BDBM50479263 Desmethylaltenusin
SMILES Cc1cc(O)c(O)cc1-c1cc(O)cc(O)c1C(O)=O
InChI Key InChIKey=LACFACJZTLCIGY-UHFFFAOYSA-N
Data 24 IC50
Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB
Found 24 hits for monomerid = 50479263
Affinity DataIC50: 1.52E+4nMAssay Description:Inhibition of recombinant EGFRMore 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: 2.46E+4nMAssay Description:Inhibition of recombinant VEGFR3More data for this Ligand-Target Pair
Affinity DataIC50: 3.62E+4nMAssay Description:Inhibition of recombinant ERBB2More data for this Ligand-Target Pair
Affinity DataIC50: 9.05E+3nMAssay Description:Inhibition of recombinant METMore data for this Ligand-Target Pair
Affinity DataIC50: 3.62E+4nMAssay Description:Inhibition of recombinant CK2alpha1More 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: 2.09E+4nMAssay Description:Inhibition of recombinant PDGFRbetaMore data for this Ligand-Target Pair
Affinity DataIC50: 3.62E+4nMAssay Description:Inhibition of recombinant CDK2/CycAMore data for this Ligand-Target Pair
Affinity DataIC50: 2.67E+4nMAssay Description:Inhibition of recombinant B-RAF-V600E mutantMore data for this Ligand-Target Pair
Affinity DataIC50: 1.08E+4nMAssay Description:Inhibition of recombinant INSRMore data for this Ligand-Target Pair
Affinity DataIC50: 2.13E+4nMAssay Description:Inhibition of recombinant EPHB4More 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: 1.59E+4nMAssay Description:Inhibition of recombinant CDK4/CycD1More data for this Ligand-Target Pair
Affinity DataIC50: 3.62E+4nMAssay Description:Inhibition of recombinant PLK1More data for this Ligand-Target Pair
Affinity DataIC50: 6.15E+3nMAssay Description:Inhibition of recombinant SAKMore data for this Ligand-Target Pair
Affinity DataIC50: 5.43E+3nMAssay Description:Inhibition of recombinant Aurora BMore data for this Ligand-Target Pair
Affinity DataIC50: 9.77E+3nMAssay Description:Inhibition of recombinant Aurora AMore data for this Ligand-Target Pair
Affinity DataIC50: 9.41E+3nMAssay Description:Inhibition of recombinant ARK5More data for this Ligand-Target Pair
Affinity DataIC50: 3.62E+4nMAssay Description:Inhibition of recombinant AKT1More 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: 3.51E+4nMAssay Description:Inhibition of recombinant COTMore data for this Ligand-Target Pair
Affinity DataIC50: 6.51E+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: 1.37E+4nMAssay Description:Inhibition of recombinant VEGFR2More data for this Ligand-Target Pair
Affinity DataIC50: 1.70E+4nMAssay Description:Inhibition of recombinant SRCMore data for this Ligand-Target Pair
Affinity DataIC50: 8.68E+3nMAssay Description:Inhibition of recombinant IGF1RMore data for this Ligand-Target Pair
Affinity DataIC50: 3.62E+4nMAssay Description:Inhibition of recombinant FAKMore data for this Ligand-Target Pair
Affinity DataIC50: 1.37E+4nMAssay Description:Inhibition of recombinant TIE2More data for this Ligand-Target Pair
