CHEMBL123349


SMILES CN1CCc2cccc(Cl)c2CC1
InChIKey RSRUDTPYRBLHEO-UHFFFAOYSA-N

Chemical properties

Hydrogen bond acceptors 1
Hydrogen bond donors 0
Rotatable bonds 0
Molecular weight (Da) 195.1

Drug properties

Molecular type Small molecule
Physiological/Surrogate Surrogate
Approved drug No

Database connections

Ligand site mutations α2A

Sankey plot

Compound is not listed as a drug.

Bioactivities

Receptor Activity Source
GTP Uniprot Species Family Class Type Min Avg Max Database
α1B ADA1B Human Adrenoceptors A pKi 6.31 6.31 6.31 ChEMBL
α1D ADA1D Human Adrenoceptors A pKi 6.9 6.9 6.9 ChEMBL
α2C ADA2C Human Adrenoceptors A pKi 7.7 7.7 7.7 ChEMBL
α1A ADA1A Human Adrenoceptors A pKi 6.35 6.35 6.35 ChEMBL
5-HT1A 5HT1A Rat 5-Hydroxytryptamine A pKi 7.0 7.0 7.0 ChEMBL
α2C ADA2C Human Adrenoceptors A pKi 8.57 8.57 8.57 PDSP Ki database
α2A ADA2A Human Adrenoceptors A pKi 8.62 8.62 8.62 PDSP Ki database
α2B ADA2B Rat Adrenoceptors A pKi 8.74 8.74 8.74 PDSP Ki database
α2A ADA2A Human Adrenoceptors A pKi 8.03 8.03 8.03 ChEMBL
α2B ADA2B Human Adrenoceptors A pKi 7.8 7.8 7.8 ChEMBL
Receptor Activity Source
GTP Uniprot Species Family Class Type Min Avg Max Database
M1 ACM1 Rat Acetylcholine (muscarinic) A Potency 4.65 4.7 4.75 ChEMBL
NPS NPSR1 Human Neuropeptide S A Potency 4.6 4.6 4.6 ChEMBL