BDBM50101979 2,6-Dihydroxyanthraquinone::2,6-dihydroxy-9,10-anthracenedione::2,6-dihydroxy-9,10-anthraquinone::2,6-dihydroxyanthra-9,10-quinone::2,6-dihydroxyanthracene-9,10-dione::Az-F::CHEMBL298398::anthraflavic acid::anthraflavin

SMILES Oc1ccc2C(=O)c3cc(O)ccc3C(=O)c2c1

InChI Key InChIKey=APAJFZPFBHMFQR-UHFFFAOYSA-N

Data  2 KI  6 IC50

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 8 hits for monomerid = 50101979   

TargetEstrogen receptor(Homo sapiens (Human))
Kyoto Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50101979(2,6-Dihydroxyanthraquinone | 2,6-dihydroxy-9,10-an...)
Affinity DataKi:  310nMAssay Description:Inhibition of binding of 17 beta-estradiol to human Estrogen receptor alphaMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetEstrogen receptor beta(Homo sapiens (Human))
Kyoto Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50101979(2,6-Dihydroxyanthraquinone | 2,6-dihydroxy-9,10-an...)
Affinity DataKi:  690nMAssay Description:Inhibition of binding of 17 beta-estradiol to human Estrogen receptor betaMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUDP-glucuronosyltransferase 1A1(Homo sapiens (Human))
University Of Minnesota

Curated by ChEMBL
LigandPNGBDBM50101979(2,6-Dihydroxyanthraquinone | 2,6-dihydroxy-9,10-an...)
Affinity DataIC50:  4.00E+3nMAssay Description:Inhibition of human recombinant UGT1A1 expressed in HEK293 cells assessed as reduction in estradiol 3-glucuronidation by LC-MS/MS methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUDP-glucuronosyltransferase 1A1(Homo sapiens (Human))
University Of Minnesota

Curated by ChEMBL
LigandPNGBDBM50101979(2,6-Dihydroxyanthraquinone | 2,6-dihydroxy-9,10-an...)
Affinity DataIC50:  3.60E+3nMAssay Description:Inhibition of human recombinant UGT1A1 expressed in HEK293 cells assessed as reduction in bilirubin glucuronidation by LC-MS/MS methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAmine oxidase [flavin-containing] B(Homo sapiens (Human))
North-West University

Curated by ChEMBL
LigandPNGBDBM50101979(2,6-Dihydroxyanthraquinone | 2,6-dihydroxy-9,10-an...)
Affinity DataIC50:  5.62E+3nMAssay Description:Inhibition of recombinant human MAO-B expressed in baculovirus infected BTI insect cells using kynuramine as substrate after 20 mins by fluorescence ...More data for this Ligand-Target Pair
In DepthDetails PubMed
TargetEstrogen receptor(Homo sapiens (Human))
Kyoto Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50101979(2,6-Dihydroxyanthraquinone | 2,6-dihydroxy-9,10-an...)
Affinity DataIC50:  1.10E+3nMAssay Description:Inhibition of binding of 17 beta-estradiol to human Estrogen receptor alphaMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAmine oxidase [flavin-containing] A(Homo sapiens (Human))
North-West University

Curated by ChEMBL
LigandPNGBDBM50101979(2,6-Dihydroxyanthraquinone | 2,6-dihydroxy-9,10-an...)
Affinity DataIC50:  1.15E+4nMAssay Description:Inhibition of recombinant human MAO-A expressed in baculovirus infected BTI insect cells using kynuramine as substrate after 20 mins by fluorescence ...More data for this Ligand-Target Pair
In DepthDetails PubMed
TargetEstrogen receptor beta(Homo sapiens (Human))
Kyoto Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50101979(2,6-Dihydroxyanthraquinone | 2,6-dihydroxy-9,10-an...)
Affinity DataIC50:  2.40E+3nMAssay Description:Inhibition of binding of 17 beta-estradiol to human Estrogen receptor betaMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed