null

SMILES COc1cc(O)c(C(O)=O)c(c1)-c1cc(O)c(O)cc1C

InChI Key InChIKey=ADPBTBPPIIKLEH-UHFFFAOYSA-N

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
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   Substructure
Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 24 hits for monomerid = 50576   

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...)copy SMILEScopy InChI
Affinity DataIC50: 3.44E+4nMAssay Description:Inhibition of recombinant CDK2/CycAMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2GB26VVPubMed
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...)copy SMILEScopy InChI
Affinity DataIC50: 3.44E+4nMAssay Description:Inhibition of recombinant ERBB2More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2GB26VVPubMed
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...)copy SMILEScopy InChI
Affinity DataIC50: 1.72E+4nMAssay Description:Inhibition of recombinant VEGFR2More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2GB26VVPubMed
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...)copy SMILEScopy InChI
Affinity DataIC50: 1.48E+4nMAssay Description:Inhibition of recombinant METMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2GB26VVPubMed
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...)copy SMILEScopy InChI
Affinity DataIC50: 3.78E+3nMAssay Description:Inhibition of recombinant Aurora BMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2GB26VVPubMed
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...)copy SMILEScopy InChI
Affinity DataIC50: 1.55E+4nMAssay Description:Inhibition of recombinant CDK4/CycD1More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2GB26VVPubMed
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...)copy SMILEScopy InChI
Affinity DataIC50: 3.44E+4nMAssay Description:Inhibition of recombinant AKT1More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2GB26VVPubMed
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...)copy SMILEScopy InChI
Affinity DataIC50: 3.37E+4nMAssay Description:Inhibition of recombinant EGFRMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2GB26VVPubMed
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...)copy SMILEScopy InChI
Affinity DataIC50: 3.23E+4nMAssay Description:Inhibition of recombinant EPHB4More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2GB26VVPubMed
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...)copy SMILEScopy InChI
Affinity DataIC50: 2.03E+4nMAssay Description:Inhibition of recombinant PDGFRbetaMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2GB26VVPubMed
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...)copy SMILEScopy InChI
Affinity DataIC50: 5.51E+3nMAssay Description:Inhibition of recombinant FLT3More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2GB26VVPubMed
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...)copy SMILEScopy InChI
Affinity DataIC50: 1.10E+4nMAssay Description:Inhibition of recombinant SAKMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2GB26VVPubMed
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...)copy SMILEScopy InChI
Affinity DataIC50: 2.44E+4nMAssay Description:Inhibition of recombinant PLK1More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2GB26VVPubMed
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...)copy SMILEScopy InChI
Affinity DataIC50: 3.44E+4nMAssay Description:Inhibition of recombinant CK2alpha1More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2GB26VVPubMed
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...)copy SMILEScopy InChI
Affinity DataIC50: 1.13E+4nMAssay Description:Inhibition of recombinant B-RAF-V600E mutantMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2GB26VVPubMed
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...)copy SMILEScopy InChI
Affinity DataIC50: 3.44E+4nMAssay Description:Inhibition of recombinant FAKMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2GB26VVPubMed
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...)copy SMILEScopy InChI
Affinity DataIC50: 1.68E+4nMAssay Description:Inhibition of recombinant IGF1RMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2GB26VVPubMed
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...)copy SMILEScopy InChI
Affinity DataIC50: 2.85E+4nMAssay Description:Inhibition of recombinant SRCMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2GB26VVPubMed
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...)copy SMILEScopy InChI
Affinity DataIC50: 3.37E+4nMAssay Description:Inhibition of recombinant TIE2More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2GB26VVPubMed
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...)copy SMILEScopy InChI
Affinity DataIC50: 3.03E+4nMAssay Description:Inhibition of recombinant COTMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2GB26VVPubMed
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...)copy SMILEScopy InChI
Affinity DataIC50: 2.27E+4nMAssay Description:Inhibition of recombinant ARK5More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2GB26VVPubMed
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...)copy SMILEScopy InChI
Affinity DataIC50: 3.44E+4nMAssay Description:Inhibition of recombinant VEGFR3More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2GB26VVPubMed
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...)copy SMILEScopy InChI
Affinity DataIC50: 6.20E+3nMAssay Description:Inhibition of recombinant Aurora AMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2GB26VVPubMed
TargetInsulin receptor(Homo sapiens (Human))
Heinrich-Heine-Universit£t

Curated by ChEMBL
LigandPNGBDBM50576(2-(4,5-dihydroxy-2-methyl-phenyl)-6-hydroxy-4-meth...)copy SMILEScopy InChI
Affinity DataIC50: 1.92E+4nMAssay Description:Inhibition of recombinant INSRMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2GB26VVPubMed