BDBM13289 2-(4-carbamimidoyl-2-{[(3S)-3-[(7-methoxynaphthalene-2-)sulfonamido]-2-oxopyrrolidin-1-yl]methyl}phenoxy)acetic acid::Sulfonamidopyrrolidinone 28::{4-(Aminoiminomethyl)-2-[3-(S)-(7-methoxynaphthalen-2-ylsulfonylamino)-2-oxopyrrolidin-1-ylmethyl]phenoxy}acetic Acid

SMILES: COc1ccc2ccc(cc2c1)S(=O)(=O)N[C@H]1CCN(Cc2cc(ccc2OCC(O)=O)C(N)=N)C1=O

InChI Key: InChIKey=LPWNNXLXMMTLKO-NRFANRHFSA-N

Data: 2 KI

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 2 hits for monomerid = 13289   

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))	BDBM13289 (2-(4-carbamimidoyl-2-{[(3S)-3-[(7-methoxynaphthale...) Show SMILES COc1ccc2ccc(cc2c1)S(=O)(=O)N[C@H]1CCN(Cc2cc(ccc2OCC(O)=O)C(N)=N)C1=O |r| Show InChI InChI=1S/C25H26N4O7S/c1-35-19-5-2-15-3-6-20(12-17(15)11-19)37(33,34)28-21-8-9-29(25(21)32)13-18-10-16(24(26)27)4-7-22(18)36-14-23(30)31/h2-7,10-12,21,28H,8-9,13-14H2,1H3,(H3,26,27)(H,30,31)/t21-/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt UniProtKB/TrEMBL B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	1.30E+3	-7.94	n/a	n/a	n/a	n/a	n/a	7.5	22
Rhone-Poulenc Rorer					Assay Description The enzyme reactions were initiated by the addition of substrate, and the color developed from the release of p-nitroanilide from each chromogenic su...				J Med Chem 42: 3572-87 (1999) Article DOI: 10.1021/jm990041+ BindingDB Entry DOI: 10.7270/Q2KW5D9R
					More data for this Ligand-Target Pair
Trypsin (Bos taurus (bovine))	BDBM13289 (2-(4-carbamimidoyl-2-{[(3S)-3-[(7-methoxynaphthale...) Show SMILES COc1ccc2ccc(cc2c1)S(=O)(=O)N[C@H]1CCN(Cc2cc(ccc2OCC(O)=O)C(N)=N)C1=O |r| Show InChI InChI=1S/C25H26N4O7S/c1-35-19-5-2-15-3-6-20(12-17(15)11-19)37(33,34)28-21-8-9-29(25(21)32)13-18-10-16(24(26)27)4-7-22(18)36-14-23(30)31/h2-7,10-12,21,28H,8-9,13-14H2,1H3,(H3,26,27)(H,30,31)/t21-/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	>2.90E+3	>-7.47	n/a	n/a	n/a	n/a	n/a	7.5	22
Rhone-Poulenc Rorer					Assay Description The enzyme reactions were initiated by the addition of substrate, and the color developed from the release of p-nitroanilide from each chromogenic su...				J Med Chem 42: 3572-87 (1999) Article DOI: 10.1021/jm990041+ BindingDB Entry DOI: 10.7270/Q2KW5D9R
					More data for this Ligand-Target Pair