BDBM50397881 CHEMBL2179491

SMILES: CN(C)S(=O)(=O)CCCn1c2CCCCc2c2cc(ccc12)S(C)(=O)=O

InChI Key: InChIKey=FZLCUDHROXCSKR-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 = 50397881   

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))	BDBM50397881 (CHEMBL2179491) Show SMILES CN(C)S(=O)(=O)CCCn1c2CCCCc2c2cc(ccc12)S(C)(=O)=O Show InChI InChI=1S/C18H26N2O4S2/c1-19(2)26(23,24)12-6-11-20-17-8-5-4-7-15(17)16-13-14(25(3,21)22)9-10-18(16)20/h9-10,13H,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	500	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