null

SMILES Oc1ccc(cc1)C(=O)N[C@@H]1CCC[C@H]1OC(=O)c1cc(O)c(C(=O)c2c(O)cccc2-c2nnn[nH]2)c(O)c1

InChI Key InChIKey=DKHPQQRGPHOKBV-DYESRHJHSA-N

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
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Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 8 hits for monomerid = 3239   

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

LigandPNGBDBM3239((1R,2R)-2-[(4-hydroxybenzene)amido]cyclopentyl 3,5...)copy SMILEScopy InChI
Affinity DataIC50: 340nMAssay 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 Article
BindingDB Entry DOI: 10.7270/Q2BG2M50PubMed
TargetProtein kinase C beta type(Homo sapiens (Human))
Sphinx Laboratories

LigandPNGBDBM3239((1R,2R)-2-[(4-hydroxybenzene)amido]cyclopentyl 3,5...)copy SMILEScopy InChI
Affinity DataIC50: 260nMAssay 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 Article
BindingDB Entry DOI: 10.7270/Q2BG2M50PubMed
TargetProtein kinase C epsilon type(Homo sapiens (Human))
Sphinx Laboratories

LigandPNGBDBM3239((1R,2R)-2-[(4-hydroxybenzene)amido]cyclopentyl 3,5...)copy SMILEScopy InChI
Affinity DataIC50: 2.00E+3nMAssay 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 Article
BindingDB Entry DOI: 10.7270/Q2BG2M50PubMed
TargetProtein kinase C beta type(Homo sapiens (Human))
Sphinx Laboratories

LigandPNGBDBM3239((1R,2R)-2-[(4-hydroxybenzene)amido]cyclopentyl 3,5...)copy SMILEScopy InChI
Affinity DataIC50: 290nMAssay Description:Inhibition of Human Protein kinase C beta 2More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2QN66R9
TargetProtein kinase C alpha type(Homo sapiens (Human))
Sphinx Laboratories

LigandPNGBDBM3239((1R,2R)-2-[(4-hydroxybenzene)amido]cyclopentyl 3,5...)copy SMILEScopy InChI
Affinity DataIC50: 340nMAssay Description:Inhibition of Human Protein kinase C alphaMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2QN66R9
TargetProtein kinase C delta type(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM3239((1R,2R)-2-[(4-hydroxybenzene)amido]cyclopentyl 3,5...)copy SMILEScopy InChI
Affinity DataIC50: 20nMAssay Description:Inhibition of Human Protein kinase C deltaMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2QN66R9
TargetProtein kinase C epsilon type(Homo sapiens (Human))
Sphinx Laboratories

LigandPNGBDBM3239((1R,2R)-2-[(4-hydroxybenzene)amido]cyclopentyl 3,5...)copy SMILEScopy InChI
Affinity DataIC50: 2.00E+3nMAssay Description:Inhibition of Human Protein kinase C epsilonMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2QN66R9
TargetcAMP-dependent protein kinase catalytic subunit alpha(Bos taurus (bovine))
Sphinx Laboratories

LigandPNGBDBM3239((1R,2R)-2-[(4-hydroxybenzene)amido]cyclopentyl 3,5...)copy SMILEScopy InChI
Affinity DataIC50: 210nMAssay 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 Article
BindingDB Entry DOI: 10.7270/Q2BG2M50PubMed