BDBM13304 4-hydroxy-3-[((3S)-2-oxo-3-{[(5-pyridin-3-ylthien-2-yl)sulfonyl]amino}pyrrolidin-1-yl)methyl]benzenecarboximidamide::4-hydroxy-3-{[(3S)-2-oxo-3-{[5-(pyridin-3-yl)thiophene-2-]sulfonamido}pyrrolidin-1-yl]methyl}benzene-1-carboximidamide::RPR130737::Sulfonamidopyrrolidinone 20b

SMILES NC(=N)c1ccc(O)c(CN2CC[C@H](NS(=O)(=O)c3ccc(s3)-c3cccnc3)C2=O)c1

InChI Key InChIKey=MKXLWSHXRLAPHM-INIZCTEOSA-N

Data  2 KI

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
Find this compound or compounds like it in BindingDB:
   Substructure
Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 13304   

TargetCoagulation factor X(Homo sapiens (Human))
Rhone-Poulenc Rorer

LigandPNGBDBM13304(4-hydroxy-3-[((3S)-2-oxo-3-{[(5-pyridin-3-ylthien-...)
Affinity DataKi:  2nMAssay 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...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSerine protease 1(Bos taurus (bovine))
Rhone-Poulenc Rorer

LigandPNGBDBM13304(4-hydroxy-3-[((3S)-2-oxo-3-{[(5-pyridin-3-ylthien-...)
Affinity DataKi:  2.90E+3nMAssay 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...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed