null

SMILES: CN1CC(CC#N)CC2C1Cc1c(Cl)[nH]c3cccc2c13

InChI Key: InChIKey=JKAHWGPTNVUTNB-UHFFFAOYSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50028672   

Target/Host (Institution)	Ligand	Target/Host Links	Ligand Links	Trg + Lig Links	Ki nM	ΔG° kcal/mole	IC50 nM	Kd nM	EC50/IC50 nM	koff s-1	kon M-1s-1	pH	Temp °C
5-hydroxytryptamine receptor 6 (RAT)	BDBM50028672 ((5-Chloro-7-methyl-4,6,6a,7,8,9,10,10a-octahydro-i...) Show SMILES CN1CC(CC#N)CC2C1Cc1c(Cl)[nH]c3cccc2c13 Show InChI InChI=1S/C17H18ClN3/c1-21-9-10(5-6-19)7-12-11-3-2-4-14-16(11)13(8-15(12)21)17(18)20-14/h2-4,10,12,15,20H,5,7-9H2,1H3	Reactome pathway UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	36.3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Alberta Curated by PDSP Ki Database									Neuropharmacology 33: 275-317 (1994) Article DOI: 10.1016/0028-3908(94)90059-0 BindingDB Entry DOI: 10.7270/Q2M043X2
					More data for this Ligand-Target Pair
5-hydroxytryptamine receptor 6 (RAT)	BDBM50028672 ((5-Chloro-7-methyl-4,6,6a,7,8,9,10,10a-octahydro-i...) Show SMILES CN1CC(CC#N)CC2C1Cc1c(Cl)[nH]c3cccc2c13 Show InChI InChI=1S/C17H18ClN3/c1-21-9-10(5-6-19)7-12-11-3-2-4-14-16(11)13(8-15(12)21)17(18)20-14/h2-4,10,12,15,20H,5,7-9H2,1H3	Reactome pathway UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	36.5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
National Institute of Neurological Disorders and Stroke Curated by PDSP Ki Database									Mol Pharmacol 43: 320-7 (1993) BindingDB Entry DOI: 10.7270/Q2ST7NCG
					More data for this Ligand-Target Pair