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
Physiological/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 4.9 5.3 5.7 Guide to Pharmacology
α2B ADA2B Human Adrenoceptors A pKi 5.2 5.45 5.7 Guide to Pharmacology
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
α2B ADA2B Human Adrenoceptors A pKi 5.46 5.46 5.46 PDSP Ki database
α2A ADA2A Human Adrenoceptors A pKi 5.24 5.24 5.24 PDSP Ki database
α2C ADA2C Human Adrenoceptors A pKi 5.0 5.0 5.0 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
α2A ADA2A Human Adrenoceptors A pEC50 6.1000000000000005 6.1 6.1 Guide to Pharmacology
α2A ADA2A Human Adrenoceptors A pIC50 6.5 6.5 6.5 Guide to Pharmacology
α2B ADA2B Human Adrenoceptors A pEC50 6.9 6.9 6.9 Guide to Pharmacology
α2B ADA2B Human Adrenoceptors A pIC50 7.7 7.7 7.7 Guide to Pharmacology
α2C ADA2C Human Adrenoceptors A pEC50 7.1 7.1 7.1 Guide to Pharmacology
α2C ADA2C Human Adrenoceptors A pIC50 6.8 6.8 6.8 Guide to Pharmacology
M1 ACM1 Rat Acetylcholine (muscarinic) A Potency 4.75 4.9 5.05 ChEMBL
TSH TSHR Human Glycoprotein hormone A Potency 4.5 4.5 4.5 ChEMBL