BDBM3206 (+/-)-anti-3-[[3,5-Dihydroxy-4-[2-hydroxy-6-(methoxycarbonyl)benzoyl]benzoyl]oxy]-4-(4-hydroxybenzyl)pyrrolidine, Trifluoroacetic Acid Salt::(3S,4R)-4-[(4-hydroxyphenyl)methyl]pyrrolidin-3-yl 3,5-dihydroxy-4-{[2-hydroxy-6-(methoxycarbonyl)phenyl]carbonyl}benzoate::Balanol Analog 35c

SMILES COC(=O)c1cccc(O)c1C(=O)c1c(O)cc(cc1O)C(=O)O[C@@H]1CNC[C@H]1Cc1ccc(O)cc1

InChI Key InChIKey=PEZLAFKDOMGSEL-UHFFFAOYSA-N

Data  15 IC50

  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 15 hits for monomerid = 3206   

TargetProtein kinase C eta type(Human)
TBA

Curated by ChEMBL
LigandPNGBDBM3206((3S,4R)-4-[(4-hydroxyphenyl)methyl]pyrrolidin-3-yl...)
Affinity DataIC50: 50nMAssay Description:Inhibition of protein kinase C etaMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/20/2010
Entry Details Article

TargetProtein kinase C delta type(Human)
TBA

Curated by ChEMBL
LigandPNGBDBM3206((3S,4R)-4-[(4-hydroxyphenyl)methyl]pyrrolidin-3-yl...)
Affinity DataIC50: 100nMAssay Description:Inhibition of protein kinase C deltaMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/20/2010
Entry Details Article

TargetProtein kinase C delta type(Human)
TBA

Curated by ChEMBL
LigandPNGBDBM3206((3S,4R)-4-[(4-hydroxyphenyl)methyl]pyrrolidin-3-yl...)
Affinity DataIC50: 100nMAssay 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 Depth
Date in BDB:
1/31/2005
Entry Details Article
PubMed
TargetProtein kinase C beta type(Human)
Sphinx Laboratories

LigandPNGBDBM3206((3S,4R)-4-[(4-hydroxyphenyl)methyl]pyrrolidin-3-yl...)
Affinity DataIC50: 110nMAssay 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 Depth
Date in BDB:
1/31/2005
Entry Details Article
PubMed
TargetProtein kinase C beta type(Human)
Sphinx Laboratories

LigandPNGBDBM3206((3S,4R)-4-[(4-hydroxyphenyl)methyl]pyrrolidin-3-yl...)
Affinity DataIC50: 110nMAssay Description:Inhibition of protein kinase C beta IIMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/20/2010
Entry Details Article

TargetProtein kinase C beta type(Human)
Sphinx Laboratories

LigandPNGBDBM3206((3S,4R)-4-[(4-hydroxyphenyl)methyl]pyrrolidin-3-yl...)
Affinity DataIC50: 250nMAssay Description:Inhibition of protein kinase C beta IIMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/20/2010
Entry Details Article

TargetProtein kinase C beta type(Human)
Sphinx Laboratories

LigandPNGBDBM3206((3S,4R)-4-[(4-hydroxyphenyl)methyl]pyrrolidin-3-yl...)
Affinity DataIC50: 250nMAssay 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 Depth
Date in BDB:
1/31/2005
Entry Details Article
PubMed
TargetProtein kinase C gamma type(Human)
TBA

Curated by ChEMBL
LigandPNGBDBM3206((3S,4R)-4-[(4-hydroxyphenyl)methyl]pyrrolidin-3-yl...)
Affinity DataIC50: 380nMAssay Description:Inhibition of protein kinase C gammaMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/20/2010
Entry Details Article

TargetProtein kinase C gamma type(Human)
TBA

Curated by ChEMBL
LigandPNGBDBM3206((3S,4R)-4-[(4-hydroxyphenyl)methyl]pyrrolidin-3-yl...)
Affinity DataIC50: 380nMAssay 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 Depth
Date in BDB:
1/31/2005
Entry Details Article
PubMed
TargetProtein kinase C eta type(Human)
TBA

Curated by ChEMBL
LigandPNGBDBM3206((3S,4R)-4-[(4-hydroxyphenyl)methyl]pyrrolidin-3-yl...)
Affinity DataIC50: 500nMAssay 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 Depth
Date in BDB:
1/31/2005
Entry Details Article
PubMed
TargetProtein kinase C alpha type(Human)
Sphinx Laboratories

LigandPNGBDBM3206((3S,4R)-4-[(4-hydroxyphenyl)methyl]pyrrolidin-3-yl...)
Affinity DataIC50: 2.20E+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 Depth
Date in BDB:
1/31/2005
Entry Details Article
PubMed
TargetProtein kinase C alpha type(Human)
Sphinx Laboratories

LigandPNGBDBM3206((3S,4R)-4-[(4-hydroxyphenyl)methyl]pyrrolidin-3-yl...)
Affinity DataIC50: 2.20E+3nMAssay Description:Inhibition of protein kinase C alphaMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/20/2010
Entry Details Article

TargetProtein kinase C epsilon type(Human)
TBA

Curated by ChEMBL
LigandPNGBDBM3206((3S,4R)-4-[(4-hydroxyphenyl)methyl]pyrrolidin-3-yl...)
Affinity DataIC50: 4.00E+3nMAssay Description:Inhibition of protein kinase C epsilonMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/20/2010
Entry Details Article

TargetProtein kinase C epsilon type(Human)
TBA

Curated by ChEMBL
LigandPNGBDBM3206((3S,4R)-4-[(4-hydroxyphenyl)methyl]pyrrolidin-3-yl...)
Affinity DataIC50: 4.00E+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 Depth
Date in BDB:
1/31/2005
Entry Details Article
PubMed
LigandPNGBDBM3206((3S,4R)-4-[(4-hydroxyphenyl)methyl]pyrrolidin-3-yl...)
Affinity DataIC50: 4.10E+3nMAssay 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 Depth
Date in BDB:
1/31/2005
Entry Details Article
PubMed