BDBM50292435 (1R,3aS,5aR,5bR,7aR,9S,11aR,11bR,13aR,13bR)-9-((E)-but-2-enoyloxy)-5a,5b,8,8,11a-pentamethyl-1-(prop-1-en-2-yl)icosahydro-1H-cyclopenta[a]chrysene-3a-carboxylic acid::Betulinic acid 3-O-crotonate::CHEMBL448637

SMILES C\C=C\C(=O)O[C@H]1CC[C@@]2(C)[C@@H](CC[C@]3(C)[C@@H]2CC[C@@H]2[C@H]4[C@@H](CC[C@@]4(CC[C@@]32C)C(O)=O)C(C)=C)C1(C)C

InChI Key InChIKey=GKLTYMVQESOHKZ-UHFFFAOYSA-N

Data  2 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 2 hits for monomerid = 50292435   

TargetProtein kinase C epsilon type(Human)
TBA

Curated by ChEMBL
LigandPNGBDBM50292435((1R,3aS,5aR,5bR,7aR,9S,11aR,11bR,13aR,13bR)-9-((E)...)
Affinity DataIC50: 1.50E+5nMAssay Description:Inhibition of PKC epsilonMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/25/2010
Entry Details Article
PubMed
TargetProtein kinase C beta type(Human)
TBA

Curated by ChEMBL
LigandPNGBDBM50292435((1R,3aS,5aR,5bR,7aR,9S,11aR,11bR,13aR,13bR)-9-((E)...)
Affinity DataIC50: 1.50E+5nMAssay Description:Inhibition of PKC beta2More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/25/2010
Entry Details Article
PubMed