xylazine


SMILES Cc1cccc(c1NC1=NCCCS1)C
InChIKey BPICBUSOMSTKRF-UHFFFAOYSA-N

Chemical properties

Hydrogen bond acceptors 3
Hydrogen bond donors 1
Rotatable bonds 1
Molecular weight (Da) 220.1

Drug properties

Molecular type Small molecule
Endogenous/Surrogate Surrogate
Approved drug Yes

Bioactivities

Receptor Activity Source
GTP Uniprot Species Family Class Type Min Avg Max Database
α2A ADA2A Human Adrenoceptors A pKi 5.24 5.24 5.24 PDSP Ki database
α2A ADA2A Human Adrenoceptors A pKi 5.7 5.7 5.7 Guide to Pharmacology
α2B ADA2B Human Adrenoceptors A pKi 5.46 5.46 5.46 PDSP Ki database
α2B ADA2B Human Adrenoceptors A pKi 5.7 5.7 5.7 Guide to Pharmacology
α2C ADA2C Human Adrenoceptors A pKi 5.0 5.0 5.0 PDSP Ki database
α2C ADA2C Human Adrenoceptors A pKi 4.8 5.35 5.9 Guide to Pharmacology
α2A ADA2A Pig Adrenoceptors A pKi 5.5 5.5 5.5 PDSP Ki database
α2A ADA2A Mouse Adrenoceptors A pKi 5.62 5.62 5.62 PDSP Ki database
Receptor Activity Source
GTP Uniprot Species Family Class Type Min Avg Max Database
TSH TSHR Human Glycoprotein hormone A Potency 4.5 4.5 4.5 ChEMBL
M1 ACM1 Rat Acetylcholine (muscarinic) A Potency 4.75 4.9 5.05 ChEMBL