LYSERGIC ACID


SMILES CN1CC(C=C2C1CC3=CNC4=CC=CC2=C34)C(=O)O
InChIKey ZAGRKAFMISFKIO-UHFFFAOYSA-N

Chemical properties

Hydrogen bond acceptors 2
Hydrogen bond donors 2
Rotatable bonds 1
Molecular weight (Da) 268.1

Drug properties

Molecular type Small molecule
Physiological/Surrogate Surrogate
Approved drug No

Database connections

Bioactivities

Receptor Activity Source
GTP Uniprot Species Family Class Type Min Avg Max Database
5-HT5A 5HT5A Mouse 5-Hydroxytryptamine A pKi 5.7 5.7 5.7 PDSP Ki database
5-HT1B 5HT1B Human 5-Hydroxytryptamine A pKi 8.41 8.41 8.41 PDSP Ki database
5-HT1D 5HT1D Human 5-Hydroxytryptamine A pKi 8.11 8.11 8.11 PDSP Ki database
5-HT1E 5HT1E Human 5-Hydroxytryptamine A pKi 7.03 7.03 7.03 PDSP Ki database
5-HT2A 5HT2A Human 5-Hydroxytryptamine A pKi 7.95 7.95 7.95 PDSP Ki database
5-HT2B 5HT2B Human 5-Hydroxytryptamine A pKi 7.52 7.52 7.52 PDSP Ki database
5-HT2C 5HT2C Human 5-Hydroxytryptamine A pKi 7.51 7.51 7.51 PDSP Ki database
5-HT5A 5HT5A Human 5-Hydroxytryptamine A pKi 8.05 8.05 8.05 PDSP Ki database
5-HT6 5HT6R Human 5-Hydroxytryptamine A pKi 8.16 8.16 8.16 PDSP Ki database
5-HT7 5HT7R Human 5-Hydroxytryptamine A pKi 8.18 8.18 8.18 PDSP Ki database
V2 V2R Human Vasopressin and oxytocin A pKi 5.0 5.0 5.0 PDSP Ki database
mGlu1 GRM1 Human Metabotropic glutamate C pKi 5.0 5.0 5.0 PDSP Ki database
mGlu2 GRM2 Human Metabotropic glutamate C pKi 5.0 5.0 5.0 PDSP Ki database
mGlu5 GRM5 Human Metabotropic glutamate C pKi 5.0 5.0 5.0 PDSP Ki database
Receptor Activity Source
GTP Uniprot Species Family Class Type Min Avg Max Database