BDBM50077655 (3S,8R,10R,12R,14R)-17-((S)-1-Hydroxy-1,5-dimethyl-hex-4-enyl)-4,4,8,10,14-pentamethyl-hexadecahydro-cyclopenta[a]phenanthrene-3,12-diol::20(S)-Protopanaxadiol::CHEMBL375563

SMILES [H][C@@]1([#6]-[#6][C@]2([#6])[C@]1([H])[#6@H](-[#8])-[#6][C@]1([H])[C@@]3([#6])[#6]-[#6]-[#6@H](-[#8])C([#6])([#6])[C@]3([H])[#6]-[#6][C@@]21[#6])[C@@]([#6])([#8])[#6]-[#6]\[#6]=[#6](\[#6])-[#6]

InChI Key InChIKey=QBNONILGYWCMII-UHFFFAOYSA-N

Data  2 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 2 hits for monomerid = 50077655   

TargetSterol O-acyltransferase 1(Rat)
Korea Research Institute of Bioscience and Biotechnology

Curated by ChEMBL
LigandPNGBDBM50077655((3S,8R,10R,12R,14R)-17-((S)-1-Hydroxy-1,5-dimethyl...)
Affinity DataIC50: 3.00E+4nMAssay Description:In vitro inhibitory activity of compound was measured on rat liver Acyl coenzyme A:cholesterol acyltransferaseMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetEstrogen receptor(Human)
Shenyang Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50077655((3S,8R,10R,12R,14R)-17-((S)-1-Hydroxy-1,5-dimethyl...)
Affinity DataIC50: 2.63E+4nMAssay Description:Displacement of [3H]-17beta-estradiol to estrogen receptor (unknown origin)More data for this Ligand-Target Pair
In Depth
Date in BDB:
4/19/2024
Entry Details
PubMed