 -1 6
Displacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in HEK cell membranes after 90 mins by liquid scintillation countingDisplacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in HEK cell membranes after 90 mins by liquid scintillation counting
ChEMBL 185 2 3 3 -0.5 OC(=O)[C@H]1[C@H]2[C@@H]1[C@](CC2)(N)C(=O)O 10.1021/acs.jmedchem.7b01481
213056 1539 None 42 Human Binding pKi = 7.0 7.0 -1 6
Displacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in HEK cell membranes after 90 mins by liquid scintillation countingDisplacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in HEK cell membranes after 90 mins by liquid scintillation counting
ChEMBL 185 2 3 3 -0.5 OC(=O)[C@H]1[C@H]2[C@@H]1[C@](CC2)(N)C(=O)O 10.1021/acs.jmedchem.7b01481
CHEMBL8759 1539 None 42 Human Binding pKi = 7.0 7.0 -1 6
Displacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in HEK cell membranes after 90 mins by liquid scintillation countingDisplacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in HEK cell membranes after 90 mins by liquid scintillation counting
ChEMBL 185 2 3 3 -0.5 OC(=O)[C@H]1[C@H]2[C@@H]1[C@](CC2)(N)C(=O)O 10.1021/acs.jmedchem.7b01481
60096194 156679 None 0 Human Binding pKi = 6.0 6.0 10 2
Displacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in HEK cell membranes after 90 mins by liquid scintillation countingDisplacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in HEK cell membranes after 90 mins by liquid scintillation counting
ChEMBL 290 5 4 4 0.3 N[C@@]1(C(=O)O)C[C@H](NCc2ccccc2)[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/acs.jmedchem.7b01481
CHEMBL4068679 156679 None 0 Human Binding pKi = 6.0 6.0 10 2
Displacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in HEK cell membranes after 90 mins by liquid scintillation countingDisplacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in HEK cell membranes after 90 mins by liquid scintillation counting
ChEMBL 290 5 4 4 0.3 N[C@@]1(C(=O)O)C[C@H](NCc2ccccc2)[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/acs.jmedchem.7b01481
1393 1539 None 42 Human Binding pKi = 6.9 6.9 -1 6
Inhibition of [3H]LY-341,495 binding to recombinant human mGlu3 receptorsInhibition of [3H]LY-341,495 binding to recombinant human mGlu3 receptors
ChEMBL 185 2 3 3 -0.5 OC(=O)[C@H]1[C@H]2[C@@H]1[C@](CC2)(N)C(=O)O 10.1021/jm050235r
1396 1539 None 42 Human Binding pKi = 6.9 6.9 -1 6
Inhibition of [3H]LY-341,495 binding to recombinant human mGlu3 receptorsInhibition of [3H]LY-341,495 binding to recombinant human mGlu3 receptors
ChEMBL 185 2 3 3 -0.5 OC(=O)[C@H]1[C@H]2[C@@H]1[C@](CC2)(N)C(=O)O 10.1021/jm050235r
213056 1539 None 42 Human Binding pKi = 6.9 6.9 -1 6
Inhibition of [3H]LY-341,495 binding to recombinant human mGlu3 receptorsInhibition of [3H]LY-341,495 binding to recombinant human mGlu3 receptors
ChEMBL 185 2 3 3 -0.5 OC(=O)[C@H]1[C@H]2[C@@H]1[C@](CC2)(N)C(=O)O 10.1021/jm050235r
CHEMBL8759 1539 None 42 Human Binding pKi = 6.9 6.9 -1 6
Inhibition of [3H]LY-341,495 binding to recombinant human mGlu3 receptorsInhibition of [3H]LY-341,495 binding to recombinant human mGlu3 receptors
ChEMBL 185 2 3 3 -0.5 OC(=O)[C@H]1[C@H]2[C@@H]1[C@](CC2)(N)C(=O)O 10.1021/jm050235r
71136653 123470 None 0 Human Binding pKi = 6.9 6.9 -2 2
Displacement of [3H]-459477 from human recombinant mGlu3 receptor expressed in AV12 cells after 90 mins by liquid scintillation countingDisplacement of [3H]-459477 from human recombinant mGlu3 receptor expressed in AV12 cells after 90 mins by liquid scintillation counting
ChEMBL 284 4 4 6 -0.6 N[C@@]1(C(=O)O)C[C@H](Sc2nnc[nH]2)[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/acs.jmedchem.5b01124
CHEMBL3616854 123470 None 0 Human Binding pKi = 6.9 6.9 -2 2
Displacement of [3H]-459477 from human recombinant mGlu3 receptor expressed in AV12 cells after 90 mins by liquid scintillation countingDisplacement of [3H]-459477 from human recombinant mGlu3 receptor expressed in AV12 cells after 90 mins by liquid scintillation counting
ChEMBL 284 4 4 6 -0.6 N[C@@]1(C(=O)O)C[C@H](Sc2nnc[nH]2)[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/acs.jmedchem.5b01124
10979251 90094 None 0 Human Binding pKi = 6.9 6.9 3 2
Displacement of [3H]-459477 from human recombinant mGlu3 receptor expressed in AV12 cells after 90 mins by liquid scintillation countingDisplacement of [3H]-459477 from human recombinant mGlu3 receptor expressed in AV12 cells after 90 mins by liquid scintillation counting
ChEMBL 293 4 3 4 1.3 N[C@@]1(C(=O)O)C[C@@H](Sc2ccccc2)[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/acs.jmedchem.5b01124
CHEMBL2381650 90094 None 0 Human Binding pKi = 6.9 6.9 3 2
Displacement of [3H]-459477 from human recombinant mGlu3 receptor expressed in AV12 cells after 90 mins by liquid scintillation countingDisplacement of [3H]-459477 from human recombinant mGlu3 receptor expressed in AV12 cells after 90 mins by liquid scintillation counting
ChEMBL 293 4 3 4 1.3 N[C@@]1(C(=O)O)C[C@@H](Sc2ccccc2)[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/acs.jmedchem.5b01124
10197984 2421 None 36 Human Binding pKi = 7.8 7.8 -2 5
Ability to displace [3H]LY-341,495 from recombinant human Metabotropic glutamate receptor 3 expressed in RGT cells.Ability to displace [3H]LY-341,495 from recombinant human Metabotropic glutamate receptor 3 expressed in RGT cells.
ChEMBL 187 2 3 4 -1.5 OC(=O)[C@H]1[C@H]2[C@@H]1[C@](CO2)(N)C(=O)O 10.1021/jm980616n
1394 2421 None 36 Human Binding pKi = 7.8 7.8 -2 5
Ability to displace [3H]LY-341,495 from recombinant human Metabotropic glutamate receptor 3 expressed in RGT cells.Ability to displace [3H]LY-341,495 from recombinant human Metabotropic glutamate receptor 3 expressed in RGT cells.
ChEMBL 187 2 3 4 -1.5 OC(=O)[C@H]1[C@H]2[C@@H]1[C@](CO2)(N)C(=O)O 10.1021/jm980616n
CHEMBL275079 2421 None 36 Human Binding pKi = 7.8 7.8 -2 5
Ability to displace [3H]LY-341,495 from recombinant human Metabotropic glutamate receptor 3 expressed in RGT cells.Ability to displace [3H]LY-341,495 from recombinant human Metabotropic glutamate receptor 3 expressed in RGT cells.
ChEMBL 187 2 3 4 -1.5 OC(=O)[C@H]1[C@H]2[C@@H]1[C@](CO2)(N)C(=O)O 10.1021/jm980616n
11298568 69397 None 1 Human Binding pKi = 6.8 6.8 6 2
Displacement of [3H]-341495 binding to membranes expressing recombinant human Metabotropic glutamate receptor 3Displacement of [3H]-341495 binding to membranes expressing recombinant human Metabotropic glutamate receptor 3
ChEMBL 199 2 3 3 -0.2 C[C@@H]1C[C@H]2[C@H](C(=O)O)[C@H]2[C@]1(N)C(=O)O 10.1021/jm040222y
CHEMBL192977 69397 None 1 Human Binding pKi = 6.8 6.8 6 2
Displacement of [3H]-341495 binding to membranes expressing recombinant human Metabotropic glutamate receptor 3Displacement of [3H]-341495 binding to membranes expressing recombinant human Metabotropic glutamate receptor 3
ChEMBL 199 2 3 3 -0.2 C[C@@H]1C[C@H]2[C@H](C(=O)O)[C@H]2[C@]1(N)C(=O)O 10.1021/jm040222y
11347391 66873 None 0 Rat Binding pKi = 7.8 7.8 -2 2
Binding affinity towards metabotropic glutamate receptor 3 of rat expressed in CHO cells was determined by using [3H]MGS-0008Binding affinity towards metabotropic glutamate receptor 3 of rat expressed in CHO cells was determined by using [3H]MGS-0008
ChEMBL 309 5 3 4 0.8 N[C@@]1(C(=O)O)[C@H](OCc2ccccc2)C[C@@H]2[C@H]1[C@@]2(F)C(=O)O 10.1021/jm0400294
CHEMBL186214 66873 None 0 Rat Binding pKi = 7.8 7.8 -2 2
Binding affinity towards metabotropic glutamate receptor 3 of rat expressed in CHO cells was determined by using [3H]MGS-0008Binding affinity towards metabotropic glutamate receptor 3 of rat expressed in CHO cells was determined by using [3H]MGS-0008
ChEMBL 309 5 3 4 0.8 N[C@@]1(C(=O)O)[C@H](OCc2ccccc2)C[C@@H]2[C@H]1[C@@]2(F)C(=O)O 10.1021/jm0400294
53240406 123463 None 21 Human Binding pKi = 6.8 6.8 -1 2
Displacement of [3H]-459477 from human recombinant mGlu3 receptor expressed in AV12 cells after 90 mins by liquid scintillation countingDisplacement of [3H]-459477 from human recombinant mGlu3 receptor expressed in AV12 cells after 90 mins by liquid scintillation counting
ChEMBL 284 4 4 6 -0.6 N[C@@]1(C(=O)O)C[C@@H](Sc2nnc[nH]2)[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/acs.jmedchem.5b01124
CHEMBL3616847 123463 None 21 Human Binding pKi = 6.8 6.8 -1 2
Displacement of [3H]-459477 from human recombinant mGlu3 receptor expressed in AV12 cells after 90 mins by liquid scintillation countingDisplacement of [3H]-459477 from human recombinant mGlu3 receptor expressed in AV12 cells after 90 mins by liquid scintillation counting
ChEMBL 284 4 4 6 -0.6 N[C@@]1(C(=O)O)C[C@@H](Sc2nnc[nH]2)[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/acs.jmedchem.5b01124
71136655 123468 None 0 Human Binding pKi = 6.8 6.8 1 2
Displacement of [3H]-459477 from human recombinant mGlu3 receptor expressed in AV12 cells after 90 mins by liquid scintillation countingDisplacement of [3H]-459477 from human recombinant mGlu3 receptor expressed in AV12 cells after 90 mins by liquid scintillation counting
ChEMBL 326 5 4 6 0.5 CC(C)c1nnc(S[C@@H]2C[C@@](N)(C(=O)O)[C@@H]3[C@@H](C(=O)O)[C@H]23)[nH]1 10.1021/acs.jmedchem.5b01124
CHEMBL3616852 123468 None 0 Human Binding pKi = 6.8 6.8 1 2
Displacement of [3H]-459477 from human recombinant mGlu3 receptor expressed in AV12 cells after 90 mins by liquid scintillation countingDisplacement of [3H]-459477 from human recombinant mGlu3 receptor expressed in AV12 cells after 90 mins by liquid scintillation counting
ChEMBL 326 5 4 6 0.5 CC(C)c1nnc(S[C@@H]2C[C@@](N)(C(=O)O)[C@@H]3[C@@H](C(=O)O)[C@H]23)[nH]1 10.1021/acs.jmedchem.5b01124
162658340 183792 None 0 Human Binding pKi = 7.8 7.8 1 2
Displacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in hamster AV12 cell membranes co-expressing rat EAAT1 incubated for 90 mins by top count scintillation methodDisplacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in hamster AV12 cell membranes co-expressing rat EAAT1 incubated for 90 mins by top count scintillation method
ChEMBL 405 6 4 5 1.9 N[C@@]1(C(=O)O)[C@H](CSCc2ccc(Cl)c(Cl)c2)[C@@H](O)[C@@H]2[C@H]1[C@H]2C(=O)O 10.1021/acs.jmedchem.6b01119
CHEMBL4760856 183792 None 0 Human Binding pKi = 7.8 7.8 1 2
Displacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in hamster AV12 cell membranes co-expressing rat EAAT1 incubated for 90 mins by top count scintillation methodDisplacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in hamster AV12 cell membranes co-expressing rat EAAT1 incubated for 90 mins by top count scintillation method
ChEMBL 405 6 4 5 1.9 N[C@@]1(C(=O)O)[C@H](CSCc2ccc(Cl)c(Cl)c2)[C@@H](O)[C@@H]2[C@H]1[C@H]2C(=O)O 10.1021/acs.jmedchem.6b01119
CHEMBL4803084 183792 None 0 Human Binding pKi = 7.8 7.8 1 2
Displacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in hamster AV12 cell membranes co-expressing rat EAAT1 incubated for 90 mins by top count scintillation methodDisplacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in hamster AV12 cell membranes co-expressing rat EAAT1 incubated for 90 mins by top count scintillation method
ChEMBL 405 6 4 5 1.9 N[C@@]1(C(=O)O)[C@H](CSCc2ccc(Cl)c(Cl)c2)[C@@H](O)[C@@H]2[C@H]1[C@H]2C(=O)O 10.1021/acs.jmedchem.6b01119
10198133 208966 None 10 Human Binding pKi = 6.8 6.8 6 2
Ability to displace [3H]LY-341,495 from recombinant human Metabotropic glutamate receptor 3 expressed in RGT cells.Ability to displace [3H]LY-341,495 from recombinant human Metabotropic glutamate receptor 3 expressed in RGT cells.
ChEMBL 203 2 3 4 -0.8 N[C@@]1(C(=O)O)CS[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/jm980616n
CHEMBL8839 208966 None 10 Human Binding pKi = 6.8 6.8 6 2
Ability to displace [3H]LY-341,495 from recombinant human Metabotropic glutamate receptor 3 expressed in RGT cells.Ability to displace [3H]LY-341,495 from recombinant human Metabotropic glutamate receptor 3 expressed in RGT cells.
ChEMBL 203 2 3 4 -0.8 N[C@@]1(C(=O)O)CS[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/jm980616n
60096211 90093 None 0 Human Binding pKi = 6.8 6.8 5 2
Displacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in HEK cell membranes after 90 mins by liquid scintillation countingDisplacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in HEK cell membranes after 90 mins by liquid scintillation counting
ChEMBL 242 3 4 4 -1.4 CC(=O)N[C@H]1C[C@@](N)(C(=O)O)[C@@H]2[C@@H](C(=O)O)[C@H]12 10.1021/acs.jmedchem.7b01481
CHEMBL2381649 90093 None 0 Human Binding pKi = 6.8 6.8 5 2
Displacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in HEK cell membranes after 90 mins by liquid scintillation countingDisplacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in HEK cell membranes after 90 mins by liquid scintillation counting
ChEMBL 242 3 4 4 -1.4 CC(=O)N[C@H]1C[C@@](N)(C(=O)O)[C@@H]2[C@@H](C(=O)O)[C@H]12 10.1021/acs.jmedchem.7b01481
162658781 183797 None 0 Human Binding pKi = 7.7 7.7 1 2
Displacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in hamster AV12 cell membranes co-expressing rat EAAT1 incubated for 90 mins by top count scintillation methodDisplacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in hamster AV12 cell membranes co-expressing rat EAAT1 incubated for 90 mins by top count scintillation method
ChEMBL 323 5 4 5 0.5 N[C@@]1(C(=O)O)[C@H](CSc2ccccc2)[C@@H](O)[C@@H]2[C@H]1[C@H]2C(=O)O 10.1021/acs.jmedchem.6b01119
CHEMBL4759209 183797 None 0 Human Binding pKi = 7.7 7.7 1 2
Displacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in hamster AV12 cell membranes co-expressing rat EAAT1 incubated for 90 mins by top count scintillation methodDisplacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in hamster AV12 cell membranes co-expressing rat EAAT1 incubated for 90 mins by top count scintillation method
ChEMBL 323 5 4 5 0.5 N[C@@]1(C(=O)O)[C@H](CSc2ccccc2)[C@@H](O)[C@@H]2[C@H]1[C@H]2C(=O)O 10.1021/acs.jmedchem.6b01119
CHEMBL4803105 183797 None 0 Human Binding pKi = 7.7 7.7 1 2
Displacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in hamster AV12 cell membranes co-expressing rat EAAT1 incubated for 90 mins by top count scintillation methodDisplacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in hamster AV12 cell membranes co-expressing rat EAAT1 incubated for 90 mins by top count scintillation method
ChEMBL 323 5 4 5 0.5 N[C@@]1(C(=O)O)[C@H](CSc2ccccc2)[C@@H](O)[C@@H]2[C@H]1[C@H]2C(=O)O 10.1021/acs.jmedchem.6b01119
60096190 158605 None 0 Human Binding pKi = 8.7 8.7 102 2
Displacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in HEK cell membranes after 90 mins by liquid scintillation countingDisplacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in HEK cell membranes after 90 mins by liquid scintillation counting
ChEMBL 322 4 4 4 0.1 N[C@@]1(C(=O)O)C[C@H](NC(=O)c2cccc(F)c2)[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/acs.jmedchem.7b01481
CHEMBL4091203 158605 None 0 Human Binding pKi = 8.7 8.7 102 2
Displacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in HEK cell membranes after 90 mins by liquid scintillation countingDisplacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in HEK cell membranes after 90 mins by liquid scintillation counting
ChEMBL 322 4 4 4 0.1 N[C@@]1(C(=O)O)C[C@H](NC(=O)c2cccc(F)c2)[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/acs.jmedchem.7b01481
60096201 158660 None 0 Human Binding pKi = 8.6 8.6 13 2
Displacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in HEK cell membranes after 90 mins by liquid scintillation countingDisplacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in HEK cell membranes after 90 mins by liquid scintillation counting
ChEMBL 320 4 5 5 -0.4 N[C@@]1(C(=O)O)C[C@H](NC(=O)c2cccc(O)c2)[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/acs.jmedchem.7b01481
CHEMBL4091735 158660 None 0 Human Binding pKi = 8.6 8.6 13 2
Displacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in HEK cell membranes after 90 mins by liquid scintillation countingDisplacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in HEK cell membranes after 90 mins by liquid scintillation counting
ChEMBL 320 4 5 5 -0.4 N[C@@]1(C(=O)O)C[C@H](NC(=O)c2cccc(O)c2)[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/acs.jmedchem.7b01481
60096250 159013 None 0 Human Binding pKi = 8.6 8.6 60 2
Displacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in HEK cell membranes after 90 mins by liquid scintillation countingDisplacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in HEK cell membranes after 90 mins by liquid scintillation counting
ChEMBL 338 4 4 4 0.6 N[C@@]1(C(=O)O)C[C@H](NC(=O)c2ccc(Cl)cc2)[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/acs.jmedchem.7b01481
CHEMBL4095567 159013 None 0 Human Binding pKi = 8.6 8.6 60 2
Displacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in HEK cell membranes after 90 mins by liquid scintillation countingDisplacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in HEK cell membranes after 90 mins by liquid scintillation counting
ChEMBL 338 4 4 4 0.6 N[C@@]1(C(=O)O)C[C@H](NC(=O)c2ccc(Cl)cc2)[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/acs.jmedchem.7b01481
69669747 183759 None 14 Human Binding pKi = 8.6 8.6 2 2
Displacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in hamster AV12 cell membranes co-expressing rat EAAT1 incubated for 90 mins by top count scintillation methodDisplacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in hamster AV12 cell membranes co-expressing rat EAAT1 incubated for 90 mins by top count scintillation method
ChEMBL 359 5 4 5 0.8 N[C@@]1(C(=O)O)[C@H](CSc2ccc(F)c(F)c2)[C@@H](O)[C@@H]2[C@H]1[C@H]2C(=O)O 10.1021/acs.jmedchem.6b01119
CHEMBL4751065 183759 None 14 Human Binding pKi = 8.6 8.6 2 2
Displacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in hamster AV12 cell membranes co-expressing rat EAAT1 incubated for 90 mins by top count scintillation methodDisplacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in hamster AV12 cell membranes co-expressing rat EAAT1 incubated for 90 mins by top count scintillation method
ChEMBL 359 5 4 5 0.8 N[C@@]1(C(=O)O)[C@H](CSc2ccc(F)c(F)c2)[C@@H](O)[C@@H]2[C@H]1[C@H]2C(=O)O 10.1021/acs.jmedchem.6b01119
CHEMBL4802733 183759 None 14 Human Binding pKi = 8.6 8.6 2 2
Displacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in hamster AV12 cell membranes co-expressing rat EAAT1 incubated for 90 mins by top count scintillation methodDisplacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in hamster AV12 cell membranes co-expressing rat EAAT1 incubated for 90 mins by top count scintillation method
ChEMBL 359 5 4 5 0.8 N[C@@]1(C(=O)O)[C@H](CSc2ccc(F)c(F)c2)[C@@H](O)[C@@H]2[C@H]1[C@H]2C(=O)O 10.1021/acs.jmedchem.6b01119
67705089 152344 None 0 Human Binding pKi = 8.6 8.6 2 2
Displacement of [3H]-LY459477 from human mGlu3 receptor expressed in hamster AV12 cell membranes co-expressing human EAAT1 after 90 mins by liquid scintillation counting methodDisplacement of [3H]-LY459477 from human mGlu3 receptor expressed in hamster AV12 cell membranes co-expressing human EAAT1 after 90 mins by liquid scintillation counting method
ChEMBL 458 7 4 7 1.9 N[C@@]1(C(=O)O)[C@H](OCc2ccc(Cl)c(Cl)c2)[C@@H](Sc2nc[nH]n2)[C@H]2[C@H](C(=O)O)[C@H]21 10.1016/j.bmcl.2016.10.067
CHEMBL3969063 152344 None 0 Human Binding pKi = 8.6 8.6 2 2
Displacement of [3H]-LY459477 from human mGlu3 receptor expressed in hamster AV12 cell membranes co-expressing human EAAT1 after 90 mins by liquid scintillation counting methodDisplacement of [3H]-LY459477 from human mGlu3 receptor expressed in hamster AV12 cell membranes co-expressing human EAAT1 after 90 mins by liquid scintillation counting method
ChEMBL 458 7 4 7 1.9 N[C@@]1(C(=O)O)[C@H](OCc2ccc(Cl)c(Cl)c2)[C@@H](Sc2nc[nH]n2)[C@H]2[C@H](C(=O)O)[C@H]21 10.1016/j.bmcl.2016.10.067
60096183 159377 None 0 Human Binding pKi = 7.6 7.6 6 2
Displacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in HEK cell membranes after 90 mins by liquid scintillation countingDisplacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in HEK cell membranes after 90 mins by liquid scintillation counting
ChEMBL 334 5 4 5 -0.1 COc1ccccc1C(=O)N[C@H]1C[C@@](N)(C(=O)O)[C@@H]2[C@@H](C(=O)O)[C@H]12 10.1021/acs.jmedchem.7b01481
CHEMBL4099470 159377 None 0 Human Binding pKi = 7.6 7.6 6 2
Displacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in HEK cell membranes after 90 mins by liquid scintillation countingDisplacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in HEK cell membranes after 90 mins by liquid scintillation counting
ChEMBL 334 5 4 5 -0.1 COc1ccccc1C(=O)N[C@H]1C[C@@](N)(C(=O)O)[C@@H]2[C@@H](C(=O)O)[C@H]12 10.1021/acs.jmedchem.7b01481
162663798 183825 None 0 Human Binding pKi = 6.6 6.6 1 2
Displacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in hamster AV12 cell membranes co-expressing rat EAAT1 incubated for 90 mins by top count scintillation methodDisplacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in hamster AV12 cell membranes co-expressing rat EAAT1 incubated for 90 mins by top count scintillation method
ChEMBL 323 5 4 5 0.5 N[C@]1(C(=O)O)[C@@H]2[C@@H](C(=O)O)[C@@H]2[C@@H](O)[C@@H]1CSc1ccccc1 10.1021/acs.jmedchem.6b01119
CHEMBL4779554 183825 None 0 Human Binding pKi = 6.6 6.6 1 2
Displacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in hamster AV12 cell membranes co-expressing rat EAAT1 incubated for 90 mins by top count scintillation methodDisplacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in hamster AV12 cell membranes co-expressing rat EAAT1 incubated for 90 mins by top count scintillation method
ChEMBL 323 5 4 5 0.5 N[C@]1(C(=O)O)[C@@H]2[C@@H](C(=O)O)[C@@H]2[C@@H](O)[C@@H]1CSc1ccccc1 10.1021/acs.jmedchem.6b01119
CHEMBL4803378 183825 None 0 Human Binding pKi = 6.6 6.6 1 2
Displacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in hamster AV12 cell membranes co-expressing rat EAAT1 incubated for 90 mins by top count scintillation methodDisplacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in hamster AV12 cell membranes co-expressing rat EAAT1 incubated for 90 mins by top count scintillation method
ChEMBL 323 5 4 5 0.5 N[C@]1(C(=O)O)[C@@H]2[C@@H](C(=O)O)[C@@H]2[C@@H](O)[C@@H]1CSc1ccccc1 10.1021/acs.jmedchem.6b01119
162666357 183837 None 0 Human Binding pKi = 7.6 7.6 1 2
Displacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in hamster AV12 cell membranes co-expressing rat EAAT1 incubated for 90 mins by top count scintillation methodDisplacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in hamster AV12 cell membranes co-expressing rat EAAT1 incubated for 90 mins by top count scintillation method
ChEMBL 341 5 4 5 0.6 N[C@@]1(C(=O)O)[C@H](CSc2cccc(F)c2)[C@@H](O)[C@@H]2[C@H]1[C@H]2C(=O)O 10.1021/acs.jmedchem.6b01119
CHEMBL4784701 183837 None 0 Human Binding pKi = 7.6 7.6 1 2
Displacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in hamster AV12 cell membranes co-expressing rat EAAT1 incubated for 90 mins by top count scintillation methodDisplacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in hamster AV12 cell membranes co-expressing rat EAAT1 incubated for 90 mins by top count scintillation method
ChEMBL 341 5 4 5 0.6 N[C@@]1(C(=O)O)[C@H](CSc2cccc(F)c2)[C@@H](O)[C@@H]2[C@H]1[C@H]2C(=O)O 10.1021/acs.jmedchem.6b01119
CHEMBL4803523 183837 None 0 Human Binding pKi = 7.6 7.6 1 2
Displacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in hamster AV12 cell membranes co-expressing rat EAAT1 incubated for 90 mins by top count scintillation methodDisplacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in hamster AV12 cell membranes co-expressing rat EAAT1 incubated for 90 mins by top count scintillation method
ChEMBL 341 5 4 5 0.6 N[C@@]1(C(=O)O)[C@H](CSc2cccc(F)c2)[C@@H](O)[C@@H]2[C@H]1[C@H]2C(=O)O 10.1021/acs.jmedchem.6b01119
162644419 183728 None 0 Human Binding pKi = 6.6 6.6 1 2
Displacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in hamster AV12 cell membranes co-expressing rat EAAT1 incubated for 90 mins by top count scintillation methodDisplacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in hamster AV12 cell membranes co-expressing rat EAAT1 incubated for 90 mins by top count scintillation method
ChEMBL 323 5 4 5 0.5 N[C@]1(C(=O)O)[C@@H]2[C@@H](C(=O)O)[C@@H]2[C@H](O)[C@@H]1CSc1ccccc1 10.1021/acs.jmedchem.6b01119
CHEMBL4778355 183728 None 0 Human Binding pKi = 6.6 6.6 1 2
Displacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in hamster AV12 cell membranes co-expressing rat EAAT1 incubated for 90 mins by top count scintillation methodDisplacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in hamster AV12 cell membranes co-expressing rat EAAT1 incubated for 90 mins by top count scintillation method
ChEMBL 323 5 4 5 0.5 N[C@]1(C(=O)O)[C@@H]2[C@@H](C(=O)O)[C@@H]2[C@H](O)[C@@H]1CSc1ccccc1 10.1021/acs.jmedchem.6b01119
CHEMBL4802356 183728 None 0 Human Binding pKi = 6.6 6.6 1 2
Displacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in hamster AV12 cell membranes co-expressing rat EAAT1 incubated for 90 mins by top count scintillation methodDisplacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in hamster AV12 cell membranes co-expressing rat EAAT1 incubated for 90 mins by top count scintillation method
ChEMBL 323 5 4 5 0.5 N[C@]1(C(=O)O)[C@@H]2[C@@H](C(=O)O)[C@@H]2[C@H](O)[C@@H]1CSc1ccccc1 10.1021/acs.jmedchem.6b01119
71136640 123469 None 0 Human Binding pKi = 6.6 6.6 -1 2
Displacement of [3H]-459477 from human recombinant mGlu3 receptor expressed in AV12 cells after 90 mins by liquid scintillation countingDisplacement of [3H]-459477 from human recombinant mGlu3 receptor expressed in AV12 cells after 90 mins by liquid scintillation counting
ChEMBL 284 4 4 6 -0.6 N[C@@]1(C(=O)O)C[C@@H](Sc2c[nH]nn2)[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/acs.jmedchem.5b01124
CHEMBL3616853 123469 None 0 Human Binding pKi = 6.6 6.6 -1 2
Displacement of [3H]-459477 from human recombinant mGlu3 receptor expressed in AV12 cells after 90 mins by liquid scintillation countingDisplacement of [3H]-459477 from human recombinant mGlu3 receptor expressed in AV12 cells after 90 mins by liquid scintillation counting
ChEMBL 284 4 4 6 -0.6 N[C@@]1(C(=O)O)C[C@@H](Sc2c[nH]nn2)[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/acs.jmedchem.5b01124
69669646 183785 None 0 Human Binding pKi = 7.6 7.6 -1 2
Displacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in hamster AV12 cell membranes co-expressing rat EAAT1 incubated for 90 mins by top count scintillation methodDisplacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in hamster AV12 cell membranes co-expressing rat EAAT1 incubated for 90 mins by top count scintillation method
ChEMBL 351 5 4 5 1.1 Cc1ccc(SC[C@@H]2[C@@H](O)[C@@H]3[C@@H]([C@H]3C(=O)O)[C@]2(N)C(=O)O)cc1C 10.1021/acs.jmedchem.6b01119
CHEMBL4757159 183785 None 0 Human Binding pKi = 7.6 7.6 -1 2
Displacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in hamster AV12 cell membranes co-expressing rat EAAT1 incubated for 90 mins by top count scintillation methodDisplacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in hamster AV12 cell membranes co-expressing rat EAAT1 incubated for 90 mins by top count scintillation method
ChEMBL 351 5 4 5 1.1 Cc1ccc(SC[C@@H]2[C@@H](O)[C@@H]3[C@@H]([C@H]3C(=O)O)[C@]2(N)C(=O)O)cc1C 10.1021/acs.jmedchem.6b01119
CHEMBL4802990 183785 None 0 Human Binding pKi = 7.6 7.6 -1 2
Displacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in hamster AV12 cell membranes co-expressing rat EAAT1 incubated for 90 mins by top count scintillation methodDisplacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in hamster AV12 cell membranes co-expressing rat EAAT1 incubated for 90 mins by top count scintillation method
ChEMBL 351 5 4 5 1.1 Cc1ccc(SC[C@@H]2[C@@H](O)[C@@H]3[C@@H]([C@H]3C(=O)O)[C@]2(N)C(=O)O)cc1C 10.1021/acs.jmedchem.6b01119
162665071 183834 None 0 Human Binding pKi = 7.6 7.6 1 2
Displacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in hamster AV12 cell membranes co-expressing rat EAAT1 incubated for 90 mins by top count scintillation methodDisplacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in hamster AV12 cell membranes co-expressing rat EAAT1 incubated for 90 mins by top count scintillation method
ChEMBL 323 5 4 5 0.5 N[C@@]1(C(=O)O)[C@H](CSc2ccccc2)[C@H](O)[C@@H]2[C@H]1[C@H]2C(=O)O 10.1021/acs.jmedchem.6b01119
CHEMBL4781638 183834 None 0 Human Binding pKi = 7.6 7.6 1 2
Displacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in hamster AV12 cell membranes co-expressing rat EAAT1 incubated for 90 mins by top count scintillation methodDisplacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in hamster AV12 cell membranes co-expressing rat EAAT1 incubated for 90 mins by top count scintillation method
ChEMBL 323 5 4 5 0.5 N[C@@]1(C(=O)O)[C@H](CSc2ccccc2)[C@H](O)[C@@H]2[C@H]1[C@H]2C(=O)O 10.1021/acs.jmedchem.6b01119
CHEMBL4803454 183834 None 0 Human Binding pKi = 7.6 7.6 1 2
Displacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in hamster AV12 cell membranes co-expressing rat EAAT1 incubated for 90 mins by top count scintillation methodDisplacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in hamster AV12 cell membranes co-expressing rat EAAT1 incubated for 90 mins by top count scintillation method
ChEMBL 323 5 4 5 0.5 N[C@@]1(C(=O)O)[C@H](CSc2ccccc2)[C@H](O)[C@@H]2[C@H]1[C@H]2C(=O)O 10.1021/acs.jmedchem.6b01119
137659992 159329 None 0 Human Binding pKi = 7.6 7.6 14 2
Displacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in HEK cell membranes after 90 mins by liquid scintillation countingDisplacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in HEK cell membranes after 90 mins by liquid scintillation counting
ChEMBL 338 4 4 4 0.6 N[C@@]1(C(=O)O)C[C@H](NC(=O)c2ccccc2Cl)[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/acs.jmedchem.7b01481
CHEMBL4098939 159329 None 0 Human Binding pKi = 7.6 7.6 14 2
Displacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in HEK cell membranes after 90 mins by liquid scintillation countingDisplacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in HEK cell membranes after 90 mins by liquid scintillation counting
ChEMBL 338 4 4 4 0.6 N[C@@]1(C(=O)O)C[C@H](NC(=O)c2ccccc2Cl)[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/acs.jmedchem.7b01481
71681826 90095 None 0 Human Binding pKi = 6.6 6.6 4 2
Displacement of [3H]-459477 from human recombinant mGlu3 receptor expressed in AV12 cells after 90 mins by liquid scintillation countingDisplacement of [3H]-459477 from human recombinant mGlu3 receptor expressed in AV12 cells after 90 mins by liquid scintillation counting
ChEMBL 293 4 3 4 1.3 N[C@@]1(C(=O)O)C[C@H](Sc2ccccc2)[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/acs.jmedchem.5b01124
CHEMBL2381651 90095 None 0 Human Binding pKi = 6.6 6.6 4 2
Displacement of [3H]-459477 from human recombinant mGlu3 receptor expressed in AV12 cells after 90 mins by liquid scintillation countingDisplacement of [3H]-459477 from human recombinant mGlu3 receptor expressed in AV12 cells after 90 mins by liquid scintillation counting
ChEMBL 293 4 3 4 1.3 N[C@@]1(C(=O)O)C[C@H](Sc2ccccc2)[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/acs.jmedchem.5b01124
137634033 156732 None 0 Human Binding pKi = 6.6 6.6 2 2
Displacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in HEK cell membranes after 90 mins by liquid scintillation countingDisplacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in HEK cell membranes after 90 mins by liquid scintillation counting
ChEMBL 332 6 4 4 0.2 N[C@@]1(C(=O)O)C[C@H](NC(=O)CCc2ccccc2)[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/acs.jmedchem.7b01481
CHEMBL4069251 156732 None 0 Human Binding pKi = 6.6 6.6 2 2
Displacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in HEK cell membranes after 90 mins by liquid scintillation countingDisplacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in HEK cell membranes after 90 mins by liquid scintillation counting
ChEMBL 332 6 4 4 0.2 N[C@@]1(C(=O)O)C[C@H](NC(=O)CCc2ccccc2)[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/acs.jmedchem.7b01481
11275666 90091 None 1 Human Binding pKi = 6.6 6.6 15 2
Displacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in HEK cell membranes after 90 mins by liquid scintillation countingDisplacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in HEK cell membranes after 90 mins by liquid scintillation counting
ChEMBL 200 2 4 4 -1.6 N[C@H]1C[C@@](N)(C(=O)O)[C@@H]2[C@@H](C(=O)O)[C@H]12 10.1021/acs.jmedchem.7b01481
CHEMBL2381647 90091 None 1 Human Binding pKi = 6.6 6.6 15 2
Displacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in HEK cell membranes after 90 mins by liquid scintillation countingDisplacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in HEK cell membranes after 90 mins by liquid scintillation counting
ChEMBL 200 2 4 4 -1.6 N[C@H]1C[C@@](N)(C(=O)O)[C@@H]2[C@@H](C(=O)O)[C@H]12 10.1021/acs.jmedchem.7b01481
11382367 66958 None 0 Rat Binding pKi = 8.5 8.5 -1 2
Binding affinity towards metabotropic glutamate receptor 3 of rat expressed in CHO cells was determined by using [3H]MGS-0008Binding affinity towards metabotropic glutamate receptor 3 of rat expressed in CHO cells was determined by using [3H]MGS-0008
ChEMBL 345 5 3 4 1.1 N[C@@]1(C(=O)O)[C@H](OCc2ccc(F)c(F)c2)C[C@@H]2[C@H]1[C@@]2(F)C(=O)O 10.1021/jm0400294
CHEMBL186630 66958 None 0 Rat Binding pKi = 8.5 8.5 -1 2
Binding affinity towards metabotropic glutamate receptor 3 of rat expressed in CHO cells was determined by using [3H]MGS-0008Binding affinity towards metabotropic glutamate receptor 3 of rat expressed in CHO cells was determined by using [3H]MGS-0008
ChEMBL 345 5 3 4 1.1 N[C@@]1(C(=O)O)[C@H](OCc2ccc(F)c(F)c2)C[C@@H]2[C@H]1[C@@]2(F)C(=O)O 10.1021/jm0400294
44361401 31349 None 0 Human Binding pKi = 8.5 8.5 7 2
Binding affinity towards metabotropic glutamate receptor 3 was determinedBinding affinity towards metabotropic glutamate receptor 3 was determined
ChEMBL 175 3 4 4 -1.9 N[C@H](C(=O)O)[C@H]1[C@@H](O)[C@@H]1C(=O)O 10.1021/jm030967o
CHEMBL140197 31349 None 0 Human Binding pKi = 8.5 8.5 7 2
Binding affinity towards metabotropic glutamate receptor 3 was determinedBinding affinity towards metabotropic glutamate receptor 3 was determined
ChEMBL 175 3 4 4 -1.9 N[C@H](C(=O)O)[C@H]1[C@@H](O)[C@@H]1C(=O)O 10.1021/jm030967o
1378 2417 None 39 Rat Binding pKi = 8.5 8.5 -5 10
Binding affinity towards metabotropic glutamate receptor 3 of rat expressed in CHO cells was determined by using [3H]MGS-0008Binding affinity towards metabotropic glutamate receptor 3 of rat expressed in CHO cells was determined by using [3H]MGS-0008
ChEMBL 353 5 3 4 2.8 OC(=O)[C@H]1C[C@@H]1[C@](C(=O)O)(CC1c2ccccc2Oc2c1cccc2)N 10.1021/jm0400294
1399 2417 None 39 Rat Binding pKi = 8.5 8.5 -5 10
Binding affinity towards metabotropic glutamate receptor 3 of rat expressed in CHO cells was determined by using [3H]MGS-0008Binding affinity towards metabotropic glutamate receptor 3 of rat expressed in CHO cells was determined by using [3H]MGS-0008
ChEMBL 353 5 3 4 2.8 OC(=O)[C@H]1C[C@@H]1[C@](C(=O)O)(CC1c2ccccc2Oc2c1cccc2)N 10.1021/jm0400294
9819927 2417 None 39 Rat Binding pKi = 8.5 8.5 -5 10
Binding affinity towards metabotropic glutamate receptor 3 of rat expressed in CHO cells was determined by using [3H]MGS-0008Binding affinity towards metabotropic glutamate receptor 3 of rat expressed in CHO cells was determined by using [3H]MGS-0008
ChEMBL 353 5 3 4 2.8 OC(=O)[C@H]1C[C@@H]1[C@](C(=O)O)(CC1c2ccccc2Oc2c1cccc2)N 10.1021/jm0400294
CHEMBL432038 2417 None 39 Rat Binding pKi = 8.5 8.5 -5 10
Binding affinity towards metabotropic glutamate receptor 3 of rat expressed in CHO cells was determined by using [3H]MGS-0008Binding affinity towards metabotropic glutamate receptor 3 of rat expressed in CHO cells was determined by using [3H]MGS-0008
ChEMBL 353 5 3 4 2.8 OC(=O)[C@H]1C[C@@H]1[C@](C(=O)O)(CC1c2ccccc2Oc2c1cccc2)N 10.1021/jm0400294
1395 2528 None 14 Rat Binding pKi = 8.4 8.4 -2 2
Tested for binding affinity against Metabotropic glutamate receptor 3 in CHO cells using [3H]-7 as radioligandTested for binding affinity against Metabotropic glutamate receptor 3 in CHO cells using [3H]-7 as radioligand
ChEMBL 217 2 3 4 -1.2 O=C1C[C@@]([C@H]2[C@@H]1[C@]2(F)C(=O)O)(N)C(=O)O 10.1021/jm000346k
9837317 2528 None 14 Rat Binding pKi = 8.4 8.4 -2 2
Tested for binding affinity against Metabotropic glutamate receptor 3 in CHO cells using [3H]-7 as radioligandTested for binding affinity against Metabotropic glutamate receptor 3 in CHO cells using [3H]-7 as radioligand
ChEMBL 217 2 3 4 -1.2 O=C1C[C@@]([C@H]2[C@@H]1[C@]2(F)C(=O)O)(N)C(=O)O 10.1021/jm000346k
CHEMBL121053 2528 None 14 Rat Binding pKi = 8.4 8.4 -2 2
Tested for binding affinity against Metabotropic glutamate receptor 3 in CHO cells using [3H]-7 as radioligandTested for binding affinity against Metabotropic glutamate receptor 3 in CHO cells using [3H]-7 as radioligand
ChEMBL 217 2 3 4 -1.2 O=C1C[C@@]([C@H]2[C@@H]1[C@]2(F)C(=O)O)(N)C(=O)O 10.1021/jm000346k
11257636 168475 None 0 Rat Binding pKi = 8.4 8.4 -1 2
Binding affinity towards metabotropic glutamate receptor 3 of rat expressed in CHO cells was determined by using [3H]MGS-0008Binding affinity towards metabotropic glutamate receptor 3 of rat expressed in CHO cells was determined by using [3H]MGS-0008
ChEMBL 385 6 3 4 2.4 N[C@@]1(C(=O)O)[C@H](OC(c2ccccc2)c2ccccc2)C[C@@H]2[C@H]1[C@@]2(F)C(=O)O 10.1021/jm0400294
CHEMBL434536 168475 None 0 Rat Binding pKi = 8.4 8.4 -1 2
Binding affinity towards metabotropic glutamate receptor 3 of rat expressed in CHO cells was determined by using [3H]MGS-0008Binding affinity towards metabotropic glutamate receptor 3 of rat expressed in CHO cells was determined by using [3H]MGS-0008
ChEMBL 385 6 3 4 2.4 N[C@@]1(C(=O)O)[C@H](OC(c2ccccc2)c2ccccc2)C[C@@H]2[C@H]1[C@@]2(F)C(=O)O 10.1021/jm0400294
11310142 2422 None 14 Human Binding pKi = 6.5 6.5 -1 2
Displacement of [3H]-341495 binding to membranes expressing recombinant human Metabotropic glutamate receptor 3Displacement of [3H]-341495 binding to membranes expressing recombinant human Metabotropic glutamate receptor 3
ChEMBL 199 2 3 3 -0.2 C[C@@H]1C[C@@]([C@H]2[C@@H]1[C@@H]2C(=O)O)(N)C(=O)O 10.1021/jm040222y
11614 2422 None 14 Human Binding pKi = 6.5 6.5 -1 2
Displacement of [3H]-341495 binding to membranes expressing recombinant human Metabotropic glutamate receptor 3Displacement of [3H]-341495 binding to membranes expressing recombinant human Metabotropic glutamate receptor 3
ChEMBL 199 2 3 3 -0.2 C[C@@H]1C[C@@]([C@H]2[C@@H]1[C@@H]2C(=O)O)(N)C(=O)O 10.1021/jm040222y
CHEMBL192051 2422 None 14 Human Binding pKi = 6.5 6.5 -1 2
Displacement of [3H]-341495 binding to membranes expressing recombinant human Metabotropic glutamate receptor 3Displacement of [3H]-341495 binding to membranes expressing recombinant human Metabotropic glutamate receptor 3
ChEMBL 199 2 3 3 -0.2 C[C@@H]1C[C@@]([C@H]2[C@@H]1[C@@H]2C(=O)O)(N)C(=O)O 10.1021/jm040222y
69669702 183781 None 0 Human Binding pKi = 7.4 7.4 -1 2
Displacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in hamster AV12 cell membranes co-expressing rat EAAT1 incubated for 90 mins by top count scintillation methodDisplacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in hamster AV12 cell membranes co-expressing rat EAAT1 incubated for 90 mins by top count scintillation method
ChEMBL 354 5 4 5 0.9 Cc1cc(SC[C@@H]2[C@@H](N)[C@H]3[C@H](C(=O)O)[C@H]3[C@]2(N)C(=O)O)ccc1F 10.1021/acs.jmedchem.6b01119
CHEMBL4756556 183781 None 0 Human Binding pKi = 7.4 7.4 -1 2
Displacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in hamster AV12 cell membranes co-expressing rat EAAT1 incubated for 90 mins by top count scintillation methodDisplacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in hamster AV12 cell membranes co-expressing rat EAAT1 incubated for 90 mins by top count scintillation method
ChEMBL 354 5 4 5 0.9 Cc1cc(SC[C@@H]2[C@@H](N)[C@H]3[C@H](C(=O)O)[C@H]3[C@]2(N)C(=O)O)ccc1F 10.1021/acs.jmedchem.6b01119
CHEMBL4802948 183781 None 0 Human Binding pKi = 7.4 7.4 -1 2
Displacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in hamster AV12 cell membranes co-expressing rat EAAT1 incubated for 90 mins by top count scintillation methodDisplacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in hamster AV12 cell membranes co-expressing rat EAAT1 incubated for 90 mins by top count scintillation method
ChEMBL 354 5 4 5 0.9 Cc1cc(SC[C@@H]2[C@@H](N)[C@H]3[C@H](C(=O)O)[C@H]3[C@]2(N)C(=O)O)ccc1F 10.1021/acs.jmedchem.6b01119
162654849 183776 None 0 Human Binding pKi = 6.4 6.4 1 2
Displacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in hamster AV12 cell membranes co-expressing rat EAAT1 incubated for 90 mins by top count scintillation methodDisplacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in hamster AV12 cell membranes co-expressing rat EAAT1 incubated for 90 mins by top count scintillation method
ChEMBL 341 5 4 5 0.6 N[C@@]1(C(=O)O)[C@H](CSc2ccccc2F)[C@@H](O)[C@@H]2[C@H]1[C@H]2C(=O)O 10.1021/acs.jmedchem.6b01119
CHEMBL4755204 183776 None 0 Human Binding pKi = 6.4 6.4 1 2
Displacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in hamster AV12 cell membranes co-expressing rat EAAT1 incubated for 90 mins by top count scintillation methodDisplacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in hamster AV12 cell membranes co-expressing rat EAAT1 incubated for 90 mins by top count scintillation method
ChEMBL 341 5 4 5 0.6 N[C@@]1(C(=O)O)[C@H](CSc2ccccc2F)[C@@H](O)[C@@H]2[C@H]1[C@H]2C(=O)O 10.1021/acs.jmedchem.6b01119
CHEMBL4802906 183776 None 0 Human Binding pKi = 6.4 6.4 1 2
Displacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in hamster AV12 cell membranes co-expressing rat EAAT1 incubated for 90 mins by top count scintillation methodDisplacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in hamster AV12 cell membranes co-expressing rat EAAT1 incubated for 90 mins by top count scintillation method
ChEMBL 341 5 4 5 0.6 N[C@@]1(C(=O)O)[C@H](CSc2ccccc2F)[C@@H](O)[C@@H]2[C@H]1[C@H]2C(=O)O 10.1021/acs.jmedchem.6b01119
10807972 35826 None 1 Rat Binding pKi = 8.4 8.4 -1 2
Tested for binding affinity against Metabotropic glutamate receptor 3 in CHO cells using [3H]-7 as radioligandTested for binding affinity against Metabotropic glutamate receptor 3 in CHO cells using [3H]-7 as radioligand
ChEMBL 353 5 3 4 2.8 N[C@@](CC1c2ccccc2Oc2ccccc21)(C(=O)O)[C@H]1C[C@@H]1C(=O)O 10.1021/jm000346k
CHEMBL144151 35826 None 1 Rat Binding pKi = 8.4 8.4 -1 2
Tested for binding affinity against Metabotropic glutamate receptor 3 in CHO cells using [3H]-7 as radioligandTested for binding affinity against Metabotropic glutamate receptor 3 in CHO cells using [3H]-7 as radioligand
ChEMBL 353 5 3 4 2.8 N[C@@](CC1c2ccccc2Oc2ccccc21)(C(=O)O)[C@H]1C[C@@H]1C(=O)O 10.1021/jm000346k
60096204 156215 None 0 Human Binding pKi = 8.4 8.4 75 2
Displacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in HEK cell membranes after 90 mins by liquid scintillation countingDisplacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in HEK cell membranes after 90 mins by liquid scintillation counting
ChEMBL 322 4 4 4 0.1 N[C@@]1(C(=O)O)C[C@H](NC(=O)c2ccc(F)cc2)[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/acs.jmedchem.7b01481
CHEMBL4063336 156215 None 0 Human Binding pKi = 8.4 8.4 75 2
Displacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in HEK cell membranes after 90 mins by liquid scintillation countingDisplacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in HEK cell membranes after 90 mins by liquid scintillation counting
ChEMBL 322 4 4 4 0.1 N[C@@]1(C(=O)O)C[C@H](NC(=O)c2ccc(F)cc2)[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/acs.jmedchem.7b01481
1397 2529 None 15 Rat Binding pKi = 8.4 8.4 -2 5
Binding affinity towards metabotropic glutamate receptor 3 of rat expressed in CHO cells was determined by using [3H]MGS-0008Binding affinity towards metabotropic glutamate receptor 3 of rat expressed in CHO cells was determined by using [3H]MGS-0008
ChEMBL 377 5 3 4 2.1 OC(=O)[C@]1(N)[C@H](OCc2ccc(c(c2)Cl)Cl)C[C@@H]2[C@H]1[C@@]2(F)C(=O)O 10.1021/jm0400294
9886034 2529 None 15 Rat Binding pKi = 8.4 8.4 -2 5
Binding affinity towards metabotropic glutamate receptor 3 of rat expressed in CHO cells was determined by using [3H]MGS-0008Binding affinity towards metabotropic glutamate receptor 3 of rat expressed in CHO cells was determined by using [3H]MGS-0008
ChEMBL 377 5 3 4 2.1 OC(=O)[C@]1(N)[C@H](OCc2ccc(c(c2)Cl)Cl)C[C@@H]2[C@H]1[C@@]2(F)C(=O)O 10.1021/jm0400294
CHEMBL186453 2529 None 15 Rat Binding pKi = 8.4 8.4 -2 5
Binding affinity towards metabotropic glutamate receptor 3 of rat expressed in CHO cells was determined by using [3H]MGS-0008Binding affinity towards metabotropic glutamate receptor 3 of rat expressed in CHO cells was determined by using [3H]MGS-0008
ChEMBL 377 5 3 4 2.1 OC(=O)[C@]1(N)[C@H](OCc2ccc(c(c2)Cl)Cl)C[C@@H]2[C@H]1[C@@]2(F)C(=O)O 10.1021/jm0400294
1397 2529 None 15 Human Binding pKi = 8.4 8.4 -2 5
Binding affinity to mGLUR3Binding affinity to mGLUR3
ChEMBL 377 5 3 4 2.1 OC(=O)[C@]1(N)[C@H](OCc2ccc(c(c2)Cl)Cl)C[C@@H]2[C@H]1[C@@]2(F)C(=O)O 10.1016/j.bmcl.2012.01.039
9886034 2529 None 15 Human Binding pKi = 8.4 8.4 -2 5
Binding affinity to mGLUR3Binding affinity to mGLUR3
ChEMBL 377 5 3 4 2.1 OC(=O)[C@]1(N)[C@H](OCc2ccc(c(c2)Cl)Cl)C[C@@H]2[C@H]1[C@@]2(F)C(=O)O 10.1016/j.bmcl.2012.01.039
CHEMBL186453 2529 None 15 Human Binding pKi = 8.4 8.4 -2 5
Binding affinity to mGLUR3Binding affinity to mGLUR3
ChEMBL 377 5 3 4 2.1 OC(=O)[C@]1(N)[C@H](OCc2ccc(c(c2)Cl)Cl)C[C@@H]2[C@H]1[C@@]2(F)C(=O)O 10.1016/j.bmcl.2012.01.039
67637415 183793 None 0 Human Binding pKi = 8.4 8.4 1 2
Displacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in hamster AV12 cell membranes co-expressing rat EAAT1 incubated for 90 mins by top count scintillation methodDisplacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in hamster AV12 cell membranes co-expressing rat EAAT1 incubated for 90 mins by top count scintillation method
ChEMBL 438 7 4 7 1.9 Cc1cc(SC[C@@H]2[C@@H](Sc3nc[nH]n3)[C@H]3[C@H](C(=O)O)[C@H]3[C@]2(N)C(=O)O)ccc1F 10.1021/acs.jmedchem.6b01119
CHEMBL4759992 183793 None 0 Human Binding pKi = 8.4 8.4 1 2
Displacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in hamster AV12 cell membranes co-expressing rat EAAT1 incubated for 90 mins by top count scintillation methodDisplacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in hamster AV12 cell membranes co-expressing rat EAAT1 incubated for 90 mins by top count scintillation method
ChEMBL 438 7 4 7 1.9 Cc1cc(SC[C@@H]2[C@@H](Sc3nc[nH]n3)[C@H]3[C@H](C(=O)O)[C@H]3[C@]2(N)C(=O)O)ccc1F 10.1021/acs.jmedchem.6b01119
CHEMBL4803099 183793 None 0 Human Binding pKi = 8.4 8.4 1 2
Displacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in hamster AV12 cell membranes co-expressing rat EAAT1 incubated for 90 mins by top count scintillation methodDisplacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in hamster AV12 cell membranes co-expressing rat EAAT1 incubated for 90 mins by top count scintillation method
ChEMBL 438 7 4 7 1.9 Cc1cc(SC[C@@H]2[C@@H](Sc3nc[nH]n3)[C@H]3[C@H](C(=O)O)[C@H]3[C@]2(N)C(=O)O)ccc1F 10.1021/acs.jmedchem.6b01119
60096246 156037 None 0 Human Binding pKi = 8.3 8.3 40 2
Displacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in HEK cell membranes after 90 mins by liquid scintillation countingDisplacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in HEK cell membranes after 90 mins by liquid scintillation counting
ChEMBL 334 5 4 5 -0.1 COc1ccc(C(=O)N[C@H]2C[C@@](N)(C(=O)O)[C@@H]3[C@@H](C(=O)O)[C@H]23)cc1 10.1021/acs.jmedchem.7b01481
CHEMBL4061162 156037 None 0 Human Binding pKi = 8.3 8.3 40 2
Displacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in HEK cell membranes after 90 mins by liquid scintillation countingDisplacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in HEK cell membranes after 90 mins by liquid scintillation counting
ChEMBL 334 5 4 5 -0.1 COc1ccc(C(=O)N[C@H]2C[C@@](N)(C(=O)O)[C@@H]3[C@@H](C(=O)O)[C@H]23)cc1 10.1021/acs.jmedchem.7b01481
10198133 208966 None 10 Human Binding pKi = 8.3 8.3 6 2
Ability to displace [3H]LY-341,495 from recombinant human Metabotropic glutamate receptor 3 expressed in RGT cells.Ability to displace [3H]LY-341,495 from recombinant human Metabotropic glutamate receptor 3 expressed in RGT cells.
ChEMBL 203 2 3 4 -0.8 N[C@@]1(C(=O)O)CS[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/jm980616n
CHEMBL8839 208966 None 10 Human Binding pKi = 8.3 8.3 6 2
Ability to displace [3H]LY-341,495 from recombinant human Metabotropic glutamate receptor 3 expressed in RGT cells.Ability to displace [3H]LY-341,495 from recombinant human Metabotropic glutamate receptor 3 expressed in RGT cells.
ChEMBL 203 2 3 4 -0.8 N[C@@]1(C(=O)O)CS[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/jm980616n
10198133 208966 None 10 Human Binding pKi = 8.3 8.3 6 2
Displacement of [3H]LY341495 from human recombinant mGluR3 in RGT cellsDisplacement of [3H]LY341495 from human recombinant mGluR3 in RGT cells
ChEMBL 203 2 3 4 -0.8 N[C@@]1(C(=O)O)CS[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/jm060917u
CHEMBL8839 208966 None 10 Human Binding pKi = 8.3 8.3 6 2
Displacement of [3H]LY341495 from human recombinant mGluR3 in RGT cellsDisplacement of [3H]LY341495 from human recombinant mGluR3 in RGT cells
ChEMBL 203 2 3 4 -0.8 N[C@@]1(C(=O)O)CS[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/jm060917u
11279365 67581 None 0 Rat Binding pKi = 8.3 8.3 -1 2
Binding affinity towards metabotropic glutamate receptor 3 of rat expressed in CHO cells was determined by using [3H]MGS-0008Binding affinity towards metabotropic glutamate receptor 3 of rat expressed in CHO cells was determined by using [3H]MGS-0008
ChEMBL 343 5 3 4 1.5 N[C@@]1(C(=O)O)[C@H](OCc2ccc(Cl)cc2)C[C@@H]2[C@H]1[C@@]2(F)C(=O)O 10.1021/jm0400294
CHEMBL189814 67581 None 0 Rat Binding pKi = 8.3 8.3 -1 2
Binding affinity towards metabotropic glutamate receptor 3 of rat expressed in CHO cells was determined by using [3H]MGS-0008Binding affinity towards metabotropic glutamate receptor 3 of rat expressed in CHO cells was determined by using [3H]MGS-0008
ChEMBL 343 5 3 4 1.5 N[C@@]1(C(=O)O)[C@H](OCc2ccc(Cl)cc2)C[C@@H]2[C@H]1[C@@]2(F)C(=O)O 10.1021/jm0400294
9815617 114563 None 3 Rat Binding pKi = 7.4 7.4 -1 2
Tested for binding affinity against Metabotropic glutamate receptor 3 in CHO cells using [3H]-7 as radioligandTested for binding affinity against Metabotropic glutamate receptor 3 in CHO cells using [3H]-7 as radioligand
ChEMBL 203 2 3 3 -0.4 N[C@@]1(C(=O)O)CC[C@@H]2[C@H]1[C@@]2(F)C(=O)O 10.1021/jm000346k
CHEMBL333519 114563 None 3 Rat Binding pKi = 7.4 7.4 -1 2
Tested for binding affinity against Metabotropic glutamate receptor 3 in CHO cells using [3H]-7 as radioligandTested for binding affinity against Metabotropic glutamate receptor 3 in CHO cells using [3H]-7 as radioligand
ChEMBL 203 2 3 3 -0.4 N[C@@]1(C(=O)O)CC[C@@H]2[C@H]1[C@@]2(F)C(=O)O 10.1021/jm000346k
137656301 158774 None 0 Human Binding pKi = 6.4 6.4 1 2
Displacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in HEK cell membranes after 90 mins by liquid scintillation countingDisplacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in HEK cell membranes after 90 mins by liquid scintillation counting
ChEMBL 324 5 4 4 0.6 N[C@@]1(C(=O)O)C[C@H](NC(=O)CC2CCCCC2)[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/acs.jmedchem.7b01481
CHEMBL4093017 158774 None 0 Human Binding pKi = 6.4 6.4 1 2
Displacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in HEK cell membranes after 90 mins by liquid scintillation countingDisplacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in HEK cell membranes after 90 mins by liquid scintillation counting
ChEMBL 324 5 4 4 0.6 N[C@@]1(C(=O)O)C[C@H](NC(=O)CC2CCCCC2)[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/acs.jmedchem.7b01481
90098428 123472 None 0 Human Binding pKi = 7.4 7.4 -5 2
Displacement of [3H]-459477 from human recombinant mGlu3 receptor expressed in AV12 cells after 90 mins by liquid scintillation countingDisplacement of [3H]-459477 from human recombinant mGlu3 receptor expressed in AV12 cells after 90 mins by liquid scintillation counting
ChEMBL 352 4 4 6 0.4 N[C@@]1(C(=O)O)C[C@H](Sc2nnc(C(F)(F)F)[nH]2)[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/acs.jmedchem.5b01124
CHEMBL3616856 123472 None 0 Human Binding pKi = 7.4 7.4 -5 2
Displacement of [3H]-459477 from human recombinant mGlu3 receptor expressed in AV12 cells after 90 mins by liquid scintillation countingDisplacement of [3H]-459477 from human recombinant mGlu3 receptor expressed in AV12 cells after 90 mins by liquid scintillation counting
ChEMBL 352 4 4 6 0.4 N[C@@]1(C(=O)O)C[C@H](Sc2nnc(C(F)(F)F)[nH]2)[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/acs.jmedchem.5b01124
10353365 83279 None 1 Human Binding pKi = 6.4 6.4 5 2
Displacement of [3H]LY341495 from human recombinant mGluR3 in RGT cellsDisplacement of [3H]LY341495 from human recombinant mGluR3 in RGT cells
ChEMBL 219 2 3 4 -1.8 N[C@@]1(C(=O)O)C[S+]([O-])[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/jm060917u
CHEMBL218710 83279 None 1 Human Binding pKi = 6.4 6.4 5 2
Displacement of [3H]LY341495 from human recombinant mGluR3 in RGT cellsDisplacement of [3H]LY341495 from human recombinant mGluR3 in RGT cells
ChEMBL 219 2 3 4 -1.8 N[C@@]1(C(=O)O)C[S+]([O-])[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/jm060917u
11405687 66478 None 0 Rat Binding pKi = 8.3 8.3 -2 2
Binding affinity towards metabotropic glutamate receptor 3 of rat expressed in CHO cells was determined by using [3H]MGS-0008Binding affinity towards metabotropic glutamate receptor 3 of rat expressed in CHO cells was determined by using [3H]MGS-0008
ChEMBL 359 5 3 4 2.0 N[C@@]1(C(=O)O)[C@H](OCc2ccc3ccccc3c2)C[C@@H]2[C@H]1[C@@]2(F)C(=O)O 10.1021/jm0400294
CHEMBL185210 66478 None 0 Rat Binding pKi = 8.3 8.3 -2 2
Binding affinity towards metabotropic glutamate receptor 3 of rat expressed in CHO cells was determined by using [3H]MGS-0008Binding affinity towards metabotropic glutamate receptor 3 of rat expressed in CHO cells was determined by using [3H]MGS-0008
ChEMBL 359 5 3 4 2.0 N[C@@]1(C(=O)O)[C@H](OCc2ccc3ccccc3c2)C[C@@H]2[C@H]1[C@@]2(F)C(=O)O 10.1021/jm0400294
60096236 158514 None 0 Human Binding pKi = 8.2 8.2 38 2
Displacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in HEK cell membranes after 90 mins by liquid scintillation countingDisplacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in HEK cell membranes after 90 mins by liquid scintillation counting
ChEMBL 322 4 4 4 0.1 N[C@@]1(C(=O)O)C[C@H](NC(=O)c2ccccc2F)[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/acs.jmedchem.7b01481
CHEMBL4090293 158514 None 0 Human Binding pKi = 8.2 8.2 38 2
Displacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in HEK cell membranes after 90 mins by liquid scintillation countingDisplacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in HEK cell membranes after 90 mins by liquid scintillation counting
ChEMBL 322 4 4 4 0.1 N[C@@]1(C(=O)O)C[C@H](NC(=O)c2ccccc2F)[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/acs.jmedchem.7b01481
10197984 2421 None 36 Human Binding pKi = 8.2 8.2 -2 5
Ability to displace [3H]LY-341,495 from recombinant human Metabotropic glutamate receptor 3 expressed in RGT cells.Ability to displace [3H]LY-341,495 from recombinant human Metabotropic glutamate receptor 3 expressed in RGT cells.
ChEMBL 187 2 3 4 -1.5 OC(=O)[C@H]1[C@H]2[C@@H]1[C@](CO2)(N)C(=O)O 10.1021/jm980616n
1394 2421 None 36 Human Binding pKi = 8.2 8.2 -2 5
Ability to displace [3H]LY-341,495 from recombinant human Metabotropic glutamate receptor 3 expressed in RGT cells.Ability to displace [3H]LY-341,495 from recombinant human Metabotropic glutamate receptor 3 expressed in RGT cells.
ChEMBL 187 2 3 4 -1.5 OC(=O)[C@H]1[C@H]2[C@@H]1[C@](CO2)(N)C(=O)O 10.1021/jm980616n
CHEMBL275079 2421 None 36 Human Binding pKi = 8.2 8.2 -2 5
Ability to displace [3H]LY-341,495 from recombinant human Metabotropic glutamate receptor 3 expressed in RGT cells.Ability to displace [3H]LY-341,495 from recombinant human Metabotropic glutamate receptor 3 expressed in RGT cells.
ChEMBL 187 2 3 4 -1.5 OC(=O)[C@H]1[C@H]2[C@@H]1[C@](CO2)(N)C(=O)O 10.1021/jm980616n
10197984 2421 None 36 Human Binding pKi = 8.2 8.2 -2 5
Displacement of [3H]LY341495 from human recombinant mGluR3 in RGT cellsDisplacement of [3H]LY341495 from human recombinant mGluR3 in RGT cells
ChEMBL 187 2 3 4 -1.5 OC(=O)[C@H]1[C@H]2[C@@H]1[C@](CO2)(N)C(=O)O 10.1021/jm060917u
1394 2421 None 36 Human Binding pKi = 8.2 8.2 -2 5
Displacement of [3H]LY341495 from human recombinant mGluR3 in RGT cellsDisplacement of [3H]LY341495 from human recombinant mGluR3 in RGT cells
ChEMBL 187 2 3 4 -1.5 OC(=O)[C@H]1[C@H]2[C@@H]1[C@](CO2)(N)C(=O)O 10.1021/jm060917u
CHEMBL275079 2421 None 36 Human Binding pKi = 8.2 8.2 -2 5
Displacement of [3H]LY341495 from human recombinant mGluR3 in RGT cellsDisplacement of [3H]LY341495 from human recombinant mGluR3 in RGT cells
ChEMBL 187 2 3 4 -1.5 OC(=O)[C@H]1[C@H]2[C@@H]1[C@](CO2)(N)C(=O)O 10.1021/jm060917u
67633340 183827 None 0 Human Binding pKi = 8.2 8.2 1 2
Displacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in hamster AV12 cell membranes co-expressing rat EAAT1 incubated for 90 mins by top count scintillation methodDisplacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in hamster AV12 cell membranes co-expressing rat EAAT1 incubated for 90 mins by top count scintillation method
ChEMBL 355 5 4 5 0.9 Cc1cc(SC[C@@H]2[C@@H](O)[C@@H]3[C@@H]([C@H]3C(=O)O)[C@]2(N)C(=O)O)ccc1F 10.1021/acs.jmedchem.6b01119
CHEMBL4780402 183827 None 0 Human Binding pKi = 8.2 8.2 1 2
Displacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in hamster AV12 cell membranes co-expressing rat EAAT1 incubated for 90 mins by top count scintillation methodDisplacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in hamster AV12 cell membranes co-expressing rat EAAT1 incubated for 90 mins by top count scintillation method
ChEMBL 355 5 4 5 0.9 Cc1cc(SC[C@@H]2[C@@H](O)[C@@H]3[C@@H]([C@H]3C(=O)O)[C@]2(N)C(=O)O)ccc1F 10.1021/acs.jmedchem.6b01119
CHEMBL4803381 183827 None 0 Human Binding pKi = 8.2 8.2 1 2
Displacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in hamster AV12 cell membranes co-expressing rat EAAT1 incubated for 90 mins by top count scintillation methodDisplacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in hamster AV12 cell membranes co-expressing rat EAAT1 incubated for 90 mins by top count scintillation method
ChEMBL 355 5 4 5 0.9 Cc1cc(SC[C@@H]2[C@@H](O)[C@@H]3[C@@H]([C@H]3C(=O)O)[C@]2(N)C(=O)O)ccc1F 10.1021/acs.jmedchem.6b01119
11344646 126844 None 0 Human Binding pKi = 6.3 6.3 1 2
Displacement of [3H]-341495 binding to membranes expressing recombinant human Metabotropic glutamate receptor 3Displacement of [3H]-341495 binding to membranes expressing recombinant human Metabotropic glutamate receptor 3
ChEMBL 199 2 3 3 -0.2 C[C@H]1C[C@@](N)(C(=O)O)[C@@H]2[C@@H](C(=O)O)[C@H]12 10.1021/jm040222y
CHEMBL365368 126844 None 0 Human Binding pKi = 6.3 6.3 1 2
Displacement of [3H]-341495 binding to membranes expressing recombinant human Metabotropic glutamate receptor 3Displacement of [3H]-341495 binding to membranes expressing recombinant human Metabotropic glutamate receptor 3
ChEMBL 199 2 3 3 -0.2 C[C@H]1C[C@@](N)(C(=O)O)[C@@H]2[C@@H](C(=O)O)[C@H]12 10.1021/jm040222y
1393 1539 None 42 Rat Binding pKi = 7.3 7.3 -2 6
Tested for binding affinity against Metabotropic glutamate receptor 3 in CHO cells using [3H]-7 as radioligandTested for binding affinity against Metabotropic glutamate receptor 3 in CHO cells using [3H]-7 as radioligand
ChEMBL 185 2 3 3 -0.5 OC(=O)[C@H]1[C@H]2[C@@H]1[C@](CC2)(N)C(=O)O 10.1021/jm000346k
1396 1539 None 42 Rat Binding pKi = 7.3 7.3 -2 6
Tested for binding affinity against Metabotropic glutamate receptor 3 in CHO cells using [3H]-7 as radioligandTested for binding affinity against Metabotropic glutamate receptor 3 in CHO cells using [3H]-7 as radioligand
ChEMBL 185 2 3 3 -0.5 OC(=O)[C@H]1[C@H]2[C@@H]1[C@](CC2)(N)C(=O)O 10.1021/jm000346k
213056 1539 None 42 Rat Binding pKi = 7.3 7.3 -2 6
Tested for binding affinity against Metabotropic glutamate receptor 3 in CHO cells using [3H]-7 as radioligandTested for binding affinity against Metabotropic glutamate receptor 3 in CHO cells using [3H]-7 as radioligand
ChEMBL 185 2 3 3 -0.5 OC(=O)[C@H]1[C@H]2[C@@H]1[C@](CC2)(N)C(=O)O 10.1021/jm000346k
CHEMBL8759 1539 None 42 Rat Binding pKi = 7.3 7.3 -2 6
Tested for binding affinity against Metabotropic glutamate receptor 3 in CHO cells using [3H]-7 as radioligandTested for binding affinity against Metabotropic glutamate receptor 3 in CHO cells using [3H]-7 as radioligand
ChEMBL 185 2 3 3 -0.5 OC(=O)[C@H]1[C@H]2[C@@H]1[C@](CC2)(N)C(=O)O 10.1021/jm000346k
71137010 123465 None 0 Human Binding pKi = 7.3 7.3 1 2
Displacement of [3H]-459477 from human recombinant mGlu3 receptor expressed in AV12 cells after 90 mins by liquid scintillation countingDisplacement of [3H]-459477 from human recombinant mGlu3 receptor expressed in AV12 cells after 90 mins by liquid scintillation counting
ChEMBL 352 4 4 6 0.4 N[C@@]1(C(=O)O)C[C@@H](Sc2nnc(C(F)(F)F)[nH]2)[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/acs.jmedchem.5b01124
CHEMBL3616849 123465 None 0 Human Binding pKi = 7.3 7.3 1 2
Displacement of [3H]-459477 from human recombinant mGlu3 receptor expressed in AV12 cells after 90 mins by liquid scintillation countingDisplacement of [3H]-459477 from human recombinant mGlu3 receptor expressed in AV12 cells after 90 mins by liquid scintillation counting
ChEMBL 352 4 4 6 0.4 N[C@@]1(C(=O)O)C[C@@H](Sc2nnc(C(F)(F)F)[nH]2)[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/acs.jmedchem.5b01124
71131322 123473 None 0 Human Binding pKi = 7.2 7.2 -4 2
Displacement of [3H]-459477 from human recombinant mGlu3 receptor expressed in AV12 cells after 90 mins by liquid scintillation countingDisplacement of [3H]-459477 from human recombinant mGlu3 receptor expressed in AV12 cells after 90 mins by liquid scintillation counting
ChEMBL 334 5 4 6 0.3 N[C@@]1(C(=O)O)C[C@H](Sc2nnc(C(F)F)[nH]2)[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/acs.jmedchem.5b01124
CHEMBL3616857 123473 None 0 Human Binding pKi = 7.2 7.2 -4 2
Displacement of [3H]-459477 from human recombinant mGlu3 receptor expressed in AV12 cells after 90 mins by liquid scintillation countingDisplacement of [3H]-459477 from human recombinant mGlu3 receptor expressed in AV12 cells after 90 mins by liquid scintillation counting
ChEMBL 334 5 4 6 0.3 N[C@@]1(C(=O)O)C[C@H](Sc2nnc(C(F)F)[nH]2)[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/acs.jmedchem.5b01124
1310 2315 None 61 Human Binding pKi = 7.2 7.2 1 18
Binding affinity to human mGluR3 receptor expressed in HEK cellsBinding affinity to human mGluR3 receptor expressed in HEK cells
ChEMBL 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N 10.1039/C1MD00186H
1369 2315 None 61 Human Binding pKi = 7.2 7.2 1 18
Binding affinity to human mGluR3 receptor expressed in HEK cellsBinding affinity to human mGluR3 receptor expressed in HEK cells
ChEMBL 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N 10.1039/C1MD00186H
33032 2315 None 61 Human Binding pKi = 7.2 7.2 1 18
Binding affinity to human mGluR3 receptor expressed in HEK cellsBinding affinity to human mGluR3 receptor expressed in HEK cells
ChEMBL 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N 10.1039/C1MD00186H
44272391 2315 None 61 Human Binding pKi = 7.2 7.2 1 18
Binding affinity to human mGluR3 receptor expressed in HEK cellsBinding affinity to human mGluR3 receptor expressed in HEK cells
ChEMBL 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N 10.1039/C1MD00186H
88747398 2315 None 61 Human Binding pKi = 7.2 7.2 1 18
Binding affinity to human mGluR3 receptor expressed in HEK cellsBinding affinity to human mGluR3 receptor expressed in HEK cells
ChEMBL 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N 10.1039/C1MD00186H
CHEMBL575060 2315 None 61 Human Binding pKi = 7.2 7.2 1 18
Binding affinity to human mGluR3 receptor expressed in HEK cellsBinding affinity to human mGluR3 receptor expressed in HEK cells
ChEMBL 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N 10.1039/C1MD00186H
DB00142 2315 None 61 Human Binding pKi = 7.2 7.2 1 18
Binding affinity to human mGluR3 receptor expressed in HEK cellsBinding affinity to human mGluR3 receptor expressed in HEK cells
ChEMBL 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N 10.1039/C1MD00186H
11310142 2422 None 14 Human Binding pKi = 6.2 6.2 -1 2
Displacement of [3H]-341495 binding to membranes expressing recombinant human Metabotropic glutamate receptor 3Displacement of [3H]-341495 binding to membranes expressing recombinant human Metabotropic glutamate receptor 3
ChEMBL 199 2 3 3 -0.2 C[C@@H]1C[C@@]([C@H]2[C@@H]1[C@@H]2C(=O)O)(N)C(=O)O 10.1021/jm040222y
11614 2422 None 14 Human Binding pKi = 6.2 6.2 -1 2
Displacement of [3H]-341495 binding to membranes expressing recombinant human Metabotropic glutamate receptor 3Displacement of [3H]-341495 binding to membranes expressing recombinant human Metabotropic glutamate receptor 3
ChEMBL 199 2 3 3 -0.2 C[C@@H]1C[C@@]([C@H]2[C@@H]1[C@@H]2C(=O)O)(N)C(=O)O 10.1021/jm040222y
CHEMBL192051 2422 None 14 Human Binding pKi = 6.2 6.2 -1 2
Displacement of [3H]-341495 binding to membranes expressing recombinant human Metabotropic glutamate receptor 3Displacement of [3H]-341495 binding to membranes expressing recombinant human Metabotropic glutamate receptor 3
ChEMBL 199 2 3 3 -0.2 C[C@@H]1C[C@@]([C@H]2[C@@H]1[C@@H]2C(=O)O)(N)C(=O)O 10.1021/jm040222y
71137012 123467 None 0 Human Binding pKi = 7.2 7.2 1 2
Displacement of [3H]-459477 from human recombinant mGlu3 receptor expressed in AV12 cells after 90 mins by liquid scintillation countingDisplacement of [3H]-459477 from human recombinant mGlu3 receptor expressed in AV12 cells after 90 mins by liquid scintillation counting
ChEMBL 299 4 5 7 -1.0 Nc1nnc(S[C@@H]2C[C@@](N)(C(=O)O)[C@@H]3[C@@H](C(=O)O)[C@H]23)[nH]1 10.1021/acs.jmedchem.5b01124
CHEMBL3616851 123467 None 0 Human Binding pKi = 7.2 7.2 1 2
Displacement of [3H]-459477 from human recombinant mGlu3 receptor expressed in AV12 cells after 90 mins by liquid scintillation countingDisplacement of [3H]-459477 from human recombinant mGlu3 receptor expressed in AV12 cells after 90 mins by liquid scintillation counting
ChEMBL 299 4 5 7 -1.0 Nc1nnc(S[C@@H]2C[C@@](N)(C(=O)O)[C@@H]3[C@@H](C(=O)O)[C@H]23)[nH]1 10.1021/acs.jmedchem.5b01124
11220424 159053 None 0 Human Binding pKi = 8.2 8.2 43 2
Displacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in HEK cell membranes after 90 mins by liquid scintillation countingDisplacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in HEK cell membranes after 90 mins by liquid scintillation counting
ChEMBL 304 4 4 4 -0.1 N[C@@]1(C(=O)O)C[C@H](NC(=O)c2ccccc2)[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/acs.jmedchem.7b01481
CHEMBL4095995 159053 None 0 Human Binding pKi = 8.2 8.2 43 2
Displacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in HEK cell membranes after 90 mins by liquid scintillation countingDisplacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in HEK cell membranes after 90 mins by liquid scintillation counting
ChEMBL 304 4 4 4 -0.1 N[C@@]1(C(=O)O)C[C@H](NC(=O)c2ccccc2)[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/acs.jmedchem.7b01481
67637138 183724 None 0 Human Binding pKi = 8.2 8.2 1 2
Displacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in hamster AV12 cell membranes co-expressing rat EAAT1 incubated for 90 mins by top count scintillation methodDisplacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in hamster AV12 cell membranes co-expressing rat EAAT1 incubated for 90 mins by top count scintillation method
ChEMBL 341 5 4 5 0.6 N[C@@]1(C(=O)O)[C@H](CSc2ccc(F)cc2)[C@@H](O)[C@@H]2[C@H]1[C@H]2C(=O)O 10.1021/acs.jmedchem.6b01119
CHEMBL4776989 183724 None 0 Human Binding pKi = 8.2 8.2 1 2
Displacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in hamster AV12 cell membranes co-expressing rat EAAT1 incubated for 90 mins by top count scintillation methodDisplacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in hamster AV12 cell membranes co-expressing rat EAAT1 incubated for 90 mins by top count scintillation method
ChEMBL 341 5 4 5 0.6 N[C@@]1(C(=O)O)[C@H](CSc2ccc(F)cc2)[C@@H](O)[C@@H]2[C@H]1[C@H]2C(=O)O 10.1021/acs.jmedchem.6b01119
CHEMBL4802329 183724 None 0 Human Binding pKi = 8.2 8.2 1 2
Displacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in hamster AV12 cell membranes co-expressing rat EAAT1 incubated for 90 mins by top count scintillation methodDisplacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in hamster AV12 cell membranes co-expressing rat EAAT1 incubated for 90 mins by top count scintillation method
ChEMBL 341 5 4 5 0.6 N[C@@]1(C(=O)O)[C@H](CSc2ccc(F)cc2)[C@@H](O)[C@@H]2[C@H]1[C@H]2C(=O)O 10.1021/acs.jmedchem.6b01119
162652146 180319 None 0 Human Binding pKi = 6.2 6.2 1 2
Displacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in hamster AV12 cell membranes co-expressing rat EAAT1 incubated for 90 mins by top count scintillation methodDisplacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in hamster AV12 cell membranes co-expressing rat EAAT1 incubated for 90 mins by top count scintillation method
ChEMBL 289 5 4 5 -0.2 CC(C)SC[C@@H]1[C@@H](O)[C@@H]2[C@@H]([C@H]2C(=O)O)[C@]1(N)C(=O)O 10.1021/acs.jmedchem.6b01119
CHEMBL4749728 180319 None 0 Human Binding pKi = 6.2 6.2 1 2
Displacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in hamster AV12 cell membranes co-expressing rat EAAT1 incubated for 90 mins by top count scintillation methodDisplacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in hamster AV12 cell membranes co-expressing rat EAAT1 incubated for 90 mins by top count scintillation method
ChEMBL 289 5 4 5 -0.2 CC(C)SC[C@@H]1[C@@H](O)[C@@H]2[C@@H]([C@H]2C(=O)O)[C@]1(N)C(=O)O 10.1021/acs.jmedchem.6b01119
71135411 123464 None 0 Human Binding pKi = 7.2 7.2 1 2
Displacement of [3H]-459477 from human recombinant mGlu3 receptor expressed in AV12 cells after 90 mins by liquid scintillation countingDisplacement of [3H]-459477 from human recombinant mGlu3 receptor expressed in AV12 cells after 90 mins by liquid scintillation counting
ChEMBL 298 4 4 6 -0.3 Cc1nnc(S[C@@H]2C[C@@](N)(C(=O)O)[C@@H]3[C@@H](C(=O)O)[C@H]23)[nH]1 10.1021/acs.jmedchem.5b01124
CHEMBL3616848 123464 None 0 Human Binding pKi = 7.2 7.2 1 2
Displacement of [3H]-459477 from human recombinant mGlu3 receptor expressed in AV12 cells after 90 mins by liquid scintillation countingDisplacement of [3H]-459477 from human recombinant mGlu3 receptor expressed in AV12 cells after 90 mins by liquid scintillation counting
ChEMBL 298 4 4 6 -0.3 Cc1nnc(S[C@@H]2C[C@@](N)(C(=O)O)[C@@H]3[C@@H](C(=O)O)[C@H]23)[nH]1 10.1021/acs.jmedchem.5b01124
71137034 123466 None 0 Human Binding pKi = 7.2 7.2 1 2
Displacement of [3H]-459477 from human recombinant mGlu3 receptor expressed in AV12 cells after 90 mins by liquid scintillation countingDisplacement of [3H]-459477 from human recombinant mGlu3 receptor expressed in AV12 cells after 90 mins by liquid scintillation counting
ChEMBL 334 5 4 6 0.3 N[C@@]1(C(=O)O)C[C@@H](Sc2nnc(C(F)F)[nH]2)[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/acs.jmedchem.5b01124
CHEMBL3616850 123466 None 0 Human Binding pKi = 7.2 7.2 1 2
Displacement of [3H]-459477 from human recombinant mGlu3 receptor expressed in AV12 cells after 90 mins by liquid scintillation countingDisplacement of [3H]-459477 from human recombinant mGlu3 receptor expressed in AV12 cells after 90 mins by liquid scintillation counting
ChEMBL 334 5 4 6 0.3 N[C@@]1(C(=O)O)C[C@@H](Sc2nnc(C(F)F)[nH]2)[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/acs.jmedchem.5b01124
71476419 123476 None 0 Human Binding pKi = 7.2 7.2 1 2
Displacement of [3H]-459477 from human recombinant mGlu3 receptor expressed in AV12 cells after 90 mins by liquid scintillation countingDisplacement of [3H]-459477 from human recombinant mGlu3 receptor expressed in AV12 cells after 90 mins by liquid scintillation counting
ChEMBL 284 4 4 6 -0.6 N[C@@]1(C(=O)O)C[C@H](Sc2c[nH]nn2)[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/acs.jmedchem.5b01124
CHEMBL3616860 123476 None 0 Human Binding pKi = 7.2 7.2 1 2
Displacement of [3H]-459477 from human recombinant mGlu3 receptor expressed in AV12 cells after 90 mins by liquid scintillation countingDisplacement of [3H]-459477 from human recombinant mGlu3 receptor expressed in AV12 cells after 90 mins by liquid scintillation counting
ChEMBL 284 4 4 6 -0.6 N[C@@]1(C(=O)O)C[C@H](Sc2c[nH]nn2)[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/acs.jmedchem.5b01124
9815616 114864 None 4 Rat Binding pKi = 7.2 7.2 -1 2
Tested for binding affinity against Metabotropic glutamate receptor 3 in CHO cells using [3H]-7 as radioligandTested for binding affinity against Metabotropic glutamate receptor 3 in CHO cells using [3H]-7 as radioligand
ChEMBL 203 2 3 3 -0.5 N[C@@]1(C(=O)O)[C@@H](F)C[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/jm000346k
CHEMBL334014 114864 None 4 Rat Binding pKi = 7.2 7.2 -1 2
Tested for binding affinity against Metabotropic glutamate receptor 3 in CHO cells using [3H]-7 as radioligandTested for binding affinity against Metabotropic glutamate receptor 3 in CHO cells using [3H]-7 as radioligand
ChEMBL 203 2 3 3 -0.5 N[C@@]1(C(=O)O)[C@@H](F)C[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/jm000346k
10130658 66774 None 0 Rat Binding pKi = 7.2 7.2 -2 2
Binding affinity towards metabotropic glutamate receptor 3 of rat expressed in CHO cells was determined by using [3H]MGS-0008Binding affinity towards metabotropic glutamate receptor 3 of rat expressed in CHO cells was determined by using [3H]MGS-0008
ChEMBL 219 2 4 4 -1.4 N[C@@]1(C(=O)O)[C@H](O)C[C@@H]2[C@H]1[C@@]2(F)C(=O)O 10.1021/jm0400294
CHEMBL185822 66774 None 0 Rat Binding pKi = 7.2 7.2 -2 2
Binding affinity towards metabotropic glutamate receptor 3 of rat expressed in CHO cells was determined by using [3H]MGS-0008Binding affinity towards metabotropic glutamate receptor 3 of rat expressed in CHO cells was determined by using [3H]MGS-0008
ChEMBL 219 2 4 4 -1.4 N[C@@]1(C(=O)O)[C@H](O)C[C@@H]2[C@H]1[C@@]2(F)C(=O)O 10.1021/jm0400294
71137011 123474 None 0 Human Binding pKi = 7.2 7.2 -2 2
Displacement of [3H]-459477 from human recombinant mGlu3 receptor expressed in AV12 cells after 90 mins by liquid scintillation countingDisplacement of [3H]-459477 from human recombinant mGlu3 receptor expressed in AV12 cells after 90 mins by liquid scintillation counting
ChEMBL 299 4 5 7 -1.0 Nc1nnc(S[C@H]2C[C@@](N)(C(=O)O)[C@@H]3[C@@H](C(=O)O)[C@H]23)[nH]1 10.1021/acs.jmedchem.5b01124
CHEMBL3616858 123474 None 0 Human Binding pKi = 7.2 7.2 -2 2
Displacement of [3H]-459477 from human recombinant mGlu3 receptor expressed in AV12 cells after 90 mins by liquid scintillation countingDisplacement of [3H]-459477 from human recombinant mGlu3 receptor expressed in AV12 cells after 90 mins by liquid scintillation counting
ChEMBL 299 4 5 7 -1.0 Nc1nnc(S[C@H]2C[C@@](N)(C(=O)O)[C@@H]3[C@@H](C(=O)O)[C@H]23)[nH]1 10.1021/acs.jmedchem.5b01124
69669820 183746 None 0 Human Binding pKi = 8.1 8.1 1 2
Displacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in hamster AV12 cell membranes co-expressing rat EAAT1 incubated for 90 mins by top count scintillation methodDisplacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in hamster AV12 cell membranes co-expressing rat EAAT1 incubated for 90 mins by top count scintillation method
ChEMBL 396 6 4 5 1.1 CC(=O)N[C@H]1[C@H]2[C@H](C(=O)O)[C@H]2[C@](N)(C(=O)O)[C@@H]1CSc1ccc(F)c(C)c1 10.1021/acs.jmedchem.6b01119
CHEMBL4746125 183746 None 0 Human Binding pKi = 8.1 8.1 1 2
Displacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in hamster AV12 cell membranes co-expressing rat EAAT1 incubated for 90 mins by top count scintillation methodDisplacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in hamster AV12 cell membranes co-expressing rat EAAT1 incubated for 90 mins by top count scintillation method
ChEMBL 396 6 4 5 1.1 CC(=O)N[C@H]1[C@H]2[C@H](C(=O)O)[C@H]2[C@](N)(C(=O)O)[C@@H]1CSc1ccc(F)c(C)c1 10.1021/acs.jmedchem.6b01119
CHEMBL4802570 183746 None 0 Human Binding pKi = 8.1 8.1 1 2
Displacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in hamster AV12 cell membranes co-expressing rat EAAT1 incubated for 90 mins by top count scintillation methodDisplacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in hamster AV12 cell membranes co-expressing rat EAAT1 incubated for 90 mins by top count scintillation method
ChEMBL 396 6 4 5 1.1 CC(=O)N[C@H]1[C@H]2[C@H](C(=O)O)[C@H]2[C@](N)(C(=O)O)[C@@H]1CSc1ccc(F)c(C)c1 10.1021/acs.jmedchem.6b01119
137635882 155984 None 0 Human Binding pKi = 6.1 6.1 1 2
Displacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in HEK cell membranes after 90 mins by liquid scintillation countingDisplacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in HEK cell membranes after 90 mins by liquid scintillation counting
ChEMBL 310 4 4 4 0.2 N[C@@]1(C(=O)O)C[C@H](NC(=O)C2CCCCC2)[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/acs.jmedchem.7b01481
CHEMBL4060567 155984 None 0 Human Binding pKi = 6.1 6.1 1 2
Displacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in HEK cell membranes after 90 mins by liquid scintillation countingDisplacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in HEK cell membranes after 90 mins by liquid scintillation counting
ChEMBL 310 4 4 4 0.2 N[C@@]1(C(=O)O)C[C@H](NC(=O)C2CCCCC2)[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/acs.jmedchem.7b01481
71137008 123471 None 0 Human Binding pKi = 7.1 7.1 2 2
Displacement of [3H]-459477 from human recombinant mGlu3 receptor expressed in AV12 cells after 90 mins by liquid scintillation countingDisplacement of [3H]-459477 from human recombinant mGlu3 receptor expressed in AV12 cells after 90 mins by liquid scintillation counting
ChEMBL 298 4 4 6 -0.3 Cc1nnc(S[C@H]2C[C@@](N)(C(=O)O)[C@@H]3[C@@H](C(=O)O)[C@H]23)[nH]1 10.1021/acs.jmedchem.5b01124
CHEMBL3616855 123471 None 0 Human Binding pKi = 7.1 7.1 2 2
Displacement of [3H]-459477 from human recombinant mGlu3 receptor expressed in AV12 cells after 90 mins by liquid scintillation countingDisplacement of [3H]-459477 from human recombinant mGlu3 receptor expressed in AV12 cells after 90 mins by liquid scintillation counting
ChEMBL 298 4 4 6 -0.3 Cc1nnc(S[C@H]2C[C@@](N)(C(=O)O)[C@@H]3[C@@H](C(=O)O)[C@H]23)[nH]1 10.1021/acs.jmedchem.5b01124
71136654 123475 None 0 Human Binding pKi = 7.1 7.1 4 2
Displacement of [3H]-459477 from human recombinant mGlu3 receptor expressed in AV12 cells after 90 mins by liquid scintillation countingDisplacement of [3H]-459477 from human recombinant mGlu3 receptor expressed in AV12 cells after 90 mins by liquid scintillation counting
ChEMBL 326 5 4 6 0.5 CC(C)c1nnc(S[C@H]2C[C@@](N)(C(=O)O)[C@@H]3[C@@H](C(=O)O)[C@H]23)[nH]1 10.1021/acs.jmedchem.5b01124
CHEMBL3616859 123475 None 0 Human Binding pKi = 7.1 7.1 4 2
Displacement of [3H]-459477 from human recombinant mGlu3 receptor expressed in AV12 cells after 90 mins by liquid scintillation countingDisplacement of [3H]-459477 from human recombinant mGlu3 receptor expressed in AV12 cells after 90 mins by liquid scintillation counting
ChEMBL 326 5 4 6 0.5 CC(C)c1nnc(S[C@H]2C[C@@](N)(C(=O)O)[C@@H]3[C@@H](C(=O)O)[C@H]23)[nH]1 10.1021/acs.jmedchem.5b01124
10192719 66135 None 0 Rat Binding pKi = 7.1 7.1 -2 2
Binding affinity towards metabotropic glutamate receptor 3 of rat expressed in CHO cells was determined by using [3H]MGS-0008Binding affinity towards metabotropic glutamate receptor 3 of rat expressed in CHO cells was determined by using [3H]MGS-0008
ChEMBL 233 3 3 4 -0.8 CO[C@@H]1C[C@@H]2[C@H]([C@]1(N)C(=O)O)[C@@]2(F)C(=O)O 10.1021/jm0400294
CHEMBL183956 66135 None 0 Rat Binding pKi = 7.1 7.1 -2 2
Binding affinity towards metabotropic glutamate receptor 3 of rat expressed in CHO cells was determined by using [3H]MGS-0008Binding affinity towards metabotropic glutamate receptor 3 of rat expressed in CHO cells was determined by using [3H]MGS-0008
ChEMBL 233 3 3 4 -0.8 CO[C@@H]1C[C@@H]2[C@H]([C@]1(N)C(=O)O)[C@@]2(F)C(=O)O 10.1021/jm0400294
60096228 156879 None 0 Human Binding pKi = 8.0 8.0 5 2
Displacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in HEK cell membranes after 90 mins by liquid scintillation countingDisplacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in HEK cell membranes after 90 mins by liquid scintillation counting
ChEMBL 320 4 5 5 -0.4 N[C@@]1(C(=O)O)C[C@H](NC(=O)c2ccc(O)cc2)[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/acs.jmedchem.7b01481
CHEMBL4070866 156879 None 0 Human Binding pKi = 8.0 8.0 5 2
Displacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in HEK cell membranes after 90 mins by liquid scintillation countingDisplacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in HEK cell membranes after 90 mins by liquid scintillation counting
ChEMBL 320 4 5 5 -0.4 N[C@@]1(C(=O)O)C[C@H](NC(=O)c2ccc(O)cc2)[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/acs.jmedchem.7b01481
10198133 208966 None 10 Human Binding pKi = 8.0 8.0 6 2
Ability to displace [3H]LY-341,495 from recombinant human Metabotropic glutamate receptor 3 expressed in RGT cells.Ability to displace [3H]LY-341,495 from recombinant human Metabotropic glutamate receptor 3 expressed in RGT cells.
ChEMBL 203 2 3 4 -0.8 N[C@@]1(C(=O)O)CS[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/jm980616n
CHEMBL8839 208966 None 10 Human Binding pKi = 8.0 8.0 6 2
Ability to displace [3H]LY-341,495 from recombinant human Metabotropic glutamate receptor 3 expressed in RGT cells.Ability to displace [3H]LY-341,495 from recombinant human Metabotropic glutamate receptor 3 expressed in RGT cells.
ChEMBL 203 2 3 4 -0.8 N[C@@]1(C(=O)O)CS[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/jm980616n
67633284 183753 None 0 Human Binding pKi = 8.0 8.0 -1 2
Displacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in hamster AV12 cell membranes co-expressing rat EAAT1 incubated for 90 mins by top count scintillation methodDisplacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in hamster AV12 cell membranes co-expressing rat EAAT1 incubated for 90 mins by top count scintillation method
ChEMBL 391 5 4 5 1.8 N[C@@]1(C(=O)O)[C@H](CSc2ccc(Cl)c(Cl)c2)[C@@H](O)[C@@H]2[C@H]1[C@H]2C(=O)O 10.1021/acs.jmedchem.6b01119
CHEMBL4748699 183753 None 0 Human Binding pKi = 8.0 8.0 -1 2
Displacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in hamster AV12 cell membranes co-expressing rat EAAT1 incubated for 90 mins by top count scintillation methodDisplacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in hamster AV12 cell membranes co-expressing rat EAAT1 incubated for 90 mins by top count scintillation method
ChEMBL 391 5 4 5 1.8 N[C@@]1(C(=O)O)[C@H](CSc2ccc(Cl)c(Cl)c2)[C@@H](O)[C@@H]2[C@H]1[C@H]2C(=O)O 10.1021/acs.jmedchem.6b01119
CHEMBL4802655 183753 None 0 Human Binding pKi = 8.0 8.0 -1 2
Displacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in hamster AV12 cell membranes co-expressing rat EAAT1 incubated for 90 mins by top count scintillation methodDisplacement of [3H]-LY459477 from recombinant human mGlu3 receptor expressed in hamster AV12 cell membranes co-expressing rat EAAT1 incubated for 90 mins by top count scintillation method
ChEMBL 391 5 4 5 1.8 N[C@@]1(C(=O)O)[C@H](CSc2ccc(Cl)c(Cl)c2)[C@@H](O)[C@@H]2[C@H]1[C@H]2C(=O)O 10.1021/acs.jmedchem.6b01119
9834591 137687 None 46 Human Binding pKi = 7.0 7.0 1 2
Displacement of [3H]LY341495 from human recombinant mGluR3 in RGT cellsDisplacement of [3H]LY341495 from human recombinant mGluR3 in RGT cells
ChEMBL 235 2 3 5 -2.1 N[C@@]1(C(=O)O)CS(=O)(=O)[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/jm060917u
CHEMBL375611 137687 None 46 Human Binding pKi = 7.0 7.0 1 2
Displacement of [3H]LY341495 from human recombinant mGluR3 in RGT cellsDisplacement of [3H]LY341495 from human recombinant mGluR3 in RGT cells
ChEMBL 235 2 3 5 -2.1 N[C@@]1(C(=O)O)CS(=O)(=O)[C@H]2[C@H](C(=O)O)[C@H]21 10.1021/jm060917u
1393 1539 None 42 Human Binding pKi = 7.0 7.0 -1 6
Displacement of [3H]-341495 binding to membranes expressing recombinant human Metabotropic glutamate receptor 3Displacement of [3H]-341495 binding to membranes expressing recombinant human Metabotropic glutamate receptor 3
ChEMBL 185 2 3 3 -0.5 OC(=O)[C@H]1[C@H]2[C@@H]1[C@](CC2)(N)C(=O)O 10.1021/jm040222y
1396 1539 None 42 Human Binding pKi = 7.0 7.0 -1 6
Displacement of [3H]-341495 binding to membranes expressing recombinant human Metabotropic glutamate receptor 3Displacement of [3H]-341495 binding to membranes expressing recombinant human Metabotropic glutamate receptor 3
ChEMBL 185 2 3 3 -0.5 OC(=O)[C@H]1[C@H]2[C@@H]1[C@](CC2)(N)C(=O)O 10.1021/jm040222y
213056 1539 None 42 Human Binding pKi = 7.0 7.0 -1 6
Displacement of [3H]-341495 binding to membranes expressing recombinant human Metabotropic glutamate receptor 3Displacement of [3H]-341495 binding to membranes expressing recombinant human Metabotropic glutamate receptor 3
ChEMBL 185 2 3 3 -0.5 OC(=O)[C@H]1[C@H]2[C@@H]1[C@](CC2)(N)C(=O)O 10.1021/jm040222y
CHEMBL8759 1539 None 42 Human Binding pKi = 7.0 7.0 -1 6
Displacement of [3H]-341495 binding to membranes expressing recombinant human Metabotropic glutamate receptor 3Displacement of [3H]-341495 binding to membranes expressing recombinant human Metabotropic glutamate receptor 3
ChEMBL 185 2 3 3 -0.5 OC(=O)[C@H]1[C@H]2[C@@H]1[C@](CC2)(N)C(=O)O 10.1021/jm040222y
1393 1539 None 42 Human Binding pKi = 7.0 7.0 -1 6
Ability to displace [3H]LY-341,495 from recombinant human Metabotropic glutamate receptor 3 expressed in RGT cells.Ability to displace [3H]LY-341,495 from recombinant human Metabotropic glutamate receptor 3 expressed in RGT cells.
ChEMBL 185 2 3 3 -0.5 OC(=O)[C@H]1[C@H]2[C@@H]1[C@](CC2)(N)C(=O)O 10.1021/jm980616n
1396 1539 None 42 Human Binding pKi = 7.0 7.0 -1 6
Ability to displace [3H]LY-341,495 from recombinant human Metabotropic glutamate receptor 3 expressed in RGT cells.Ability to displace [3H]LY-341,495 from recombinant human Metabotropic glutamate receptor 3 expressed in RGT cells.
ChEMBL 185 2 3 3 -0.5 OC(=O)[C@H]1[C@H]2[C@@H]1[C@](CC2)(N)C(=O)O 10.1021/jm980616n
213056 1539 None 42 Human Binding pKi = 7.0 7.0 -1 6
Ability to displace [3H]LY-341,495 from recombinant human Metabotropic glutamate receptor 3 expressed in RGT cells.Ability to displace [3H]LY-341,495 from recombinant human Metabotropic glutamate receptor 3 expressed in RGT cells.
ChEMBL 185 2 3 3 -0.5 OC(=O)[C@H]1[C@H]2[C@@H]1[C@](CC2)(N)C(=O)O 10.1021/jm980616n
CHEMBL8759 1539 None 42 Human Binding pKi = 7.0 7.0 -1 6
Ability to displace [3H]LY-341,495 from recombinant human Metabotropic glutamate receptor 3 expressed in RGT cells.Ability to displace [3H]LY-341,495 from recombinant human Metabotropic glutamate receptor 3 expressed in RGT cells.
ChEMBL 185 2 3 3 -0.5 OC(=O)[C@H]1[C@H]2[C@@H]1[C@](CC2)(N)C(=O)O 10.1021/jm980616n
1393 1539 None 42 Human Binding pKi = 7.0 7.0 -1 6
Displacement of [3H]LY341495 from human recombinant mGluR3 in RGT cellsDisplacement of [3H]LY341495 from human recombinant mGluR3 in RGT cells
ChEMBL 185 2 3 3 -0.5 OC(=O)[C@H]1[C@H]2[C@@H]1[C@](CC2)(N)C(=O)O 10.1021/jm060917u
1396 1539 None 42 Human Binding pKi = 7.0 7.0 -1 6
Displacement of [3H]LY341495 from human recombinant mGluR3 in RGT cellsDisplacement of [3H]LY341495 from human recombinant mGluR3 in RGT cells
ChEMBL 185 2 3 3 -0.5 OC(=O)[C@H]1[C@H]2[C@@H]1[C@](CC2)(N)C(=O)O 10.1021/jm060917u
213056 1539 None 42 Human Binding pKi = 7.0 7.0 -1 6
Displacement of [3H]LY341495 from human recombinant mGluR3 in RGT cellsDisplacement of [3H]LY341495 from human recombinant mGluR3 in RGT cells
ChEMBL 185 2 3 3 -0.5 OC(=O)[C@H]1[C@H]2[C@@H]1[C@](CC2)(N)C(=O)O 10.1021/jm060917u
CHEMBL8759 1539 None 42 Human Binding pKi = 7.0 7.0 -1 6
Displacement of [3H]LY341495 from human recombinant mGluR3 in RGT cellsDisplacement of [3H]LY341495 from human recombinant mGluR3 in RGT cells
ChEMBL 185 2 3 3 -0.5 OC(=O)[C@H]1[C@H]2[C@@H]1[C@](CC2)(N)C(=O)O 10.1021/jm060917u
1378 2417 None 39 Rat Binding pKd None 7.3 7.3 -5 10
UnclassifiedUnclassified
Guide to Pharmacology 353 5 3 4 2.8 OC(=O)[C@H]1C[C@@H]1[C@](C(=O)O)(CC1c2ccccc2Oc2c1cccc2)N 10884552
1399 2417 None 39 Rat Binding pKd None 7.3 7.3 -5 10
UnclassifiedUnclassified
Guide to Pharmacology 353 5 3 4 2.8 OC(=O)[C@H]1C[C@@H]1[C@](C(=O)O)(CC1c2ccccc2Oc2c1cccc2)N 10884552
9819927 2417 None 39 Rat Binding pKd None 7.3 7.3 -5 10
UnclassifiedUnclassified
Guide to Pharmacology 353 5 3 4 2.8 OC(=O)[C@H]1C[C@@H]1[C@](C(=O)O)(CC1c2ccccc2Oc2c1cccc2)N 10884552
CHEMBL432038 2417 None 39 Rat Binding pKd None 7.3 7.3 -5 10
UnclassifiedUnclassified
Guide to Pharmacology 353 5 3 4 2.8 OC(=O)[C@H]1C[C@@H]1[C@](C(=O)O)(CC1c2ccccc2Oc2c1cccc2)N 10884552
1378 2417 None 39 Human Binding pKd None 9.1 9.1 1 10
UnclassifiedUnclassified
Guide to Pharmacology 353 5 3 4 2.8 OC(=O)[C@H]1C[C@@H]1[C@](C(=O)O)(CC1c2ccccc2Oc2c1cccc2)N 10530814
1399 2417 None 39 Human Binding pKd None 9.1 9.1 1 10
UnclassifiedUnclassified
Guide to Pharmacology 353 5 3 4 2.8 OC(=O)[C@H]1C[C@@H]1[C@](C(=O)O)(CC1c2ccccc2Oc2c1cccc2)N 10530814
9819927 2417 None 39 Human Binding pKd None 9.1 9.1 1 10
UnclassifiedUnclassified
Guide to Pharmacology 353 5 3 4 2.8 OC(=O)[C@H]1C[C@@H]1[C@](C(=O)O)(CC1c2ccccc2Oc2c1cccc2)N 10530814
CHEMBL432038 2417 None 39 Human Binding pKd None 9.1 9.1 1 10
UnclassifiedUnclassified
Guide to Pharmacology 353 5 3 4 2.8 OC(=O)[C@H]1C[C@@H]1[C@](C(=O)O)(CC1c2ccccc2Oc2c1cccc2)N 10530814
12310764 1970 Functional 46 Human Binding pKi = 5 5.0 -14 8
NoneNone
PDSP KiDatabase 158 2 3 4 -0.9 OC(=O)C(c1o[nH]c(=O)c1)N None
1233 1970 Functional 46 Human Binding pKi = 5 5.0 -14 8
NoneNone
PDSP KiDatabase 158 2 3 4 -0.9 OC(=O)C(c1o[nH]c(=O)c1)N None
1371 1970 Functional 46 Human Binding pKi = 5 5.0 -14 8
NoneNone
PDSP KiDatabase 158 2 3 4 -0.9 OC(=O)C(c1o[nH]c(=O)c1)N None
CHEMBL284895 1970 Functional 46 Human Binding pKi = 5 5.0 -14 8
NoneNone
PDSP KiDatabase 158 2 3 4 -0.9 OC(=O)C(c1o[nH]c(=O)c1)N None
1370 3263 Functional 42 Human Binding pKi = 5 5.0 -1202 8
NoneNone
PDSP KiDatabase 189 3 3 6 -2.5 OC(=O)[C@H](Cn1oc(=O)[nH]c1=O)N None
1372 3263 Functional 42 Human Binding pKi = 5 5.0 -1202 8
NoneNone
PDSP KiDatabase 189 3 3 6 -2.5 OC(=O)[C@H](Cn1oc(=O)[nH]c1=O)N None
40539 3263 Functional 42 Human Binding pKi = 5 5.0 -1202 8
NoneNone
PDSP KiDatabase 189 3 3 6 -2.5 OC(=O)[C@H](Cn1oc(=O)[nH]c1=O)N None
6971145 3263 Functional 42 Human Binding pKi = 5 5.0 -1202 8
NoneNone
PDSP KiDatabase 189 3 3 6 -2.5 OC(=O)[C@H](Cn1oc(=O)[nH]c1=O)N None
CHEMBL279956 3263 Functional 42 Human Binding pKi = 5 5.0 -1202 8
NoneNone
PDSP KiDatabase 189 3 3 6 -2.5 OC(=O)[C@H](Cn1oc(=O)[nH]c1=O)N None
DB02999 3263 Functional 42 Human Binding pKi = 5 5.0 -1202 8
NoneNone
PDSP KiDatabase 189 3 3 6 -2.5 OC(=O)[C@H](Cn1oc(=O)[nH]c1=O)N None
139054390 207381 Functional 56 Human Binding pKi = 5 5.0 -1 5
NoneNone
PDSP KiDatabase 147 4 3 3 -0.7 N[C@H](CCC(=O)O)C(=O)O None
23327 207381 Functional 56 Human Binding pKi = 5 5.0 -1 5
NoneNone
PDSP KiDatabase 147 4 3 3 -0.7 N[C@H](CCC(=O)O)C(=O)O None
CHEMBL76232 207381 Functional 56 Human Binding pKi = 5 5.0 -1 5
NoneNone
PDSP KiDatabase 147 4 3 3 -0.7 N[C@H](CCC(=O)O)C(=O)O None
114827 218819 3H-LY341495 0 Human Binding pKi = 6.9 6.9 -4 3
NoneNone
PDSP KiDatabase 185 2 3 3 -0.5 C1CC(C2C1C2C(=O)O)(C(=O)O)N None
None 218821 Functional 0 Human Binding pKi = 6.7 6.7 -3 3
NoneNone
PDSP KiDatabase 203 4 4 4 -1.6 C1(C(C1C(=O)O)C(=O)O)C(C(=O)O)N None
210320 220219 None 0 Human Binding pKi = 8.3 8.3 - 1
NoneNone
Drug Central 304 9 5 5 -1.6 CC(=O)N[C@@H](CC(=O)N[C@@H](CCC(O)=O)C(O)=O)C(O)=O None
1310 2315 Functional 61 Human Binding pKi = 5.4 5.4 1 18
NoneNone
PDSP KiDatabase 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N None
1369 2315 Functional 61 Human Binding pKi = 5.4 5.4 1 18
NoneNone
PDSP KiDatabase 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N None
33032 2315 Functional 61 Human Binding pKi = 5.4 5.4 1 18
NoneNone
PDSP KiDatabase 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N None
44272391 2315 Functional 61 Human Binding pKi = 5.4 5.4 1 18
NoneNone
PDSP KiDatabase 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N None
88747398 2315 Functional 61 Human Binding pKi = 5.4 5.4 1 18
NoneNone
PDSP KiDatabase 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N None
CHEMBL575060 2315 Functional 61 Human Binding pKi = 5.4 5.4 1 18
NoneNone
PDSP KiDatabase 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N None
DB00142 2315 Functional 61 Human Binding pKi = 5.4 5.4 1 18
NoneNone
PDSP KiDatabase 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N None
1310 2315 None 61 Human Binding pKi = 8.1 8.1 1 18
NoneNone
Drug Central 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N None
1369 2315 None 61 Human Binding pKi = 8.1 8.1 1 18
NoneNone
Drug Central 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N None
33032 2315 None 61 Human Binding pKi = 8.1 8.1 1 18
NoneNone
Drug Central 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N None
44272391 2315 None 61 Human Binding pKi = 8.1 8.1 1 18
NoneNone
Drug Central 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N None
88747398 2315 None 61 Human Binding pKi = 8.1 8.1 1 18
NoneNone
Drug Central 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N None
CHEMBL575060 2315 None 61 Human Binding pKi = 8.1 8.1 1 18
NoneNone
Drug Central 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N None
DB00142 2315 None 61 Human Binding pKi = 8.1 8.1 1 18
NoneNone
Drug Central 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N None
None 218660 Functional 0 Human Binding pKi = 5.1 5.1 -1 7
NoneNone
PDSP KiDatabase 173 2 3 3 -0.3 C1CC(CC1C(=O)O)(C(=O)O)N None
1405 2709 None 0 Human Binding pKi = 4.7 4.7 - 1
UnclassifiedUnclassified
Guide to Pharmacology 304 9 5 5 -1.6 OC(=O)CC[C@@H](C(=O)O)NC(=O)[C@@H](NC(=O)C)CC(=O)O 10884552
188803 2709 None 0 Human Binding pKi = 4.7 4.7 - 1
UnclassifiedUnclassified
Guide to Pharmacology 304 9 5 5 -1.6 OC(=O)CC[C@@H](C(=O)O)NC(=O)[C@@H](NC(=O)C)CC(=O)O 10884552
CHEMBL1329032 2709 None 0 Human Binding pKi = 4.7 4.7 - 1
UnclassifiedUnclassified
Guide to Pharmacology 304 9 5 5 -1.6 OC(=O)CC[C@@H](C(=O)O)NC(=O)[C@@H](NC(=O)C)CC(=O)O 10884552
11310142 2422 None 14 Human Binding pKi = 6.5 6.5 -1 2
UnclassifiedUnclassified
Guide to Pharmacology 199 2 3 3 -0.2 C[C@@H]1C[C@@]([C@H]2[C@@H]1[C@@H]2C(=O)O)(N)C(=O)O 26341392
11614 2422 None 14 Human Binding pKi = 6.5 6.5 -1 2
UnclassifiedUnclassified
Guide to Pharmacology 199 2 3 3 -0.2 C[C@@H]1C[C@@]([C@H]2[C@@H]1[C@@H]2C(=O)O)(N)C(=O)O 26341392
CHEMBL192051 2422 None 14 Human Binding pKi = 6.5 6.5 -1 2
UnclassifiedUnclassified
Guide to Pharmacology 199 2 3 3 -0.2 C[C@@H]1C[C@@]([C@H]2[C@@H]1[C@@H]2C(=O)O)(N)C(=O)O 26341392
1373 2475 None 35 Human Binding pKi None 3.8 3.8 -6 5
UnclassifiedUnclassified
Guide to Pharmacology 209 3 3 3 0.6 OC(=O)c1ccc(cc1)[C@@](C(=O)O)(N)C 10530814
139055582 2475 None 35 Human Binding pKi None 3.8 3.8 -6 5
UnclassifiedUnclassified
Guide to Pharmacology 209 3 3 3 0.6 OC(=O)c1ccc(cc1)[C@@](C(=O)O)(N)C 10530814
446355 2475 None 35 Human Binding pKi None 3.8 3.8 -6 5
UnclassifiedUnclassified
Guide to Pharmacology 209 3 3 3 0.6 OC(=O)c1ccc(cc1)[C@@](C(=O)O)(N)C 10530814
CHEMBL257626 2475 None 35 Human Binding pKi None 3.8 3.8 -6 5
UnclassifiedUnclassified
Guide to Pharmacology 209 3 3 3 0.6 OC(=O)c1ccc(cc1)[C@@](C(=O)O)(N)C 10530814
DB04256 2475 None 35 Human Binding pKi None 3.8 3.8 -6 5
UnclassifiedUnclassified
Guide to Pharmacology 209 3 3 3 0.6 OC(=O)c1ccc(cc1)[C@@](C(=O)O)(N)C 10530814
104766 33 None 30 Human Binding pKi None 4.7 4.7 -12 11
UnclassifiedUnclassified
Guide to Pharmacology 173 2 3 3 -0.3 OC(=O)[C@@H]1CC[C@@](C1)(N)C(=O)O 10530814
1365 33 None 30 Human Binding pKi None 4.7 4.7 -12 11
UnclassifiedUnclassified
Guide to Pharmacology 173 2 3 3 -0.3 OC(=O)[C@@H]1CC[C@@](C1)(N)C(=O)O 10530814
CHEMBL34453 33 None 30 Human Binding pKi None 4.7 4.7 -12 11
UnclassifiedUnclassified
Guide to Pharmacology 173 2 3 3 -0.3 OC(=O)[C@@H]1CC[C@@](C1)(N)C(=O)O 10530814
104766 33 None 30 Rat Binding pKi None 4.8 4.8 -10 11
UnclassifiedUnclassified
Guide to Pharmacology 173 2 3 3 -0.3 OC(=O)[C@@H]1CC[C@@](C1)(N)C(=O)O 10884552
1365 33 None 30 Rat Binding pKi None 4.8 4.8 -10 11
UnclassifiedUnclassified
Guide to Pharmacology 173 2 3 3 -0.3 OC(=O)[C@@H]1CC[C@@](C1)(N)C(=O)O 10884552
CHEMBL34453 33 None 30 Rat Binding pKi None 4.8 4.8 -10 11
UnclassifiedUnclassified
Guide to Pharmacology 173 2 3 3 -0.3 OC(=O)[C@@H]1CC[C@@](C1)(N)C(=O)O 10884552
10197984 2421 None 36 Human Binding pKi None 4.8 4.8 -2 5
UnclassifiedUnclassified
Guide to Pharmacology 187 2 3 4 -1.5 OC(=O)[C@H]1[C@H]2[C@@H]1[C@](CO2)(N)C(=O)O 10090786
1394 2421 None 36 Human Binding pKi None 4.8 4.8 -2 5
UnclassifiedUnclassified
Guide to Pharmacology 187 2 3 4 -1.5 OC(=O)[C@H]1[C@H]2[C@@H]1[C@](CO2)(N)C(=O)O 10090786
CHEMBL275079 2421 None 36 Human Binding pKi None 4.8 4.8 -2 5
UnclassifiedUnclassified
Guide to Pharmacology 187 2 3 4 -1.5 OC(=O)[C@H]1[C@H]2[C@@H]1[C@](CO2)(N)C(=O)O 10090786
1392 73 None 32 Human Binding pKi None 5.3 5.3 1 2
UnclassifiedUnclassified
Guide to Pharmacology 174 2 4 4 -1.8 OC(=O)[C@@H]1NC[C@@](C1)(N)C(=O)O 10530814
5310984 73 None 32 Human Binding pKi None 5.3 5.3 1 2
UnclassifiedUnclassified
Guide to Pharmacology 174 2 4 4 -1.8 OC(=O)[C@@H]1NC[C@@](C1)(N)C(=O)O 10530814
CHEMBL40086 73 None 32 Human Binding pKi None 5.3 5.3 1 2
UnclassifiedUnclassified
Guide to Pharmacology 174 2 4 4 -1.8 OC(=O)[C@@H]1NC[C@@](C1)(N)C(=O)O 10530814
1400 1538 None 0 Rat Binding pKi None 5.4 5.4 7 2
UnclassifiedUnclassified
Guide to Pharmacology 175 5 3 3 0.0 CC[C@@](C(=O)O)(CCC(=O)O)N 10884552
5311079 1538 None 0 Rat Binding pKi None 5.4 5.4 7 2
UnclassifiedUnclassified
Guide to Pharmacology 175 5 3 3 0.0 CC[C@@](C(=O)O)(CCC(=O)O)N 10884552
CHEMBL1450466 1538 None 0 Rat Binding pKi None 5.4 5.4 7 2
UnclassifiedUnclassified
Guide to Pharmacology 175 5 3 3 0.0 CC[C@@](C(=O)O)(CCC(=O)O)N 10884552
1310 2315 None 61 Rat Binding pKi None 6.4 6.4 -1 18
UnclassifiedUnclassified
Guide to Pharmacology 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N 10884552
1369 2315 None 61 Rat Binding pKi None 6.4 6.4 -1 18
UnclassifiedUnclassified
Guide to Pharmacology 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N 10884552
33032 2315 None 61 Rat Binding pKi None 6.4 6.4 -1 18
UnclassifiedUnclassified
Guide to Pharmacology 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N 10884552
44272391 2315 None 61 Rat Binding pKi None 6.4 6.4 -1 18
UnclassifiedUnclassified
Guide to Pharmacology 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N 10884552
88747398 2315 None 61 Rat Binding pKi None 6.4 6.4 -1 18
UnclassifiedUnclassified
Guide to Pharmacology 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N 10884552
CHEMBL575060 2315 None 61 Rat Binding pKi None 6.4 6.4 -1 18
UnclassifiedUnclassified
Guide to Pharmacology 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N 10884552
DB00142 2315 None 61 Rat Binding pKi None 6.4 6.4 -1 18
UnclassifiedUnclassified
Guide to Pharmacology 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N 10884552
1368 2290 None 30 Rat Binding pKi None 6.5 6.5 -2 11
UnclassifiedUnclassified
Guide to Pharmacology 159 3 3 3 -0.9 N[C@@H]([C@H]1C[C@@H]1C(=O)O)C(=O)O 10884552
5310956 2290 None 30 Rat Binding pKi None 6.5 6.5 -2 11
UnclassifiedUnclassified
Guide to Pharmacology 159 3 3 3 -0.9 N[C@@H]([C@H]1C[C@@H]1C(=O)O)C(=O)O 10884552
CHEMBL280563 2290 None 30 Rat Binding pKi None 6.5 6.5 -2 11
UnclassifiedUnclassified
Guide to Pharmacology 159 3 3 3 -0.9 N[C@@H]([C@H]1C[C@@H]1C(=O)O)C(=O)O 10884552
1377 1340 None 23 Rat Binding pKi None 6.8 6.8 -2 6
UnclassifiedUnclassified
Guide to Pharmacology 203 4 4 4 -1.6 N[C@@H](C1[C@H]([C@@H]1C(=O)O)C(=O)O)C(=O)O 10884552
5310979 1340 None 23 Rat Binding pKi None 6.8 6.8 -2 6
UnclassifiedUnclassified
Guide to Pharmacology 203 4 4 4 -1.6 N[C@@H](C1[C@H]([C@@H]1C(=O)O)C(=O)O)C(=O)O 10884552
CHEMBL284193 1340 None 23 Rat Binding pKi None 6.8 6.8 -2 6
UnclassifiedUnclassified
Guide to Pharmacology 203 4 4 4 -1.6 N[C@@H](C1[C@H]([C@@H]1C(=O)O)C(=O)O)C(=O)O 10884552
1377 1340 None 23 Human Binding pKi None 7.2 7.2 1 6
UnclassifiedUnclassified
Guide to Pharmacology 203 4 4 4 -1.6 N[C@@H](C1[C@H]([C@@H]1C(=O)O)C(=O)O)C(=O)O 10530814
5310979 1340 None 23 Human Binding pKi None 7.2 7.2 1 6
UnclassifiedUnclassified
Guide to Pharmacology 203 4 4 4 -1.6 N[C@@H](C1[C@H]([C@@H]1C(=O)O)C(=O)O)C(=O)O 10530814
CHEMBL284193 1340 None 23 Human Binding pKi None 7.2 7.2 1 6
UnclassifiedUnclassified
Guide to Pharmacology 203 4 4 4 -1.6 N[C@@H](C1[C@H]([C@@H]1C(=O)O)C(=O)O)C(=O)O 10530814
1393 1539 None 42 Rat Binding pKi None 7.3 7.3 -2 6
UnclassifiedUnclassified
Guide to Pharmacology 185 2 3 3 -0.5 OC(=O)[C@H]1[C@H]2[C@@H]1[C@](CC2)(N)C(=O)O 10884552
1396 1539 None 42 Rat Binding pKi None 7.3 7.3 -2 6
UnclassifiedUnclassified
Guide to Pharmacology 185 2 3 3 -0.5 OC(=O)[C@H]1[C@H]2[C@@H]1[C@](CC2)(N)C(=O)O 10884552
213056 1539 None 42 Rat Binding pKi None 7.3 7.3 -2 6
UnclassifiedUnclassified
Guide to Pharmacology 185 2 3 3 -0.5 OC(=O)[C@H]1[C@H]2[C@@H]1[C@](CC2)(N)C(=O)O 10884552
CHEMBL8759 1539 None 42 Rat Binding pKi None 7.3 7.3 -2 6
UnclassifiedUnclassified
Guide to Pharmacology 185 2 3 3 -0.5 OC(=O)[C@H]1[C@H]2[C@@H]1[C@](CC2)(N)C(=O)O 10884552
1368 2290 None 30 Human Binding pKi None 7.4 7.4 -1 11
UnclassifiedUnclassified
Guide to Pharmacology 159 3 3 3 -0.9 N[C@@H]([C@H]1C[C@@H]1C(=O)O)C(=O)O 10530814
5310956 2290 None 30 Human Binding pKi None 7.4 7.4 -1 11
UnclassifiedUnclassified
Guide to Pharmacology 159 3 3 3 -0.9 N[C@@H]([C@H]1C[C@@H]1C(=O)O)C(=O)O 10530814
CHEMBL280563 2290 None 30 Human Binding pKi None 7.4 7.4 -1 11
UnclassifiedUnclassified
Guide to Pharmacology 159 3 3 3 -0.9 N[C@@H]([C@H]1C[C@@H]1C(=O)O)C(=O)O 10530814
1310 2315 None 61 Human Binding pKi None 7.4 7.4 1 18
UnclassifiedUnclassified
Guide to Pharmacology 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N 10530814
1369 2315 None 61 Human Binding pKi None 7.4 7.4 1 18
UnclassifiedUnclassified
Guide to Pharmacology 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N 10530814
33032 2315 None 61 Human Binding pKi None 7.4 7.4 1 18
UnclassifiedUnclassified
Guide to Pharmacology 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N 10530814
44272391 2315 None 61 Human Binding pKi None 7.4 7.4 1 18
UnclassifiedUnclassified
Guide to Pharmacology 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N 10530814
88747398 2315 None 61 Human Binding pKi None 7.4 7.4 1 18
UnclassifiedUnclassified
Guide to Pharmacology 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N 10530814
CHEMBL575060 2315 None 61 Human Binding pKi None 7.4 7.4 1 18
UnclassifiedUnclassified
Guide to Pharmacology 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N 10530814
DB00142 2315 None 61 Human Binding pKi None 7.4 7.4 1 18
UnclassifiedUnclassified
Guide to Pharmacology 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N 10530814
1378 2417 None 39 Rat Binding pKi None 8 8.0 -5 10
UnclassifiedUnclassified
Guide to Pharmacology 353 5 3 4 2.8 OC(=O)[C@H]1C[C@@H]1[C@](C(=O)O)(CC1c2ccccc2Oc2c1cccc2)N 10884552
1399 2417 None 39 Rat Binding pKi None 8 8.0 -5 10
UnclassifiedUnclassified
Guide to Pharmacology 353 5 3 4 2.8 OC(=O)[C@H]1C[C@@H]1[C@](C(=O)O)(CC1c2ccccc2Oc2c1cccc2)N 10884552
9819927 2417 None 39 Rat Binding pKi None 8 8.0 -5 10
UnclassifiedUnclassified
Guide to Pharmacology 353 5 3 4 2.8 OC(=O)[C@H]1C[C@@H]1[C@](C(=O)O)(CC1c2ccccc2Oc2c1cccc2)N 10884552
CHEMBL432038 2417 None 39 Rat Binding pKi None 8 8.0 -5 10
UnclassifiedUnclassified
Guide to Pharmacology 353 5 3 4 2.8 OC(=O)[C@H]1C[C@@H]1[C@](C(=O)O)(CC1c2ccccc2Oc2c1cccc2)N 10884552
1397 2529 None 15 Rat Binding pKi None 8.4 8.4 -2 5
UnclassifiedUnclassified
Guide to Pharmacology 377 5 3 4 2.1 OC(=O)[C@]1(N)[C@H](OCc2ccc(c(c2)Cl)Cl)C[C@@H]2[C@H]1[C@@]2(F)C(=O)O 14975669
1397 2529 None 15 Rat Binding pKi None 8.4 8.4 -2 5
UnclassifiedUnclassified
Guide to Pharmacology 377 5 3 4 2.1 OC(=O)[C@]1(N)[C@H](OCc2ccc(c(c2)Cl)Cl)C[C@@H]2[C@H]1[C@@]2(F)C(=O)O 15317467
9886034 2529 None 15 Rat Binding pKi None 8.4 8.4 -2 5
UnclassifiedUnclassified
Guide to Pharmacology 377 5 3 4 2.1 OC(=O)[C@]1(N)[C@H](OCc2ccc(c(c2)Cl)Cl)C[C@@H]2[C@H]1[C@@]2(F)C(=O)O 14975669
9886034 2529 None 15 Rat Binding pKi None 8.4 8.4 -2 5
UnclassifiedUnclassified
Guide to Pharmacology 377 5 3 4 2.1 OC(=O)[C@]1(N)[C@H](OCc2ccc(c(c2)Cl)Cl)C[C@@H]2[C@H]1[C@@]2(F)C(=O)O 15317467
CHEMBL186453 2529 None 15 Rat Binding pKi None 8.4 8.4 -2 5
UnclassifiedUnclassified
Guide to Pharmacology 377 5 3 4 2.1 OC(=O)[C@]1(N)[C@H](OCc2ccc(c(c2)Cl)Cl)C[C@@H]2[C@H]1[C@@]2(F)C(=O)O 14975669
CHEMBL186453 2529 None 15 Rat Binding pKi None 8.4 8.4 -2 5
UnclassifiedUnclassified
Guide to Pharmacology 377 5 3 4 2.1 OC(=O)[C@]1(N)[C@H](OCc2ccc(c(c2)Cl)Cl)C[C@@H]2[C@H]1[C@@]2(F)C(=O)O 15317467
1393 1539 None 42 Human Binding pKi None 8.9 8.9 -1 6
UnclassifiedUnclassified
Guide to Pharmacology 185 2 3 3 -0.5 OC(=O)[C@H]1[C@H]2[C@@H]1[C@](CC2)(N)C(=O)O 10530814
1396 1539 None 42 Human Binding pKi None 8.9 8.9 -1 6
UnclassifiedUnclassified
Guide to Pharmacology 185 2 3 3 -0.5 OC(=O)[C@H]1[C@H]2[C@@H]1[C@](CC2)(N)C(=O)O 10530814
213056 1539 None 42 Human Binding pKi None 8.9 8.9 -1 6
UnclassifiedUnclassified
Guide to Pharmacology 185 2 3 3 -0.5 OC(=O)[C@H]1[C@H]2[C@@H]1[C@](CC2)(N)C(=O)O 10530814
CHEMBL8759 1539 None 42 Human Binding pKi None 8.9 8.9 -1 6
UnclassifiedUnclassified
Guide to Pharmacology 185 2 3 3 -0.5 OC(=O)[C@H]1[C@H]2[C@@H]1[C@](CC2)(N)C(=O)O 10530814
1378 2417 None 39 Human Binding pKi None 8.9 8.9 1 10
UnclassifiedUnclassified
Guide to Pharmacology 353 5 3 4 2.8 OC(=O)[C@H]1C[C@@H]1[C@](C(=O)O)(CC1c2ccccc2Oc2c1cccc2)N 10530814
1399 2417 None 39 Human Binding pKi None 8.9 8.9 1 10
UnclassifiedUnclassified
Guide to Pharmacology 353 5 3 4 2.8 OC(=O)[C@H]1C[C@@H]1[C@](C(=O)O)(CC1c2ccccc2Oc2c1cccc2)N 10530814
9819927 2417 None 39 Human Binding pKi None 8.9 8.9 1 10
UnclassifiedUnclassified
Guide to Pharmacology 353 5 3 4 2.8 OC(=O)[C@H]1C[C@@H]1[C@](C(=O)O)(CC1c2ccccc2Oc2c1cccc2)N 10530814
CHEMBL432038 2417 None 39 Human Binding pKi None 8.9 8.9 1 10
UnclassifiedUnclassified
Guide to Pharmacology 353 5 3 4 2.8 OC(=O)[C@H]1C[C@@H]1[C@](C(=O)O)(CC1c2ccccc2Oc2c1cccc2)N 10530814