Found 31 hits for monomerid = 50576 Target/Host (Institution) | Ligand | Target/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 | pH | Temp °C |
Induced myeloid leukemia cell differentiation protein Mcl-1
(Homo sapiens (Human)) | BDBM50576
(2-(4,5-dihydroxy-2-methyl-phenyl)-6-hydroxy-4-meth...)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) | PDB MMDB
NCI pathway KEGG
UniProtKB/SwissProt
B.MOAD antibodypedia GoogleScholar AffyNet
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| PCBioAssay
| n/a | n/a | 4.15E+3 | n/a | n/a | n/a | n/a | n/a | n/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
(2-(4,5-dihydroxy-2-methyl-phenyl)-6-hydroxy-4-meth...)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) | PDB MMDB
KEGG
UniProtKB/SwissProt
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Similars
| Article PubMed
| n/a | n/a | 5.60 | n/a | n/a | n/a | n/a | n/a | n/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
(2-(4,5-dihydroxy-2-methyl-phenyl)-6-hydroxy-4-meth...)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) | KEGG
UniProtKB/SwissProt
GoogleScholar AffyNet
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Similars
| PCBioAssay
| n/a | n/a | n/a | n/a | 3.00E+5 | n/a | n/a | n/a | n/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
(2-(4,5-dihydroxy-2-methyl-phenyl)-6-hydroxy-4-meth...)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) | UniProtKB/TrEMBL
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| PCBioAssay
| n/a | n/a | 3.75E+3 | n/a | n/a | n/a | n/a | n/a | n/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
(2-(4,5-dihydroxy-2-methyl-phenyl)-6-hydroxy-4-meth...)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) | PDB
UniProtKB/SwissProt UniProtKB/TrEMBL
antibodypedia GoogleScholar AffyNet
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| PCBioAssay
| n/a | n/a | 3.10E+4 | n/a | n/a | n/a | n/a | n/a | n/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
(2-(4,5-dihydroxy-2-methyl-phenyl)-6-hydroxy-4-meth...)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) | UniProtKB/TrEMBL
GoogleScholar AffyNet
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| PCBioAssay
| n/a | n/a | >8.00E+4 | n/a | n/a | n/a | n/a | n/a | n/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
(2-(4,5-dihydroxy-2-methyl-phenyl)-6-hydroxy-4-meth...)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) | UniProtKB/TrEMBL
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| PCBioAssay
| n/a | n/a | 1.94E+4 | n/a | n/a | n/a | n/a | n/a | n/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
(2-(4,5-dihydroxy-2-methyl-phenyl)-6-hydroxy-4-meth...)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) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt UniProtKB/TrEMBL
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| Article PubMed
| n/a | n/a | >1 | n/a | n/a | n/a | n/a | n/a | n/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
(2-(4,5-dihydroxy-2-methyl-phenyl)-6-hydroxy-4-meth...)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) | PDB MMDB
UniProtKB/SwissProt UniProtKB/TrEMBL
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Similars
| Article PubMed
| n/a | n/a | >1 | n/a | n/a | n/a | n/a | n/a | n/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
(2-(4,5-dihydroxy-2-methyl-phenyl)-6-hydroxy-4-meth...)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) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
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| Article PubMed
| n/a | n/a | 5 | n/a | n/a | n/a | n/a | n/a | n/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
(2-(4,5-dihydroxy-2-methyl-phenyl)-6-hydroxy-4-meth...)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) | PDB MMDB
KEGG
UniProtKB/SwissProt UniProtKB/TrEMBL
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Similars
| Article PubMed
| n/a | n/a | 4.30 | n/a | n/a | n/a | n/a | n/a | n/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
(2-(4,5-dihydroxy-2-methyl-phenyl)-6-hydroxy-4-meth...)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) | PDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD antibodypedia GoogleScholar AffyNet
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PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 1.10 | n/a | n/a | n/a | n/a | n/a | n/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
(2-(4,5-dihydroxy-2-methyl-phenyl)-6-hydroxy-4-meth...)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) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt UniProtKB/TrEMBL
B.MOAD DrugBank antibodypedia antibodypedia GoogleScholar AffyNet
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Similars
| Article PubMed
| n/a | n/a | 4.5 | n/a | n/a | n/a | n/a | n/a | n/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
(2-(4,5-dihydroxy-2-methyl-phenyl)-6-hydroxy-4-meth...)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) | PDB
UniProtKB/SwissProt UniProtKB/TrEMBL
antibodypedia GoogleScholar AffyNet
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Similars
| Article PubMed
| n/a | n/a | >1 | n/a | n/a | n/a | n/a | n/a | n/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
(2-(4,5-dihydroxy-2-methyl-phenyl)-6-hydroxy-4-meth...)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) | PDB MMDB
KEGG
UniProtKB/SwissProt
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PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 9.80 | n/a | n/a | n/a | n/a | n/a | n/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
(2-(4,5-dihydroxy-2-methyl-phenyl)-6-hydroxy-4-meth...)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) | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt UniProtKB/TrEMBL
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
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PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 9.40 | n/a | n/a | n/a | n/a | n/a | n/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
(2-(4,5-dihydroxy-2-methyl-phenyl)-6-hydroxy-4-meth...)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) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
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PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 5.90 | n/a | n/a | n/a | n/a | n/a | n/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
(2-(4,5-dihydroxy-2-methyl-phenyl)-6-hydroxy-4-meth...)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) | PDB MMDB
KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
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PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 1.60 | n/a | n/a | n/a | n/a | n/a | n/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
(2-(4,5-dihydroxy-2-methyl-phenyl)-6-hydroxy-4-meth...)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) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD antibodypedia GoogleScholar AffyNet
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PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 3.20 | n/a | n/a | n/a | n/a | n/a | n/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
(2-(4,5-dihydroxy-2-methyl-phenyl)-6-hydroxy-4-meth...)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) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
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PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 7.10 | n/a | n/a | n/a | n/a | n/a | n/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
(2-(4,5-dihydroxy-2-methyl-phenyl)-6-hydroxy-4-meth...)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) | PDB
UniProtKB/SwissProt
antibodypedia GoogleScholar AffyNet
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Similars
| Article PubMed
| n/a | n/a | >1 | n/a | n/a | n/a | n/a | n/a | n/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
(2-(4,5-dihydroxy-2-methyl-phenyl)-6-hydroxy-4-meth...)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) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
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PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 3.30 | n/a | n/a | n/a | n/a | n/a | n/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
(2-(4,5-dihydroxy-2-methyl-phenyl)-6-hydroxy-4-meth...)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) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
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PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | >1 | n/a | n/a | n/a | n/a | n/a | n/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
(2-(4,5-dihydroxy-2-methyl-phenyl)-6-hydroxy-4-meth...)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) | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
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PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 4.90 | n/a | n/a | n/a | n/a | n/a | n/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
(2-(4,5-dihydroxy-2-methyl-phenyl)-6-hydroxy-4-meth...)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) | PDB MMDB
KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
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PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 8.30 | n/a | n/a | n/a | n/a | n/a | n/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
(2-(4,5-dihydroxy-2-methyl-phenyl)-6-hydroxy-4-meth...)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) | PDB MMDB
KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
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PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 9.80 | n/a | n/a | n/a | n/a | n/a | n/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
(2-(4,5-dihydroxy-2-methyl-phenyl)-6-hydroxy-4-meth...)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) | PDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
antibodypedia GoogleScholar AffyNet
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PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 8.80 | n/a | n/a | n/a | n/a | n/a | n/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
(2-(4,5-dihydroxy-2-methyl-phenyl)-6-hydroxy-4-meth...)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) | KEGG
UniProtKB/SwissProt UniProtKB/TrEMBL
antibodypedia GoogleScholar AffyNet
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PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 6.60 | n/a | n/a | n/a | n/a | n/a | n/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
(2-(4,5-dihydroxy-2-methyl-phenyl)-6-hydroxy-4-meth...)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) | PDB
KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
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PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | >1 | n/a | n/a | n/a | n/a | n/a | n/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
(2-(4,5-dihydroxy-2-methyl-phenyl)-6-hydroxy-4-meth...)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) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| Purchase
PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 1.80 | n/a | n/a | n/a | n/a | n/a | n/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
(2-(4,5-dihydroxy-2-methyl-phenyl)-6-hydroxy-4-meth...)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) | PDB
KEGG
UniProtKB/TrEMBL
GoogleScholar AffyNet
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PC cid PC sid UniChem
Similars
| PCBioAssay
| n/a | n/a | n/a | n/a | 3.10E+4 | n/a | n/a | n/a | n/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 | |