BDBM50356307 CHEMBL1911231

SMILES: CCc1ccc(cc1)C(=O)Nc1ccc(cc1)S(=O)(=O)NC(N)=N

InChI Key: InChIKey=OPWMXDRPYRMRMZ-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 = 50356307   

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
Acrosin (Homo sapiens (Human))	BDBM50356307 (CHEMBL1911231) Show SMILES CCc1ccc(cc1)C(=O)Nc1ccc(cc1)S(=O)(=O)NC(N)=N Show InChI InChI=1S/C16H18N4O3S/c1-2-11-3-5-12(6-4-11)15(21)19-13-7-9-14(10-8-13)24(22,23)20-16(17)18/h3-10H,2H2,1H3,(H,19,21)(H4,17,18,20)	Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	2.10E+5	n/a	n/a	n/a	n/a	n/a	n/a
Second Military Medical University Curated by ChEMBL					Assay Description Inhibition of acrosin activity in human spermatozoa using N-alpha-benzoyl-DL-arginine para-nitroanilide-HCI as a substrate after 3 hrs by spectrophot...				Bioorg Med Chem Lett 21: 6674-7 (2011) Article DOI: 10.1016/j.bmcl.2011.09.060 BindingDB Entry DOI: 10.7270/Q2TT4RBF
					More data for this Ligand-Target Pair