null

SMILES CS(=O)(=O)c1ccccc1-c1ccc(NC(=O)[C@H]2C[C@@H](O)CN2C(=O)Nc2ccc(Cl)cc2)c(F)c1

InChI Key InChIKey=SAWKEKRFHJVBDD-XMSQKQJNSA-N

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

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 3 hits for monomerid = 50328728   

TargetCoagulation factor X(Homo sapiens (Human))
Pfizer Global Research and Development,

LigandPNGBDBM50328728((2R,4R)-N1-(4-chlorophenyl)-N2-(3-fluoro-2'-(methy...)copy SMILEScopy InChI
Affinity DataIC50: 0.380nMAssay Description:FXa inhibition were determined by using an inhibition assay.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PZ5799PubMed
TargetCoagulation factor X(Homo sapiens (Human))
Pfizer Global Research and Development,

LigandPNGBDBM50328728((2R,4R)-N1-(4-chlorophenyl)-N2-(3-fluoro-2'-(methy...)copy SMILEScopy InChI
Affinity DataIC50: 0.380nMAssay Description:Inhibition of factor 10aMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2CR5VBBPubMed
TargetCoagulation factor X(Homo sapiens (Human))
Pfizer Global Research and Development,

LigandPNGBDBM50328728((2R,4R)-N1-(4-chlorophenyl)-N2-(3-fluoro-2'-(methy...)copy SMILEScopy InChI
Affinity DataIC50: 6.10nMAssay Description:FXa inhibition were determined by using an inhibition assay.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PZ5799PubMed