BDBM50397883 CHEMBL2179489

SMILES: Cc1cc(C)nc(OCCCn2c3CCCCc3c3cc(ccc23)S(C)(=O)=O)n1

InChI Key: InChIKey=KXXPUAQHPRBNNR-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 = 50397883   

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))	BDBM50397883 (CHEMBL2179489) Show SMILES Cc1cc(C)nc(OCCCn2c3CCCCc3c3cc(ccc23)S(C)(=O)=O)n1 Show InChI InChI=1S/C22H27N3O3S/c1-15-13-16(2)24-22(23-15)28-12-6-11-25-20-8-5-4-7-18(20)19-14-17(29(3,26)27)9-10-21(19)25/h9-10,13-14H,4-8,11-12H2,1-3H3	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