tyramine


SMILES NCCc1ccc(cc1)O
InChIKey DZGWFCGJZKJUFP-UHFFFAOYSA-N

Chemical properties

Hydrogen bond acceptors 2
Hydrogen bond donors 2
Rotatable bonds 2
Molecular weight (Da) 137.1

Drug properties

Molecular type Small molecule
Physiological/Surrogate Endogenous
Approved drug Yes

Database connections

Ligand site mutations D2

Bioactivities

Receptor Activity Source
GTP Uniprot Species Family Class Type Min Avg Max Database
TA1 TAAR1 Human Trace amine A pKd 7.7 7.7 7.7 Guide to Pharmacology
TA1 TAAR1 Rat Trace amine A pKi 7.2 7.2 7.2 Guide to Pharmacology
TA1 TAAR1 Mouse Trace amine A pKi 6.4 6.4 6.4 Guide to Pharmacology
TA1 TAAR1 Human Trace amine A pKi 7.47 7.47 7.47 PDSP Ki database
5-HT2B 5HT2B Rat 5-Hydroxytryptamine A pKd 5.1 5.1 5.1 ChEMBL
Receptor Activity Source
GTP Uniprot Species Family Class Type Min Avg Max Database
TA1 TAAR1 Human Trace amine A pEC50 5.8 6.25 6.7 Guide to Pharmacology
TA1 TAAR1 Rat Trace amine A pEC50 6.9 7.05 7.2 Guide to Pharmacology
TA1 TAAR1 Mouse Trace amine A pEC50 6.2 6.65 7.1 Guide to Pharmacology
TA1 TAAR1 Rat Trace amine A pEC50 7.16 7.34 7.52 ChEMBL
TA1 TAAR1 Human Trace amine A pEC50 6.0 6.5 7.12 ChEMBL
TA1 TAAR1 Human Trace amine A pIC50 6.05 6.05 6.05 ChEMBL
TA1 TAAR1 Mouse Trace amine A pEC50 6.55 6.55 6.55 ChEMBL
M1 ACM1 Rat Acetylcholine (muscarinic) A Potency 7.3 7.3 7.3 ChEMBL
TA1 TAAR1 Human Trace amine A pEC50 8.15 8.15 8.15 Drug Central
TA1 TAAR1 Rat Trace amine A pEC50 8.14 8.14 8.14 Drug Central
TA1 TAAR1 Mouse Trace amine A pEC50 8.15 8.15 8.15 Drug Central