BDBM50296259 (S)-2-cyano-1-(naphthalen-2-yl)-3-(2-oxo-1-(2-oxo-2-(pyrrolidin-1-yl)ethyl)azepan-3-yl)guanidine::CHEMBL560714

SMILES: O=C(CN1CCCC[C@H](NC(NC#N)=Nc2ccc3ccccc3c2)C1=O)N1CCCC1

InChI Key: InChIKey=PTTOJPLBWDWABA-NRFANRHFSA-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 = 50296259   

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))	BDBM50296259 ((S)-2-cyano-1-(naphthalen-2-yl)-3-(2-oxo-1-(2-oxo-...) Show SMILES O=C(CN1CCCC[C@H](NC(NC#N)=Nc2ccc3ccccc3c2)C1=O)N1CCCC1 |r,w:14.14| Show InChI InChI=1S/C24H28N6O2/c25-17-26-24(27-20-11-10-18-7-1-2-8-19(18)15-20)28-21-9-3-4-14-30(23(21)32)16-22(31)29-12-5-6-13-29/h1-2,7-8,10-11,15,21H,3-6,9,12-14,16H2,(H2,26,27,28)/t21-/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	780	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-mediated cleavage of synthetic substrate S-2222				Bioorg Med Chem Lett 19: 4034-41 (2009) Article DOI: 10.1016/j.bmcl.2009.06.014 BindingDB Entry DOI: 10.7270/Q2TQ61KM
					More data for this Ligand-Target Pair