BDBM3212 (3R,4R)-3-[(4-hydroxybenzene)amido]azepan-4-yl 4-[(2,6-dihydroxyphenyl)carbonyl]-3,5-dihydroxybenzoate::Modified Benzophenone Ring, Balanol Analog 12::trans-4-[3,5-Dihydroxy-4-(2,6-dihydroxybenzoyloxy)]-3-(4-hydroxybenzamido)azepane

SMILES Oc1ccc(cc1)C(=O)N[C@@H]1CNCCC[C@H]1OC(=O)c1cc(O)c(C(=O)c2c(O)cccc2O)c(O)c1

InChI Key InChIKey=FZNVHMDFJAWXTJ-VGOFRKELSA-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 = 3212   

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

LigandPNGBDBM3212((3R,4R)-3-[(4-hydroxybenzene)amido]azepan-4-yl 4-[...)
Affinity DataIC50:  860nMpH: 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

LigandPNGBDBM3212((3R,4R)-3-[(4-hydroxybenzene)amido]azepan-4-yl 4-[...)
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

LigandPNGBDBM3212((3R,4R)-3-[(4-hydroxybenzene)amido]azepan-4-yl 4-[...)
Affinity DataIC50:  2.10E+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

LigandPNGBDBM3212((3R,4R)-3-[(4-hydroxybenzene)amido]azepan-4-yl 4-[...)
Affinity DataIC50:  7.60E+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