BDBM50276157 Alternariol 5-O-Methyl Ether::CHEMBL483526
SMILES COc1cc(O)c2c(c1)c1c(C)cc(O)cc1oc2=O
InChI Key InChIKey=LCSDQFNUYFTXMT-UHFFFAOYSA-N
Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB
Found 29 hits for monomerid = 50276157
Affinity DataIC50: 3.67E+4nMAssay Description:Inhibition of recombinant CK2alpha1More data for this Ligand-Target Pair
Affinity DataIC50: 8.00E+4nMAssay Description:Inhibition of human MAO-BMore data for this Ligand-Target Pair
Affinity DataIC50: 1.71E+3nMAssay Description:Inhibition of human MAO-AMore data for this Ligand-Target Pair
TargetPlatelet-derived growth factor receptor beta(Human)
Heinrich-Heine-Universit£T
Curated by ChEMBL
Heinrich-Heine-Universit£T
Curated by ChEMBL
Affinity DataIC50: 6.61E+3nMAssay Description:Inhibition of recombinant PDGFRbetaMore data for this Ligand-Target Pair
Affinity DataIC50: 9.18E+3nMAssay Description:Inhibition of recombinant SAKMore data for this Ligand-Target Pair
Affinity DataIC50: 3.67E+3nMAssay Description:Inhibition of recombinant FLT3More data for this Ligand-Target Pair
TargetVascular endothelial growth factor receptor 2(Human)
Heinrich-Heine-Universit£T
Curated by ChEMBL
Heinrich-Heine-Universit£T
Curated by ChEMBL
Affinity DataIC50: 4.04E+3nMAssay Description:Inhibition of recombinant VEGFR2More data for this Ligand-Target Pair
Affinity DataIC50: 5.14E+3nMAssay Description:Inhibition of recombinant EPHB4More data for this Ligand-Target Pair
Affinity DataIC50: 4.77E+3nMAssay Description:Inhibition of recombinant Aurora BMore data for this Ligand-Target Pair
Affinity DataIC50: 6.24E+3nMAssay Description:Inhibition of recombinant EGFRMore data for this Ligand-Target Pair
Affinity DataIC50: 3.01E+4nMAssay Description:Inhibition of recombinant PLK1More data for this Ligand-Target Pair
Affinity DataIC50: 2.90E+4nMAssay Description:Inhibition of recombinant INSRMore data for this Ligand-Target Pair
TargetCyclin-dependent kinase 4/G1/S-specific cyclin-D1(Human)
Heinrich-Heine-Universit£T
Curated by ChEMBL
Heinrich-Heine-Universit£T
Curated by ChEMBL
Affinity DataIC50: 7.71E+3nMAssay Description:Inhibition of recombinant CDK4/CycD1More data for this Ligand-Target Pair
Affinity DataIC50: 1.32E+4nMAssay Description:Inhibition of recombinant CDK2/CycAMore data for this Ligand-Target Pair
Affinity DataIC50: 1.71E+3nMAssay Description:Inhibition of recombinant human MAO-A using kynuramine as substrate incubated for 10 mins by spectrophotometric methodMore data for this Ligand-Target Pair
Affinity DataIC50: 1.83E+4nMAssay Description:Inhibition of recombinant Aurora AMore data for this Ligand-Target Pair
Affinity DataIC50: 1.46E+4nMAssay Description:Inhibition of recombinant ARK5More data for this Ligand-Target Pair
TargetMitogen-activated protein kinase kinase kinase 8(Human)
Heinrich-Heine-Universit£T
Curated by ChEMBL
Heinrich-Heine-Universit£T
Curated by ChEMBL
Affinity DataIC50: 9.54E+3nMAssay Description:Inhibition of recombinant COTMore data for this Ligand-Target Pair
Affinity DataIC50: 1.76E+4nMAssay Description:Inhibition of recombinant B-RAF-V600E mutantMore data for this Ligand-Target Pair
TargetVascular endothelial growth factor receptor 3(Human)
Heinrich-Heine-Universit£T
Curated by ChEMBL
Heinrich-Heine-Universit£T
Curated by ChEMBL
Affinity DataIC50: 3.52E+3nMAssay Description:Inhibition of recombinant VEGFR3More data for this Ligand-Target Pair
Affinity DataIC50: 4.40E+3nMAssay Description:Inhibition of recombinant SRCMore data for this Ligand-Target Pair
Affinity DataIC50: 6.24E+3nMAssay Description:Inhibition of recombinant IGF1RMore data for this Ligand-Target Pair
Affinity DataIC50: 2.90E+4nMAssay Description:Inhibition of recombinant AKT1More data for this Ligand-Target Pair
Affinity DataIC50: 3.26E+4nMAssay Description:Inhibition of recombinant FAKMore data for this Ligand-Target Pair
Affinity DataIC50: 1.65E+4nMAssay Description:Inhibition of recombinant ERBB2More data for this Ligand-Target Pair
Affinity DataIC50: 3.67E+4nMAssay Description:Inhibition of recombinant METMore data for this Ligand-Target Pair
Affinity DataIC50: 1.28E+4nMAssay Description:Inhibition of recombinant TIE2More data for this Ligand-Target Pair
Affinity DataIC50: 1.71E+3nMAssay Description:Inhibition of human recombinant MAOA using kynuramine as substrate preincubated for 30 mins followed by substrate additionMore data for this Ligand-Target Pair
Affinity DataKi: 340nMAssay Description:Mixed type inhibition of human MAO-A assessed as inhibition constant by Lineweaver-Burk plot analysisMore data for this Ligand-Target Pair