BDBM13669 2-bromo-3-[2-(2,4-dichlorophenyl)ethoxy]-5-({[1-(pyridin-4-yl)piperidin-4-yl]methyl}carbamoyl)phenyl acetate::3-Oxybenzamide 55

SMILES CC(=O)Oc1cc(cc(OCCc2ccc(Cl)cc2Cl)c1Br)C(=O)NCC1CCN(CC1)c1ccncc1

InChI Key InChIKey=AFXSBHYPZXEQNT-UHFFFAOYSA-N

Data  2 KI

  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 2 hits for monomerid = 13669   

TargetCoagulation factor X(Homo sapiens (Human))
Sanofi-Aventis Deutschland

Curated by ChEMBL
LigandPNGBDBM13669(2-bromo-3-[2-(2,4-dichlorophenyl)ethoxy]-5-({[1-(p...)
Affinity DataKi:  285nMAssay Description:Binding affinity to human factor 10a using S-2765 as substrate preincubated for 15 mins followed by substrate addition measured between 1 and 5 mins ...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCoagulation factor X(Homo sapiens (Human))
Sanofi-Aventis Deutschland

Curated by ChEMBL
LigandPNGBDBM13669(2-bromo-3-[2-(2,4-dichlorophenyl)ethoxy]-5-({[1-(p...)
Affinity DataKi:  285nMAssay Description:The inhibitory effect of test compound for human fXa was determined by using the chromogenic substrates S-2765. The hydrolysis rates of chromogenic s...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed