BDBM50175877 2-hydroxyethyl (4aS,6aS,6bR,8aR,10R,11R,12aR,12bR,14bS)-10,11-dihydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,2,3,4,4a,5,6,6a,6b,7,8,8a,9,10,11,12,12a,12b,13,14b-icosahydropicene-4a-carboxylate::CHEMBL204906

SMILES CC1(C)CC[C@@]2(CC[C@]3(C)C(=CC[C@@H]4[C@@]5(C)C[C@@H](O)[C@H](O)C(C)(C)[C@@H]5CC[C@@]34C)[C@@H]2C1)C(=O)OCCO

InChI Key InChIKey=VWOCPYLNQOWOQM-UHFFFAOYSA-N

Data  2 KI  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 4 hits for monomerid = 50175877   

TargetCholinesterase(Horse)
Martin-Luther-Universit£T Halle-Wittenberg

Curated by ChEMBL
LigandPNGBDBM50175877(2-hydroxyethyl (4aS,6aS,6bR,8aR,10R,11R,12aR,12bR,...)
Affinity DataKi: >1.00E+5nMAssay Description:Inhibition of equine serum BChE using butyrylthiocholine iodide as substrate preincubated for 20mins before the addition of substrate by Ellman's met...More data for this Ligand-Target Pair
In Depth
Date in BDB:
7/2/2017
Entry Details Article
PubMed
TargetAcetylcholinesterase(Electric eel)
Martin-Luther-Universit£T Halle-Wittenberg

Curated by ChEMBL
LigandPNGBDBM50175877(2-hydroxyethyl (4aS,6aS,6bR,8aR,10R,11R,12aR,12bR,...)
Affinity DataKi: >1.00E+5nMAssay Description:Inhibition of Electrophorus electricus AChE using acetylthiocholine iodide as substrate preincubated for 20mins before the addition of substrate by E...More data for this Ligand-Target Pair
In Depth
Date in BDB:
7/2/2017
Entry Details Article
PubMed
TargetGlycogen phosphorylase, muscle form(Rabbit)
Chinese Academy of Sciences

Curated by ChEMBL
LigandPNGBDBM50175877(2-hydroxyethyl (4aS,6aS,6bR,8aR,10R,11R,12aR,12bR,...)
Affinity DataIC50: 1.51E+5nMAssay Description:Inhibition of rabbit muscle glycogen phosphorylase A assessed as release of phosphate from glucose-1-phosphate after 25 mins by microplate reader bas...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/23/2012
Entry Details Article
PubMed
TargetGlycogen phosphorylase, muscle form(Rabbit)
Chinese Academy of Sciences

Curated by ChEMBL
LigandPNGBDBM50175877(2-hydroxyethyl (4aS,6aS,6bR,8aR,10R,11R,12aR,12bR,...)
Affinity DataIC50: 1.53E+5nMAssay Description:Inhibitory activity against rabbit muscle GPaMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed