BDBM50362523 CHEMBL1940993

SMILES CC(=O)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](COC(C)=O)O[C@H]([C@H](OC(C)=O)[C@H]2OC(C)=O)n2[se]c3ccccc3c2=O)[C@H](OC(C)=O)[C@@H](OC(C)=O)[C@H]1OC(C)=O

InChI Key InChIKey=QRBQWXYKYOJHCY-CVTNGHOSSA-N

Data  3 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 3 hits for monomerid = 50362523   

TargetProtein kinase C alpha type(Homo sapiens (Human))
Institute Of The Sir Mortimer Jewish General Hospital

Curated by ChEMBL
LigandPNGBDBM50362523(CHEMBL1940993)
Affinity DataIC50:  220nMAssay Description:Inhibition of PKCalphaMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFocal adhesion kinase 1(Homo sapiens (Human))
Institute Of The Sir Mortimer Jewish General Hospital

Curated by ChEMBL
LigandPNGBDBM50362523(CHEMBL1940993)
Affinity DataIC50:  420nMAssay Description:Inhibition of human recombinant full-length FAK using ATP and Poly Glu:Tyr as substrate after 4 hrs by luminescence analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetRAC-alpha serine/threonine-protein kinase(Homo sapiens (Human))
Institute Of The Sir Mortimer Jewish General Hospital

Curated by ChEMBL
LigandPNGBDBM50362523(CHEMBL1940993)
Affinity DataIC50:  830nMAssay Description:Inhibition of AKT-1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed