BDBM50397875 CHEMBL2179496

SMILES: N#Cc1ccc2n(CCCc3nc4ccccc4[nH]3)c3CCCCc3c2c1

InChI Key: InChIKey=INZZLTCMGWYMQT-UHFFFAOYSA-N

Data: 1 IC50

Find this compound or compounds like it in BindingDB or PDB:

Substructure Similarity at least:  must be >=0.5 Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 1 hit for monomerid = 50397875   

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
Scavenger receptor class B member 1 (Homo sapiens (Human))	BDBM50397875 (CHEMBL2179496) Show SMILES N#Cc1ccc2n(CCCc3nc4ccccc4[nH]3)c3CCCCc3c2c1 Show InChI InChI=1S/C23H22N4/c24-15-16-11-12-22-18(14-16)17-6-1-4-9-21(17)27(22)13-5-10-23-25-19-7-2-3-8-20(19)26-23/h2-3,7-8,11-12,14H,1,4-6,9-10,13H2,(H,25,26)	KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	50	n/a	n/a	n/a	n/a	n/a	n/a
iTherX Pharmaceuticals, Inc. Curated by ChEMBL					Assay Description Inhibition of human SRB1-mediated Hepatitis C virus genotype 2a entry into human HuH7.5 cells by luciferase reporter gene assay				Bioorg Med Chem Lett 22: 4955-61 (2012) Article DOI: 10.1016/j.bmcl.2012.06.038 BindingDB Entry DOI: 10.7270/Q20R9QH1
					More data for this Ligand-Target Pair