Compile Data Set for Download or QSAR
maximum 50k data
Found 29 of ic50 for monomerid = 50576
TargetGlucose-6-phosphate dehydrogenase-6-phosphogluconolactonase(Plasmodium falciparum 3D7)
Burnham Center For Chemical Genomics

Curated by PubChem BioAssay
LigandPNGBDBM50576(2-(4,5-dihydroxy-2-methyl-phenyl)-6-hydroxy-4-meth...)
Affinity DataIC50:  3.75E+3nMAssay Description:Data Source: Sanford-Burnham Center for Chemical Genomics (SBCCG) Source Affiliation: Sanford-Burnham Medical Research Institute (SBMRI, San Diego CA...More data for this Ligand-Target Pair
In DepthDetails PCBioAssay
TargetAurora kinase B(Homo sapiens (Human))
Heinrich-Heine-Universit£T

Curated by ChEMBL
LigandPNGBDBM50576(2-(4,5-dihydroxy-2-methyl-phenyl)-6-hydroxy-4-meth...)
Affinity DataIC50:  3.78E+3nMAssay Description:Inhibition of recombinant Aurora BMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetInduced myeloid leukemia cell differentiation protein Mcl-1(Homo sapiens (Human))
Emory University

Curated by PubChem BioAssay
LigandPNGBDBM50576(2-(4,5-dihydroxy-2-methyl-phenyl)-6-hydroxy-4-meth...)
Affinity DataIC50:  4.15E+3nMAssay Description:NIH Molecular Libraries Screening Centers Network [MLSCN] Emory Chemical Biology Discovery Center in MLSCN Assay provider: Nikolovska-Coleska, Univer...More data for this Ligand-Target Pair
In DepthDetails PCBioAssay
TargetReceptor-type tyrosine-protein kinase FLT3(Homo sapiens (Human))
Heinrich-Heine-Universit£T

Curated by ChEMBL
LigandPNGBDBM50576(2-(4,5-dihydroxy-2-methyl-phenyl)-6-hydroxy-4-meth...)
Affinity DataIC50:  5.51E+3nMAssay Description:Inhibition of recombinant FLT3More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAurora kinase A(Homo sapiens (Human))
Heinrich-Heine-Universit£T

Curated by ChEMBL
LigandPNGBDBM50576(2-(4,5-dihydroxy-2-methyl-phenyl)-6-hydroxy-4-meth...)
Affinity DataIC50:  6.20E+3nMAssay Description:Inhibition of recombinant Aurora AMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSerine/threonine-protein kinase PLK4(Homo sapiens (Human))
Heinrich-Heine-Universit£T

Curated by ChEMBL
LigandPNGBDBM50576(2-(4,5-dihydroxy-2-methyl-phenyl)-6-hydroxy-4-meth...)
Affinity DataIC50:  1.10E+4nMAssay Description:Inhibition of recombinant SAKMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSerine/threonine-protein kinase B-raf(Homo sapiens (Human))
Heinrich-Heine-Universit£T

Curated by ChEMBL
LigandPNGBDBM50576(2-(4,5-dihydroxy-2-methyl-phenyl)-6-hydroxy-4-meth...)
Affinity DataIC50:  1.13E+4nMAssay Description:Inhibition of recombinant B-RAF-V600E mutantMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHepatocyte growth factor receptor(Homo sapiens (Human))
Heinrich-Heine-Universit£T

Curated by ChEMBL
LigandPNGBDBM50576(2-(4,5-dihydroxy-2-methyl-phenyl)-6-hydroxy-4-meth...)
Affinity DataIC50:  1.48E+4nMAssay Description:Inhibition of recombinant METMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCyclin-dependent kinase 4/G1/S-specific cyclin-D1(Homo sapiens (Human))
Heinrich-Heine-Universit£T

Curated by ChEMBL
LigandPNGBDBM50576(2-(4,5-dihydroxy-2-methyl-phenyl)-6-hydroxy-4-meth...)
Affinity DataIC50:  1.55E+4nMAssay Description:Inhibition of recombinant CDK4/CycD1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetInsulin-like growth factor 1 receptor(Homo sapiens (Human))
Heinrich-Heine-Universit£T

Curated by ChEMBL
LigandPNGBDBM50576(2-(4,5-dihydroxy-2-methyl-phenyl)-6-hydroxy-4-meth...)
Affinity DataIC50:  1.68E+4nMAssay Description:Inhibition of recombinant IGF1RMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetVascular endothelial growth factor receptor 2(Homo sapiens (Human))
Heinrich-Heine-Universit£T

Curated by ChEMBL
LigandPNGBDBM50576(2-(4,5-dihydroxy-2-methyl-phenyl)-6-hydroxy-4-meth...)
Affinity DataIC50:  1.72E+4nMAssay Description:Inhibition of recombinant VEGFR2More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetInsulin receptor(Homo sapiens (Human))
Heinrich-Heine-Universit£T

Curated by ChEMBL
LigandPNGBDBM50576(2-(4,5-dihydroxy-2-methyl-phenyl)-6-hydroxy-4-meth...)
Affinity DataIC50:  1.92E+4nMAssay Description:Inhibition of recombinant INSRMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGlucose-6-phosphate dehydrogenase-6-phosphogluconolactonase(Plasmodium falciparum 3D7)
Burnham Center For Chemical Genomics

Curated by PubChem BioAssay
LigandPNGBDBM50576(2-(4,5-dihydroxy-2-methyl-phenyl)-6-hydroxy-4-meth...)
Affinity DataIC50:  1.94E+4nMAssay Description:Data Source: Sanford-Burnham Center for Chemical Genomics (SBCCG) Source Affiliation: Sanford-Burnham Medical Research Institute (SBMRI, San Diego CA...More data for this Ligand-Target Pair
In DepthDetails PCBioAssay
TargetPlatelet-derived growth factor receptor beta(Homo sapiens (Human))
Heinrich-Heine-Universit£T

Curated by ChEMBL
LigandPNGBDBM50576(2-(4,5-dihydroxy-2-methyl-phenyl)-6-hydroxy-4-meth...)
Affinity DataIC50:  2.03E+4nMAssay Description:Inhibition of recombinant PDGFRbetaMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetNUAK family SNF1-like kinase 1(Homo sapiens (Human))
Heinrich-Heine-Universit£T

Curated by ChEMBL
LigandPNGBDBM50576(2-(4,5-dihydroxy-2-methyl-phenyl)-6-hydroxy-4-meth...)
Affinity DataIC50:  2.27E+4nMAssay Description:Inhibition of recombinant ARK5More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSerine/threonine-protein kinase PLK1(Homo sapiens (Human))
Heinrich-Heine-Universit£T

Curated by ChEMBL
LigandPNGBDBM50576(2-(4,5-dihydroxy-2-methyl-phenyl)-6-hydroxy-4-meth...)
Affinity DataIC50:  2.44E+4nMAssay Description:Inhibition of recombinant PLK1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
Heinrich-Heine-Universit£T

Curated by ChEMBL
LigandPNGBDBM50576(2-(4,5-dihydroxy-2-methyl-phenyl)-6-hydroxy-4-meth...)
Affinity DataIC50:  2.85E+4nMAssay Description:Inhibition of recombinant SRCMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMitogen-activated protein kinase kinase kinase 8(Homo sapiens (Human))
Heinrich-Heine-Universit£T

Curated by ChEMBL
LigandPNGBDBM50576(2-(4,5-dihydroxy-2-methyl-phenyl)-6-hydroxy-4-meth...)
Affinity DataIC50:  3.03E+4nMAssay Description:Inhibition of recombinant COTMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGlucose-6-phosphate 1-dehydrogenase(Homo sapiens (Human))
Burnham Center For Chemical Genomics

Curated by PubChem BioAssay
LigandPNGBDBM50576(2-(4,5-dihydroxy-2-methyl-phenyl)-6-hydroxy-4-meth...)
Affinity DataIC50:  3.10E+4nMAssay Description:Data Source: Sanford-Burnham Center for Chemical Genomics (SBCCG) Source Affiliation: Sanford-Burnham Medical Research Institute (SBMRI, San Diego CA...More data for this Ligand-Target Pair
In DepthDetails PCBioAssay
TargetEphrin type-B receptor 4(Homo sapiens (Human))
Heinrich-Heine-Universit£T

Curated by ChEMBL
LigandPNGBDBM50576(2-(4,5-dihydroxy-2-methyl-phenyl)-6-hydroxy-4-meth...)
Affinity DataIC50:  3.23E+4nMAssay Description:Inhibition of recombinant EPHB4More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAngiopoietin-1 receptor(Homo sapiens (Human))
Heinrich-Heine-Universit£T

Curated by ChEMBL
LigandPNGBDBM50576(2-(4,5-dihydroxy-2-methyl-phenyl)-6-hydroxy-4-meth...)
Affinity DataIC50:  3.37E+4nMAssay Description:Inhibition of recombinant TIE2More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetEpidermal growth factor receptor(Homo sapiens (Human))
Heinrich-Heine-Universit£T

Curated by ChEMBL
LigandPNGBDBM50576(2-(4,5-dihydroxy-2-methyl-phenyl)-6-hydroxy-4-meth...)
Affinity DataIC50:  3.37E+4nMAssay Description:Inhibition of recombinant EGFRMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFocal adhesion kinase 1(Homo sapiens (Human))
Heinrich-Heine-Universit£T

Curated by ChEMBL
LigandPNGBDBM50576(2-(4,5-dihydroxy-2-methyl-phenyl)-6-hydroxy-4-meth...)
Affinity DataIC50: >3.44E+4nMAssay Description:Inhibition of recombinant FAKMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCyclin-dependent kinase 2(Homo sapiens (Human))
Heinrich-Heine-Universit£T

Curated by ChEMBL
LigandPNGBDBM50576(2-(4,5-dihydroxy-2-methyl-phenyl)-6-hydroxy-4-meth...)
Affinity DataIC50: >3.44E+4nMAssay Description:Inhibition of recombinant CDK2/CycAMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCasein kinase II subunit alpha(Homo sapiens (Human))
Heinrich-Heine-Universit£T

Curated by ChEMBL
LigandPNGBDBM50576(2-(4,5-dihydroxy-2-methyl-phenyl)-6-hydroxy-4-meth...)
Affinity DataIC50: >3.44E+4nMAssay Description:Inhibition of recombinant CK2alpha1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetReceptor tyrosine-protein kinase erbB-2(Homo sapiens (Human))
Heinrich-Heine-Universit£T

Curated by ChEMBL
LigandPNGBDBM50576(2-(4,5-dihydroxy-2-methyl-phenyl)-6-hydroxy-4-meth...)
Affinity DataIC50: >3.44E+4nMAssay Description:Inhibition of recombinant ERBB2More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetRAC-alpha serine/threonine-protein kinase(Homo sapiens (Human))
Heinrich-Heine-Universit£T

Curated by ChEMBL
LigandPNGBDBM50576(2-(4,5-dihydroxy-2-methyl-phenyl)-6-hydroxy-4-meth...)
Affinity DataIC50: >3.44E+4nMAssay Description:Inhibition of recombinant AKT1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetVascular endothelial growth factor receptor 3(Homo sapiens (Human))
Heinrich-Heine-Universit£T

Curated by ChEMBL
LigandPNGBDBM50576(2-(4,5-dihydroxy-2-methyl-phenyl)-6-hydroxy-4-meth...)
Affinity DataIC50: >3.44E+4nMAssay Description:Inhibition of recombinant VEGFR3More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGlucose-6-phosphate dehydrogenase-6-phosphogluconolactonase(Plasmodium falciparum 3D7)
Burnham Center For Chemical Genomics

Curated by PubChem BioAssay
LigandPNGBDBM50576(2-(4,5-dihydroxy-2-methyl-phenyl)-6-hydroxy-4-meth...)
Affinity DataIC50: >8.00E+4nMAssay Description:Data Source: Sanford-Burnham Center for Chemical Genomics (SBCCG) Source Affiliation: Sanford-Burnham Medical Research Institute (SBMRI, San Diego CA...More data for this Ligand-Target Pair
In DepthDetails PCBioAssay