BDBM50129579 2,5-Dihydroxy-3-[7-(2-methyl-benzyl)-1H-indol-3-yl]-[1,4]benzoquinone::CHEMBL87763

SMILES Cc1ccccc1Cc1cccc2c(c[nH]c12)C1C(=O)C(=O)CC(=O)C1=O

InChI Key InChIKey=PWWGOYLRXNCWLL-UHFFFAOYSA-N

Data  3 IC50

  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 3 hits for monomerid = 50129579   

TargetM-phase inducer phosphatase 1(Homo sapiens (Human))
Duke University

Curated by ChEMBL
LigandPNGBDBM50129579(2,5-Dihydroxy-3-[7-(2-methyl-benzyl)-1H-indol-3-yl...)
Affinity DataIC50:  1.00E+3nMAssay Description:Eight point inhibitory concentration against Cell division cycle 25A was determinedMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetM-phase inducer phosphatase 3(Homo sapiens (Human))
Duke University

Curated by ChEMBL
LigandPNGBDBM50129579(2,5-Dihydroxy-3-[7-(2-methyl-benzyl)-1H-indol-3-yl...)
Affinity DataIC50:  3.50E+3nMAssay Description:Eight point inhibitory concentration against Cell division cycle 25 degree C was determinedMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetM-phase inducer phosphatase 2(Homo sapiens (Human))
Duke University

Curated by ChEMBL
LigandPNGBDBM50129579(2,5-Dihydroxy-3-[7-(2-methyl-benzyl)-1H-indol-3-yl...)
Affinity DataIC50:  1.00E+3nMAssay Description:Eight point inhibitory concentration against Cell division cycle 25B was determinedMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed