BDBM13306 4-Hydroxy-3-[3-(S)-(5-isoxazol-3-ylthiophene-2-ylsulfonylamino)2-oxopyrrolidin-1-ylmethyl]benzamidine::4-hydroxy-3-{[(3S)-3-{[5-(1,2-oxazol-3-yl)thiophene-2-]sulfonamido}-2-oxopyrrolidin-1-yl]methyl}benzene-1-carboximidamide::Sulfonamidopyrrolidinone 20c

SMILES NC(=N)c1ccc(O)c(CN2CC[C@H](NS(=O)(=O)c3ccc(s3)-c3ccon3)C2=O)c1

InChI Key InChIKey=UPZCVHMIYOGCHJ-UHFFFAOYSA-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 = 13306   

TargetCoagulation factor X(Human)
Rhone-Poulenc Rorer

LigandPNGBDBM13306(4-hydroxy-3-{[(3S)-3-{[5-(1,2-oxazol-3-yl)thiophen...)
Affinity DataKi:  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 Depth
Date in BDB:
1/22/2007
Entry Details Article
PubMed
TargetSerine protease 1(Bovine)
Rhone-Poulenc Rorer

LigandPNGBDBM13306(4-hydroxy-3-{[(3S)-3-{[5-(1,2-oxazol-3-yl)thiophen...)
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 Depth
Date in BDB:
1/22/2007
Entry Details Article
PubMed