BDBM50234133 CHEMBL4087128

SMILES [H][C@@]1(O[C@H]2[C@H](O)[C@@H](NS([O-])(=O)=O)[C@@H](OC)O[C@@H]2COS([O-])(=O)=O)O[C@@H](C([O-])=O)[C@@]([H])(O[C@@H]2O[C@H](COS([O-])(=O)=O)[C@@]([H])(O[C@@H]3O[C@H](C([O-])=O)[C@@]([H])(O[C@H]4O[C@H](COS([O-])(=O)=O)[C@@H](O)[C@H](O)[C@H]4N)[C@H](O)[C@H]3O)[C@H](OS([O-])(=O)=O)[C@H]2N)[C@H](O)[C@H]1OS([O-])(=O)=O

InChI Key InChIKey=DPAMEDAMXPKHCQ-UHFFFAOYSA-F

Data  1 IC50

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 1 hit for monomerid = 50234133   

TargetCoagulation factor X(Human)
Nankai University

Curated by ChEMBL
LigandPNGBDBM50234133(CHEMBL4087128)
Affinity DataIC50: 966nMAssay Description:Inhibition of factor 10a (unknown origin) using S-2765 as substrate preincubated with AT-3 followed by factor 10a addition for 60 secs and subsequent...More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/11/2019
Entry Details Article
PubMed