ERGOCORNINE
SMILES | CC(C)[C@H]1C(=O)N2CCC[C@H]2[C@]2(O)O[C@](NC(=O)[C@@H]3C=C4c5cccc6[nH]cc(c56)C[C@H]4N(C)C3)(C(C)C)C(=O)N12 |
InChIKey | UJYGDMFEEDNVBF-OGGGUQDZSA-N |
Chemical properties
Hydrogen bond acceptors | 6 |
Hydrogen bond donors | 3 |
Rotatable bonds | 4 |
Molecular weight (Da) | 561.3 |
Drug properties
Molecular type | Small molecule |
Physiological/Surrogate | Surrogate |
Approved drug | No |
Database connections
Ligand site mutations | 5-HT2A |
Bioactivities
Receptor | Activity | Source | |||||||
---|---|---|---|---|---|---|---|---|---|
GTP | Uniprot | Species | Family | Class | Type | Min | Avg | Max | Database |
5-HT1B | 5HT1B | Rat | 5-Hydroxytryptamine | A | pKi | 7.72 | 7.72 | 7.72 | ChEMBL |
α1B | ADA1B | Rat | Adrenoceptors | A | pKi | 8.54 | 8.54 | 8.54 | ChEMBL |
α1A | ADA1A | Rat | Adrenoceptors | A | pKi | 8.35 | 8.35 | 8.35 | ChEMBL |
α1D | ADA1D | Human | Adrenoceptors | A | pKi | 8.06 | 8.06 | 8.06 | ChEMBL |
α2B | ADA2B | Human | Adrenoceptors | A | pKi | 8.86 | 8.86 | 8.86 | ChEMBL |
α2C | ADA2C | Human | Adrenoceptors | A | pKi | 8.62 | 8.62 | 8.62 | ChEMBL |
5-HT1A | 5HT1A | Rat | 5-Hydroxytryptamine | A | pKi | 8.75 | 8.75 | 8.75 | ChEMBL |
α2A | ADA2A | Human | Adrenoceptors | A | pKi | 8.63 | 8.63 | 8.63 | ChEMBL |
D1 | DRD1 | Human | Dopamine | A | pKi | 6.83 | 6.83 | 6.83 | ChEMBL |
5-HT6 | 5HT6R | Human | 5-Hydroxytryptamine | A | pKi | 8.15 | 8.15 | 8.15 | ChEMBL |
5-HT2B | 5HT2B | Human | 5-Hydroxytryptamine | A | pKi | 8.16 | 8.16 | 8.16 | ChEMBL |
5-HT2C | 5HT2C | Human | 5-Hydroxytryptamine | A | pKi | 7.26 | 7.26 | 7.26 | ChEMBL |
D3 | DRD3 | Human | Dopamine | A | pKi | 9.01 | 9.01 | 9.01 | ChEMBL |
5-HT2A | 5HT2A | Human | 5-Hydroxytryptamine | A | pKi | 8.1 | 8.1 | 8.1 | ChEMBL |
D2 | DRD2 | Human | Dopamine | A | pKi | 8.78 | 8.78 | 8.78 | ChEMBL |
D2 | DRD2 | Bovine | Dopamine | A | pKi | 9.15 | 9.15 | 9.15 | PDSP Ki database |
D1 | DRD1 | Bovine | Dopamine | A | pKi | 7.44 | 7.44 | 7.44 | PDSP Ki database |
Receptor | Activity | Source | |||||||
---|---|---|---|---|---|---|---|---|---|
GTP | Uniprot | Species | Family | Class | Type | Min | Avg | Max | Database |
5-HT1B | 5HT1B | Rat | 5-Hydroxytryptamine | A | pIC50 | 7.52 | 7.52 | 7.52 | ChEMBL |
α1B | ADA1B | Rat | Adrenoceptors | A | pIC50 | 8.29 | 8.29 | 8.29 | ChEMBL |
α1A | ADA1A | Rat | Adrenoceptors | A | pIC50 | 7.96 | 7.96 | 7.96 | ChEMBL |
α1D | ADA1D | Human | Adrenoceptors | A | pIC50 | 7.75 | 7.75 | 7.75 | ChEMBL |
α2B | ADA2B | Human | Adrenoceptors | A | pIC50 | 8.52 | 8.52 | 8.52 | ChEMBL |
α2C | ADA2C | Human | Adrenoceptors | A | pIC50 | 7.77 | 7.77 | 7.77 | ChEMBL |
5-HT1A | 5HT1A | Rat | 5-Hydroxytryptamine | A | pIC50 | 8.51 | 8.51 | 8.51 | ChEMBL |
α2A | ADA2A | Human | Adrenoceptors | A | pIC50 | 8.2 | 8.2 | 8.2 | ChEMBL |
D1 | DRD1 | Human | Dopamine | A | pIC50 | 6.53 | 6.53 | 6.53 | ChEMBL |
5-HT6 | 5HT6R | Human | 5-Hydroxytryptamine | A | pIC50 | 7.82 | 7.82 | 7.82 | ChEMBL |
5-HT2B | 5HT2B | Human | 5-Hydroxytryptamine | A | pIC50 | 7.96 | 7.96 | 7.96 | ChEMBL |
5-HT2C | 5HT2C | Human | 5-Hydroxytryptamine | A | pIC50 | 6.98 | 6.98 | 6.98 | ChEMBL |
D3 | DRD3 | Human | Dopamine | A | pIC50 | 8.54 | 8.54 | 8.54 | ChEMBL |
5-HT2A | 5HT2A | Human | 5-Hydroxytryptamine | A | pIC50 | 7.55 | 7.55 | 7.55 | ChEMBL |
NPS | NPSR1 | Human | Neuropeptide S | A | Potency | 5.4 | 6.56 | 8.0 | ChEMBL |
D2 | DRD2 | Human | Dopamine | A | pIC50 | 8.3 | 8.3 | 8.3 | ChEMBL |