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Experimentally measured binding affinity data (IC50) for protein-ligand complexes derived from PDB
Assay data:4302 Active, 250 Activity ≤ 1 nM, 2931 Activity ≤ 1 µM, 4302 Tested
SummaryCompounds, ActiveCompounds, activity ≤ 1 µMPubMed CitationRelated BioAssays by DepositorRelated BioAssays by Target
Inhibition of recombinant BRAF V600E mutant using GSTP1-MEK1 and [gamma-32P]ATP as substrate after 30 mins by scintillation counting
Assay data:8 Active, 8 Activity ≤ 1 µM, 8 Tested
SummaryCompounds, ActiveCompounds, activity ≤ 1 µMPubMed CitationRelated BioAssays by Target
Inhibition of VEGFR2
Inhibition of BRAF V600E mutant in human HT-29 cells assessed as reduction of MRK phosphorylation
Assay data:7 Active, 8 Activity ≤ 1 µM, 8 Tested
Inhibition of VEGFR2 in HUVEC assessed as reduction of VGF-stimulated cell proliferation after 5 days
Assay data:1 Active, 1 Activity ≤ 1 µM, 1 Tested
Inhibition of wild type human BRAF (445 to 726) expressed in Sf9 insect cells
Inhibition of c-RAF
Inhibition of FGFR3
Inhibition of PDGFRbeta
Inhibition of PDGFRalpha
Inhibition of HER2
Assay data:1 Active, 1 Tested
SummaryCompounds, ActivePubMed CitationRelated BioAssays by Target
Inhibition of TIE2
Inhibition of c-Kit
Inhibition of Src
Inhibition of IKKbeta
Inhibition of CDK1
Inhibition of aurora B
Inhibition of p38alpha
Inhibition of MEK1
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