Ligand source activities (1 row/activity)





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DOI

60096224 156545 0 None 43 2 Human 9.8 pEC50 = 9.8 Functional
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 156545 0 None 43 2 Human 9.8 pEC50 = 9.8 Functional
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 157655 15 None 48 4 Human 9.3 pEC50 = 9.3 Functional
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 157655 15 None 48 4 Human 9.3 pEC50 = 9.3 Functional
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 158568 0 None 5 2 Human 9.2 pEC50 = 9.2 Functional
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 158568 0 None 5 2 Human 9.2 pEC50 = 9.2 Functional
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 156881 0 None 10 2 Human 9.1 pEC50 = 9.1 Functional
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 156881 0 None 10 2 Human 9.1 pEC50 = 9.1 Functional
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 83247 1 None -13 3 Human 8.9 pEC50 = 8.9 Functional
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 83247 1 None -13 3 Human 8.9 pEC50 = 8.9 Functional
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 35817 1 None -6 4 Rat 7.0 pEC50 = 7 Functional
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 35817 1 None -6 4 Rat 7.0 pEC50 = 7 Functional
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 110 None -251 17 Human 6.0 pEC50 = 6 Functional
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 110 None -251 17 Human 6.0 pEC50 = 6 Functional
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 110 None -251 17 Human 6.0 pEC50 = 6 Functional
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 110 None -251 17 Human 6.0 pEC50 = 6 Functional
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 110 None -251 17 Human 6.0 pEC50 = 6 Functional
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 110 None -251 17 Human 6.0 pEC50 = 6 Functional
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 110 None -251 17 Human 6.0 pEC50 = 6 Functional
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 123397 0 None -5 2 Human 7.0 pEC50 = 7.0 Functional
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 123397 0 None -5 2 Human 7.0 pEC50 = 7.0 Functional
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 0 None -10 2 Human 5.0 pEC50 = 5.0 Functional
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 0 None -10 2 Human 5.0 pEC50 = 5.0 Functional
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 0 None -10 2 Human 5.0 pEC50 = 5.0 Functional
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 123397 0 None -5 2 Human 7.0 pEC50 = 7.0 Functional
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 123397 0 None -5 2 Human 7.0 pEC50 = 7.0 Functional
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 31341 0 None -1 5 Rat 8.0 pEC50 = 8.0 Functional
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 31341 0 None -1 5 Rat 8.0 pEC50 = 8.0 Functional
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 157655 15 None 48 4 Human 7.9 pEC50 = 7.9 Functional
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 157655 15 None 48 4 Human 7.9 pEC50 = 7.9 Functional
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 123407 0 None -58 2 Human 7.0 pEC50 = 7.0 Functional
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 123407 0 None -58 2 Human 7.0 pEC50 = 7.0 Functional
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 123396 17 None -107 4 Human 5.9 pEC50 = 5.9 Functional
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 123396 17 None -107 4 Human 5.9 pEC50 = 5.9 Functional
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 123396 17 None -107 4 Human 6.9 pEC50 = 6.9 Functional
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 123396 17 None -107 4 Human 6.9 pEC50 = 6.9 Functional
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 0 None -16 2 Human 4.9 pEC50 = 4.9 Functional
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 0 None -16 2 Human 4.9 pEC50 = 4.9 Functional
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 0 None -16 2 Human 4.9 pEC50 = 4.9 Functional
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 64 None -4 6 Human 6.9 pEC50 = 6.9 Functional
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 64 None -4 6 Human 6.9 pEC50 = 6.9 Functional
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 64 None -4 6 Human 6.9 pEC50 = 6.9 Functional
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 64 None -4 6 Human 6.9 pEC50 = 6.9 Functional
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 110 None -251 17 Human 5.8 pEC50 = 5.8 Functional
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 110 None -251 17 Human 5.8 pEC50 = 5.8 Functional
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 110 None -251 17 Human 5.8 pEC50 = 5.8 Functional
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 110 None -251 17 Human 5.8 pEC50 = 5.8 Functional
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 110 None -251 17 Human 5.8 pEC50 = 5.8 Functional
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 110 None -251 17 Human 5.8 pEC50 = 5.8 Functional
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 110 None -251 17 Human 5.8 pEC50 = 5.8 Functional
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 137075 0 None -2 2 Human 6.8 pEC50 = 6.8 Functional
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 137075 0 None -2 2 Human 6.8 pEC50 = 6.8 Functional
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 48 None -5 4 Rat 5.8 pEC50 = 5.8 Functional
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 48 None -5 4 Rat 5.8 pEC50 = 5.8 Functional
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 48 None -5 4 Rat 5.8 pEC50 = 5.8 Functional
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 111866 0 None -25 2 Rat 5.8 pEC50 = 5.8 Functional
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 111866 0 None -25 2 Rat 5.8 pEC50 = 5.8 Functional
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 90059 0 None 1 4 Human 6.7 pEC50 = 6.7 Functional
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 90059 0 None 1 4 Human 6.7 pEC50 = 6.7 Functional
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 158513 0 None 9 2 Human 8.7 pEC50 = 8.7 Functional
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 158513 0 None 9 2 Human 8.7 pEC50 = 8.7 Functional
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 15 None -3 4 Human 8.7 pEC50 = 8.7 Functional
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 15 None -3 4 Human 8.7 pEC50 = 8.7 Functional
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 15 None -3 4 Human 8.7 pEC50 = 8.7 Functional
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 15 None -3 4 Rat 8.7 pEC50 = 8.7 Functional
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 15 None -3 4 Rat 8.7 pEC50 = 8.7 Functional
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 15 None -3 4 Rat 8.7 pEC50 = 8.7 Functional
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 156787 0 None 2 2 Human 8.7 pEC50 = 8.7 Functional
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 156787 0 None 2 2 Human 8.7 pEC50 = 8.7 Functional
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 155947 0 None 6 2 Human 8.6 pEC50 = 8.6 Functional
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 155947 0 None 6 2 Human 8.6 pEC50 = 8.6 Functional
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 26 None -1 8 Rat 6.7 pEC50 = 6.7 Functional
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 26 None -1 8 Rat 6.7 pEC50 = 6.7 Functional
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 26 None -1 8 Rat 6.7 pEC50 = 6.7 Functional
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 83247 1 None -13 3 Human 6.7 pEC50 = 6.7 Functional
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 83247 1 None -13 3 Human 6.7 pEC50 = 6.7 Functional
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 123396 17 None -107 4 Human 5.7 pEC50 = 5.7 Functional
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 123396 17 None -107 4 Human 5.7 pEC50 = 5.7 Functional
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 123403 0 None -51 2 Human 6.6 pEC50 = 6.6 Functional
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 123403 0 None -51 2 Human 6.6 pEC50 = 6.6 Functional
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 123402 0 None -60 2 Human 6.6 pEC50 = 6.6 Functional
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 123402 0 None -60 2 Human 6.6 pEC50 = 6.6 Functional
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 64 None -4 6 Human 7.6 pEC50 = 7.6 Functional
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 64 None -4 6 Human 7.6 pEC50 = 7.6 Functional
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 64 None -4 6 Human 7.6 pEC50 = 7.6 Functional
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 64 None -4 6 Human 7.6 pEC50 = 7.6 Functional
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 90057 1 None -1 3 Human 7.6 pEC50 = 7.6 Functional
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 90057 1 None -1 3 Human 7.6 pEC50 = 7.6 Functional
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 110 None -251 17 Human 5.6 pEC50 = 5.6 Functional
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 110 None -251 17 Human 5.6 pEC50 = 5.6 Functional
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 110 None -251 17 Human 5.6 pEC50 = 5.6 Functional
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 110 None -251 17 Human 5.6 pEC50 = 5.6 Functional
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 110 None -251 17 Human 5.6 pEC50 = 5.6 Functional
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 110 None -251 17 Human 5.6 pEC50 = 5.6 Functional
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 110 None -251 17 Human 5.6 pEC50 = 5.6 Functional
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 123406 0 None -43 2 Human 7.6 pEC50 = 7.6 Functional
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 123406 0 None -43 2 Human 7.6 pEC50 = 7.6 Functional
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 64 None -4 6 Human 7.6 pEC50 = 7.6 Functional
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 64 None -4 6 Human 7.6 pEC50 = 7.6 Functional
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 64 None -4 6 Human 7.6 pEC50 = 7.6 Functional
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 64 None -4 6 Human 7.6 pEC50 = 7.6 Functional
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 64 None -4 6 Human 7.6 pEC50 = 7.6 Functional
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 64 None -4 6 Human 7.6 pEC50 = 7.6 Functional
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 64 None -4 6 Human 7.6 pEC50 = 7.6 Functional
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 64 None -4 6 Human 7.6 pEC50 = 7.6 Functional
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 123401 0 None -12 2 Human 6.6 pEC50 = 6.6 Functional
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 123401 0 None -12 2 Human 6.6 pEC50 = 6.6 Functional
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 123396 17 None -107 4 Human 5.6 pEC50 = 5.6 Functional
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 123396 17 None -107 4 Human 5.6 pEC50 = 5.6 Functional
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 137104 0 None 1 2 Human 6.5 pEC50 = 6.5 Functional
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 137104 0 None 1 2 Human 6.5 pEC50 = 6.5 Functional
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 123405 0 None -60 2 Human 7.5 pEC50 = 7.5 Functional
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 123405 0 None -60 2 Human 7.5 pEC50 = 7.5 Functional
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 48 None -9 4 Human 5.5 pEC50 = 5.5 Functional
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 48 None -9 4 Human 5.5 pEC50 = 5.5 Functional
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 48 None -9 4 Human 5.5 pEC50 = 5.5 Functional
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 42 None -8 14 Human 4.5 pEC50 = 4.5 Functional
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 42 None -8 14 Human 4.5 pEC50 = 4.5 Functional
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 42 None -8 14 Human 4.5 pEC50 = 4.5 Functional
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 120125 1 None - 1 Human 4.5 pEC50 = 4.5 Functional
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 120125 1 None - 1 Human 4.5 pEC50 = 4.5 Functional
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 137081 0 None -21 2 Human 5.5 pEC50 = 5.5 Functional
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 137081 0 None -21 2 Human 5.5 pEC50 = 5.5 Functional
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 136981 0 None 3 2 Human 7.5 pEC50 = 7.5 Functional
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 136981 0 None 3 2 Human 7.5 pEC50 = 7.5 Functional
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 126776 1 None -2 3 Human 7.5 pEC50 = 7.5 Functional
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 126776 1 None -2 3 Human 7.5 pEC50 = 7.5 Functional
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 156588 0 None 1 2 Human 6.5 pEC50 = 6.5 Functional
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 156588 0 None 1 2 Human 6.5 pEC50 = 6.5 Functional
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 13378 0 None 1 2 Rat 4.4 pEC50 = 4.4 Functional
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 13378 0 None 1 2 Rat 4.4 pEC50 = 4.4 Functional
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 13378 0 None 1 2 Rat 4.4 pEC50 = 4.4 Functional
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 64 None -4 6 Human 7.4 pEC50 = 7.4 Functional
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 64 None -4 6 Human 7.4 pEC50 = 7.4 Functional
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 64 None -4 6 Human 7.4 pEC50 = 7.4 Functional
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 64 None -4 6 Human 7.4 pEC50 = 7.4 Functional
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 64 None -5 6 Rat 7.4 pEC50 = 7.4 Functional
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 64 None -5 6 Rat 7.4 pEC50 = 7.4 Functional
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 64 None -5 6 Rat 7.4 pEC50 = 7.4 Functional
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 64 None -5 6 Rat 7.4 pEC50 = 7.4 Functional
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 64 None -4 6 Human 7.4 pEC50 = 7.4 Functional
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 64 None -4 6 Human 7.4 pEC50 = 7.4 Functional
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 64 None -4 6 Human 7.4 pEC50 = 7.4 Functional
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 64 None -4 6 Human 7.4 pEC50 = 7.4 Functional
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 64 None -4 6 Human 7.4 pEC50 = 7.4 Functional
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 64 None -4 6 Human 7.4 pEC50 = 7.4 Functional
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 64 None -4 6 Human 7.4 pEC50 = 7.4 Functional
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 64 None -4 6 Human 7.4 pEC50 = 7.4 Functional
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 114827 1 None -4 4 Rat 7.4 pEC50 = 7.4 Functional
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 114827 1 None -4 4 Rat 7.4 pEC50 = 7.4 Functional
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 25134 23 None - 1 Human 4.4 pEC50 = 4.4 Functional
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 25134 23 None - 1 Human 4.4 pEC50 = 4.4 Functional
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 44 None -1 5 Human 8.3 pEC50 = 8.3 Functional
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 44 None -1 5 Human 8.3 pEC50 = 8.3 Functional
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 44 None -1 5 Human 8.3 pEC50 = 8.3 Functional
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 44 None -1 5 Human 8.3 pEC50 = 8.3 Functional
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 44 None -1 5 Human 8.3 pEC50 = 8.3 Functional
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 44 None -1 5 Human 8.3 pEC50 = 8.3 Functional
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 44 None -1 5 Human 8.3 pEC50 = 8.3 Functional
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 44 None -1 5 Human 8.3 pEC50 = 8.3 Functional
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 44 None -1 5 Human 8.3 pEC50 = 8.3 Functional
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 158961 0 None 3 2 Human 8.3 pEC50 = 8.3 Functional
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 158961 0 None 3 2 Human 8.3 pEC50 = 8.3 Functional
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 159236 0 None 8 2 Human 8.3 pEC50 = 8.3 Functional
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 159236 0 None 8 2 Human 8.3 pEC50 = 8.3 Functional
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 110 None -251 17 Human 5.4 pEC50 = 5.4 Functional
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 110 None -251 17 Human 5.4 pEC50 = 5.4 Functional
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 110 None -251 17 Human 5.4 pEC50 = 5.4 Functional
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 110 None -251 17 Human 5.4 pEC50 = 5.4 Functional
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 110 None -251 17 Human 5.4 pEC50 = 5.4 Functional
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 110 None -251 17 Human 5.4 pEC50 = 5.4 Functional
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 110 None -251 17 Human 5.4 pEC50 = 5.4 Functional
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 114800 6 None 1 4 Rat 7.3 pEC50 = 7.3 Functional
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 114800 6 None 1 4 Rat 7.3 pEC50 = 7.3 Functional
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 25134 23 None - 1 Human 4.4 pEC50 = 4.4 Functional
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 25134 23 None - 1 Human 4.4 pEC50 = 4.4 Functional
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 137600 69 None -2 3 Human 7.3 pEC50 = 7.3 Functional
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 137600 69 None -2 3 Human 7.3 pEC50 = 7.3 Functional
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 158422 0 None 3 2 Human 8.3 pEC50 = 8.3 Functional
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 158422 0 None 3 2 Human 8.3 pEC50 = 8.3 Functional
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 158921 0 None 1 2 Human 8.3 pEC50 = 8.3 Functional
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 158921 0 None 1 2 Human 8.3 pEC50 = 8.3 Functional
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 25134 23 None - 1 Human 4.3 pEC50 = 4.3 Functional
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 25134 23 None - 1 Human 4.3 pEC50 = 4.3 Functional
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 110 None -251 17 Human 5.3 pEC50 = 5.3 Functional
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 110 None -251 17 Human 5.3 pEC50 = 5.3 Functional
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 110 None -251 17 Human 5.3 pEC50 = 5.3 Functional
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 110 None -251 17 Human 5.3 pEC50 = 5.3 Functional
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 110 None -251 17 Human 5.3 pEC50 = 5.3 Functional
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 110 None -251 17 Human 5.3 pEC50 = 5.3 Functional
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 110 None -251 17 Human 5.3 pEC50 = 5.3 Functional
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 101382 1 None -10 2 Human 4.3 pEC50 = 4.3 Functional
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 101382 1 None -10 2 Human 4.3 pEC50 = 4.3 Functional
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 137024 0 None -3 2 Human 6.3 pEC50 = 6.3 Functional
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 137024 0 None -3 2 Human 6.3 pEC50 = 6.3 Functional
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 123396 17 None -107 4 Human 5.3 pEC50 = 5.3 Functional
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 123396 17 None -107 4 Human 5.3 pEC50 = 5.3 Functional
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 156124 0 None 2 2 Human 8.2 pEC50 = 8.2 Functional
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 156124 0 None 2 2 Human 8.2 pEC50 = 8.2 Functional
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 37 None -1 11 Rat 6.2 pEC50 = 6.2 Functional
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 37 None -1 11 Rat 6.2 pEC50 = 6.2 Functional
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 37 None -1 11 Rat 6.2 pEC50 = 6.2 Functional
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 64 None -5 6 Rat 7.2 pEC50 = 7.2 Functional
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 64 None -5 6 Rat 7.2 pEC50 = 7.2 Functional
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 64 None -5 6 Rat 7.2 pEC50 = 7.2 Functional
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 64 None -5 6 Rat 7.2 pEC50 = 7.2 Functional
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 170346 0 None 1 3 Human 6.2 pEC50 = 6.2 Functional
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 170346 0 None 1 3 Human 6.2 pEC50 = 6.2 Functional
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 137029 0 None -52 2 Human 5.2 pEC50 = 5.2 Functional
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 137029 0 None -52 2 Human 5.2 pEC50 = 5.2 Functional
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 13459 0 None -1 2 Rat 5.2 pEC50 = 5.2 Functional
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 13459 0 None -1 2 Rat 5.2 pEC50 = 5.2 Functional
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 13459 0 None -1 2 Rat 5.2 pEC50 = 5.2 Functional
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 31341 0 None -1 5 Rat 8.2 pEC50 = 8.2 Functional
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 31341 0 None -1 5 Rat 8.2 pEC50 = 8.2 Functional
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 159284 0 None 3 2 Human 8.2 pEC50 = 8.2 Functional
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 159284 0 None 3 2 Human 8.2 pEC50 = 8.2 Functional
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 206508 12 None -1 4 Human 8.1 pEC50 = 8.1 Functional
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 206508 12 None -1 4 Human 8.1 pEC50 = 8.1 Functional
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 206508 12 None -1 4 Human 8.1 pEC50 = 8.1 Functional
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 206508 12 None -1 4 Human 8.1 pEC50 = 8.1 Functional
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 123400 0 None -11 2 Human 7.1 pEC50 = 7.1 Functional
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 123400 0 None -11 2 Human 7.1 pEC50 = 7.1 Functional
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 137122 0 None -1 2 Human 7.1 pEC50 = 7.1 Functional
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 137122 0 None -1 2 Human 7.1 pEC50 = 7.1 Functional
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 114800 6 None -1 4 Human 7.1 pEC50 = 7.1 Functional
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 114800 6 None -1 4 Human 7.1 pEC50 = 7.1 Functional
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 13355 0 None 3 3 Rat 5.1 pEC50 = 5.1 Functional
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 13355 0 None 3 3 Rat 5.1 pEC50 = 5.1 Functional
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 13355 0 None 3 3 Rat 5.1 pEC50 = 5.1 Functional
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 123399 0 None -7 2 Human 7.1 pEC50 = 7.1 Functional
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 123399 0 None -7 2 Human 7.1 pEC50 = 7.1 Functional
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 123408 0 None -3 2 Human 7.1 pEC50 = 7.1 Functional
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 123408 0 None -3 2 Human 7.1 pEC50 = 7.1 Functional
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 123398 0 None -5 2 Human 7.1 pEC50 = 7.1 Functional
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 123398 0 None -5 2 Human 7.1 pEC50 = 7.1 Functional
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 114499 7 None 1 2 Rat 7.1 pEC50 = 7.1 Functional
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 114499 7 None 1 2 Rat 7.1 pEC50 = 7.1 Functional
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 123398 0 None -5 2 Human 7.1 pEC50 = 7.1 Functional
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 123398 0 None -5 2 Human 7.1 pEC50 = 7.1 Functional
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 142312 3 None -32 2 Human 6.1 pEC50 = 6.1 Functional
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 142312 3 None -32 2 Human 6.1 pEC50 = 6.1 Functional
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 4 None -5 2 Human 5.1 pEC50 = 5.1 Functional
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 4 None -5 2 Human 5.1 pEC50 = 5.1 Functional
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 4 None -5 2 Human 5.1 pEC50 = 5.1 Functional
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 123409 0 None -51 2 Human 7.0 pEC50 = 7.0 Functional
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 123409 0 None -51 2 Human 7.0 pEC50 = 7.0 Functional
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 123404 0 None -7 2 Human 7.0 pEC50 = 7.0 Functional
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 123404 0 None -7 2 Human 7.0 pEC50 = 7.0 Functional
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 114800 6 None 1 4 Rat 7.0 pEC50 = 7.0 Functional
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 114800 6 None 1 4 Rat 7.0 pEC50 = 7.0 Functional
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 54 None 2 14 Human 8.0 pIC50 = 8 Functional
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 54 None 2 14 Human 8.0 pIC50 = 8 Functional
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 54 None 2 14 Human 8.0 pIC50 = 8 Functional
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 54 None 2 14 Human 8.0 pIC50 = 8 Functional
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 112544 0 None 3 5 Rat 7.0 pIC50 = 7 Functional
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 112544 0 None 3 5 Rat 7.0 pIC50 = 7 Functional
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 208051 0 None 1 4 Rat 6.0 pIC50 = 6 Functional
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 208051 0 None 1 4 Rat 6.0 pIC50 = 6 Functional
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 162946 0 None -2 2 Rat 6.0 pIC50 = 6.0 Functional
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 162946 0 None -2 2 Rat 6.0 pIC50 = 6.0 Functional
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 162946 0 None -2 2 Rat 6.0 pIC50 = 6.0 Functional
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 162946 0 None -2 2 Rat 6.0 pIC50 = 6.0 Functional
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 90327 0 None - 1 Rat 5.0 pIC50 = 5.0 Functional
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 90327 0 None - 1 Rat 5.0 pIC50 = 5.0 Functional
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 123453 0 None 1 2 Rat 6.0 pIC50 = 6.0 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123453 0 None 1 2 Rat 6.0 pIC50 = 6.0 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123453 0 None 1 2 Rat 6.0 pIC50 = 6.0 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123453 0 None 1 2 Rat 6.0 pIC50 = 6.0 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 19 None -13 3 Human 6.0 pIC50 = 6.0 Functional
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 19 None -13 3 Human 6.0 pIC50 = 6.0 Functional
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 19 None -13 3 Human 6.0 pIC50 = 6.0 Functional
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 90060 0 None -1 3 Human 6.0 pIC50 = 6.0 Functional
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 90060 0 None -1 3 Human 6.0 pIC50 = 6.0 Functional
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 147500 0 None 1 2 Human 6.0 pIC50 = 6.0 Functional
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 147500 0 None 1 2 Human 6.0 pIC50 = 6.0 Functional
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 123459 0 None 3 2 Rat 6.0 pIC50 = 6.0 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123459 0 None 3 2 Rat 6.0 pIC50 = 6.0 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 90329 0 None - 1 Rat 6.0 pIC50 = 6.0 Functional
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 90329 0 None - 1 Rat 6.0 pIC50 = 6.0 Functional
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 150823 0 None 3 2 Human 7.0 pIC50 = 7.0 Functional
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 150823 0 None 3 2 Human 7.0 pIC50 = 7.0 Functional
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 123459 0 None 3 2 Rat 6.0 pIC50 = 6.0 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123459 0 None 3 2 Rat 6.0 pIC50 = 6.0 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 90323 0 None - 1 Rat 6.0 pIC50 = 6.0 Functional
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 90323 0 None - 1 Rat 6.0 pIC50 = 6.0 Functional
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 123457 0 None - 1 Rat 5.9 pIC50 = 5.9 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123457 0 None - 1 Rat 5.9 pIC50 = 5.9 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123457 0 None - 1 Rat 5.9 pIC50 = 5.9 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123457 0 None - 1 Rat 5.9 pIC50 = 5.9 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123450 0 None -1 2 Rat 5.9 pIC50 = 5.9 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123450 0 None -1 2 Rat 5.9 pIC50 = 5.9 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123450 0 None -1 2 Rat 5.9 pIC50 = 5.9 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123450 0 None -1 2 Rat 5.9 pIC50 = 5.9 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 111994 0 None 2 2 Rat 5.9 pIC50 = 5.9 Functional
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 111994 0 None 2 2 Rat 5.9 pIC50 = 5.9 Functional
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 123447 0 None -1 2 Rat 5.9 pIC50 = 5.9 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123447 0 None -1 2 Rat 5.9 pIC50 = 5.9 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 183640 0 None 2 2 Human 7.9 pIC50 = 7.9 Functional
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 183640 0 None 2 2 Human 7.9 pIC50 = 7.9 Functional
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 183640 0 None 2 2 Human 7.9 pIC50 = 7.9 Functional
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 78738 0 None 1 2 Human 5.9 pIC50 = 5.9 Functional
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 78738 0 None 1 2 Human 5.9 pIC50 = 5.9 Functional
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 123447 0 None -1 2 Rat 5.9 pIC50 = 5.9 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123447 0 None -1 2 Rat 5.9 pIC50 = 5.9 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 155778 0 None -4 2 Rat 6.9 pIC50 = 6.9 Functional
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 155778 0 None -4 2 Rat 6.9 pIC50 = 6.9 Functional
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 108274 0 None 6 7 Rat 6.9 pIC50 = 6.9 Functional
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 108274 0 None 6 7 Rat 6.9 pIC50 = 6.9 Functional
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 123510 0 None - 1 Rat 6.9 pIC50 = 6.9 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123510 0 None - 1 Rat 6.9 pIC50 = 6.9 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123510 0 None - 1 Rat 6.9 pIC50 = 6.9 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123510 0 None - 1 Rat 6.9 pIC50 = 6.9 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123520 0 None 2 2 Rat 5.9 pIC50 = 5.9 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123520 0 None 2 2 Rat 5.9 pIC50 = 5.9 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 162294 0 None - 1 Rat 5.9 pIC50 = 5.9 Functional
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 162294 0 None - 1 Rat 5.9 pIC50 = 5.9 Functional
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 123520 0 None 2 2 Rat 5.9 pIC50 = 5.9 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123520 0 None 2 2 Rat 5.9 pIC50 = 5.9 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 162294 0 None - 1 Rat 5.9 pIC50 = 5.9 Functional
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 162294 0 None - 1 Rat 5.9 pIC50 = 5.9 Functional
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 107879 0 None 7 5 Rat 6.9 pIC50 = 6.9 Functional
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 107879 0 None 7 5 Rat 6.9 pIC50 = 6.9 Functional
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 112000 0 None -1 2 Rat 5.9 pIC50 = 5.9 Functional
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 112000 0 None -1 2 Rat 5.9 pIC50 = 5.9 Functional
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 142446 0 None 1 2 Human 6.9 pIC50 = 6.9 Functional
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 142446 0 None 1 2 Human 6.9 pIC50 = 6.9 Functional
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 123452 0 None 1 2 Rat 5.9 pIC50 = 5.9 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123452 0 None 1 2 Rat 5.9 pIC50 = 5.9 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123452 0 None 1 2 Rat 5.9 pIC50 = 5.9 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123452 0 None 1 2 Rat 5.9 pIC50 = 5.9 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 83602 0 None 2 2 Rat 5.9 pIC50 = 5.9 Functional
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 83602 0 None 2 2 Rat 5.9 pIC50 = 5.9 Functional
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 54 None 2 14 Human 7.9 pIC50 = 7.9 Functional
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 54 None 2 14 Human 7.9 pIC50 = 7.9 Functional
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 54 None 2 14 Human 7.9 pIC50 = 7.9 Functional
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 54 None 2 14 Human 7.9 pIC50 = 7.9 Functional
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 56408 0 None -1 3 Rat 7.9 pIC50 = 7.9 Functional
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 56408 0 None -1 3 Rat 7.9 pIC50 = 7.9 Functional
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 145339 0 None 1 2 Human 7.8 pIC50 = 7.8 Functional
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 145339 0 None 1 2 Human 7.8 pIC50 = 7.8 Functional
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 78731 0 None -1 2 Human 5.9 pIC50 = 5.9 Functional
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 78731 0 None -1 2 Human 5.9 pIC50 = 5.9 Functional
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 123500 0 None 7 2 Rat 6.9 pIC50 = 6.9 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123500 0 None 7 2 Rat 6.9 pIC50 = 6.9 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123500 0 None 7 2 Rat 6.9 pIC50 = 6.9 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123500 0 None 7 2 Rat 6.9 pIC50 = 6.9 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123501 0 None 12 2 Rat 6.8 pIC50 = 6.8 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123501 0 None 12 2 Rat 6.8 pIC50 = 6.8 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123446 0 None - 1 Rat 5.8 pIC50 = 5.8 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123446 0 None - 1 Rat 5.8 pIC50 = 5.8 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123446 0 None - 1 Rat 5.8 pIC50 = 5.8 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123446 0 None - 1 Rat 5.8 pIC50 = 5.8 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 162966 0 None 5 2 Rat 5.8 pIC50 = 5.8 Functional
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 162966 0 None 5 2 Rat 5.8 pIC50 = 5.8 Functional
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 152510 0 None 1 2 Human 6.8 pIC50 = 6.8 Functional
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 152510 0 None 1 2 Human 6.8 pIC50 = 6.8 Functional
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 123501 0 None 12 2 Rat 6.8 pIC50 = 6.8 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123501 0 None 12 2 Rat 6.8 pIC50 = 6.8 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 162966 0 None 5 2 Rat 5.8 pIC50 = 5.8 Functional
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 162966 0 None 5 2 Rat 5.8 pIC50 = 5.8 Functional
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 144789 0 None 1 2 Human 6.8 pIC50 = 6.8 Functional
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 144789 0 None 1 2 Human 6.8 pIC50 = 6.8 Functional
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 123399 0 None -7 2 Human 6.8 pIC50 = 6.8 Functional
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 123399 0 None -7 2 Human 6.8 pIC50 = 6.8 Functional
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 123469 0 None - 1 Rat 5.8 pIC50 = 5.8 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123469 0 None - 1 Rat 5.8 pIC50 = 5.8 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123469 0 None - 1 Rat 5.8 pIC50 = 5.8 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123469 0 None - 1 Rat 5.8 pIC50 = 5.8 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 35817 1 None 3 4 Human 7.8 pIC50 = 7.8 Functional
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 35817 1 None 3 4 Human 7.8 pIC50 = 7.8 Functional
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 54 None -2 14 Rat 7.8 pIC50 = 7.8 Functional
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 54 None -2 14 Rat 7.8 pIC50 = 7.8 Functional
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 54 None -2 14 Rat 7.8 pIC50 = 7.8 Functional
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 54 None -2 14 Rat 7.8 pIC50 = 7.8 Functional
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 183687 0 None -2 2 Human 7.8 pIC50 = 7.8 Functional
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 183687 0 None -2 2 Human 7.8 pIC50 = 7.8 Functional
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 183687 0 None -2 2 Human 7.8 pIC50 = 7.8 Functional
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 118494 0 None 2 2 Human 6.8 pIC50 = 6.8 Functional
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 118494 0 None 2 2 Human 6.8 pIC50 = 6.8 Functional
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 100846 0 None 2 2 Human 4.8 pIC50 = 4.8 Functional
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 100846 0 None 2 2 Human 4.8 pIC50 = 4.8 Functional
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 123498 0 None - 1 Rat 6.8 pIC50 = 6.8 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123498 0 None - 1 Rat 6.8 pIC50 = 6.8 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123498 0 None - 1 Rat 6.8 pIC50 = 6.8 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123498 0 None - 1 Rat 6.8 pIC50 = 6.8 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123449 0 None - 1 Rat 5.8 pIC50 = 5.8 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123449 0 None - 1 Rat 5.8 pIC50 = 5.8 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123449 0 None - 1 Rat 5.8 pIC50 = 5.8 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123449 0 None - 1 Rat 5.8 pIC50 = 5.8 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 183675 0 None -3 2 Human 6.8 pIC50 = 6.8 Functional
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 183675 0 None -3 2 Human 6.8 pIC50 = 6.8 Functional
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 183675 0 None -3 2 Human 6.8 pIC50 = 6.8 Functional
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 111991 0 None 5 2 Rat 6.8 pIC50 = 6.8 Functional
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 111991 0 None 5 2 Rat 6.8 pIC50 = 6.8 Functional
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 123463 0 None - 1 Rat 5.8 pIC50 = 5.8 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123463 0 None - 1 Rat 5.8 pIC50 = 5.8 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123463 0 None - 1 Rat 5.8 pIC50 = 5.8 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123463 0 None - 1 Rat 5.8 pIC50 = 5.8 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 90323 0 None - 1 Rat 5.8 pIC50 = 5.8 Functional
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 90323 0 None - 1 Rat 5.8 pIC50 = 5.8 Functional
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 95864 0 None 2 2 Rat 7.8 pIC50 = 7.8 Functional
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 95864 0 None 2 2 Rat 7.8 pIC50 = 7.8 Functional
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 56308 0 None 1 3 Rat 7.8 pIC50 = 7.8 Functional
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 56308 0 None 1 3 Rat 7.8 pIC50 = 7.8 Functional
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 16604 0 None 1 2 Human 6.8 pIC50 = 6.8 Functional
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 16604 0 None 1 2 Human 6.8 pIC50 = 6.8 Functional
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 150394 0 None 1 2 Human 6.8 pIC50 = 6.8 Functional
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 150394 0 None 1 2 Human 6.8 pIC50 = 6.8 Functional
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 114585 0 None -1 2 Human 6.8 pIC50 = 6.8 Functional
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 114585 0 None -1 2 Human 6.8 pIC50 = 6.8 Functional
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 117012 0 None 1 2 Human 6.8 pIC50 = 6.8 Functional
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 117012 0 None 1 2 Human 6.8 pIC50 = 6.8 Functional
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 117012 0 None 1 2 Human 6.8 pIC50 = 6.8 Functional
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 162226 0 None 1 2 Rat 6.8 pIC50 = 6.8 Functional
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 162226 0 None 1 2 Rat 6.8 pIC50 = 6.8 Functional
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 113350 0 None -1 2 Human 5.8 pIC50 = 5.8 Functional
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 113350 0 None -1 2 Human 5.8 pIC50 = 5.8 Functional
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 123511 0 None 6 2 Rat 6.7 pIC50 = 6.7 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123511 0 None 6 2 Rat 6.7 pIC50 = 6.7 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123511 0 None 6 2 Rat 6.7 pIC50 = 6.7 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123511 0 None 6 2 Rat 6.7 pIC50 = 6.7 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 162226 0 None 1 2 Rat 6.7 pIC50 = 6.7 Functional
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 162226 0 None 1 2 Rat 6.7 pIC50 = 6.7 Functional
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 123509 0 None 11 2 Rat 6.7 pIC50 = 6.7 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123509 0 None 11 2 Rat 6.7 pIC50 = 6.7 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 153463 0 None 2 2 Human 6.7 pIC50 = 6.7 Functional
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 153463 0 None 2 2 Human 6.7 pIC50 = 6.7 Functional
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 123454 0 None - 1 Rat 5.7 pIC50 = 5.7 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123454 0 None - 1 Rat 5.7 pIC50 = 5.7 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123509 0 None 11 2 Rat 6.7 pIC50 = 6.7 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123509 0 None 11 2 Rat 6.7 pIC50 = 6.7 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123454 0 None - 1 Rat 5.7 pIC50 = 5.7 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123454 0 None - 1 Rat 5.7 pIC50 = 5.7 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123499 0 None 14 2 Rat 6.7 pIC50 = 6.7 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123499 0 None 14 2 Rat 6.7 pIC50 = 6.7 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123499 0 None 14 2 Rat 6.7 pIC50 = 6.7 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123499 0 None 14 2 Rat 6.7 pIC50 = 6.7 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123502 0 None 1 2 Rat 6.7 pIC50 = 6.7 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123502 0 None 1 2 Rat 6.7 pIC50 = 6.7 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 208358 0 None 11 3 Rat 6.7 pIC50 = 6.7 Functional
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 208358 0 None 11 3 Rat 6.7 pIC50 = 6.7 Functional
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 123502 0 None 1 2 Rat 6.7 pIC50 = 6.7 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123502 0 None 1 2 Rat 6.7 pIC50 = 6.7 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123507 0 None - 1 Rat 6.7 pIC50 = 6.7 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123507 0 None - 1 Rat 6.7 pIC50 = 6.7 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123507 0 None - 1 Rat 6.7 pIC50 = 6.7 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123507 0 None - 1 Rat 6.7 pIC50 = 6.7 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 111998 0 None 1 2 Rat 5.7 pIC50 = 5.7 Functional
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 111998 0 None 1 2 Rat 5.7 pIC50 = 5.7 Functional
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 183653 11 None 2 4 Human 8.6 pIC50 = 8.6 Functional
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 183653 11 None 2 4 Human 8.6 pIC50 = 8.6 Functional
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 183653 11 None 2 4 Human 8.6 pIC50 = 8.6 Functional
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 54 None 2 14 Human 8.6 pIC50 = 8.6 Functional
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 54 None 2 14 Human 8.6 pIC50 = 8.6 Functional
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 54 None 2 14 Human 8.6 pIC50 = 8.6 Functional
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 54 None 2 14 Human 8.6 pIC50 = 8.6 Functional
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 148642 0 None -1 2 Human 7.7 pIC50 = 7.7 Functional
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 148642 0 None -1 2 Human 7.7 pIC50 = 7.7 Functional
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 16564 0 None 15 2 Human 6.7 pIC50 = 6.7 Functional
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 16564 0 None 15 2 Human 6.7 pIC50 = 6.7 Functional
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 183691 0 None -1 2 Human 6.7 pIC50 = 6.7 Functional
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 183691 0 None -1 2 Human 6.7 pIC50 = 6.7 Functional
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 183691 0 None -1 2 Human 6.7 pIC50 = 6.7 Functional
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 123517 0 None 29 2 Rat 6.7 pIC50 = 6.7 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123517 0 None 29 2 Rat 6.7 pIC50 = 6.7 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 156641 0 None 1 2 Human 5.7 pIC50 = 5.7 Functional
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 156641 0 None 1 2 Human 5.7 pIC50 = 5.7 Functional
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 123517 0 None 29 2 Rat 6.7 pIC50 = 6.7 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123517 0 None 29 2 Rat 6.7 pIC50 = 6.7 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123462 0 None - 1 Rat 5.7 pIC50 = 5.7 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123462 0 None - 1 Rat 5.7 pIC50 = 5.7 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123462 0 None - 1 Rat 5.7 pIC50 = 5.7 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123462 0 None - 1 Rat 5.7 pIC50 = 5.7 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 116882 0 None -1 2 Human 6.7 pIC50 = 6.7 Functional
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 116882 0 None -1 2 Human 6.7 pIC50 = 6.7 Functional
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 12951 0 None 1 3 Rat 4.7 pIC50 = 4.7 Functional
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 12951 0 None 1 3 Rat 4.7 pIC50 = 4.7 Functional
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 12951 0 None 1 3 Rat 4.7 pIC50 = 4.7 Functional
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 123504 0 None - 1 Rat 6.7 pIC50 = 6.7 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123504 0 None - 1 Rat 6.7 pIC50 = 6.7 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123504 0 None - 1 Rat 6.7 pIC50 = 6.7 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123504 0 None - 1 Rat 6.7 pIC50 = 6.7 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 183719 0 None -1 2 Human 5.7 pIC50 = 5.7 Functional
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 183719 0 None -1 2 Human 5.7 pIC50 = 5.7 Functional
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 183719 0 None -1 2 Human 5.7 pIC50 = 5.7 Functional
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 123516 0 None 14 2 Rat 6.7 pIC50 = 6.7 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123516 0 None 14 2 Rat 6.7 pIC50 = 6.7 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123532 0 None 6 2 Rat 6.7 pIC50 = 6.7 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123532 0 None 6 2 Rat 6.7 pIC50 = 6.7 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123532 0 None 6 2 Rat 6.7 pIC50 = 6.7 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123532 0 None 6 2 Rat 6.7 pIC50 = 6.7 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123516 0 None 14 2 Rat 6.7 pIC50 = 6.7 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123516 0 None 14 2 Rat 6.7 pIC50 = 6.7 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 152255 0 None -1 2 Human 7.6 pIC50 = 7.6 Functional
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 152255 0 None -1 2 Human 7.6 pIC50 = 7.6 Functional
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 13013 0 None 1 2 Rat 4.6 pIC50 = 4.6 Functional
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 13013 0 None 1 2 Rat 4.6 pIC50 = 4.6 Functional
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 13013 0 None 1 2 Rat 4.6 pIC50 = 4.6 Functional
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 123468 0 None - 1 Rat 5.6 pIC50 = 5.6 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123468 0 None - 1 Rat 5.6 pIC50 = 5.6 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123408 0 None -3 2 Human 5.6 pIC50 = 5.6 Functional
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 123408 0 None -3 2 Human 5.6 pIC50 = 5.6 Functional
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 123468 0 None - 1 Rat 5.6 pIC50 = 5.6 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123468 0 None - 1 Rat 5.6 pIC50 = 5.6 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123467 0 None -1 2 Rat 5.6 pIC50 = 5.6 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123467 0 None -1 2 Rat 5.6 pIC50 = 5.6 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123402 0 None -60 2 Human 5.6 pIC50 = 5.6 Functional
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 123402 0 None -60 2 Human 5.6 pIC50 = 5.6 Functional
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 150637 0 None 1 2 Human 6.6 pIC50 = 6.6 Functional
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 150637 0 None 1 2 Human 6.6 pIC50 = 6.6 Functional
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 123467 0 None -1 2 Rat 5.6 pIC50 = 5.6 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123467 0 None -1 2 Rat 5.6 pIC50 = 5.6 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 15 None -1 8 Human 7.6 pIC50 = 7.6 Functional
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 15 None -1 8 Human 7.6 pIC50 = 7.6 Functional
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 15 None -1 8 Human 7.6 pIC50 = 7.6 Functional
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 183622 0 None -186 2 Human 5.6 pIC50 = 5.6 Functional
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 183622 0 None -186 2 Human 5.6 pIC50 = 5.6 Functional
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 183622 0 None -186 2 Human 5.6 pIC50 = 5.6 Functional
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 123406 0 None -43 2 Human 6.6 pIC50 = 6.6 Functional
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 123406 0 None -43 2 Human 6.6 pIC50 = 6.6 Functional
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 162817 6 None - 1 Rat 6.6 pIC50 = 6.6 Functional
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 162817 6 None - 1 Rat 6.6 pIC50 = 6.6 Functional
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 162817 6 None - 1 Rat 6.6 pIC50 = 6.6 Functional
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 162817 6 None - 1 Rat 6.6 pIC50 = 6.6 Functional
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 162817 6 None - 1 Rat 6.6 pIC50 = 6.6 Functional
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 162817 6 None - 1 Rat 6.6 pIC50 = 6.6 Functional
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 111992 0 None 6 2 Rat 6.6 pIC50 = 6.6 Functional
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 111992 0 None 6 2 Rat 6.6 pIC50 = 6.6 Functional
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 78736 0 None 2 2 Human 5.6 pIC50 = 5.6 Functional
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 78736 0 None 2 2 Human 5.6 pIC50 = 5.6 Functional
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 123396 17 None -107 4 Human 4.6 pIC50 = 4.6 Functional
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 123396 17 None -107 4 Human 4.6 pIC50 = 4.6 Functional
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 123451 0 None - 1 Rat 5.6 pIC50 = 5.6 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123451 0 None - 1 Rat 5.6 pIC50 = 5.6 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123540 0 None - 1 Rat 6.6 pIC50 = 6.6 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123540 0 None - 1 Rat 6.6 pIC50 = 6.6 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123451 0 None - 1 Rat 5.6 pIC50 = 5.6 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123451 0 None - 1 Rat 5.6 pIC50 = 5.6 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 16781 0 None 3 2 Human 6.6 pIC50 = 6.6 Functional
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 16781 0 None 3 2 Human 6.6 pIC50 = 6.6 Functional
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 123540 0 None - 1 Rat 6.6 pIC50 = 6.6 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123540 0 None - 1 Rat 6.6 pIC50 = 6.6 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123440 0 None -5 2 Rat 6.6 pIC50 = 6.6 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123440 0 None -5 2 Rat 6.6 pIC50 = 6.6 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123505 0 None - 1 Rat 6.6 pIC50 = 6.6 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123505 0 None - 1 Rat 6.6 pIC50 = 6.6 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123440 0 None -5 2 Rat 6.6 pIC50 = 6.6 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123440 0 None -5 2 Rat 6.6 pIC50 = 6.6 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123505 0 None - 1 Rat 6.6 pIC50 = 6.6 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123505 0 None - 1 Rat 6.6 pIC50 = 6.6 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 162883 0 None 4 2 Rat 6.6 pIC50 = 6.6 Functional
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 162883 0 None 4 2 Rat 6.6 pIC50 = 6.6 Functional
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 183721 0 None -1 2 Human 7.6 pIC50 = 7.6 Functional
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 183721 0 None -1 2 Human 7.6 pIC50 = 7.6 Functional
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 183721 0 None -1 2 Human 7.6 pIC50 = 7.6 Functional
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 162883 0 None 4 2 Rat 6.6 pIC50 = 6.6 Functional
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 162883 0 None 4 2 Rat 6.6 pIC50 = 6.6 Functional
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 14186 0 None -4 3 Rat 4.6 pIC50 = 4.6 Functional
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 14186 0 None -4 3 Rat 4.6 pIC50 = 4.6 Functional
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 14186 0 None -4 3 Rat 4.6 pIC50 = 4.6 Functional
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 183731 0 None -3 2 Human 6.6 pIC50 = 6.6 Functional
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 183731 0 None -3 2 Human 6.6 pIC50 = 6.6 Functional
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 183731 0 None -3 2 Human 6.6 pIC50 = 6.6 Functional
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 123396 17 None -107 4 Human 5.6 pIC50 = 5.6 Functional
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 123396 17 None -107 4 Human 5.6 pIC50 = 5.6 Functional
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 90330 0 None - 1 Rat 5.6 pIC50 = 5.6 Functional
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 90330 0 None - 1 Rat 5.6 pIC50 = 5.6 Functional
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 90326 0 None - 1 Rat 4.6 pIC50 = 4.6 Functional
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 90326 0 None - 1 Rat 4.6 pIC50 = 4.6 Functional
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 123409 0 None -51 2 Human 5.6 pIC50 = 5.6 Functional
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 123409 0 None -51 2 Human 5.6 pIC50 = 5.6 Functional
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 86122 0 None 15 2 Human 6.6 pIC50 = 6.6 Functional
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 86122 0 None 15 2 Human 6.6 pIC50 = 6.6 Functional
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 123531 0 None 9 2 Rat 6.6 pIC50 = 6.6 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123531 0 None 9 2 Rat 6.6 pIC50 = 6.6 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 78743 0 None -6 2 Human 5.6 pIC50 = 5.6 Functional
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 78743 0 None -6 2 Human 5.6 pIC50 = 5.6 Functional
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 123531 0 None 9 2 Rat 6.6 pIC50 = 6.6 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123531 0 None 9 2 Rat 6.6 pIC50 = 6.6 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 56304 0 None 1 3 Rat 7.5 pIC50 = 7.5 Functional
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 56304 0 None 1 3 Rat 7.5 pIC50 = 7.5 Functional
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 207754 0 None 16 6 Rat 7.5 pIC50 = 7.5 Functional
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 207754 0 None 16 6 Rat 7.5 pIC50 = 7.5 Functional
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 149765 0 None -1 2 Human 7.5 pIC50 = 7.5 Functional
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 149765 0 None -1 2 Human 7.5 pIC50 = 7.5 Functional
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 162299 0 None 4 2 Rat 6.5 pIC50 = 6.5 Functional
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 162299 0 None 4 2 Rat 6.5 pIC50 = 6.5 Functional
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 111996 0 None 1 2 Rat 6.5 pIC50 = 6.5 Functional
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 111996 0 None 1 2 Rat 6.5 pIC50 = 6.5 Functional
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 123331 0 None - 1 Rat 6.5 pIC50 = 6.5 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123331 0 None - 1 Rat 6.5 pIC50 = 6.5 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 19 None -13 3 Human 5.5 pIC50 = 5.5 Functional
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 19 None -13 3 Human 5.5 pIC50 = 5.5 Functional
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 19 None -13 3 Human 5.5 pIC50 = 5.5 Functional
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 123460 0 None - 1 Rat 5.5 pIC50 = 5.5 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123460 0 None - 1 Rat 5.5 pIC50 = 5.5 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123331 0 None - 1 Rat 6.5 pIC50 = 6.5 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123331 0 None - 1 Rat 6.5 pIC50 = 6.5 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 162299 0 None 4 2 Rat 6.5 pIC50 = 6.5 Functional
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 162299 0 None 4 2 Rat 6.5 pIC50 = 6.5 Functional
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 123460 0 None - 1 Rat 5.5 pIC50 = 5.5 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123460 0 None - 1 Rat 5.5 pIC50 = 5.5 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 56309 0 None 2 3 Rat 8.5 pIC50 = 8.5 Functional
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 56309 0 None 2 3 Rat 8.5 pIC50 = 8.5 Functional
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 56307 0 None -10 3 Rat 7.5 pIC50 = 7.5 Functional
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 56307 0 None -10 3 Rat 7.5 pIC50 = 7.5 Functional
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 147944 11 None -6 2 Human 4.5 pIC50 = 4.5 Functional
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 147944 11 None -6 2 Human 4.5 pIC50 = 4.5 Functional
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 147944 11 None -6 2 Human 4.5 pIC50 = 4.5 Functional
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 147944 11 None -6 2 Human 4.5 pIC50 = 4.5 Functional
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 90324 0 None - 1 Rat 6.5 pIC50 = 6.5 Functional
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 90324 0 None - 1 Rat 6.5 pIC50 = 6.5 Functional
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 90324 0 None - 1 Rat 6.5 pIC50 = 6.5 Functional
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 123403 0 None -51 2 Human 5.5 pIC50 = 5.5 Functional
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 123403 0 None -51 2 Human 5.5 pIC50 = 5.5 Functional
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 123525 0 None 16 2 Rat 6.5 pIC50 = 6.5 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123525 0 None 16 2 Rat 6.5 pIC50 = 6.5 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123535 0 None 3 2 Rat 6.5 pIC50 = 6.5 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123535 0 None 3 2 Rat 6.5 pIC50 = 6.5 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 112002 0 None 1 2 Rat 5.5 pIC50 = 5.5 Functional
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 112002 0 None 1 2 Rat 5.5 pIC50 = 5.5 Functional
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 123525 0 None 16 2 Rat 6.5 pIC50 = 6.5 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123525 0 None 16 2 Rat 6.5 pIC50 = 6.5 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123535 0 None 3 2 Rat 6.5 pIC50 = 6.5 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123535 0 None 3 2 Rat 6.5 pIC50 = 6.5 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123508 0 None 4 2 Rat 6.5 pIC50 = 6.5 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123508 0 None 4 2 Rat 6.5 pIC50 = 6.5 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123508 0 None 4 2 Rat 6.5 pIC50 = 6.5 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123508 0 None 4 2 Rat 6.5 pIC50 = 6.5 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123518 0 None 16 2 Rat 6.5 pIC50 = 6.5 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123518 0 None 16 2 Rat 6.5 pIC50 = 6.5 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123536 0 None - 1 Rat 6.5 pIC50 = 6.5 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123536 0 None - 1 Rat 6.5 pIC50 = 6.5 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 96172 0 None -2 2 Rat 7.5 pIC50 = 7.5 Functional
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 96172 0 None -2 2 Rat 7.5 pIC50 = 7.5 Functional
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 96308 0 None -1 2 Rat 7.5 pIC50 = 7.5 Functional
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 96308 0 None -1 2 Rat 7.5 pIC50 = 7.5 Functional
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 123518 0 None 16 2 Rat 6.5 pIC50 = 6.5 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123518 0 None 16 2 Rat 6.5 pIC50 = 6.5 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123536 0 None - 1 Rat 6.5 pIC50 = 6.5 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123536 0 None - 1 Rat 6.5 pIC50 = 6.5 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 90061 0 None -1 3 Human 5.5 pIC50 = 5.5 Functional
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 90061 0 None -1 3 Human 5.5 pIC50 = 5.5 Functional
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 90061 0 None -1 3 Human 5.5 pIC50 = 5.5 Functional
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 90061 0 None -1 3 Human 5.5 pIC50 = 5.5 Functional
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 123506 0 None -1 2 Rat 6.5 pIC50 = 6.5 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123506 0 None -1 2 Rat 6.5 pIC50 = 6.5 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 162205 0 None 18 2 Rat 6.5 pIC50 = 6.5 Functional
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 162205 0 None 18 2 Rat 6.5 pIC50 = 6.5 Functional
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 123506 0 None -1 2 Rat 6.5 pIC50 = 6.5 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123506 0 None -1 2 Rat 6.5 pIC50 = 6.5 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 90058 0 None 1 3 Human 5.5 pIC50 = 5.5 Functional
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 90058 0 None 1 3 Human 5.5 pIC50 = 5.5 Functional
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 162205 0 None 18 2 Rat 6.5 pIC50 = 6.5 Functional
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 162205 0 None 18 2 Rat 6.5 pIC50 = 6.5 Functional
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 19 None -13 3 Human 5.5 pIC50 = 5.5 Functional
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 19 None -13 3 Human 5.5 pIC50 = 5.5 Functional
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 19 None -13 3 Human 5.5 pIC50 = 5.5 Functional
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 123503 0 None - 1 Rat 6.5 pIC50 = 6.5 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123503 0 None - 1 Rat 6.5 pIC50 = 6.5 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123503 0 None - 1 Rat 6.5 pIC50 = 6.5 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123503 0 None - 1 Rat 6.5 pIC50 = 6.5 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123515 0 None 28 2 Rat 6.5 pIC50 = 6.5 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123515 0 None 28 2 Rat 6.5 pIC50 = 6.5 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 162746 0 None 4 2 Rat 6.5 pIC50 = 6.5 Functional
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 162746 0 None 4 2 Rat 6.5 pIC50 = 6.5 Functional
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 123515 0 None 28 2 Rat 6.5 pIC50 = 6.5 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123515 0 None 28 2 Rat 6.5 pIC50 = 6.5 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 162746 0 None 4 2 Rat 6.5 pIC50 = 6.5 Functional
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 162746 0 None 4 2 Rat 6.5 pIC50 = 6.5 Functional
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 123404 0 None -7 2 Human 5.5 pIC50 = 5.5 Functional
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 123404 0 None -7 2 Human 5.5 pIC50 = 5.5 Functional
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 123538 0 None - 1 Rat 6.4 pIC50 = 6.4 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123538 0 None - 1 Rat 6.4 pIC50 = 6.4 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123538 0 None - 1 Rat 6.4 pIC50 = 6.4 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123538 0 None - 1 Rat 6.4 pIC50 = 6.4 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123464 0 None - 1 Rat 5.4 pIC50 = 5.4 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123464 0 None - 1 Rat 5.4 pIC50 = 5.4 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123464 0 None - 1 Rat 5.4 pIC50 = 5.4 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123464 0 None - 1 Rat 5.4 pIC50 = 5.4 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 153248 0 None -2 2 Human 7.4 pIC50 = 7.4 Functional
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 153248 0 None -2 2 Human 7.4 pIC50 = 7.4 Functional
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 123407 0 None -58 2 Human 5.4 pIC50 = 5.4 Functional
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 123407 0 None -58 2 Human 5.4 pIC50 = 5.4 Functional
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 20 None 1 2 Rat 6.4 pIC50 = 6.4 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 20 None 1 2 Rat 6.4 pIC50 = 6.4 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 20 None 1 2 Rat 6.4 pIC50 = 6.4 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123522 0 None 9 2 Rat 6.4 pIC50 = 6.4 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123522 0 None 9 2 Rat 6.4 pIC50 = 6.4 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 162727 0 None 5 2 Rat 6.4 pIC50 = 6.4 Functional
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 162727 0 None 5 2 Rat 6.4 pIC50 = 6.4 Functional
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 162727 0 None 5 2 Rat 6.4 pIC50 = 6.4 Functional
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 162727 0 None 5 2 Rat 6.4 pIC50 = 6.4 Functional
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 20 None 1 2 Rat 6.4 pIC50 = 6.4 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 20 None 1 2 Rat 6.4 pIC50 = 6.4 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 20 None 1 2 Rat 6.4 pIC50 = 6.4 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123522 0 None 9 2 Rat 6.4 pIC50 = 6.4 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123522 0 None 9 2 Rat 6.4 pIC50 = 6.4 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 207980 0 None 9 5 Rat 7.4 pIC50 = 7.4 Functional
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 207980 0 None 9 5 Rat 7.4 pIC50 = 7.4 Functional
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 200916 0 None 1 2 Human 4.4 pIC50 = 4.4 Functional
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 200916 0 None 1 2 Human 4.4 pIC50 = 4.4 Functional
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 123523 0 None - 1 Rat 6.4 pIC50 = 6.4 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123523 0 None - 1 Rat 6.4 pIC50 = 6.4 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123544 0 None - 1 Rat 6.4 pIC50 = 6.4 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123544 0 None - 1 Rat 6.4 pIC50 = 6.4 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123458 0 None - 1 Rat 5.4 pIC50 = 5.4 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123458 0 None - 1 Rat 5.4 pIC50 = 5.4 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123458 0 None - 1 Rat 5.4 pIC50 = 5.4 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123458 0 None - 1 Rat 5.4 pIC50 = 5.4 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123544 0 None - 1 Rat 6.4 pIC50 = 6.4 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123544 0 None - 1 Rat 6.4 pIC50 = 6.4 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 183618 0 None -2 2 Human 7.4 pIC50 = 7.4 Functional
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 183618 0 None -2 2 Human 7.4 pIC50 = 7.4 Functional
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 183618 0 None -2 2 Human 7.4 pIC50 = 7.4 Functional
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 123523 0 None - 1 Rat 6.4 pIC50 = 6.4 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123523 0 None - 1 Rat 6.4 pIC50 = 6.4 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123444 0 None -1 2 Rat 6.4 pIC50 = 6.4 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123444 0 None -1 2 Rat 6.4 pIC50 = 6.4 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123533 0 None - 1 Rat 6.4 pIC50 = 6.4 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123533 0 None - 1 Rat 6.4 pIC50 = 6.4 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123444 0 None -1 2 Rat 6.4 pIC50 = 6.4 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123444 0 None -1 2 Rat 6.4 pIC50 = 6.4 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 96308 0 None -1 2 Rat 7.4 pIC50 = 7.4 Functional
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 96308 0 None -1 2 Rat 7.4 pIC50 = 7.4 Functional
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 16566 0 None -1 2 Human 6.4 pIC50 = 6.4 Functional
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 16566 0 None -1 2 Human 6.4 pIC50 = 6.4 Functional
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 123533 0 None - 1 Rat 6.4 pIC50 = 6.4 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123533 0 None - 1 Rat 6.4 pIC50 = 6.4 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 3 None 31 2 Human 5.4 pIC50 = 5.4 Functional
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 3 None 31 2 Human 5.4 pIC50 = 5.4 Functional
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 3 None 31 2 Human 5.4 pIC50 = 5.4 Functional
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 123527 0 None 11 2 Rat 6.4 pIC50 = 6.4 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123527 0 None 11 2 Rat 6.4 pIC50 = 6.4 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123403 0 None -51 2 Human 5.4 pIC50 = 5.4 Functional
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 123403 0 None -51 2 Human 5.4 pIC50 = 5.4 Functional
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 123527 0 None 11 2 Rat 6.4 pIC50 = 6.4 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123527 0 None 11 2 Rat 6.4 pIC50 = 6.4 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123513 0 None - 1 Rat 6.4 pIC50 = 6.4 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123513 0 None - 1 Rat 6.4 pIC50 = 6.4 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123513 0 None - 1 Rat 6.4 pIC50 = 6.4 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123513 0 None - 1 Rat 6.4 pIC50 = 6.4 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123526 0 None 10 2 Rat 6.4 pIC50 = 6.4 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123526 0 None 10 2 Rat 6.4 pIC50 = 6.4 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123526 0 None 10 2 Rat 6.4 pIC50 = 6.4 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123526 0 None 10 2 Rat 6.4 pIC50 = 6.4 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 162082 0 None 17 2 Rat 6.4 pIC50 = 6.4 Functional
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 162082 0 None 17 2 Rat 6.4 pIC50 = 6.4 Functional
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 162082 0 None 17 2 Rat 6.4 pIC50 = 6.4 Functional
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 162082 0 None 17 2 Rat 6.4 pIC50 = 6.4 Functional
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 30 None - 1 Rat 6.4 pIC50 = 6.4 Functional
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 30 None - 1 Rat 6.4 pIC50 = 6.4 Functional
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 30 None - 1 Rat 6.4 pIC50 = 6.4 Functional
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 112005 0 None - 1 Rat 5.4 pIC50 = 5.4 Functional
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 112005 0 None - 1 Rat 5.4 pIC50 = 5.4 Functional
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 90332 0 None - 1 Rat 6.3 pIC50 = 6.3 Functional
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 90332 0 None - 1 Rat 6.3 pIC50 = 6.3 Functional
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 180213 0 None -1 2 Human 5.3 pIC50 = 5.3 Functional
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 180213 0 None -1 2 Human 5.3 pIC50 = 5.3 Functional
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 123443 0 None -5 2 Rat 6.3 pIC50 = 6.3 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123443 0 None -5 2 Rat 6.3 pIC50 = 6.3 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 90332 0 None - 1 Rat 6.3 pIC50 = 6.3 Functional
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 90332 0 None - 1 Rat 6.3 pIC50 = 6.3 Functional
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 123399 0 None -7 2 Human 6.3 pIC50 = 6.3 Functional
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 123399 0 None -7 2 Human 6.3 pIC50 = 6.3 Functional
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 149627 0 None -1 5 Human 7.3 pIC50 = 7.3 Functional
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 149627 0 None -1 5 Human 7.3 pIC50 = 7.3 Functional
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 123443 0 None -5 2 Rat 6.3 pIC50 = 6.3 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123443 0 None -5 2 Rat 6.3 pIC50 = 6.3 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 78741 0 None -1 2 Human 6.3 pIC50 = 6.3 Functional
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 78741 0 None -1 2 Human 6.3 pIC50 = 6.3 Functional
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 123541 0 None - 1 Rat 6.3 pIC50 = 6.3 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123541 0 None - 1 Rat 6.3 pIC50 = 6.3 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123542 0 None - 1 Rat 6.3 pIC50 = 6.3 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123542 0 None - 1 Rat 6.3 pIC50 = 6.3 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123542 0 None - 1 Rat 6.3 pIC50 = 6.3 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123542 0 None - 1 Rat 6.3 pIC50 = 6.3 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123541 0 None - 1 Rat 6.3 pIC50 = 6.3 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123541 0 None - 1 Rat 6.3 pIC50 = 6.3 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 112003 0 None 3 2 Rat 6.3 pIC50 = 6.3 Functional
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 112003 0 None 3 2 Rat 6.3 pIC50 = 6.3 Functional
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 123441 0 None -2 2 Rat 6.3 pIC50 = 6.3 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123441 0 None -2 2 Rat 6.3 pIC50 = 6.3 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123534 0 None - 1 Rat 6.3 pIC50 = 6.3 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123534 0 None - 1 Rat 6.3 pIC50 = 6.3 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123398 0 None -5 2 Human 6.3 pIC50 = 6.3 Functional
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 123398 0 None -5 2 Human 6.3 pIC50 = 6.3 Functional
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 123534 0 None - 1 Rat 6.3 pIC50 = 6.3 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123534 0 None - 1 Rat 6.3 pIC50 = 6.3 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 111995 0 None 3 2 Rat 6.3 pIC50 = 6.3 Functional
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 111995 0 None 3 2 Rat 6.3 pIC50 = 6.3 Functional
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 123441 0 None -2 2 Rat 6.3 pIC50 = 6.3 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123441 0 None -2 2 Rat 6.3 pIC50 = 6.3 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123448 0 None -1 2 Rat 6.3 pIC50 = 6.3 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123448 0 None -1 2 Rat 6.3 pIC50 = 6.3 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123448 0 None -1 2 Rat 6.3 pIC50 = 6.3 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123448 0 None -1 2 Rat 6.3 pIC50 = 6.3 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123465 0 None - 1 Rat 6.3 pIC50 = 6.3 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123465 0 None - 1 Rat 6.3 pIC50 = 6.3 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123529 0 None 6 2 Rat 6.3 pIC50 = 6.3 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123529 0 None 6 2 Rat 6.3 pIC50 = 6.3 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123465 0 None - 1 Rat 6.3 pIC50 = 6.3 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123465 0 None - 1 Rat 6.3 pIC50 = 6.3 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123529 0 None 6 2 Rat 6.3 pIC50 = 6.3 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123529 0 None 6 2 Rat 6.3 pIC50 = 6.3 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 147948 0 None -1 2 Human 7.3 pIC50 = 7.3 Functional
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 147948 0 None -1 2 Human 7.3 pIC50 = 7.3 Functional
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 183728 0 None -1 2 Human 6.3 pIC50 = 6.3 Functional
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 183728 0 None -1 2 Human 6.3 pIC50 = 6.3 Functional
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 183728 0 None -1 2 Human 6.3 pIC50 = 6.3 Functional
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 90322 0 None - 1 Rat 5.3 pIC50 = 5.3 Functional
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 90322 0 None - 1 Rat 5.3 pIC50 = 5.3 Functional
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 90331 0 None - 1 Rat 5.3 pIC50 = 5.3 Functional
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 90331 0 None - 1 Rat 5.3 pIC50 = 5.3 Functional
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 78742 0 None 1 2 Human 6.3 pIC50 = 6.3 Functional
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 78742 0 None 1 2 Human 6.3 pIC50 = 6.3 Functional
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 123402 0 None -60 2 Human 5.3 pIC50 = 5.3 Functional
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 123402 0 None -60 2 Human 5.3 pIC50 = 5.3 Functional
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 123519 0 None 5 2 Rat 6.3 pIC50 = 6.3 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123519 0 None 5 2 Rat 6.3 pIC50 = 6.3 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 183647 0 None -5 2 Human 7.3 pIC50 = 7.3 Functional
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 183647 0 None -5 2 Human 7.3 pIC50 = 7.3 Functional
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 183647 0 None -5 2 Human 7.3 pIC50 = 7.3 Functional
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 123519 0 None 5 2 Rat 6.3 pIC50 = 6.3 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123519 0 None 5 2 Rat 6.3 pIC50 = 6.3 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 78739 0 None 1 2 Human 6.2 pIC50 = 6.2 Functional
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 78739 0 None 1 2 Human 6.2 pIC50 = 6.2 Functional
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 123521 0 None 3 2 Rat 6.2 pIC50 = 6.2 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123521 0 None 3 2 Rat 6.2 pIC50 = 6.2 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123521 0 None 3 2 Rat 6.2 pIC50 = 6.2 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123521 0 None 3 2 Rat 6.2 pIC50 = 6.2 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 30 None - 1 Rat 6.2 pIC50 = 6.2 Functional
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 30 None - 1 Rat 6.2 pIC50 = 6.2 Functional
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 30 None - 1 Rat 6.2 pIC50 = 6.2 Functional
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 56305 0 None 1 3 Rat 8.2 pIC50 = 8.2 Functional
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 56305 0 None 1 3 Rat 8.2 pIC50 = 8.2 Functional
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 183653 11 None 2 4 Human 8.2 pIC50 = 8.2 Functional
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 183653 11 None 2 4 Human 8.2 pIC50 = 8.2 Functional
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 183653 11 None 2 4 Human 8.2 pIC50 = 8.2 Functional
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 123466 0 None 4 2 Rat 6.2 pIC50 = 6.2 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123466 0 None 4 2 Rat 6.2 pIC50 = 6.2 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123537 0 None - 1 Rat 6.2 pIC50 = 6.2 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123537 0 None - 1 Rat 6.2 pIC50 = 6.2 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123543 0 None - 1 Rat 6.2 pIC50 = 6.2 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123543 0 None - 1 Rat 6.2 pIC50 = 6.2 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 30 None - 1 Rat 6.2 pIC50 = 6.2 Functional
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 30 None - 1 Rat 6.2 pIC50 = 6.2 Functional
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 30 None - 1 Rat 6.2 pIC50 = 6.2 Functional
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 123466 0 None 4 2 Rat 6.2 pIC50 = 6.2 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123466 0 None 4 2 Rat 6.2 pIC50 = 6.2 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123543 0 None - 1 Rat 6.2 pIC50 = 6.2 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123543 0 None - 1 Rat 6.2 pIC50 = 6.2 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123537 0 None - 1 Rat 6.2 pIC50 = 6.2 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123537 0 None - 1 Rat 6.2 pIC50 = 6.2 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 183679 0 None -2 2 Human 7.2 pIC50 = 7.2 Functional
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 183679 0 None -2 2 Human 7.2 pIC50 = 7.2 Functional
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 183679 0 None -2 2 Human 7.2 pIC50 = 7.2 Functional
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 154974 1 None 1 2 Human 5.2 pIC50 = 5.2 Functional
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 154974 1 None 1 2 Human 5.2 pIC50 = 5.2 Functional
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 183686 0 None -1 2 Human 7.2 pIC50 = 7.2 Functional
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 183686 0 None -1 2 Human 7.2 pIC50 = 7.2 Functional
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 183686 0 None -1 2 Human 7.2 pIC50 = 7.2 Functional
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 123405 0 None -60 2 Human 6.2 pIC50 = 6.2 Functional
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 123405 0 None -60 2 Human 6.2 pIC50 = 6.2 Functional
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 102731 0 None -1 2 Human 4.2 pIC50 = 4.2 Functional
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 102731 0 None -1 2 Human 4.2 pIC50 = 4.2 Functional
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 112001 0 None 1 2 Rat 6.2 pIC50 = 6.2 Functional
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 112001 0 None 1 2 Rat 6.2 pIC50 = 6.2 Functional
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 78740 0 None 1 2 Human 6.2 pIC50 = 6.2 Functional
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 78740 0 None 1 2 Human 6.2 pIC50 = 6.2 Functional
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 78740 0 None 1 2 Human 6.2 pIC50 = 6.2 Functional
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 78740 0 None 1 2 Human 6.2 pIC50 = 6.2 Functional
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 90324 0 None - 1 Rat 6.2 pIC50 = 6.2 Functional
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 90324 0 None - 1 Rat 6.2 pIC50 = 6.2 Functional
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 90324 0 None - 1 Rat 6.2 pIC50 = 6.2 Functional
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 41 None -1 2 Human 6.2 pIC50 = 6.2 Functional
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 41 None -1 2 Human 6.2 pIC50 = 6.2 Functional
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 41 None -1 2 Human 6.2 pIC50 = 6.2 Functional
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 90324 0 None - 1 Rat 6.2 pIC50 = 6.2 Functional
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 90324 0 None - 1 Rat 6.2 pIC50 = 6.2 Functional
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 90324 0 None - 1 Rat 6.2 pIC50 = 6.2 Functional
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 111999 0 None 6 2 Rat 7.2 pIC50 = 7.2 Functional
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 111999 0 None 6 2 Rat 7.2 pIC50 = 7.2 Functional
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 123539 0 None - 1 Rat 6.2 pIC50 = 6.2 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123539 0 None - 1 Rat 6.2 pIC50 = 6.2 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123461 0 None - 1 Rat 5.2 pIC50 = 5.2 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123461 0 None - 1 Rat 5.2 pIC50 = 5.2 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123461 0 None - 1 Rat 5.2 pIC50 = 5.2 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123461 0 None - 1 Rat 5.2 pIC50 = 5.2 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123539 0 None - 1 Rat 6.2 pIC50 = 6.2 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123539 0 None - 1 Rat 6.2 pIC50 = 6.2 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 161322 16 None -1 2 Rat 4.2 pIC50 = 4.2 Functional
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 161322 16 None -1 2 Rat 4.2 pIC50 = 4.2 Functional
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 123524 0 None - 1 Rat 6.2 pIC50 = 6.2 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123524 0 None - 1 Rat 6.2 pIC50 = 6.2 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123524 0 None - 1 Rat 6.2 pIC50 = 6.2 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123524 0 None - 1 Rat 6.2 pIC50 = 6.2 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 111993 0 None 1 2 Rat 6.2 pIC50 = 6.2 Functional
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 111993 0 None 1 2 Rat 6.2 pIC50 = 6.2 Functional
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 54 None 2 14 Human 8.1 pIC50 = 8.1 Functional
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 54 None 2 14 Human 8.1 pIC50 = 8.1 Functional
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 54 None 2 14 Human 8.1 pIC50 = 8.1 Functional
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 54 None 2 14 Human 8.1 pIC50 = 8.1 Functional
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 151361 0 None -1 2 Human 7.2 pIC50 = 7.2 Functional
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 151361 0 None -1 2 Human 7.2 pIC50 = 7.2 Functional
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 90329 0 None - 1 Rat 6.2 pIC50 = 6.2 Functional
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 90329 0 None - 1 Rat 6.2 pIC50 = 6.2 Functional
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 123445 0 None 2 2 Rat 6.1 pIC50 = 6.1 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123445 0 None 2 2 Rat 6.1 pIC50 = 6.1 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123445 0 None 2 2 Rat 6.1 pIC50 = 6.1 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123445 0 None 2 2 Rat 6.1 pIC50 = 6.1 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 90325 0 None - 1 Rat 5.1 pIC50 = 5.1 Functional
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 90325 0 None - 1 Rat 5.1 pIC50 = 5.1 Functional
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 90328 0 None - 1 Rat 5.1 pIC50 = 5.1 Functional
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 90328 0 None - 1 Rat 5.1 pIC50 = 5.1 Functional
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 169083 0 None 33 5 Rat 7.1 pIC50 = 7.1 Functional
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 169083 0 None 33 5 Rat 7.1 pIC50 = 7.1 Functional
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 150823 0 None 3 2 Human 7.1 pIC50 = 7.1 Functional
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 150823 0 None 3 2 Human 7.1 pIC50 = 7.1 Functional
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 78744 0 None -3 2 Human 6.1 pIC50 = 6.1 Functional
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 78744 0 None -3 2 Human 6.1 pIC50 = 6.1 Functional
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 83602 0 None 2 2 Rat 6.1 pIC50 = 6.1 Functional
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 83602 0 None 2 2 Rat 6.1 pIC50 = 6.1 Functional
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 90060 0 None -1 3 Human 5.1 pIC50 = 5.1 Functional
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 90060 0 None -1 3 Human 5.1 pIC50 = 5.1 Functional
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 112004 0 None 3 2 Rat 7.1 pIC50 = 7.1 Functional
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 112004 0 None 3 2 Rat 7.1 pIC50 = 7.1 Functional
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 13659 0 None 1 2 Rat 4.1 pIC50 = 4.1 Functional
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 13659 0 None 1 2 Rat 4.1 pIC50 = 4.1 Functional
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 13659 0 None 1 2 Rat 4.1 pIC50 = 4.1 Functional
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 123442 0 None -10 2 Rat 6.1 pIC50 = 6.1 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123442 0 None -10 2 Rat 6.1 pIC50 = 6.1 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123442 0 None -10 2 Rat 6.1 pIC50 = 6.1 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123442 0 None -10 2 Rat 6.1 pIC50 = 6.1 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123456 0 None 2 2 Rat 6.1 pIC50 = 6.1 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123456 0 None 2 2 Rat 6.1 pIC50 = 6.1 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 112004 0 None 3 2 Rat 7.1 pIC50 = 7.1 Functional
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 112004 0 None 3 2 Rat 7.1 pIC50 = 7.1 Functional
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
122190327 123456 0 None 2 2 Rat 6.1 pIC50 = 6.1 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123456 0 None 2 2 Rat 6.1 pIC50 = 6.1 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 16785 0 None 2 2 Human 7.1 pIC50 = 7.1 Functional
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 16785 0 None 2 2 Human 7.1 pIC50 = 7.1 Functional
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 78765 0 None 22 2 Human 7.1 pIC50 = 7.1 Functional
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 78765 0 None 22 2 Human 7.1 pIC50 = 7.1 Functional
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 123528 0 None - 1 Rat 6.1 pIC50 = 6.1 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123528 0 None - 1 Rat 6.1 pIC50 = 6.1 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 145959 0 None 1 2 Human 7.1 pIC50 = 7.1 Functional
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 145959 0 None 1 2 Human 7.1 pIC50 = 7.1 Functional
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 123455 0 None 3 2 Rat 6.1 pIC50 = 6.1 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123455 0 None 3 2 Rat 6.1 pIC50 = 6.1 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123455 0 None 3 2 Rat 6.1 pIC50 = 6.1 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123455 0 None 3 2 Rat 6.1 pIC50 = 6.1 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123528 0 None - 1 Rat 6.1 pIC50 = 6.1 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123528 0 None - 1 Rat 6.1 pIC50 = 6.1 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 147068 0 None 2 2 Human 7.1 pIC50 = 7.1 Functional
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 147068 0 None 2 2 Human 7.1 pIC50 = 7.1 Functional
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 123530 0 None 7 2 Rat 6.1 pIC50 = 6.1 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123530 0 None 7 2 Rat 6.1 pIC50 = 6.1 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123530 0 None 7 2 Rat 6.1 pIC50 = 6.1 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123530 0 None 7 2 Rat 6.1 pIC50 = 6.1 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 102126 0 None 2 2 Human 5.1 pIC50 = 5.1 Functional
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 102126 0 None 2 2 Human 5.1 pIC50 = 5.1 Functional
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 123401 0 None -12 2 Human 6.1 pIC50 = 6.1 Functional
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 123401 0 None -12 2 Human 6.1 pIC50 = 6.1 Functional
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 123514 0 None - 1 Rat 6.1 pIC50 = 6.1 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123514 0 None - 1 Rat 6.1 pIC50 = 6.1 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 111990 0 None 2 2 Rat 6.1 pIC50 = 6.1 Functional
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 111990 0 None 2 2 Rat 6.1 pIC50 = 6.1 Functional
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 123514 0 None - 1 Rat 6.1 pIC50 = 6.1 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123514 0 None - 1 Rat 6.1 pIC50 = 6.1 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 90060 0 None -1 3 Human 6.1 pIC50 = 6.1 Functional
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 90060 0 None -1 3 Human 6.1 pIC50 = 6.1 Functional
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 123512 0 None 3 2 Rat 6.0 pIC50 = 6.0 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123512 0 None 3 2 Rat 6.0 pIC50 = 6.0 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123512 0 None 3 2 Rat 6.0 pIC50 = 6.0 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 123512 0 None 3 2 Rat 6.0 pIC50 = 6.0 Functional
Negative allosteric modulation of rat mGlu3 receptor assessed 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 162449 0 None -1 2 Rat 6.0 pIC50 = 6.0 Functional
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 162449 0 None -1 2 Rat 6.0 pIC50 = 6.0 Functional
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 13032 0 None -2 3 Rat 4.0 pIC50 = 4.0 Functional
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 13032 0 None -2 3 Rat 4.0 pIC50 = 4.0 Functional
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 13032 0 None -2 3 Rat 4.0 pIC50 = 4.0 Functional
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 162449 0 None -1 2 Rat 6.0 pIC50 = 6.0 Functional
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 162449 0 None -1 2 Rat 6.0 pIC50 = 6.0 Functional
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 123400 0 None -11 2 Human 7.0 pIC50 = 7.0 Functional
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 123400 0 None -11 2 Human 7.0 pIC50 = 7.0 Functional
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 183670 0 None 1 2 Human 6.0 pIC50 = 6.0 Functional
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 183670 0 None 1 2 Human 6.0 pIC50 = 6.0 Functional
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 183670 0 None 1 2 Human 6.0 pIC50 = 6.0 Functional
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 69375 1 None -5 2 Human 5.0 pIC50 = 5.0 Functional
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 69375 1 None -5 2 Human 5.0 pIC50 = 5.0 Functional
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 155894 0 None -1 2 Human 5.0 pIC50 = 5 Functional
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 155894 0 None -1 2 Human 5.0 pIC50 = 5 Functional
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 112571 0 None - 0 Human 7.0 pKi = 7 Functional
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 112571 0 None - 0 Human 7.0 pKi = 7 Functional
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 54 None 2 14 Human 7.9 pKi = 7.9 Functional
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 54 None 2 14 Human 7.9 pKi = 7.9 Functional
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 54 None 2 14 Human 7.9 pKi = 7.9 Functional
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 54 None 2 14 Human 7.9 pKi = 7.9 Functional
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 206866 1 None - 0 Human 6.7 pKi = 6.7 Functional
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 206866 1 None - 0 Human 6.7 pKi = 6.7 Functional
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 206837 1 None - 0 Human 5.7 pKi = 5.7 Functional
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 206837 1 None - 0 Human 5.7 pKi = 5.7 Functional
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 147944 11 None -6 2 Human 4.5 pKi = 4.5 Functional
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 147944 11 None -6 2 Human 4.5 pKi = 4.5 Functional
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 64 None -4 6 Human 7.4 pKi = 7.4 Functional
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 64 None -4 6 Human 7.4 pKi = 7.4 Functional
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 64 None -4 6 Human 7.4 pKi = 7.4 Functional
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 64 None -4 6 Human 7.4 pKi = 7.4 Functional
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 44 None -1 5 Human 8.3 pKi = 8.3 Functional
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 44 None -1 5 Human 8.3 pKi = 8.3 Functional
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 44 None -1 5 Human 8.3 pKi = 8.3 Functional
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 67 None - 6 Human 4.4 pKi = 4.4 Functional
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 67 None - 6 Human 4.4 pKi = 4.4 Functional
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 67 None - 6 Human 4.4 pKi = 4.4 Functional
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 67 None - 6 Human 4.4 pKi = 4.4 Functional
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 67 None - 6 Human 4.4 pKi = 4.4 Functional
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 67 None - 6 Human 4.4 pKi = 4.4 Functional
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 48 None -9 4 Human 6.4 pKi = 6.4 Functional
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 48 None -9 4 Human 6.4 pKi = 6.4 Functional
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 48 None -9 4 Human 6.4 pKi = 6.4 Functional
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 37 None - 11 Human 6.4 pKi = 6.4 Functional
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 37 None - 11 Human 6.4 pKi = 6.4 Functional
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 37 None - 11 Human 6.4 pKi = 6.4 Functional
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 101382 1 None -10 2 Human 4.3 pKi = 4.3 Functional
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 101382 1 None -10 2 Human 4.3 pKi = 4.3 Functional
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 154974 1 None 1 2 Human 5.2 pKi = 5.2 Functional
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 154974 1 None 1 2 Human 5.2 pKi = 5.2 Functional
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 206603 1 None - 0 Human 8.1 pKi = 8.1 Functional
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 206603 1 None - 0 Human 8.1 pKi = 8.1 Functional
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 110 None -251 17 Human 5.1 pKi = 5.1 Functional
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 110 None -251 17 Human 5.1 pKi = 5.1 Functional
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 110 None -251 17 Human 5.1 pKi = 5.1 Functional
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 110 None -251 17 Human 5.1 pKi = 5.1 Functional
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 110 None -251 17 Human 5.1 pKi = 5.1 Functional
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 110 None -251 17 Human 5.1 pKi = 5.1 Functional
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 110 None -251 17 Human 5.1 pKi = 5.1 Functional
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 110 None -29 17 Rat 8.3 pEC50 = 8.3 Functional
NoneNone
Drug Central 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N None
1369 2315 110 None -29 17 Rat 8.3 pEC50 = 8.3 Functional
NoneNone
Drug Central 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N None
33032 2315 110 None -29 17 Rat 8.3 pEC50 = 8.3 Functional
NoneNone
Drug Central 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N None
44272391 2315 110 None -29 17 Rat 8.3 pEC50 = 8.3 Functional
NoneNone
Drug Central 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N None
88747398 2315 110 None -29 17 Rat 8.3 pEC50 = 8.3 Functional
NoneNone
Drug Central 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N None
CHEMBL575060 2315 110 None -29 17 Rat 8.3 pEC50 = 8.3 Functional
NoneNone
Drug Central 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N None
DB00142 2315 110 None -29 17 Rat 8.3 pEC50 = 8.3 Functional
NoneNone
Drug Central 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N None
49836087 1061 0 None -16 2 Human 4.9 pEC50 = 4.9 Functional
UnclassifiedUnclassified
Guide to Pharmacology 328 2 2 4 3.3 O/N=C\1/c2ccccc2OC2(C1C2)C(=O)Nc1ccc(cc1)Cl 21105727
6222 1061 0 None -16 2 Human 4.9 pEC50 = 4.9 Functional
UnclassifiedUnclassified
Guide to Pharmacology 328 2 2 4 3.3 O/N=C\1/c2ccccc2OC2(C1C2)C(=O)Nc1ccc(cc1)Cl 21105727
CHEMBL1630805 1061 0 None -16 2 Human 4.9 pEC50 = 4.9 Functional
UnclassifiedUnclassified
Guide to Pharmacology 328 2 2 4 3.3 O/N=C\1/c2ccccc2OC2(C1C2)C(=O)Nc1ccc(cc1)Cl 21105727
49858118 1110 0 None -10 2 Human 5.0 pEC50 = 5.0 Functional
UnclassifiedUnclassified
Guide to Pharmacology 324 3 2 5 2.7 O/N=C\1/c2ccccc2OC2(C1C2)C(=O)Nc1ccc(cc1)OC 21105727
6224 1110 0 None -10 2 Human 5.0 pEC50 = 5.0 Functional
UnclassifiedUnclassified
Guide to Pharmacology 324 3 2 5 2.7 O/N=C\1/c2ccccc2OC2(C1C2)C(=O)Nc1ccc(cc1)OC 21105727
CHEMBL1630807 1110 0 None -10 2 Human 5.0 pEC50 = 5.0 Functional
UnclassifiedUnclassified
Guide to Pharmacology 324 3 2 5 2.7 O/N=C\1/c2ccccc2OC2(C1C2)C(=O)Nc1ccc(cc1)OC 21105727
49858117 1089 4 None -5 2 Human 5.1 pEC50 = 5.1 Functional
UnclassifiedUnclassified
Guide to Pharmacology 308 2 2 4 3.0 O/N=C\1/c2ccccc2OC2(C1C2)C(=O)Nc1ccc(cc1)C 21105727
6223 1089 4 None -5 2 Human 5.1 pEC50 = 5.1 Functional
UnclassifiedUnclassified
Guide to Pharmacology 308 2 2 4 3.0 O/N=C\1/c2ccccc2OC2(C1C2)C(=O)Nc1ccc(cc1)C 21105727
CHEMBL1630806 1089 4 None -5 2 Human 5.1 pEC50 = 5.1 Functional
UnclassifiedUnclassified
Guide to Pharmacology 308 2 2 4 3.0 O/N=C\1/c2ccccc2OC2(C1C2)C(=O)Nc1ccc(cc1)C 21105727
1310 2315 110 None -251 17 Human 5.4 pEC50 = 5.4 Functional
UnclassifiedUnclassified
Guide to Pharmacology 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N 10443583
1369 2315 110 None -251 17 Human 5.4 pEC50 = 5.4 Functional
UnclassifiedUnclassified
Guide to Pharmacology 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N 10443583
33032 2315 110 None -251 17 Human 5.4 pEC50 = 5.4 Functional
UnclassifiedUnclassified
Guide to Pharmacology 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N 10443583
44272391 2315 110 None -251 17 Human 5.4 pEC50 = 5.4 Functional
UnclassifiedUnclassified
Guide to Pharmacology 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N 10443583
88747398 2315 110 None -251 17 Human 5.4 pEC50 = 5.4 Functional
UnclassifiedUnclassified
Guide to Pharmacology 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N 10443583
CHEMBL575060 2315 110 None -251 17 Human 5.4 pEC50 = 5.4 Functional
UnclassifiedUnclassified
Guide to Pharmacology 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N 10443583
DB00142 2315 110 None -251 17 Human 5.4 pEC50 = 5.4 Functional
UnclassifiedUnclassified
Guide to Pharmacology 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N 10443583
6219 2585 0 None -1 3 Rat 7.5 pEC50 = 7.5 Functional
UnclassifiedUnclassified
Guide to Pharmacology 401 1 1 3 4.0 N#Cc1cccc(c1)C1=Nc2ccc(cc2NC(=O)CC1)I 17416742
73755191 2585 0 None -1 3 Rat 7.5 pEC50 = 7.5 Functional
UnclassifiedUnclassified
Guide to Pharmacology 401 1 1 3 4.0 N#Cc1cccc(c1)C1=Nc2ccc(cc2NC(=O)CC1)I 17416742
11158623 3351 11 None -1 4 Rat 8.0 pIC50 < 8 Functional
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 11 None -1 4 Rat 8.0 pIC50 < 8 Functional
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 11 None -1 4 Rat 8.0 pIC50 < 8 Functional
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 3 None 31 2 Human 6.7 pIC50 = 6.7 Functional
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 3 None 31 2 Human 6.7 pIC50 = 6.7 Functional
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 3 None 31 2 Human 6.7 pIC50 = 6.7 Functional
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 41 None 1 2 Rat 6.0 pIC50 = 6 Functional
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 41 None 1 2 Rat 6.0 pIC50 = 6 Functional
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 41 None 1 2 Rat 6.0 pIC50 = 6 Functional
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 30 None - 1 Rat 6.2 pIC50 = 6.2 Functional
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 30 None - 1 Rat 6.2 pIC50 = 6.2 Functional
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 30 None - 1 Rat 6.2 pIC50 = 6.2 Functional
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 20 None -1 2 Human 6.4 pIC50 = 6.4 Functional
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 20 None -1 2 Human 6.4 pIC50 = 6.4 Functional
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 20 None -1 2 Human 6.4 pIC50 = 6.4 Functional
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 11 None -50 4 Human 6.6 pIC50 = 6.6 Functional
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 11 None -50 4 Human 6.6 pIC50 = 6.6 Functional
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 11 None -50 4 Human 6.6 pIC50 = 6.6 Functional
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 0 None -1 3 Rat 7.7 pIC50 = 7.7 Functional
UnclassifiedUnclassified
Guide to Pharmacology 405 2 1 3 5.4 O=C1CCC(=Nc2c(N1)ccc(c2)Br)c1cccc(c1)c1ccncc1 17416742
73755192 2586 0 None -1 3 Rat 7.7 pIC50 = 7.7 Functional
UnclassifiedUnclassified
Guide to Pharmacology 405 2 1 3 5.4 O=C1CCC(=Nc2c(N1)ccc(c2)Br)c1cccc(c1)c1ccncc1 17416742
6221 2587 0 None -1 3 Rat 7.7 pIC50 = 7.7 Functional
UnclassifiedUnclassified
Guide to Pharmacology 354 1 1 4 3.6 N#Cc1nccc(c1)C1=Nc2ccc(cc2NC(=O)CC1)Br 17416742
73755193 2587 0 None -1 3 Rat 7.7 pIC50 = 7.7 Functional
UnclassifiedUnclassified
Guide to Pharmacology 354 1 1 4 3.6 N#Cc1nccc(c1)C1=Nc2ccc(cc2NC(=O)CC1)Br 17416742




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DOI

9794208 90050 4 None - 0 Human 10.0 pEC50 = 10.0 Binding
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 90050 4 None - 0 Human 10.0 pEC50 = 10.0 Binding
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 90062 2 None - 0 Human 9.6 pEC50 = 9.6 Binding
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 90062 2 None - 0 Human 9.6 pEC50 = 9.6 Binding
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 90062 2 None - 0 Human 9.6 pEC50 = 9.6 Binding
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 102201 23 None - 0 Rat 5.0 pEC50 = 5 Binding
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 102201 23 None - 0 Rat 5.0 pEC50 = 5 Binding
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 102201 23 None - 0 Rat 5.0 pEC50 = 5 Binding
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 111873 0 None - 0 Rat 6.0 pEC50 = 6.0 Binding
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 111873 0 None - 0 Rat 6.0 pEC50 = 6.0 Binding
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 184575 0 None - 0 Rat 6.0 pEC50 = 6.0 Binding
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 184575 0 None - 0 Rat 6.0 pEC50 = 6.0 Binding
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 186200 0 None - 0 Rat 6.0 pEC50 = 6.0 Binding
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 186200 0 None - 0 Rat 6.0 pEC50 = 6.0 Binding
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 185532 0 None - 0 Rat 6.0 pEC50 = 6.0 Binding
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 185532 0 None - 0 Rat 6.0 pEC50 = 6.0 Binding
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 185873 0 None - 0 Rat 6.0 pEC50 = 6.0 Binding
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 185873 0 None - 0 Rat 6.0 pEC50 = 6.0 Binding
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 185529 0 None - 0 Rat 6.0 pEC50 = 6.0 Binding
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 185529 0 None - 0 Rat 6.0 pEC50 = 6.0 Binding
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 111868 0 None - 0 Rat 5.9 pEC50 = 5.9 Binding
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 111868 0 None - 0 Rat 5.9 pEC50 = 5.9 Binding
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 184754 0 None - 0 Rat 5.9 pEC50 = 5.9 Binding
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 184754 0 None - 0 Rat 5.9 pEC50 = 5.9 Binding
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 90054 0 None - 0 Human 7.9 pEC50 = 7.9 Binding
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 90054 0 None - 0 Human 7.9 pEC50 = 7.9 Binding
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 186381 0 None - 0 Rat 5.9 pEC50 = 5.9 Binding
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 186381 0 None - 0 Rat 5.9 pEC50 = 5.9 Binding
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 185130 0 None - 0 Rat 5.9 pEC50 = 5.9 Binding
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 185130 0 None - 0 Rat 5.9 pEC50 = 5.9 Binding
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 184441 0 None - 0 Rat 6.9 pEC50 = 6.9 Binding
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 184441 0 None - 0 Rat 6.9 pEC50 = 6.9 Binding
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 184579 0 None - 0 Rat 5.9 pEC50 = 5.9 Binding
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 184579 0 None - 0 Rat 5.9 pEC50 = 5.9 Binding
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 185114 0 None - 0 Rat 5.9 pEC50 = 5.9 Binding
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 185114 0 None - 0 Rat 5.9 pEC50 = 5.9 Binding
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 90052 2 None - 1 Human 7.9 pEC50 = 7.9 Binding
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 90052 2 None - 1 Human 7.9 pEC50 = 7.9 Binding
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 111864 0 None - 0 Rat 5.9 pEC50 = 5.9 Binding
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 111864 0 None - 0 Rat 5.9 pEC50 = 5.9 Binding
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 111849 0 None - 0 Rat 5.8 pEC50 = 5.8 Binding
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 111849 0 None - 0 Rat 5.8 pEC50 = 5.8 Binding
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 184616 0 None - 0 Rat 5.8 pEC50 = 5.8 Binding
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 184616 0 None - 0 Rat 5.8 pEC50 = 5.8 Binding
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 90051 2 None - 0 Human 7.8 pEC50 = 7.8 Binding
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 90051 2 None - 0 Human 7.8 pEC50 = 7.8 Binding
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 111894 0 None - 0 Rat 6.8 pEC50 = 6.8 Binding
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 111894 0 None - 0 Rat 6.8 pEC50 = 6.8 Binding
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 185444 0 None - 0 Rat 5.8 pEC50 = 5.8 Binding
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 185444 0 None - 0 Rat 5.8 pEC50 = 5.8 Binding
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 185485 0 None - 0 Rat 5.8 pEC50 = 5.8 Binding
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 185485 0 None - 0 Rat 5.8 pEC50 = 5.8 Binding
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 126776 1 None 1 2 Human 6.8 pEC50 = 6.8 Binding
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 126776 1 None 1 2 Human 6.8 pEC50 = 6.8 Binding
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 185251 0 None - 0 Rat 6.8 pEC50 = 6.8 Binding
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 185251 0 None - 0 Rat 6.8 pEC50 = 6.8 Binding
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 111889 0 None - 0 Rat 5.7 pEC50 = 5.7 Binding
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 111889 0 None - 0 Rat 5.7 pEC50 = 5.7 Binding
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 185267 0 None - 0 Rat 5.7 pEC50 = 5.7 Binding
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 185267 0 None - 0 Rat 5.7 pEC50 = 5.7 Binding
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 111862 0 None - 0 Rat 5.7 pEC50 = 5.7 Binding
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 111862 0 None - 0 Rat 5.7 pEC50 = 5.7 Binding
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 111867 0 None - 0 Rat 5.7 pEC50 = 5.7 Binding
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 111867 0 None - 0 Rat 5.7 pEC50 = 5.7 Binding
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 90059 0 None 5 2 Human 6.7 pEC50 = 6.7 Binding
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 90059 0 None 5 2 Human 6.7 pEC50 = 6.7 Binding
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 111856 0 None - 0 Rat 5.7 pEC50 = 5.7 Binding
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 111856 0 None - 0 Rat 5.7 pEC50 = 5.7 Binding
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 186029 0 None - 0 Rat 5.7 pEC50 = 5.7 Binding
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 186029 0 None - 0 Rat 5.7 pEC50 = 5.7 Binding
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 185184 0 None - 0 Rat 5.7 pEC50 = 5.7 Binding
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 185184 0 None - 0 Rat 5.7 pEC50 = 5.7 Binding
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 111857 0 None - 0 Rat 5.7 pEC50 = 5.7 Binding
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 111857 0 None - 0 Rat 5.7 pEC50 = 5.7 Binding
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 90055 0 None - 0 Human 7.6 pEC50 = 7.6 Binding
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 90055 0 None - 0 Human 7.6 pEC50 = 7.6 Binding
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 90057 1 None 15 2 Human 7.6 pEC50 = 7.6 Binding
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 90057 1 None 15 2 Human 7.6 pEC50 = 7.6 Binding
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 184890 0 None - 0 Rat 5.6 pEC50 = 5.6 Binding
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 184890 0 None - 0 Rat 5.6 pEC50 = 5.6 Binding
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 111859 0 None - 0 Rat 5.6 pEC50 = 5.6 Binding
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 111859 0 None - 0 Rat 5.6 pEC50 = 5.6 Binding
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 111897 0 None - 0 Rat 6.6 pEC50 = 6.6 Binding
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 111897 0 None - 0 Rat 6.6 pEC50 = 6.6 Binding
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 64 None -1 6 Human 7.6 pEC50 = 7.6 Binding
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 64 None -1 6 Human 7.6 pEC50 = 7.6 Binding
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 64 None -1 6 Human 7.6 pEC50 = 7.6 Binding
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 64 None -1 6 Human 7.6 pEC50 = 7.6 Binding
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 111847 0 None - 0 Rat 5.6 pEC50 = 5.6 Binding
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 111847 0 None - 0 Rat 5.6 pEC50 = 5.6 Binding
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 26 None -2 6 Rat 6.5 pEC50 = 6.5 Binding
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 26 None -2 6 Rat 6.5 pEC50 = 6.5 Binding
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 26 None -2 6 Rat 6.5 pEC50 = 6.5 Binding
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 111896 0 None - 0 Rat 6.5 pEC50 = 6.5 Binding
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 111896 0 None - 0 Rat 6.5 pEC50 = 6.5 Binding
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 110 None -1 18 Rat 5.5 pEC50 = 5.5 Binding
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 110 None -1 18 Rat 5.5 pEC50 = 5.5 Binding
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 110 None -1 18 Rat 5.5 pEC50 = 5.5 Binding
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 110 None -1 18 Rat 5.5 pEC50 = 5.5 Binding
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 110 None -1 18 Rat 5.5 pEC50 = 5.5 Binding
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 110 None -1 18 Rat 5.5 pEC50 = 5.5 Binding
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 110 None -1 18 Rat 5.5 pEC50 = 5.5 Binding
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 101400 35 None - 0 Human 4.5 pEC50 = 4.5 Binding
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 101400 35 None - 0 Human 4.5 pEC50 = 4.5 Binding
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 186384 0 None - 0 Rat 6.5 pEC50 = 6.5 Binding
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 186384 0 None - 0 Rat 6.5 pEC50 = 6.5 Binding
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 111895 0 None - 0 Rat 6.5 pEC50 = 6.5 Binding
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 111895 0 None - 0 Rat 6.5 pEC50 = 6.5 Binding
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 110 None -1 18 Rat 5.5 pEC50 = 5.5 Binding
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 110 None -1 18 Rat 5.5 pEC50 = 5.5 Binding
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 110 None -1 18 Rat 5.5 pEC50 = 5.5 Binding
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 110 None -1 18 Rat 5.5 pEC50 = 5.5 Binding
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 110 None -1 18 Rat 5.5 pEC50 = 5.5 Binding
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 110 None -1 18 Rat 5.5 pEC50 = 5.5 Binding
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 110 None -1 18 Rat 5.5 pEC50 = 5.5 Binding
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 111850 0 None - 0 Rat 5.5 pEC50 = 5.5 Binding
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 111850 0 None - 0 Rat 5.5 pEC50 = 5.5 Binding
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 185720 0 None - 0 Rat 5.4 pEC50 = 5.4 Binding
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 185720 0 None - 0 Rat 5.4 pEC50 = 5.4 Binding
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 185065 0 None - 0 Rat 6.4 pEC50 = 6.4 Binding
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 185065 0 None - 0 Rat 6.4 pEC50 = 6.4 Binding
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 111870 0 None - 0 Rat 5.4 pEC50 = 5.4 Binding
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 111870 0 None - 0 Rat 5.4 pEC50 = 5.4 Binding
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 186057 0 None - 0 Rat 5.4 pEC50 = 5.4 Binding
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 186057 0 None - 0 Rat 5.4 pEC50 = 5.4 Binding
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 67 None - 8 Rat 4.4 pEC50 = 4.4 Binding
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 67 None - 8 Rat 4.4 pEC50 = 4.4 Binding
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 67 None - 8 Rat 4.4 pEC50 = 4.4 Binding
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 67 None - 8 Rat 4.4 pEC50 = 4.4 Binding
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 67 None - 8 Rat 4.4 pEC50 = 4.4 Binding
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 67 None - 8 Rat 4.4 pEC50 = 4.4 Binding
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 111892 0 None - 0 Rat 6.4 pEC50 = 6.4 Binding
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 111892 0 None - 0 Rat 6.4 pEC50 = 6.4 Binding
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 184948 0 None - 0 Rat 6.3 pEC50 = 6.3 Binding
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 184948 0 None - 0 Rat 6.3 pEC50 = 6.3 Binding
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 184467 0 None - 0 Rat 6.3 pEC50 = 6.3 Binding
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 184467 0 None - 0 Rat 6.3 pEC50 = 6.3 Binding
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 111890 0 None - 0 Rat 6.3 pEC50 = 6.3 Binding
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 111890 0 None - 0 Rat 6.3 pEC50 = 6.3 Binding
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 184925 0 None - 0 Rat 6.3 pEC50 = 6.3 Binding
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 184925 0 None - 0 Rat 6.3 pEC50 = 6.3 Binding
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 90056 0 None - 0 Human 7.2 pEC50 = 7.2 Binding
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 90056 0 None - 0 Human 7.2 pEC50 = 7.2 Binding
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 110 None -1 18 Rat 7.2 pEC50 = 7.2 Binding
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 110 None -1 18 Rat 7.2 pEC50 = 7.2 Binding
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 110 None -1 18 Rat 7.2 pEC50 = 7.2 Binding
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 110 None -1 18 Rat 7.2 pEC50 = 7.2 Binding
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 110 None -1 18 Rat 7.2 pEC50 = 7.2 Binding
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 110 None -1 18 Rat 7.2 pEC50 = 7.2 Binding
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 110 None -1 18 Rat 7.2 pEC50 = 7.2 Binding
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 111885 0 None - 0 Rat 6.2 pEC50 = 6.2 Binding
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 111885 0 None - 0 Rat 6.2 pEC50 = 6.2 Binding
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 90053 2 None - 1 Human 8.2 pEC50 = 8.2 Binding
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 90053 2 None - 1 Human 8.2 pEC50 = 8.2 Binding
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 110 None 1 18 Human 7.2 pEC50 = 7.2 Binding
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 110 None 1 18 Human 7.2 pEC50 = 7.2 Binding
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 110 None 1 18 Human 7.2 pEC50 = 7.2 Binding
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 110 None 1 18 Human 7.2 pEC50 = 7.2 Binding
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 110 None 1 18 Human 7.2 pEC50 = 7.2 Binding
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 110 None 1 18 Human 7.2 pEC50 = 7.2 Binding
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 110 None 1 18 Human 7.2 pEC50 = 7.2 Binding
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 110 None -1 18 Rat 7.2 pEC50 = 7.2 Binding
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 110 None -1 18 Rat 7.2 pEC50 = 7.2 Binding
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 110 None -1 18 Rat 7.2 pEC50 = 7.2 Binding
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 110 None -1 18 Rat 7.2 pEC50 = 7.2 Binding
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 110 None -1 18 Rat 7.2 pEC50 = 7.2 Binding
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 110 None -1 18 Rat 7.2 pEC50 = 7.2 Binding
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 110 None -1 18 Rat 7.2 pEC50 = 7.2 Binding
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 111866 0 None - 0 Rat 6.2 pEC50 = 6.2 Binding
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 111866 0 None - 0 Rat 6.2 pEC50 = 6.2 Binding
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 111880 0 None - 0 Rat 5.2 pEC50 = 5.2 Binding
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 111880 0 None - 0 Rat 5.2 pEC50 = 5.2 Binding
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 186211 0 None - 0 Rat 6.2 pEC50 = 6.2 Binding
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 186211 0 None - 0 Rat 6.2 pEC50 = 6.2 Binding
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 184952 0 None - 0 Rat 6.2 pEC50 = 6.2 Binding
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 184952 0 None - 0 Rat 6.2 pEC50 = 6.2 Binding
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 111872 0 None - 0 Rat 6.1 pEC50 = 6.1 Binding
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 111872 0 None - 0 Rat 6.1 pEC50 = 6.1 Binding
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 185565 0 None - 0 Rat 7.1 pEC50 = 7.1 Binding
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 185565 0 None - 0 Rat 7.1 pEC50 = 7.1 Binding
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 26 None -2 6 Rat 7.1 pEC50 = 7.1 Binding
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 26 None -2 6 Rat 7.1 pEC50 = 7.1 Binding
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 26 None -2 6 Rat 7.1 pEC50 = 7.1 Binding
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 42 None -10 11 Rat 5.1 pEC50 = 5.1 Binding
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 42 None -10 11 Rat 5.1 pEC50 = 5.1 Binding
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 42 None -10 11 Rat 5.1 pEC50 = 5.1 Binding
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 185391 0 None - 0 Rat 6.1 pEC50 = 6.1 Binding
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 185391 0 None - 0 Rat 6.1 pEC50 = 6.1 Binding
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 185769 0 None - 0 Rat 6.1 pEC50 = 6.1 Binding
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 185769 0 None - 0 Rat 6.1 pEC50 = 6.1 Binding
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 185742 0 None - 0 Rat 6.1 pEC50 = 6.1 Binding
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 185742 0 None - 0 Rat 6.1 pEC50 = 6.1 Binding
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 204923 106 None - 5 Rat 5.1 pEC50 = 5.1 Binding
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 204923 106 None - 5 Rat 5.1 pEC50 = 5.1 Binding
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 204923 106 None - 5 Rat 5.1 pEC50 = 5.1 Binding
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 111858 0 None - 0 Rat 6.0 pEC50 = 6.0 Binding
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 111858 0 None - 0 Rat 6.0 pEC50 = 6.0 Binding
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 90052 2 None - 1 Human 8.0 pIC50 = 8.0 Binding
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 90052 2 None - 1 Human 8.0 pIC50 = 8.0 Binding
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 162817 6 None - 0 Rat 5.9 pIC50 = 5.9 Binding
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 162817 6 None - 0 Rat 5.9 pIC50 = 5.9 Binding
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 7527 0 None - 1 Rat 5.9 pIC50 = 5.9 Binding
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 7527 0 None - 1 Rat 5.9 pIC50 = 5.9 Binding
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 171824 0 None - 0 Rat 5.9 pIC50 = 5.9 Binding
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 171824 0 None - 0 Rat 5.9 pIC50 = 5.9 Binding
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 174499 0 None - 0 Rat 5.9 pIC50 = 5.9 Binding
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 174499 0 None - 0 Rat 5.9 pIC50 = 5.9 Binding
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 54 None -5 10 Rat 7.9 pIC50 = 7.9 Binding
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 54 None -5 10 Rat 7.9 pIC50 = 7.9 Binding
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 54 None -5 10 Rat 7.9 pIC50 = 7.9 Binding
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 54 None -5 10 Rat 7.9 pIC50 = 7.9 Binding
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 173126 0 None - 0 Rat 5.9 pIC50 = 5.9 Binding
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 173126 0 None - 0 Rat 5.9 pIC50 = 5.9 Binding
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 41 None - 0 Human 5.8 pIC50 = 5.8 Binding
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 41 None - 0 Human 5.8 pIC50 = 5.8 Binding
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 41 None - 0 Human 5.8 pIC50 = 5.8 Binding
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 41 None - 0 Human 5.8 pIC50 = 5.8 Binding
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 41 None - 0 Human 5.8 pIC50 = 5.8 Binding
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 41 None - 0 Human 5.8 pIC50 = 5.8 Binding
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 175289 0 None - 0 Rat 5.8 pIC50 = 5.8 Binding
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 175289 0 None - 0 Rat 5.8 pIC50 = 5.8 Binding
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 54 None -5 10 Rat 7.8 pIC50 = 7.8 Binding
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 54 None -5 10 Rat 7.8 pIC50 = 7.8 Binding
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 54 None -5 10 Rat 7.8 pIC50 = 7.8 Binding
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 54 None -5 10 Rat 7.8 pIC50 = 7.8 Binding
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 3 None - 0 Human 6.7 pIC50 = 6.7 Binding
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 3 None - 0 Human 6.7 pIC50 = 6.7 Binding
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 3 None - 0 Human 6.7 pIC50 = 6.7 Binding
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
53393868 83604 7 None - 0 Human 5.7 pIC50 = 5.7 Binding
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 83604 7 None - 0 Human 5.7 pIC50 = 5.7 Binding
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 83604 7 None - 0 Human 5.7 pIC50 = 5.7 Binding
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 83604 7 None - 0 Human 5.7 pIC50 = 5.7 Binding
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 15 None -2 5 Rat 7.6 pIC50 = 7.6 Binding
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 15 None -2 5 Rat 7.6 pIC50 = 7.6 Binding
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 15 None -2 5 Rat 7.6 pIC50 = 7.6 Binding
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 83602 0 None - 0 Human 5.6 pIC50 = 5.6 Binding
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 83602 0 None - 0 Human 5.6 pIC50 = 5.6 Binding
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 83602 0 None - 0 Human 5.6 pIC50 = 5.6 Binding
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 83602 0 None - 0 Human 5.6 pIC50 = 5.6 Binding
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 64 None -1 6 Human 7.6 pIC50 = 7.6 Binding
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 64 None -1 6 Human 7.6 pIC50 = 7.6 Binding
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 64 None -1 6 Human 7.6 pIC50 = 7.6 Binding
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 64 None -1 6 Human 7.6 pIC50 = 7.6 Binding
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 11 None - 2 Human 6.6 pIC50 = 6.6 Binding
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 11 None - 2 Human 6.6 pIC50 = 6.6 Binding
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 11 None - 2 Human 6.6 pIC50 = 6.6 Binding
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 11 None - 2 Human 6.6 pIC50 = 6.6 Binding
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 11 None - 2 Human 6.6 pIC50 = 6.6 Binding
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 11 None - 2 Human 6.6 pIC50 = 6.6 Binding
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 173379 0 None - 0 Rat 5.6 pIC50 = 5.6 Binding
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 173379 0 None - 0 Rat 5.6 pIC50 = 5.6 Binding
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 117654 0 None - 0 Human 6.5 pIC50 = 6.5 Binding
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 117654 0 None - 0 Human 6.5 pIC50 = 6.5 Binding
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 173261 0 None - 0 Rat 5.5 pIC50 = 5.5 Binding
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 173261 0 None - 0 Rat 5.5 pIC50 = 5.5 Binding
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 173068 0 None - 0 Rat 5.5 pIC50 = 5.5 Binding
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 173068 0 None - 0 Rat 5.5 pIC50 = 5.5 Binding
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 170268 0 None - 0 Rat 5.5 pIC50 = 5.5 Binding
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 170268 0 None - 0 Rat 5.5 pIC50 = 5.5 Binding
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 175900 0 None - 0 Rat 5.5 pIC50 = 5.5 Binding
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 175900 0 None - 0 Rat 5.5 pIC50 = 5.5 Binding
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 83605 2 None - 0 Human 5.5 pIC50 = 5.5 Binding
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 83605 2 None - 0 Human 5.5 pIC50 = 5.5 Binding
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 83600 0 None - 0 Human 5.4 pIC50 = 5.4 Binding
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 83600 0 None - 0 Human 5.4 pIC50 = 5.4 Binding
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 83600 0 None - 0 Human 5.4 pIC50 = 5.4 Binding
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 83600 0 None - 0 Human 5.4 pIC50 = 5.4 Binding
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 169662 0 None - 0 Rat 5.4 pIC50 = 5.4 Binding
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 169662 0 None - 0 Rat 5.4 pIC50 = 5.4 Binding
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 3 None - 0 Human 5.4 pIC50 = 5.4 Binding
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 3 None - 0 Human 5.4 pIC50 = 5.4 Binding
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 3 None - 0 Human 5.4 pIC50 = 5.4 Binding
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 83601 0 None - 0 Human 5.3 pIC50 = 5.3 Binding
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 83601 0 None - 0 Human 5.3 pIC50 = 5.3 Binding
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 83601 0 None - 0 Human 5.3 pIC50 = 5.3 Binding
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 83601 0 None - 0 Human 5.3 pIC50 = 5.3 Binding
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 170661 0 None - 0 Rat 6.3 pIC50 = 6.3 Binding
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 170661 0 None - 0 Rat 6.3 pIC50 = 6.3 Binding
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 83605 2 None - 0 Human 5.3 pIC50 = 5.3 Binding
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 83605 2 None - 0 Human 5.3 pIC50 = 5.3 Binding
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 83603 0 None - 0 Human 5.2 pIC50 = 5.2 Binding
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 83603 0 None - 0 Human 5.2 pIC50 = 5.2 Binding
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 83603 0 None - 0 Human 5.2 pIC50 = 5.2 Binding
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 83603 0 None - 0 Human 5.2 pIC50 = 5.2 Binding
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 90053 2 None - 1 Human 8.2 pIC50 = 8.2 Binding
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 90053 2 None - 1 Human 8.2 pIC50 = 8.2 Binding
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 117637 0 None - 0 Human 6.2 pIC50 = 6.2 Binding
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 117637 0 None - 0 Human 6.2 pIC50 = 6.2 Binding
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 110538 0 None - 1 Rat 7.1 pIC50 = 7.1 Binding
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 110538 0 None - 1 Rat 7.1 pIC50 = 7.1 Binding
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 170238 0 None - 0 Rat 5.1 pIC50 = 5.1 Binding
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 170238 0 None - 0 Rat 5.1 pIC50 = 5.1 Binding
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 172236 0 None - 0 Rat 6.0 pIC50 = 6.0 Binding
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 172236 0 None - 0 Rat 6.0 pIC50 = 6.0 Binding
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 83247 1 None 5 2 Human 9.8 pKi = 9.8 Binding
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 83247 1 None 5 2 Human 9.8 pKi = 9.8 Binding
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 156881 0 None 181 2 Human 9.3 pKi = 9.3 Binding
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 156881 0 None 181 2 Human 9.3 pKi = 9.3 Binding
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 157655 15 None 446 2 Human 9.0 pKi = 9.0 Binding
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 157655 15 None 446 2 Human 9.0 pKi = 9.0 Binding
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 54 None 1 10 Human 8.9 pKi = 8.9 Binding
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 54 None 1 10 Human 8.9 pKi = 8.9 Binding
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 54 None 1 10 Human 8.9 pKi = 8.9 Binding
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 54 None 1 10 Human 8.9 pKi = 8.9 Binding
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 156545 0 None 32 2 Human 8.8 pKi = 8.8 Binding
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 156545 0 None 32 2 Human 8.8 pKi = 8.8 Binding
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 44 None -2 5 Human 6.0 pKi = 6.0 Binding
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 44 None -2 5 Human 6.0 pKi = 6.0 Binding
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 44 None -2 5 Human 6.0 pKi = 6.0 Binding
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 64 None -1 6 Human 7.0 pKi = 7.0 Binding
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 64 None -1 6 Human 7.0 pKi = 7.0 Binding
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 64 None -1 6 Human 7.0 pKi = 7.0 Binding
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 64 None -1 6 Human 7.0 pKi = 7.0 Binding
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 64 None -1 6 Human 7.0 pKi = 7.0 Binding
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 64 None -1 6 Human 7.0 pKi = 7.0 Binding
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 64 None -1 6 Human 7.0 pKi = 7.0 Binding
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 64 None -1 6 Human 7.0 pKi = 7.0 Binding
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 156588 0 None 10 2 Human 6.0 pKi = 6.0 Binding
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 156588 0 None 10 2 Human 6.0 pKi = 6.0 Binding
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 64 None -1 6 Human 6.9 pKi = 6.9 Binding
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 64 None -1 6 Human 6.9 pKi = 6.9 Binding
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 64 None -1 6 Human 6.9 pKi = 6.9 Binding
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 64 None -1 6 Human 6.9 pKi = 6.9 Binding
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 123403 0 None -2 2 Human 6.9 pKi = 6.9 Binding
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 123403 0 None -2 2 Human 6.9 pKi = 6.9 Binding
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 90060 0 None 3 2 Human 6.9 pKi = 6.9 Binding
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 90060 0 None 3 2 Human 6.9 pKi = 6.9 Binding
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 44 None -2 5 Human 7.8 pKi = 7.8 Binding
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 44 None -2 5 Human 7.8 pKi = 7.8 Binding
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 44 None -2 5 Human 7.8 pKi = 7.8 Binding
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 69375 1 None 6 2 Human 6.8 pKi = 6.8 Binding
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 69375 1 None 6 2 Human 6.8 pKi = 6.8 Binding
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 66852 0 None -2 2 Rat 7.8 pKi = 7.8 Binding
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 66852 0 None -2 2 Rat 7.8 pKi = 7.8 Binding
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 123396 17 None -1 2 Human 6.8 pKi = 6.8 Binding
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 123396 17 None -1 2 Human 6.8 pKi = 6.8 Binding
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 123401 0 None 1 2 Human 6.8 pKi = 6.8 Binding
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 123401 0 None 1 2 Human 6.8 pKi = 6.8 Binding
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 183686 0 None 1 2 Human 7.8 pKi = 7.8 Binding
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 183686 0 None 1 2 Human 7.8 pKi = 7.8 Binding
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 183686 0 None 1 2 Human 7.8 pKi = 7.8 Binding
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 206508 12 None 6 2 Human 6.8 pKi = 6.8 Binding
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 206508 12 None 6 2 Human 6.8 pKi = 6.8 Binding
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 90059 0 None 5 2 Human 6.8 pKi = 6.8 Binding
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 90059 0 None 5 2 Human 6.8 pKi = 6.8 Binding
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 183691 0 None 1 2 Human 7.7 pKi = 7.7 Binding
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 183691 0 None 1 2 Human 7.7 pKi = 7.7 Binding
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 183691 0 None 1 2 Human 7.7 pKi = 7.7 Binding
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 158513 0 None 102 2 Human 8.7 pKi = 8.7 Binding
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 158513 0 None 102 2 Human 8.7 pKi = 8.7 Binding
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 158568 0 None 13 2 Human 8.6 pKi = 8.6 Binding
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 158568 0 None 13 2 Human 8.6 pKi = 8.6 Binding
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 158921 0 None 60 2 Human 8.6 pKi = 8.6 Binding
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 158921 0 None 60 2 Human 8.6 pKi = 8.6 Binding
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 183653 11 None 2 2 Human 8.6 pKi = 8.6 Binding
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 183653 11 None 2 2 Human 8.6 pKi = 8.6 Binding
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 183653 11 None 2 2 Human 8.6 pKi = 8.6 Binding
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 152255 0 None 2 2 Human 8.6 pKi = 8.6 Binding
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 152255 0 None 2 2 Human 8.6 pKi = 8.6 Binding
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 159284 0 None 6 2 Human 7.6 pKi = 7.6 Binding
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 159284 0 None 6 2 Human 7.6 pKi = 7.6 Binding
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 183719 0 None 1 2 Human 6.6 pKi = 6.6 Binding
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 183719 0 None 1 2 Human 6.6 pKi = 6.6 Binding
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 183719 0 None 1 2 Human 6.6 pKi = 6.6 Binding
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 183731 0 None 1 2 Human 7.6 pKi = 7.6 Binding
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 183731 0 None 1 2 Human 7.6 pKi = 7.6 Binding
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 183731 0 None 1 2 Human 7.6 pKi = 7.6 Binding
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 183622 0 None 1 2 Human 6.6 pKi = 6.6 Binding
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 183622 0 None 1 2 Human 6.6 pKi = 6.6 Binding
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 183622 0 None 1 2 Human 6.6 pKi = 6.6 Binding
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 123402 0 None -1 2 Human 6.6 pKi = 6.6 Binding
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 123402 0 None -1 2 Human 6.6 pKi = 6.6 Binding
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 183679 0 None -1 2 Human 7.6 pKi = 7.6 Binding
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 183679 0 None -1 2 Human 7.6 pKi = 7.6 Binding
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 183679 0 None -1 2 Human 7.6 pKi = 7.6 Binding
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 183728 0 None 1 2 Human 7.6 pKi = 7.6 Binding
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 183728 0 None 1 2 Human 7.6 pKi = 7.6 Binding
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 183728 0 None 1 2 Human 7.6 pKi = 7.6 Binding
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 159236 0 None 14 2 Human 7.6 pKi = 7.6 Binding
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 159236 0 None 14 2 Human 7.6 pKi = 7.6 Binding
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 90061 0 None 4 2 Human 6.6 pKi = 6.6 Binding
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 90061 0 None 4 2 Human 6.6 pKi = 6.6 Binding
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 156641 0 None 2 2 Human 6.6 pKi = 6.6 Binding
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 156641 0 None 2 2 Human 6.6 pKi = 6.6 Binding
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 90057 1 None 15 2 Human 6.6 pKi = 6.6 Binding
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 90057 1 None 15 2 Human 6.6 pKi = 6.6 Binding
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 66937 0 None -1 2 Rat 8.5 pKi = 8.5 Binding
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 66937 0 None -1 2 Rat 8.5 pKi = 8.5 Binding
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 31341 0 None 7 2 Human 8.5 pKi = 8.5 Binding
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 31341 0 None 7 2 Human 8.5 pKi = 8.5 Binding
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 54 None -5 10 Rat 8.5 pKi = 8.5 Binding
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 54 None -5 10 Rat 8.5 pKi = 8.5 Binding
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 54 None -5 10 Rat 8.5 pKi = 8.5 Binding
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 54 None -5 10 Rat 8.5 pKi = 8.5 Binding
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 15 None -2 2 Rat 8.4 pKi = 8.4 Binding
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 15 None -2 2 Rat 8.4 pKi = 8.4 Binding
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 15 None -2 2 Rat 8.4 pKi = 8.4 Binding
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 168372 0 None -1 2 Rat 8.4 pKi = 8.4 Binding
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 168372 0 None -1 2 Rat 8.4 pKi = 8.4 Binding
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 19 None -1 2 Human 6.5 pKi = 6.5 Binding
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 19 None -1 2 Human 6.5 pKi = 6.5 Binding
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 19 None -1 2 Human 6.5 pKi = 6.5 Binding
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 183675 0 None -1 2 Human 7.4 pKi = 7.4 Binding
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 183675 0 None -1 2 Human 7.4 pKi = 7.4 Binding
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 183675 0 None -1 2 Human 7.4 pKi = 7.4 Binding
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 183670 0 None 1 2 Human 6.4 pKi = 6.4 Binding
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 183670 0 None 1 2 Human 6.4 pKi = 6.4 Binding
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 183670 0 None 1 2 Human 6.4 pKi = 6.4 Binding
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 35817 1 None -1 2 Rat 8.4 pKi = 8.4 Binding
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 35817 1 None -1 2 Rat 8.4 pKi = 8.4 Binding
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 156124 0 None 75 2 Human 8.4 pKi = 8.4 Binding
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 156124 0 None 75 2 Human 8.4 pKi = 8.4 Binding
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 15 None -2 5 Rat 8.4 pKi = 8.4 Binding
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 15 None -2 5 Rat 8.4 pKi = 8.4 Binding
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 15 None -2 5 Rat 8.4 pKi = 8.4 Binding
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 15 None -2 5 Human 8.4 pKi = 8.4 Binding
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 15 None -2 5 Human 8.4 pKi = 8.4 Binding
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 15 None -2 5 Human 8.4 pKi = 8.4 Binding
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 183687 0 None 1 2 Human 8.4 pKi = 8.4 Binding
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 183687 0 None 1 2 Human 8.4 pKi = 8.4 Binding
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 183687 0 None 1 2 Human 8.4 pKi = 8.4 Binding
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 155947 0 None 40 2 Human 8.3 pKi = 8.3 Binding
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 155947 0 None 40 2 Human 8.3 pKi = 8.3 Binding
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 206508 12 None 6 2 Human 8.3 pKi = 8.3 Binding
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 206508 12 None 6 2 Human 8.3 pKi = 8.3 Binding
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 206508 12 None 6 2 Human 8.3 pKi = 8.3 Binding
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 206508 12 None 6 2 Human 8.3 pKi = 8.3 Binding
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 67560 0 None -1 2 Rat 8.3 pKi = 8.3 Binding
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 67560 0 None -1 2 Rat 8.3 pKi = 8.3 Binding
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 114499 7 None -1 2 Rat 7.4 pKi = 7.4 Binding
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 114499 7 None -1 2 Rat 7.4 pKi = 7.4 Binding
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 158682 0 None 1 2 Human 6.4 pKi = 6.4 Binding
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 158682 0 None 1 2 Human 6.4 pKi = 6.4 Binding
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 123405 0 None -5 2 Human 7.4 pKi = 7.4 Binding
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 123405 0 None -5 2 Human 7.4 pKi = 7.4 Binding
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 83247 1 None 5 2 Human 6.4 pKi = 6.4 Binding
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 83247 1 None 5 2 Human 6.4 pKi = 6.4 Binding
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 66457 0 None -2 2 Rat 8.3 pKi = 8.3 Binding
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 66457 0 None -2 2 Rat 8.3 pKi = 8.3 Binding
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 158422 0 None 38 2 Human 8.2 pKi = 8.2 Binding
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 158422 0 None 38 2 Human 8.2 pKi = 8.2 Binding
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 44 None -2 5 Human 8.2 pKi = 8.2 Binding
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 44 None -2 5 Human 8.2 pKi = 8.2 Binding
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 44 None -2 5 Human 8.2 pKi = 8.2 Binding
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 44 None -2 5 Human 8.2 pKi = 8.2 Binding
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 44 None -2 5 Human 8.2 pKi = 8.2 Binding
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 44 None -2 5 Human 8.2 pKi = 8.2 Binding
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 183721 0 None 1 2 Human 8.2 pKi = 8.2 Binding
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 183721 0 None 1 2 Human 8.2 pKi = 8.2 Binding
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 183721 0 None 1 2 Human 8.2 pKi = 8.2 Binding
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 126776 1 None 1 2 Human 6.3 pKi = 6.3 Binding
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 126776 1 None 1 2 Human 6.3 pKi = 6.3 Binding
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 64 None -2 6 Rat 7.3 pKi = 7.3 Binding
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 64 None -2 6 Rat 7.3 pKi = 7.3 Binding
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 64 None -2 6 Rat 7.3 pKi = 7.3 Binding
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 64 None -2 6 Rat 7.3 pKi = 7.3 Binding
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 123398 0 None 1 2 Human 7.3 pKi = 7.3 Binding
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 123398 0 None 1 2 Human 7.3 pKi = 7.3 Binding
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 123406 0 None -4 2 Human 7.2 pKi = 7.2 Binding
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 123406 0 None -4 2 Human 7.2 pKi = 7.2 Binding
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 110 None 1 18 Human 7.2 pKi = 7.2 Binding
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 110 None 1 18 Human 7.2 pKi = 7.2 Binding
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 110 None 1 18 Human 7.2 pKi = 7.2 Binding
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 110 None 1 18 Human 7.2 pKi = 7.2 Binding
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 110 None 1 18 Human 7.2 pKi = 7.2 Binding
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 110 None 1 18 Human 7.2 pKi = 7.2 Binding
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 110 None 1 18 Human 7.2 pKi = 7.2 Binding
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 19 None -1 2 Human 6.2 pKi = 6.2 Binding
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 19 None -1 2 Human 6.2 pKi = 6.2 Binding
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 19 None -1 2 Human 6.2 pKi = 6.2 Binding
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 123400 0 None 1 2 Human 7.2 pKi = 7.2 Binding
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 123400 0 None 1 2 Human 7.2 pKi = 7.2 Binding
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 158961 0 None 43 2 Human 8.2 pKi = 8.2 Binding
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 158961 0 None 43 2 Human 8.2 pKi = 8.2 Binding
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 183618 0 None 1 2 Human 8.2 pKi = 8.2 Binding
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 183618 0 None 1 2 Human 8.2 pKi = 8.2 Binding
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 183618 0 None 1 2 Human 8.2 pKi = 8.2 Binding
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 180213 0 None 1 2 Human 6.2 pKi = 6.2 Binding
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 180213 0 None 1 2 Human 6.2 pKi = 6.2 Binding
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 123397 0 None 1 2 Human 7.2 pKi = 7.2 Binding
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 123397 0 None 1 2 Human 7.2 pKi = 7.2 Binding
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 123399 0 None 1 2 Human 7.2 pKi = 7.2 Binding
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 123399 0 None 1 2 Human 7.2 pKi = 7.2 Binding
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 123409 0 None 1 2 Human 7.2 pKi = 7.2 Binding
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 123409 0 None 1 2 Human 7.2 pKi = 7.2 Binding
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 114800 6 None -1 2 Rat 7.2 pKi = 7.2 Binding
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 114800 6 None -1 2 Rat 7.2 pKi = 7.2 Binding
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 66753 0 None -2 2 Rat 7.2 pKi = 7.2 Binding
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 66753 0 None -2 2 Rat 7.2 pKi = 7.2 Binding
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 123407 0 None -2 2 Human 7.2 pKi = 7.2 Binding
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 123407 0 None -2 2 Human 7.2 pKi = 7.2 Binding
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 183640 0 None 1 2 Human 8.1 pKi = 8.1 Binding
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 183640 0 None 1 2 Human 8.1 pKi = 8.1 Binding
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 183640 0 None 1 2 Human 8.1 pKi = 8.1 Binding
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 155894 0 None 1 2 Human 6.1 pKi = 6.1 Binding
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 155894 0 None 1 2 Human 6.1 pKi = 6.1 Binding
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 123404 0 None 2 2 Human 7.1 pKi = 7.1 Binding
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 123404 0 None 2 2 Human 7.1 pKi = 7.1 Binding
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 123408 0 None 4 2 Human 7.1 pKi = 7.1 Binding
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 123408 0 None 4 2 Human 7.1 pKi = 7.1 Binding
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 66114 0 None -2 2 Rat 7.1 pKi = 7.1 Binding
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 66114 0 None -2 2 Rat 7.1 pKi = 7.1 Binding
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 156787 0 None 5 2 Human 8.0 pKi = 8.0 Binding
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 156787 0 None 5 2 Human 8.0 pKi = 8.0 Binding
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 206508 12 None 6 2 Human 8.0 pKi = 8.0 Binding
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 206508 12 None 6 2 Human 8.0 pKi = 8.0 Binding
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 183647 0 None -1 2 Human 8.0 pKi = 8.0 Binding
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 183647 0 None -1 2 Human 8.0 pKi = 8.0 Binding
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 183647 0 None -1 2 Human 8.0 pKi = 8.0 Binding
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 137600 69 None 1 2 Human 7.0 pKi = 7.0 Binding
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 137600 69 None 1 2 Human 7.0 pKi = 7.0 Binding
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 64 None -1 6 Human 7.0 pKi = 7.0 Binding
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 64 None -1 6 Human 7.0 pKi = 7.0 Binding
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 64 None -1 6 Human 7.0 pKi = 7.0 Binding
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 64 None -1 6 Human 7.0 pKi = 7.0 Binding
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 64 None -1 6 Human 7.0 pKi = 7.0 Binding
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 64 None -1 6 Human 7.0 pKi = 7.0 Binding
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 64 None -1 6 Human 7.0 pKi = 7.0 Binding
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 64 None -1 6 Human 7.0 pKi = 7.0 Binding
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 64 None -1 6 Human 7.0 pKi = 7.0 Binding
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 64 None -1 6 Human 7.0 pKi = 7.0 Binding
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 64 None -1 6 Human 7.0 pKi = 7.0 Binding
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 64 None -1 6 Human 7.0 pKi = 7.0 Binding
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 54 None -5 10 Rat 7.3 pKd None 7.3 Binding
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 54 None -5 10 Rat 7.3 pKd None 7.3 Binding
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 54 None -5 10 Rat 7.3 pKd None 7.3 Binding
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 54 None -5 10 Rat 7.3 pKd None 7.3 Binding
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 54 None 1 10 Human 9.1 pKd None 9.1 Binding
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 54 None 1 10 Human 9.1 pKd None 9.1 Binding
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 54 None 1 10 Human 9.1 pKd None 9.1 Binding
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 54 None 1 10 Human 9.1 pKd None 9.1 Binding
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 64 Functional -14 8 Human 5.0 pKi = 5 Binding
NoneNone
PDSP KiDatabase 158 2 3 4 -0.9 OC(=O)C(c1o[nH]c(=O)c1)N None
1233 1970 64 Functional -14 8 Human 5.0 pKi = 5 Binding
NoneNone
PDSP KiDatabase 158 2 3 4 -0.9 OC(=O)C(c1o[nH]c(=O)c1)N None
1371 1970 64 Functional -14 8 Human 5.0 pKi = 5 Binding
NoneNone
PDSP KiDatabase 158 2 3 4 -0.9 OC(=O)C(c1o[nH]c(=O)c1)N None
CHEMBL284895 1970 64 Functional -14 8 Human 5.0 pKi = 5 Binding
NoneNone
PDSP KiDatabase 158 2 3 4 -0.9 OC(=O)C(c1o[nH]c(=O)c1)N None
1370 3263 67 Functional -1202 8 Human 5.0 pKi = 5 Binding
NoneNone
PDSP KiDatabase 189 3 3 6 -2.5 OC(=O)[C@H](Cn1oc(=O)[nH]c1=O)N None
1372 3263 67 Functional -1202 8 Human 5.0 pKi = 5 Binding
NoneNone
PDSP KiDatabase 189 3 3 6 -2.5 OC(=O)[C@H](Cn1oc(=O)[nH]c1=O)N None
40539 3263 67 Functional -1202 8 Human 5.0 pKi = 5 Binding
NoneNone
PDSP KiDatabase 189 3 3 6 -2.5 OC(=O)[C@H](Cn1oc(=O)[nH]c1=O)N None
6971145 3263 67 Functional -1202 8 Human 5.0 pKi = 5 Binding
NoneNone
PDSP KiDatabase 189 3 3 6 -2.5 OC(=O)[C@H](Cn1oc(=O)[nH]c1=O)N None
CHEMBL279956 3263 67 Functional -1202 8 Human 5.0 pKi = 5 Binding
NoneNone
PDSP KiDatabase 189 3 3 6 -2.5 OC(=O)[C@H](Cn1oc(=O)[nH]c1=O)N None
DB02999 3263 67 Functional -1202 8 Human 5.0 pKi = 5 Binding
NoneNone
PDSP KiDatabase 189 3 3 6 -2.5 OC(=O)[C@H](Cn1oc(=O)[nH]c1=O)N None
139054390 204923 106 Functional -1 5 Human 5.0 pKi = 5 Binding
NoneNone
PDSP KiDatabase 147 4 3 3 -0.7 N[C@H](CCC(=O)O)C(=O)O None
23327 204923 106 Functional -1 5 Human 5.0 pKi = 5 Binding
NoneNone
PDSP KiDatabase 147 4 3 3 -0.7 N[C@H](CCC(=O)O)C(=O)O None
CHEMBL76232 204923 106 Functional -1 5 Human 5.0 pKi = 5 Binding
NoneNone
PDSP KiDatabase 147 4 3 3 -0.7 N[C@H](CCC(=O)O)C(=O)O None
114827 216332 0 3H-LY341495 -4 3 Human 6.9 pKi = 6.9 Binding
NoneNone
PDSP KiDatabase 185 2 3 3 -0.5 C1CC(C2C1C2C(=O)O)(C(=O)O)N None
None 216334 0 Functional -3 3 Human 6.7 pKi = 6.7 Binding
NoneNone
PDSP KiDatabase 203 4 4 4 -1.6 C1(C(C1C(=O)O)C(=O)O)C(C(=O)O)N None
210320 217733 0 None - 1 Human 8.3 pKi = 8.3 Binding
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 110 Functional 1 18 Human 5.4 pKi = 5.4 Binding
NoneNone
PDSP KiDatabase 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N None
1369 2315 110 Functional 1 18 Human 5.4 pKi = 5.4 Binding
NoneNone
PDSP KiDatabase 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N None
33032 2315 110 Functional 1 18 Human 5.4 pKi = 5.4 Binding
NoneNone
PDSP KiDatabase 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N None
44272391 2315 110 Functional 1 18 Human 5.4 pKi = 5.4 Binding
NoneNone
PDSP KiDatabase 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N None
88747398 2315 110 Functional 1 18 Human 5.4 pKi = 5.4 Binding
NoneNone
PDSP KiDatabase 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N None
CHEMBL575060 2315 110 Functional 1 18 Human 5.4 pKi = 5.4 Binding
NoneNone
PDSP KiDatabase 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N None
DB00142 2315 110 Functional 1 18 Human 5.4 pKi = 5.4 Binding
NoneNone
PDSP KiDatabase 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N None
1310 2315 110 None 1 18 Human 8.1 pKi = 8.1 Binding
NoneNone
Drug Central 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N None
1369 2315 110 None 1 18 Human 8.1 pKi = 8.1 Binding
NoneNone
Drug Central 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N None
33032 2315 110 None 1 18 Human 8.1 pKi = 8.1 Binding
NoneNone
Drug Central 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N None
44272391 2315 110 None 1 18 Human 8.1 pKi = 8.1 Binding
NoneNone
Drug Central 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N None
88747398 2315 110 None 1 18 Human 8.1 pKi = 8.1 Binding
NoneNone
Drug Central 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N None
CHEMBL575060 2315 110 None 1 18 Human 8.1 pKi = 8.1 Binding
NoneNone
Drug Central 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N None
DB00142 2315 110 None 1 18 Human 8.1 pKi = 8.1 Binding
NoneNone
Drug Central 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N None
None 216172 0 Functional -1 7 Human 5.1 pKi = 5.1 Binding
NoneNone
PDSP KiDatabase 173 2 3 3 -0.3 C1CC(CC1C(=O)O)(C(=O)O)N None
1405 2709 0 None - 1 Human 4.7 pKi = 4.7 Binding
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 0 None - 1 Human 4.7 pKi = 4.7 Binding
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 0 None - 1 Human 4.7 pKi = 4.7 Binding
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 19 None -1 2 Human 6.5 pKi = 6.5 Binding
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 19 None -1 2 Human 6.5 pKi = 6.5 Binding
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 19 None -1 2 Human 6.5 pKi = 6.5 Binding
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 51 None -6 5 Human 3.8 pKi None 3.8 Binding
UnclassifiedUnclassified
Guide to Pharmacology 209 3 3 3 0.6 OC(=O)c1ccc(cc1)[C@@](C(=O)O)(N)C 10530814
139055582 2475 51 None -6 5 Human 3.8 pKi None 3.8 Binding
UnclassifiedUnclassified
Guide to Pharmacology 209 3 3 3 0.6 OC(=O)c1ccc(cc1)[C@@](C(=O)O)(N)C 10530814
446355 2475 51 None -6 5 Human 3.8 pKi None 3.8 Binding
UnclassifiedUnclassified
Guide to Pharmacology 209 3 3 3 0.6 OC(=O)c1ccc(cc1)[C@@](C(=O)O)(N)C 10530814
CHEMBL257626 2475 51 None -6 5 Human 3.8 pKi None 3.8 Binding
UnclassifiedUnclassified
Guide to Pharmacology 209 3 3 3 0.6 OC(=O)c1ccc(cc1)[C@@](C(=O)O)(N)C 10530814
DB04256 2475 51 None -6 5 Human 3.8 pKi None 3.8 Binding
UnclassifiedUnclassified
Guide to Pharmacology 209 3 3 3 0.6 OC(=O)c1ccc(cc1)[C@@](C(=O)O)(N)C 10530814
104766 33 42 None -12 11 Human 4.7 pKi None 4.7 Binding
UnclassifiedUnclassified
Guide to Pharmacology 173 2 3 3 -0.3 OC(=O)[C@@H]1CC[C@@](C1)(N)C(=O)O 10530814
1365 33 42 None -12 11 Human 4.7 pKi None 4.7 Binding
UnclassifiedUnclassified
Guide to Pharmacology 173 2 3 3 -0.3 OC(=O)[C@@H]1CC[C@@](C1)(N)C(=O)O 10530814
CHEMBL34453 33 42 None -12 11 Human 4.7 pKi None 4.7 Binding
UnclassifiedUnclassified
Guide to Pharmacology 173 2 3 3 -0.3 OC(=O)[C@@H]1CC[C@@](C1)(N)C(=O)O 10530814
104766 33 42 None -10 11 Rat 4.8 pKi None 4.8 Binding
UnclassifiedUnclassified
Guide to Pharmacology 173 2 3 3 -0.3 OC(=O)[C@@H]1CC[C@@](C1)(N)C(=O)O 10884552
1365 33 42 None -10 11 Rat 4.8 pKi None 4.8 Binding
UnclassifiedUnclassified
Guide to Pharmacology 173 2 3 3 -0.3 OC(=O)[C@@H]1CC[C@@](C1)(N)C(=O)O 10884552
CHEMBL34453 33 42 None -10 11 Rat 4.8 pKi None 4.8 Binding
UnclassifiedUnclassified
Guide to Pharmacology 173 2 3 3 -0.3 OC(=O)[C@@H]1CC[C@@](C1)(N)C(=O)O 10884552
10197984 2421 44 None -2 5 Human 4.8 pKi None 4.8 Binding
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 44 None -2 5 Human 4.8 pKi None 4.8 Binding
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 44 None -2 5 Human 4.8 pKi None 4.8 Binding
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 48 None 1 2 Human 5.3 pKi None 5.3 Binding
UnclassifiedUnclassified
Guide to Pharmacology 174 2 4 4 -1.8 OC(=O)[C@@H]1NC[C@@](C1)(N)C(=O)O 10530814
5310984 73 48 None 1 2 Human 5.3 pKi None 5.3 Binding
UnclassifiedUnclassified
Guide to Pharmacology 174 2 4 4 -1.8 OC(=O)[C@@H]1NC[C@@](C1)(N)C(=O)O 10530814
CHEMBL40086 73 48 None 1 2 Human 5.3 pKi None 5.3 Binding
UnclassifiedUnclassified
Guide to Pharmacology 174 2 4 4 -1.8 OC(=O)[C@@H]1NC[C@@](C1)(N)C(=O)O 10530814
1400 1538 0 None 7 2 Rat 5.4 pKi None 5.4 Binding
UnclassifiedUnclassified
Guide to Pharmacology 175 5 3 3 0.0 CC[C@@](C(=O)O)(CCC(=O)O)N 10884552
5311079 1538 0 None 7 2 Rat 5.4 pKi None 5.4 Binding
UnclassifiedUnclassified
Guide to Pharmacology 175 5 3 3 0.0 CC[C@@](C(=O)O)(CCC(=O)O)N 10884552
CHEMBL1450466 1538 0 None 7 2 Rat 5.4 pKi None 5.4 Binding
UnclassifiedUnclassified
Guide to Pharmacology 175 5 3 3 0.0 CC[C@@](C(=O)O)(CCC(=O)O)N 10884552
1310 2315 110 None -1 18 Rat 6.4 pKi None 6.4 Binding
UnclassifiedUnclassified
Guide to Pharmacology 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N 10884552
1369 2315 110 None -1 18 Rat 6.4 pKi None 6.4 Binding
UnclassifiedUnclassified
Guide to Pharmacology 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N 10884552
33032 2315 110 None -1 18 Rat 6.4 pKi None 6.4 Binding
UnclassifiedUnclassified
Guide to Pharmacology 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N 10884552
44272391 2315 110 None -1 18 Rat 6.4 pKi None 6.4 Binding
UnclassifiedUnclassified
Guide to Pharmacology 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N 10884552
88747398 2315 110 None -1 18 Rat 6.4 pKi None 6.4 Binding
UnclassifiedUnclassified
Guide to Pharmacology 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N 10884552
CHEMBL575060 2315 110 None -1 18 Rat 6.4 pKi None 6.4 Binding
UnclassifiedUnclassified
Guide to Pharmacology 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N 10884552
DB00142 2315 110 None -1 18 Rat 6.4 pKi None 6.4 Binding
UnclassifiedUnclassified
Guide to Pharmacology 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N 10884552
1368 2290 37 None -2 11 Rat 6.5 pKi None 6.5 Binding
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 37 None -2 11 Rat 6.5 pKi None 6.5 Binding
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 37 None -2 11 Rat 6.5 pKi None 6.5 Binding
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 26 None -2 6 Rat 6.8 pKi None 6.8 Binding
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 26 None -2 6 Rat 6.8 pKi None 6.8 Binding
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 26 None -2 6 Rat 6.8 pKi None 6.8 Binding
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 26 None 1 6 Human 7.2 pKi None 7.2 Binding
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 26 None 1 6 Human 7.2 pKi None 7.2 Binding
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 26 None 1 6 Human 7.2 pKi None 7.2 Binding
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 64 None -2 6 Rat 7.3 pKi None 7.3 Binding
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 64 None -2 6 Rat 7.3 pKi None 7.3 Binding
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 64 None -2 6 Rat 7.3 pKi None 7.3 Binding
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 64 None -2 6 Rat 7.3 pKi None 7.3 Binding
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 37 None -1 11 Human 7.4 pKi None 7.4 Binding
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 37 None -1 11 Human 7.4 pKi None 7.4 Binding
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 37 None -1 11 Human 7.4 pKi None 7.4 Binding
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 110 None 1 18 Human 7.4 pKi None 7.4 Binding
UnclassifiedUnclassified
Guide to Pharmacology 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N 10530814
1369 2315 110 None 1 18 Human 7.4 pKi None 7.4 Binding
UnclassifiedUnclassified
Guide to Pharmacology 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N 10530814
33032 2315 110 None 1 18 Human 7.4 pKi None 7.4 Binding
UnclassifiedUnclassified
Guide to Pharmacology 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N 10530814
44272391 2315 110 None 1 18 Human 7.4 pKi None 7.4 Binding
UnclassifiedUnclassified
Guide to Pharmacology 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N 10530814
88747398 2315 110 None 1 18 Human 7.4 pKi None 7.4 Binding
UnclassifiedUnclassified
Guide to Pharmacology 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N 10530814
CHEMBL575060 2315 110 None 1 18 Human 7.4 pKi None 7.4 Binding
UnclassifiedUnclassified
Guide to Pharmacology 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N 10530814
DB00142 2315 110 None 1 18 Human 7.4 pKi None 7.4 Binding
UnclassifiedUnclassified
Guide to Pharmacology 147 4 3 3 -0.7 OC(=O)CC[C@@H](C(=O)O)N 10530814
1378 2417 54 None -5 10 Rat 8.0 pKi None 8 Binding
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 54 None -5 10 Rat 8.0 pKi None 8 Binding
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 54 None -5 10 Rat 8.0 pKi None 8 Binding
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 54 None -5 10 Rat 8.0 pKi None 8 Binding
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 15 None -2 5 Rat 8.4 pKi None 8.4 Binding
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 15 None -2 5 Rat 8.4 pKi None 8.4 Binding
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 15 None -2 5 Rat 8.4 pKi None 8.4 Binding
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 15 None -2 5 Rat 8.4 pKi None 8.4 Binding
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 15 None -2 5 Rat 8.4 pKi None 8.4 Binding
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 15 None -2 5 Rat 8.4 pKi None 8.4 Binding
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 64 None -1 6 Human 8.9 pKi None 8.9 Binding
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 64 None -1 6 Human 8.9 pKi None 8.9 Binding
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 64 None -1 6 Human 8.9 pKi None 8.9 Binding
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 64 None -1 6 Human 8.9 pKi None 8.9 Binding
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 54 None 1 10 Human 8.9 pKi None 8.9 Binding
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 54 None 1 10 Human 8.9 pKi None 8.9 Binding
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 54 None 1 10 Human 8.9 pKi None 8.9 Binding
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 54 None 1 10 Human 8.9 pKi None 8.9 Binding
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