ALTANSERIN


SMILES O=C(c1ccc(F)cc1)C1CCN(CCn2c(=S)[nH]c3ccccc3c2=O)CC1
InChIKey SMYALUSCZJXWHG-UHFFFAOYSA-N

Chemical properties

Hydrogen bond acceptors 5
Hydrogen bond donors 1
Rotatable bonds 5
Molecular weight (Da) 411.1

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
α1A ADA1A Rat Adrenoceptors A pKi 8.3 8.3 8.3 ChEMBL
D2 DRD2 Rat Dopamine A pKi 7.21 7.21 7.21 ChEMBL
5-HT2C 5HT2C Human 5-Hydroxytryptamine A pKi 7.4 7.4 7.4 ChEMBL
5-HT2A 5HT2A Human 5-Hydroxytryptamine A pKi 9.52 9.71 9.89 ChEMBL
5-HT1A 5HT1A Human 5-Hydroxytryptamine A pKi 5.8 5.8 5.8 ChEMBL
5-HT1B 5HT1B Rat 5-Hydroxytryptamine A pKi 5.98 5.98 5.98 PDSP Ki database
D2 DRD2 Human Dopamine A pKi 7.21 7.21 7.21 ChEMBL
5-HT2A 5HT2A Rat 5-Hydroxytryptamine A pKi 8.58 9.01 9.85 PDSP Ki database
5-HT2C K7GSR7 Pig 5-Hydroxytryptamine A pKi 6.9 6.92 6.93 PDSP Ki database
Receptor Activity Source
GTP Uniprot Species Family Class Type Min Avg Max Database
5-HT2A 5HT2A Human 5-Hydroxytryptamine A pIC50 8.82 8.82 8.82 ChEMBL
TSH TSHR Human Glycoprotein hormone A Potency 4.4 4.4 4.4 ChEMBL