BDBM50357538 CHEMBL1914863

SMILES: CC(C)OC(=O)c1ccc2n(CCCN3C[C@H](C)N[C@H](C)C3)c3ccccc3c2c1

InChI Key: InChIKey=DWQGPIJJNQYVIL-KDURUIRLSA-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 = 50357538   

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))	BDBM50357538 (CHEMBL1914863) Show SMILES CC(C)OC(=O)c1ccc2n(CCCN3C[C@H](C)N[C@H](C)C3)c3ccccc3c2c1 |r| Show InChI InChI=1S/C25H33N3O2/c1-17(2)30-25(29)20-10-11-24-22(14-20)21-8-5-6-9-23(21)28(24)13-7-12-27-15-18(3)26-19(4)16-27/h5-6,8-11,14,17-19,26H,7,12-13,15-16H2,1-4H3/t18-,19+	KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	630	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 293T cells by immunoblotting				Bioorg Med Chem Lett 21: 6852-5 (2011) Article DOI: 10.1016/j.bmcl.2011.09.019 BindingDB Entry DOI: 10.7270/Q2319W93
					More data for this Ligand-Target Pair