BDBM3211 (3R,4R)-3-[(4-hydroxybenzene)amido]azepan-4-yl 3,5-dihydroxy-4-[(2-hydroxyphenyl)carbonyl]benzoate::4-trans-[4-(2-Hydroxybenzoyl)-3,5-dihydroxybenzoyloxy]-3-(4-hydroxybenzamido)azepane::Modified Benzophenone Ring, Balanol Analog 11

SMILES Oc1ccc(cc1)C(=O)N[C@@H]1CNCCC[C@H]1OC(=O)c1cc(O)c(C(=O)c2ccccc2O)c(O)c1

InChI Key InChIKey=SDXJATDGAWWJQA-AUSIDOKSSA-N

Data  4 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 4 hits for monomerid = 3211   

TargetProtein kinase C alpha type(Homo sapiens (Human))
Sphinx Laboratories

LigandPNGBDBM3211((3R,4R)-3-[(4-hydroxybenzene)amido]azepan-4-yl 3,5...)
Affinity DataIC50:  9.70E+4nMpH: 7.5 T: 2°CAssay Description:PKC was assayed by quantitating the incorporation of 32P from [gamma-32P]ATP into histone type IIIs.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetcAMP-dependent protein kinase catalytic subunit alpha(Bos taurus (bovine))
Sphinx Laboratories

LigandPNGBDBM3211((3R,4R)-3-[(4-hydroxybenzene)amido]azepan-4-yl 3,5...)
Affinity DataIC50:  440nMpH: 7.5 T: 2°CAssay Description:The activity of PKA, activated by cAMP, is measured by its ability to transfer phosphate from [gamma-32P]ATP to histone.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProtein kinase C epsilon type(Homo sapiens (Human))
Sphinx Laboratories

LigandPNGBDBM3211((3R,4R)-3-[(4-hydroxybenzene)amido]azepan-4-yl 3,5...)
Affinity DataIC50:  8.00E+3nMpH: 7.5 T: 2°CAssay Description:PKC was assayed by quantitating the incorporation of 32P from [gamma-32P]ATP into histone type IIIs.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProtein kinase C beta type(Homo sapiens (Human))
Sphinx Laboratories

LigandPNGBDBM3211((3R,4R)-3-[(4-hydroxybenzene)amido]azepan-4-yl 3,5...)
Affinity DataIC50:  3.80E+4nMpH: 7.5 T: 2°CAssay Description:PKC was assayed by quantitating the incorporation of 32P from [gamma-32P]ATP into histone type IIIs.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed