null

SMILES OC[C@H](NC(=O)[C@H](Cc1ccc(OP(O)(O)=O)cc1)NC(=O)Cc1ccccc1)c1nc(Cc2ccc(Cl)c(Cl)c2)no1

InChI Key InChIKey=OBKJDPLCBADFLQ-ZEQRLZLVSA-N

  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 3 hits for monomerid = 5105   

TargetTyrosine-protein kinase ZAP-70(Homo sapiens (Human))
ARIAD Pharmaceuticals, Inc.

LigandPNGBDBM5105(1,2,4-Oxadiazole Analogue 15b | 4-[(2S)-2-{[(1S)-1...)copy SMILEScopy InChI
Affinity DataIC50: 2.00E+3nMAssay Description:Fluorescence polarization competitive binding assays were used to measure the IC50s of compounds binding to the different SH2 domains. The difference...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q27D2SBPPubMed
TargetGrowth factor receptor-bound protein 2(Homo sapiens (Human))
ARIAD Pharmaceuticals, Inc.

LigandPNGBDBM5105(1,2,4-Oxadiazole Analogue 15b | 4-[(2S)-2-{[(1S)-1...)copy SMILEScopy InChI
Affinity DataIC50: 2.63E+5nMAssay Description:Fluorescence polarization competitive binding assays were used to measure the IC50s of compounds binding to the different SH2 domains. The difference...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q27D2SBPPubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
ARIAD Pharmaceuticals, Inc.

LigandPNGBDBM5105(1,2,4-Oxadiazole Analogue 15b | 4-[(2S)-2-{[(1S)-1...)copy SMILEScopy InChI
Affinity DataIC50: 3.50E+4nMAssay Description:Fluorescence polarization competitive binding assays were used to measure the IC50s of compounds binding to the different SH2 domains. The difference...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q27D2SBPPubMed