BDBM50358856 CHEMBL1923441

SMILES: Cc1cc2cc(ccc2o1)S(=O)(=O)N[C@H]1CCCN(CC(=O)N2CCCC2)C1=O

InChI Key: InChIKey=MZBBGGHIUUATCY-KRWDZBQOSA-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 = 50358856   

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
Coagulation factor X (Homo sapiens (Human))	BDBM50358856 (CHEMBL1923441) Show SMILES Cc1cc2cc(ccc2o1)S(=O)(=O)N[C@H]1CCCN(CC(=O)N2CCCC2)C1=O |r| Show InChI InChI=1S/C20H25N3O5S/c1-14-11-15-12-16(6-7-18(15)28-14)29(26,27)21-17-5-4-10-23(20(17)25)13-19(24)22-8-2-3-9-22/h6-7,11-12,17,21H,2-5,8-10,13H2,1H3/t17-/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt UniProtKB/TrEMBL B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	1.11E+3	n/a	n/a	n/a	n/a	n/a	n/a
Bristol-Myers Squibb Company Curated by ChEMBL					Assay Description Inhibition of human factor 10a using phenyl-Ile-Glu-Gly-Arg-pNA as substrate preincubated for 3 mins prior to substrate addition by spectrophotometry				Bioorg Med Chem Lett 21: 7516-21 (2011) Article DOI: 10.1016/j.bmcl.2011.06.098 BindingDB Entry DOI: 10.7270/Q2MK6DBS
					More data for this Ligand-Target Pair