rizatriptan


SMILES CN(CCc1c[nH]c2c1cc(cc2)Cn1cncn1)C
InChIKey ULFRLSNUDGIQQP-UHFFFAOYSA-N

Chemical properties

Hydrogen bond acceptors 4
Hydrogen bond donors 1
Rotatable bonds 5
Molecular weight (Da) 269.2

Drug properties

Molecular type Small molecule
Physiological/Surrogate Surrogate
Approved drug Yes

Bioactivities

Receptor Activity Source
GTP Uniprot Species Family Class Type Min Avg Max Database
5-HT1A 5HT1A Human 5-Hydroxytryptamine A pKi 6.4 6.4 6.4 Guide to Pharmacology
5-HT1B 5HT1B Human 5-Hydroxytryptamine A pKi 6.9 6.9 6.9 Guide to Pharmacology
5-HT1E 5HT1E Human 5-Hydroxytryptamine A pKi 6.8 6.8 6.8 Guide to Pharmacology
5-HT1F 5HT1F Human 5-Hydroxytryptamine A pKi 6.4 6.6 6.8 Guide to Pharmacology
5-HT1B 5HT1B Human 5-Hydroxytryptamine A pKi 8.0 8.0 8.0 ChEMBL
5-HT1D 5HT1D Human 5-Hydroxytryptamine A pKi 7.4 7.88 8.37 ChEMBL
5-HT1A 5HT1A Human 5-Hydroxytryptamine A pKi 6.53 6.69 6.85 ChEMBL
5-HT1A 5HT1A Human 5-Hydroxytryptamine A pKi 8.16 8.16 8.16 Drug Central
5-HT1B 5HT1B Human 5-Hydroxytryptamine A pKi 8.16 8.16 8.16 Drug Central
5-HT1D 5HT1D Human 5-Hydroxytryptamine A pKi 8.1 8.1 8.1 Drug Central
5-HT1E 5HT1E Human 5-Hydroxytryptamine A pKi 8.17 8.17 8.17 Drug Central
5-HT1F 5HT1F Human 5-Hydroxytryptamine A pKi 8.17 8.17 8.17 Drug Central
5-HT1D 5HT1D Human 5-Hydroxytryptamine A pKi 7.9 7.9 7.9 Guide to Pharmacology
Receptor Activity Source
GTP Uniprot Species Family Class Type Min Avg Max Database
5-HT1B 5HT1B Human 5-Hydroxytryptamine A pIC50 7.39 7.39 7.39 ChEMBL
5-HT1D 5HT1D Human 5-Hydroxytryptamine A pIC50 7.1 7.53 7.96 ChEMBL
5-HT1D 5HT1D Human 5-Hydroxytryptamine A pEC50 8.08 8.3 8.52 ChEMBL
5-HT2C 5HT2C Human 5-Hydroxytryptamine A pIC50 5.1 5.1 5.1 ChEMBL
5-HT2A 5HT2A Human 5-Hydroxytryptamine A pIC50 5.1 5.1 5.1 ChEMBL
5-HT1A 5HT1A Human 5-Hydroxytryptamine A pIC50 6.4 6.45 6.5 ChEMBL
5-HT2C 5HT2C Human 5-Hydroxytryptamine A pIC50 8.29 8.29 8.29 Drug Central
5-HT2A 5HT2A Rat 5-Hydroxytryptamine A pIC50 8.28 8.28 8.28 Drug Central
5-HT2A 5HT2A Human 5-Hydroxytryptamine A pIC50 8.29 8.29 8.29 Drug Central