BDBM50479264 Alternariol 5-O-Sulfate::CHEMBL483525
SMILES Cc1cc(O)cc2oc(=O)c3c(O)cc(OS(O)(=O)=O)cc3c12
InChI Key InChIKey=IOBDCMVQCAWFQQ-UHFFFAOYSA-N
Data 24 IC50
Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB
Found 24 hits for monomerid = 50479264
TargetSerine/threonine-protein kinase PLK4(Homo sapiens (Human))
Heinrich-Heine-Universit£T
Curated by ChEMBL
Heinrich-Heine-Universit£T
Curated by ChEMBL
Affinity DataIC50: 1.12E+3nMAssay Description:Inhibition of recombinant SAKMore data for this Ligand-Target Pair
TargetHepatocyte growth factor receptor(Homo sapiens (Human))
Heinrich-Heine-Universit£T
Curated by ChEMBL
Heinrich-Heine-Universit£T
Curated by ChEMBL
Affinity DataIC50: 2.24E+4nMAssay Description:Inhibition of recombinant METMore data for this Ligand-Target Pair
TargetVascular endothelial growth factor receptor 2(Homo sapiens (Human))
Heinrich-Heine-Universit£T
Curated by ChEMBL
Heinrich-Heine-Universit£T
Curated by ChEMBL
Affinity DataIC50: 2.06E+3nMAssay Description:Inhibition of recombinant VEGFR2More data for this Ligand-Target Pair
TargetReceptor-type tyrosine-protein kinase FLT3(Homo sapiens (Human))
Heinrich-Heine-Universit£T
Curated by ChEMBL
Heinrich-Heine-Universit£T
Curated by ChEMBL
Affinity DataIC50: 975nMAssay Description:Inhibition of recombinant FLT3More data for this Ligand-Target Pair
TargetSerine/threonine-protein kinase B-raf(Homo sapiens (Human))
Heinrich-Heine-Universit£T
Curated by ChEMBL
Heinrich-Heine-Universit£T
Curated by ChEMBL
Affinity DataIC50: 2.18E+3nMAssay Description:Inhibition of recombinant B-RAF-V600E mutantMore data for this Ligand-Target Pair
TargetNUAK family SNF1-like kinase 1(Homo sapiens (Human))
Heinrich-Heine-Universit£T
Curated by ChEMBL
Heinrich-Heine-Universit£T
Curated by ChEMBL
Affinity DataIC50: 2.21E+3nMAssay Description:Inhibition of recombinant ARK5More data for this Ligand-Target Pair
TargetEpidermal growth factor receptor(Homo sapiens (Human))
Heinrich-Heine-Universit£T
Curated by ChEMBL
Heinrich-Heine-Universit£T
Curated by ChEMBL
Affinity DataIC50: 1.24E+4nMAssay Description:Inhibition of recombinant EGFRMore data for this Ligand-Target Pair
TargetPlatelet-derived growth factor receptor beta(Homo sapiens (Human))
Heinrich-Heine-Universit£T
Curated by ChEMBL
Heinrich-Heine-Universit£T
Curated by ChEMBL
Affinity DataIC50: 3.84E+3nMAssay Description:Inhibition of recombinant PDGFRbetaMore data for this Ligand-Target Pair
TargetSerine/threonine-protein kinase PLK1(Homo sapiens (Human))
Heinrich-Heine-Universit£T
Curated by ChEMBL
Heinrich-Heine-Universit£T
Curated by ChEMBL
Affinity DataIC50: 1.30E+4nMAssay Description:Inhibition of recombinant PLK1More data for this Ligand-Target Pair
TargetCasein kinase II subunit alpha(Homo sapiens (Human))
Heinrich-Heine-Universit£T
Curated by ChEMBL
Heinrich-Heine-Universit£T
Curated by ChEMBL
Affinity DataIC50: 5.91E+3nMAssay Description:Inhibition of recombinant CK2alpha1More data for this Ligand-Target Pair
TargetVascular endothelial growth factor receptor 3(Homo sapiens (Human))
Heinrich-Heine-Universit£T
Curated by ChEMBL
Heinrich-Heine-Universit£T
Curated by ChEMBL
Affinity DataIC50: 5.02E+3nMAssay Description:Inhibition of recombinant VEGFR3More data for this Ligand-Target Pair
Affinity DataIC50: 8.57E+3nMAssay Description:Inhibition of recombinant INSRMore data for this Ligand-Target Pair
TargetRAC-alpha serine/threonine-protein kinase(Homo sapiens (Human))
Heinrich-Heine-Universit£T
Curated by ChEMBL
Heinrich-Heine-Universit£T
Curated by ChEMBL
Affinity DataIC50: >2.95E+4nMAssay Description:Inhibition of recombinant AKT1More data for this Ligand-Target Pair
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
Heinrich-Heine-Universit£T
Curated by ChEMBL
Heinrich-Heine-Universit£T
Curated by ChEMBL
Affinity DataIC50: 1.65E+4nMAssay Description:Inhibition of recombinant SRCMore data for this Ligand-Target Pair
TargetMitogen-activated protein kinase kinase kinase 8(Homo sapiens (Human))
Heinrich-Heine-Universit£T
Curated by ChEMBL
Heinrich-Heine-Universit£T
Curated by ChEMBL
Affinity DataIC50: 2.21E+4nMAssay Description:Inhibition of recombinant COTMore data for this Ligand-Target Pair
Affinity DataIC50: 650nMAssay Description:Inhibition of recombinant Aurora BMore data for this Ligand-Target Pair
Affinity DataIC50: 2.48E+3nMAssay Description:Inhibition of recombinant CDK2/CycAMore data for this Ligand-Target Pair
TargetCyclin-dependent kinase 4/G1/S-specific cyclin-D1(Homo sapiens (Human))
Heinrich-Heine-Universit£T
Curated by ChEMBL
Heinrich-Heine-Universit£T
Curated by ChEMBL
Affinity DataIC50: 7.98E+3nMAssay Description:Inhibition of recombinant CDK4/CycD1More data for this Ligand-Target Pair
Affinity DataIC50: 1.15E+3nMAssay Description:Inhibition of recombinant Aurora AMore data for this Ligand-Target Pair
TargetReceptor tyrosine-protein kinase erbB-2(Homo sapiens (Human))
Heinrich-Heine-Universit£T
Curated by ChEMBL
Heinrich-Heine-Universit£T
Curated by ChEMBL
Affinity DataIC50: 2.48E+4nMAssay Description:Inhibition of recombinant ERBB2More data for this Ligand-Target Pair
Affinity DataIC50: 6.20E+3nMAssay Description:Inhibition of recombinant FAKMore data for this Ligand-Target Pair
Affinity DataIC50: 2.01E+4nMAssay Description:Inhibition of recombinant TIE2More data for this Ligand-Target Pair
TargetInsulin-like growth factor 1 receptor(Homo sapiens (Human))
Heinrich-Heine-Universit£T
Curated by ChEMBL
Heinrich-Heine-Universit£T
Curated by ChEMBL
Affinity DataIC50: 1.44E+4nMAssay Description:Inhibition of recombinant IGF1RMore data for this Ligand-Target Pair
Affinity DataIC50: 9.16E+3nMAssay Description:Inhibition of recombinant EPHB4More data for this Ligand-Target Pair