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BDBM50576 2-(4,5-dihydroxy-2-methyl-phenyl)-6-hydroxy-4-methoxy-benzoic acid::2-(4,5-dihydroxy-2-methylphenyl)-6-hydroxy-4-methoxybenzoic acid::4-methoxy-2-[2-methyl-4,5-bis(oxidanyl)phenyl]-6-oxidanyl-benzoic acid::MLS000877038::SMR000440664::cid_6918469

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

InChI Key: InChIKey=ADPBTBPPIIKLEH-UHFFFAOYSA-N

Data: 29 IC50  2 EC50

Find this compound or compounds like it in BindingDB or PDB:
   Substructure
Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 31 hits for monomerid = 50576   
Target/Host
(Institution)
LigandTarget/Host
Links
Ligand
Links
Trg + Lig
Links
Ki
nM
ΔG°
kcal/mole
IC50
nM
Kd
nM
EC50/IC50
nM
koff
s-1
kon
M-1s-1
pHTemp
°C
Induced myeloid leukemia cell differentiation protein Mcl-1


(Homo sapiens (Human))
BDBM50576
PNG
(2-(4,5-dihydroxy-2-methyl-phenyl)-6-hydroxy-4-meth...)
Show SMILES COc1cc(O)c(C(O)=O)c(c1)-c1cc(O)c(O)cc1C
Show InChI InChI=1S/C15H14O6/c1-7-3-11(16)12(17)6-9(7)10-4-8(21-2)5-13(18)14(10)15(19)20/h3-6,16-18H,1-2H3,(H,19,20)
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n/an/a 4.15E+3n/an/an/an/an/an/a



Emory University Molecular Libraries Screening Center

Curated by PubChem BioAssay


Assay Description
NIH Molecular Libraries Screening Centers Network [MLSCN] Emory Chemical Biology Discovery Center in MLSCN Assay provider: Nikolovska-Coleska, Univer...


PubChem Bioassay (2008)


BindingDB Entry DOI: 10.7270/Q23X8539
More data for this
Ligand-Target Pair
Insulin receptor


(Homo sapiens (Human))
BDBM50576
PNG
(2-(4,5-dihydroxy-2-methyl-phenyl)-6-hydroxy-4-meth...)
Show SMILES COc1cc(O)c(C(O)=O)c(c1)-c1cc(O)c(O)cc1C
Show InChI InChI=1S/C15H14O6/c1-7-3-11(16)12(17)6-9(7)10-4-8(21-2)5-13(18)14(10)15(19)20/h3-6,16-18H,1-2H3,(H,19,20)
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n/an/a 5.60n/an/an/an/an/an/a



Heinrich-Heine-Universit£t

Curated by ChEMBL


Assay Description
Inhibition of recombinant INSR


J Nat Prod 71: 972-80 (2008)


Article DOI: 10.1021/np070447m
BindingDB Entry DOI: 10.7270/Q2GB26VV
More data for this
Ligand-Target Pair
RecName: Full=Zinc finger protein mex-5


(Caenorhabditis elegans)
BDBM50576
PNG
(2-(4,5-dihydroxy-2-methyl-phenyl)-6-hydroxy-4-meth...)
Show SMILES COc1cc(O)c(C(O)=O)c(c1)-c1cc(O)c(O)cc1C
Show InChI InChI=1S/C15H14O6/c1-7-3-11(16)12(17)6-9(7)10-4-8(21-2)5-13(18)14(10)15(19)20/h3-6,16-18H,1-2H3,(H,19,20)
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n/an/an/an/a 3.00E+5n/an/an/an/a



Broad Institute

Curated by PubChem BioAssay


Assay Description
Broad Institute: MLPCN maternal gene expression Project ID: 2024 Keywords: Zinc finger, C. elegans, maternal gene expression, RNA-protein interac...


PubChem Bioassay (2009)


BindingDB Entry DOI: 10.7270/Q2D798VP
More data for this
Ligand-Target Pair
glucose-6-phosphate dehydrogenase-6-phosphogluconolactonase


(Plasmodium falciparum 3D7)
BDBM50576
PNG
(2-(4,5-dihydroxy-2-methyl-phenyl)-6-hydroxy-4-meth...)
Show SMILES COc1cc(O)c(C(O)=O)c(c1)-c1cc(O)c(O)cc1C
Show InChI InChI=1S/C15H14O6/c1-7-3-11(16)12(17)6-9(7)10-4-8(21-2)5-13(18)14(10)15(19)20/h3-6,16-18H,1-2H3,(H,19,20)
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n/an/a 3.75E+3n/an/an/an/an/an/a



Burnham Center for Chemical Genomics

Curated by PubChem BioAssay


Assay Description
Data Source: Sanford-Burnham Center for Chemical Genomics (SBCCG) Source Affiliation: Sanford-Burnham Medical Research Institute (SBMRI, San Diego CA...


PubChem Bioassay (2011)


BindingDB Entry DOI: 10.7270/Q2ZS2TZG
More data for this
Ligand-Target Pair
Glucose 6-phosphate dehydrogenase (G6PD)


(Homo sapiens (Human))
BDBM50576
PNG
(2-(4,5-dihydroxy-2-methyl-phenyl)-6-hydroxy-4-meth...)
Show SMILES COc1cc(O)c(C(O)=O)c(c1)-c1cc(O)c(O)cc1C
Show InChI InChI=1S/C15H14O6/c1-7-3-11(16)12(17)6-9(7)10-4-8(21-2)5-13(18)14(10)15(19)20/h3-6,16-18H,1-2H3,(H,19,20)
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n/an/a 3.10E+4n/an/an/an/an/an/a



Burnham Center for Chemical Genomics

Curated by PubChem BioAssay


Assay Description
Data Source: Sanford-Burnham Center for Chemical Genomics (SBCCG) Source Affiliation: Sanford-Burnham Medical Research Institute (SBMRI, San Diego CA...


PubChem Bioassay (2011)


BindingDB Entry DOI: 10.7270/Q2V12389
More data for this
Ligand-Target Pair
glucose-6-phosphate dehydrogenase-6-phosphogluconolactonase


(Plasmodium falciparum 3D7)
BDBM50576
PNG
(2-(4,5-dihydroxy-2-methyl-phenyl)-6-hydroxy-4-meth...)
Show SMILES COc1cc(O)c(C(O)=O)c(c1)-c1cc(O)c(O)cc1C
Show InChI InChI=1S/C15H14O6/c1-7-3-11(16)12(17)6-9(7)10-4-8(21-2)5-13(18)14(10)15(19)20/h3-6,16-18H,1-2H3,(H,19,20)
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n/an/a>8.00E+4n/an/an/an/an/an/a



Burnham Center for Chemical Genomics

Curated by PubChem BioAssay


Assay Description
Data Source: Sanford-Burnham Center for Chemical Genomics (SBCCG) Source Affiliation: Sanford-Burnham Medical Research Institute (SBMRI, San Diego CA...


PubChem Bioassay (2011)


BindingDB Entry DOI: 10.7270/Q27H1H3W
More data for this
Ligand-Target Pair
glucose-6-phosphate dehydrogenase-6-phosphogluconolactonase


(Plasmodium falciparum 3D7)
BDBM50576
PNG
(2-(4,5-dihydroxy-2-methyl-phenyl)-6-hydroxy-4-meth...)
Show SMILES COc1cc(O)c(C(O)=O)c(c1)-c1cc(O)c(O)cc1C
Show InChI InChI=1S/C15H14O6/c1-7-3-11(16)12(17)6-9(7)10-4-8(21-2)5-13(18)14(10)15(19)20/h3-6,16-18H,1-2H3,(H,19,20)
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n/an/a 1.94E+4n/an/an/an/an/an/a



Burnham Center for Chemical Genomics

Curated by PubChem BioAssay


Assay Description
Data Source: Sanford-Burnham Center for Chemical Genomics (SBCCG) Source Affiliation: Sanford-Burnham Medical Research Institute (SBMRI, San Diego CA...


PubChem Bioassay (2011)


BindingDB Entry DOI: 10.7270/Q23T9FQ1
More data for this
Ligand-Target Pair
Cyclin-dependent kinase 2


(Homo sapiens (Human))
BDBM50576
PNG
(2-(4,5-dihydroxy-2-methyl-phenyl)-6-hydroxy-4-meth...)
Show SMILES COc1cc(O)c(C(O)=O)c(c1)-c1cc(O)c(O)cc1C
Show InChI InChI=1S/C15H14O6/c1-7-3-11(16)12(17)6-9(7)10-4-8(21-2)5-13(18)14(10)15(19)20/h3-6,16-18H,1-2H3,(H,19,20)
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n/an/a>1n/an/an/an/an/an/a



Heinrich-Heine-Universit£t

Curated by ChEMBL


Assay Description
Inhibition of recombinant CDK2/CycA


J Nat Prod 71: 972-80 (2008)


Article DOI: 10.1021/np070447m
BindingDB Entry DOI: 10.7270/Q2GB26VV
More data for this
Ligand-Target Pair
Receptor tyrosine-protein kinase erbB-2


(Homo sapiens (Human))
BDBM50576
PNG
(2-(4,5-dihydroxy-2-methyl-phenyl)-6-hydroxy-4-meth...)
Show SMILES COc1cc(O)c(C(O)=O)c(c1)-c1cc(O)c(O)cc1C
Show InChI InChI=1S/C15H14O6/c1-7-3-11(16)12(17)6-9(7)10-4-8(21-2)5-13(18)14(10)15(19)20/h3-6,16-18H,1-2H3,(H,19,20)
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n/an/a>1n/an/an/an/an/an/a



Heinrich-Heine-Universit£t

Curated by ChEMBL


Assay Description
Inhibition of recombinant ERBB2


J Nat Prod 71: 972-80 (2008)


Article DOI: 10.1021/np070447m
BindingDB Entry DOI: 10.7270/Q2GB26VV
More data for this
Ligand-Target Pair
Vascular endothelial growth factor receptor 2


(Homo sapiens (Human))
BDBM50576
PNG
(2-(4,5-dihydroxy-2-methyl-phenyl)-6-hydroxy-4-meth...)
Show SMILES COc1cc(O)c(C(O)=O)c(c1)-c1cc(O)c(O)cc1C
Show InChI InChI=1S/C15H14O6/c1-7-3-11(16)12(17)6-9(7)10-4-8(21-2)5-13(18)14(10)15(19)20/h3-6,16-18H,1-2H3,(H,19,20)
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n/an/a 5n/an/an/an/an/an/a



Heinrich-Heine-Universit£t

Curated by ChEMBL


Assay Description
Inhibition of recombinant VEGFR2


J Nat Prod 71: 972-80 (2008)


Article DOI: 10.1021/np070447m
BindingDB Entry DOI: 10.7270/Q2GB26VV
More data for this
Ligand-Target Pair
Hepatocyte growth factor receptor


(Homo sapiens (Human))
BDBM50576
PNG
(2-(4,5-dihydroxy-2-methyl-phenyl)-6-hydroxy-4-meth...)
Show SMILES COc1cc(O)c(C(O)=O)c(c1)-c1cc(O)c(O)cc1C
Show InChI InChI=1S/C15H14O6/c1-7-3-11(16)12(17)6-9(7)10-4-8(21-2)5-13(18)14(10)15(19)20/h3-6,16-18H,1-2H3,(H,19,20)
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n/an/a 4.30n/an/an/an/an/an/a



Heinrich-Heine-Universit£t

Curated by ChEMBL


Assay Description
Inhibition of recombinant MET


J Nat Prod 71: 972-80 (2008)


Article DOI: 10.1021/np070447m
BindingDB Entry DOI: 10.7270/Q2GB26VV
More data for this
Ligand-Target Pair
Aurora kinase B


(Homo sapiens (Human))
BDBM50576
PNG
(2-(4,5-dihydroxy-2-methyl-phenyl)-6-hydroxy-4-meth...)
Show SMILES COc1cc(O)c(C(O)=O)c(c1)-c1cc(O)c(O)cc1C
Show InChI InChI=1S/C15H14O6/c1-7-3-11(16)12(17)6-9(7)10-4-8(21-2)5-13(18)14(10)15(19)20/h3-6,16-18H,1-2H3,(H,19,20)
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n/an/a 1.10n/an/an/an/an/an/a



Heinrich-Heine-Universit£t

Curated by ChEMBL


Assay Description
Inhibition of recombinant Aurora B


J Nat Prod 71: 972-80 (2008)


Article DOI: 10.1021/np070447m
BindingDB Entry DOI: 10.7270/Q2GB26VV
More data for this
Ligand-Target Pair
Cyclin-Dependent Kinase 4 (CDK4)


(Homo sapiens (Human))
BDBM50576
PNG
(2-(4,5-dihydroxy-2-methyl-phenyl)-6-hydroxy-4-meth...)
Show SMILES COc1cc(O)c(C(O)=O)c(c1)-c1cc(O)c(O)cc1C
Show InChI InChI=1S/C15H14O6/c1-7-3-11(16)12(17)6-9(7)10-4-8(21-2)5-13(18)14(10)15(19)20/h3-6,16-18H,1-2H3,(H,19,20)
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n/an/a 4.5n/an/an/an/an/an/a



Heinrich-Heine-Universit£t

Curated by ChEMBL


Assay Description
Inhibition of recombinant CDK4/CycD1


J Nat Prod 71: 972-80 (2008)


Article DOI: 10.1021/np070447m
BindingDB Entry DOI: 10.7270/Q2GB26VV
More data for this
Ligand-Target Pair
RAC-alpha serine/threonine-protein kinase


(Homo sapiens (Human))
BDBM50576
PNG
(2-(4,5-dihydroxy-2-methyl-phenyl)-6-hydroxy-4-meth...)
Show SMILES COc1cc(O)c(C(O)=O)c(c1)-c1cc(O)c(O)cc1C
Show InChI InChI=1S/C15H14O6/c1-7-3-11(16)12(17)6-9(7)10-4-8(21-2)5-13(18)14(10)15(19)20/h3-6,16-18H,1-2H3,(H,19,20)
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n/an/a>1n/an/an/an/an/an/a



Heinrich-Heine-Universit£t

Curated by ChEMBL


Assay Description
Inhibition of recombinant AKT1


J Nat Prod 71: 972-80 (2008)


Article DOI: 10.1021/np070447m
BindingDB Entry DOI: 10.7270/Q2GB26VV
More data for this
Ligand-Target Pair
Epidermal growth factor receptor


(Homo sapiens (Human))
BDBM50576
PNG
(2-(4,5-dihydroxy-2-methyl-phenyl)-6-hydroxy-4-meth...)
Show SMILES COc1cc(O)c(C(O)=O)c(c1)-c1cc(O)c(O)cc1C
Show InChI InChI=1S/C15H14O6/c1-7-3-11(16)12(17)6-9(7)10-4-8(21-2)5-13(18)14(10)15(19)20/h3-6,16-18H,1-2H3,(H,19,20)
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n/an/a 9.80n/an/an/an/an/an/a



Heinrich-Heine-Universit£t

Curated by ChEMBL


Assay Description
Inhibition of recombinant EGFR


J Nat Prod 71: 972-80 (2008)


Article DOI: 10.1021/np070447m
BindingDB Entry DOI: 10.7270/Q2GB26VV
More data for this
Ligand-Target Pair
Ephrin type-B receptor 4


(Homo sapiens (Human))
BDBM50576
PNG
(2-(4,5-dihydroxy-2-methyl-phenyl)-6-hydroxy-4-meth...)
Show SMILES COc1cc(O)c(C(O)=O)c(c1)-c1cc(O)c(O)cc1C
Show InChI InChI=1S/C15H14O6/c1-7-3-11(16)12(17)6-9(7)10-4-8(21-2)5-13(18)14(10)15(19)20/h3-6,16-18H,1-2H3,(H,19,20)
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n/an/a 9.40n/an/an/an/an/an/a



Heinrich-Heine-Universit£t

Curated by ChEMBL


Assay Description
Inhibition of recombinant EPHB4


J Nat Prod 71: 972-80 (2008)


Article DOI: 10.1021/np070447m
BindingDB Entry DOI: 10.7270/Q2GB26VV
More data for this
Ligand-Target Pair
Platelet-derived growth factor receptor beta


(Homo sapiens (Human))
BDBM50576
PNG
(2-(4,5-dihydroxy-2-methyl-phenyl)-6-hydroxy-4-meth...)
Show SMILES COc1cc(O)c(C(O)=O)c(c1)-c1cc(O)c(O)cc1C
Show InChI InChI=1S/C15H14O6/c1-7-3-11(16)12(17)6-9(7)10-4-8(21-2)5-13(18)14(10)15(19)20/h3-6,16-18H,1-2H3,(H,19,20)
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n/an/a 5.90n/an/an/an/an/an/a



Heinrich-Heine-Universit£t

Curated by ChEMBL


Assay Description
Inhibition of recombinant PDGFRbeta


J Nat Prod 71: 972-80 (2008)


Article DOI: 10.1021/np070447m
BindingDB Entry DOI: 10.7270/Q2GB26VV
More data for this
Ligand-Target Pair
Receptor-type tyrosine-protein kinase FLT3


(Homo sapiens (Human))
BDBM50576
PNG
(2-(4,5-dihydroxy-2-methyl-phenyl)-6-hydroxy-4-meth...)
Show SMILES COc1cc(O)c(C(O)=O)c(c1)-c1cc(O)c(O)cc1C
Show InChI InChI=1S/C15H14O6/c1-7-3-11(16)12(17)6-9(7)10-4-8(21-2)5-13(18)14(10)15(19)20/h3-6,16-18H,1-2H3,(H,19,20)
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n/an/a 1.60n/an/an/an/an/an/a



Heinrich-Heine-Universit£t

Curated by ChEMBL


Assay Description
Inhibition of recombinant FLT3


J Nat Prod 71: 972-80 (2008)


Article DOI: 10.1021/np070447m
BindingDB Entry DOI: 10.7270/Q2GB26VV
More data for this
Ligand-Target Pair
Serine/threonine-protein kinase PLK4


(Homo sapiens (Human))
BDBM50576
PNG
(2-(4,5-dihydroxy-2-methyl-phenyl)-6-hydroxy-4-meth...)
Show SMILES COc1cc(O)c(C(O)=O)c(c1)-c1cc(O)c(O)cc1C
Show InChI InChI=1S/C15H14O6/c1-7-3-11(16)12(17)6-9(7)10-4-8(21-2)5-13(18)14(10)15(19)20/h3-6,16-18H,1-2H3,(H,19,20)
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n/an/a 3.20n/an/an/an/an/an/a



Heinrich-Heine-Universit£t

Curated by ChEMBL


Assay Description
Inhibition of recombinant SAK


J Nat Prod 71: 972-80 (2008)


Article DOI: 10.1021/np070447m
BindingDB Entry DOI: 10.7270/Q2GB26VV
More data for this
Ligand-Target Pair
Serine/threonine-protein kinase PLK1


(Homo sapiens (Human))
BDBM50576
PNG
(2-(4,5-dihydroxy-2-methyl-phenyl)-6-hydroxy-4-meth...)
Show SMILES COc1cc(O)c(C(O)=O)c(c1)-c1cc(O)c(O)cc1C
Show InChI InChI=1S/C15H14O6/c1-7-3-11(16)12(17)6-9(7)10-4-8(21-2)5-13(18)14(10)15(19)20/h3-6,16-18H,1-2H3,(H,19,20)
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n/an/a 7.10n/an/an/an/an/an/a



Heinrich-Heine-Universit£t

Curated by ChEMBL


Assay Description
Inhibition of recombinant PLK1


J Nat Prod 71: 972-80 (2008)


Article DOI: 10.1021/np070447m
BindingDB Entry DOI: 10.7270/Q2GB26VV
More data for this
Ligand-Target Pair
Casein kinase II subunit alpha


(Homo sapiens (Human))
BDBM50576
PNG
(2-(4,5-dihydroxy-2-methyl-phenyl)-6-hydroxy-4-meth...)
Show SMILES COc1cc(O)c(C(O)=O)c(c1)-c1cc(O)c(O)cc1C
Show InChI InChI=1S/C15H14O6/c1-7-3-11(16)12(17)6-9(7)10-4-8(21-2)5-13(18)14(10)15(19)20/h3-6,16-18H,1-2H3,(H,19,20)
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n/an/a>1n/an/an/an/an/an/a



Heinrich-Heine-Universit£t

Curated by ChEMBL


Assay Description
Inhibition of recombinant CK2alpha1


J Nat Prod 71: 972-80 (2008)


Article DOI: 10.1021/np070447m
BindingDB Entry DOI: 10.7270/Q2GB26VV
More data for this
Ligand-Target Pair
Serine/threonine-protein kinase B-raf


(Homo sapiens (Human))
BDBM50576
PNG
(2-(4,5-dihydroxy-2-methyl-phenyl)-6-hydroxy-4-meth...)
Show SMILES COc1cc(O)c(C(O)=O)c(c1)-c1cc(O)c(O)cc1C
Show InChI InChI=1S/C15H14O6/c1-7-3-11(16)12(17)6-9(7)10-4-8(21-2)5-13(18)14(10)15(19)20/h3-6,16-18H,1-2H3,(H,19,20)
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n/an/a 3.30n/an/an/an/an/an/a



Heinrich-Heine-Universit£t

Curated by ChEMBL


Assay Description
Inhibition of recombinant B-RAF-V600E mutant


J Nat Prod 71: 972-80 (2008)


Article DOI: 10.1021/np070447m
BindingDB Entry DOI: 10.7270/Q2GB26VV
More data for this
Ligand-Target Pair
Focal adhesion kinase 1/vascular endothelial growth factor receptor 3


(Homo sapiens (Human))
BDBM50576
PNG
(2-(4,5-dihydroxy-2-methyl-phenyl)-6-hydroxy-4-meth...)
Show SMILES COc1cc(O)c(C(O)=O)c(c1)-c1cc(O)c(O)cc1C
Show InChI InChI=1S/C15H14O6/c1-7-3-11(16)12(17)6-9(7)10-4-8(21-2)5-13(18)14(10)15(19)20/h3-6,16-18H,1-2H3,(H,19,20)
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n/an/a>1n/an/an/an/an/an/a



Heinrich-Heine-Universit£t

Curated by ChEMBL


Assay Description
Inhibition of recombinant FAK


J Nat Prod 71: 972-80 (2008)


Article DOI: 10.1021/np070447m
BindingDB Entry DOI: 10.7270/Q2GB26VV
More data for this
Ligand-Target Pair
Insulin-like growth factor I receptor


(Homo sapiens (Human))
BDBM50576
PNG
(2-(4,5-dihydroxy-2-methyl-phenyl)-6-hydroxy-4-meth...)
Show SMILES COc1cc(O)c(C(O)=O)c(c1)-c1cc(O)c(O)cc1C
Show InChI InChI=1S/C15H14O6/c1-7-3-11(16)12(17)6-9(7)10-4-8(21-2)5-13(18)14(10)15(19)20/h3-6,16-18H,1-2H3,(H,19,20)
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n/an/a 4.90n/an/an/an/an/an/a



Heinrich-Heine-Universit£t

Curated by ChEMBL


Assay Description
Inhibition of recombinant IGF1R


J Nat Prod 71: 972-80 (2008)


Article DOI: 10.1021/np070447m
BindingDB Entry DOI: 10.7270/Q2GB26VV
More data for this
Ligand-Target Pair
Calmodulin/Proto-oncogene tyrosine-protein kinase Src


(Homo sapiens (Human))
BDBM50576
PNG
(2-(4,5-dihydroxy-2-methyl-phenyl)-6-hydroxy-4-meth...)
Show SMILES COc1cc(O)c(C(O)=O)c(c1)-c1cc(O)c(O)cc1C
Show InChI InChI=1S/C15H14O6/c1-7-3-11(16)12(17)6-9(7)10-4-8(21-2)5-13(18)14(10)15(19)20/h3-6,16-18H,1-2H3,(H,19,20)
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n/an/a 8.30n/an/an/an/an/an/a



Heinrich-Heine-Universit£t

Curated by ChEMBL


Assay Description
Inhibition of recombinant SRC


J Nat Prod 71: 972-80 (2008)


Article DOI: 10.1021/np070447m
BindingDB Entry DOI: 10.7270/Q2GB26VV
More data for this
Ligand-Target Pair
Vascular endothelial growth factor receptor 2 and tyrosine-protein kinase TIE-2 (KDR and TIE2)


(Homo sapiens (Human))
BDBM50576
PNG
(2-(4,5-dihydroxy-2-methyl-phenyl)-6-hydroxy-4-meth...)
Show SMILES COc1cc(O)c(C(O)=O)c(c1)-c1cc(O)c(O)cc1C
Show InChI InChI=1S/C15H14O6/c1-7-3-11(16)12(17)6-9(7)10-4-8(21-2)5-13(18)14(10)15(19)20/h3-6,16-18H,1-2H3,(H,19,20)
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n/an/a 9.80n/an/an/an/an/an/a



Heinrich-Heine-Universit£t

Curated by ChEMBL


Assay Description
Inhibition of recombinant TIE2


J Nat Prod 71: 972-80 (2008)


Article DOI: 10.1021/np070447m
BindingDB Entry DOI: 10.7270/Q2GB26VV
More data for this
Ligand-Target Pair
Mitogen-activated protein kinase kinase kinase 8


(Homo sapiens (Human))
BDBM50576
PNG
(2-(4,5-dihydroxy-2-methyl-phenyl)-6-hydroxy-4-meth...)
Show SMILES COc1cc(O)c(C(O)=O)c(c1)-c1cc(O)c(O)cc1C
Show InChI InChI=1S/C15H14O6/c1-7-3-11(16)12(17)6-9(7)10-4-8(21-2)5-13(18)14(10)15(19)20/h3-6,16-18H,1-2H3,(H,19,20)
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n/an/a 8.80n/an/an/an/an/an/a



Heinrich-Heine-Universit£t

Curated by ChEMBL


Assay Description
Inhibition of recombinant COT


J Nat Prod 71: 972-80 (2008)


Article DOI: 10.1021/np070447m
BindingDB Entry DOI: 10.7270/Q2GB26VV
More data for this
Ligand-Target Pair
NUAK family SNF1-like kinase 1


(Homo sapiens (Human))
BDBM50576
PNG
(2-(4,5-dihydroxy-2-methyl-phenyl)-6-hydroxy-4-meth...)
Show SMILES COc1cc(O)c(C(O)=O)c(c1)-c1cc(O)c(O)cc1C
Show InChI InChI=1S/C15H14O6/c1-7-3-11(16)12(17)6-9(7)10-4-8(21-2)5-13(18)14(10)15(19)20/h3-6,16-18H,1-2H3,(H,19,20)
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n/an/a 6.60n/an/an/an/an/an/a



Heinrich-Heine-Universit£t

Curated by ChEMBL


Assay Description
Inhibition of recombinant ARK5


J Nat Prod 71: 972-80 (2008)


Article DOI: 10.1021/np070447m
BindingDB Entry DOI: 10.7270/Q2GB26VV
More data for this
Ligand-Target Pair
Focal adhesion kinase 1/vascular endothelial growth factor receptor 3


(Homo sapiens (Human))
BDBM50576
PNG
(2-(4,5-dihydroxy-2-methyl-phenyl)-6-hydroxy-4-meth...)
Show SMILES COc1cc(O)c(C(O)=O)c(c1)-c1cc(O)c(O)cc1C
Show InChI InChI=1S/C15H14O6/c1-7-3-11(16)12(17)6-9(7)10-4-8(21-2)5-13(18)14(10)15(19)20/h3-6,16-18H,1-2H3,(H,19,20)
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n/an/a>1n/an/an/an/an/an/a



Heinrich-Heine-Universit£t

Curated by ChEMBL


Assay Description
Inhibition of recombinant VEGFR3


J Nat Prod 71: 972-80 (2008)


Article DOI: 10.1021/np070447m
BindingDB Entry DOI: 10.7270/Q2GB26VV
More data for this
Ligand-Target Pair
Aurora kinase A


(Homo sapiens (Human))
BDBM50576
PNG
(2-(4,5-dihydroxy-2-methyl-phenyl)-6-hydroxy-4-meth...)
Show SMILES COc1cc(O)c(C(O)=O)c(c1)-c1cc(O)c(O)cc1C
Show InChI InChI=1S/C15H14O6/c1-7-3-11(16)12(17)6-9(7)10-4-8(21-2)5-13(18)14(10)15(19)20/h3-6,16-18H,1-2H3,(H,19,20)
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n/an/a 1.80n/an/an/an/an/an/a



Heinrich-Heine-Universit£t

Curated by ChEMBL


Assay Description
Inhibition of recombinant Aurora A


J Nat Prod 71: 972-80 (2008)


Article DOI: 10.1021/np070447m
BindingDB Entry DOI: 10.7270/Q2GB26VV
More data for this
Ligand-Target Pair
POsterior Segregation family member (pos-1)


(Caenorhabditis elegans)
BDBM50576
PNG
(2-(4,5-dihydroxy-2-methyl-phenyl)-6-hydroxy-4-meth...)
Show SMILES COc1cc(O)c(C(O)=O)c(c1)-c1cc(O)c(O)cc1C
Show InChI InChI=1S/C15H14O6/c1-7-3-11(16)12(17)6-9(7)10-4-8(21-2)5-13(18)14(10)15(19)20/h3-6,16-18H,1-2H3,(H,19,20)
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n/an/an/an/a 3.10E+4n/an/an/an/a



Broad Institute

Curated by PubChem BioAssay


Assay Description
Broad Institute: MLPCN maternal gene expression Project ID: 2024 Keywords: Zinc finger, C. elegans, maternal gene expression, RNA-protein interac...


PubChem Bioassay (2009)


BindingDB Entry DOI: 10.7270/Q28G8J4C
More data for this
Ligand-Target Pair