BDBM50250341 23-hydroxyursolic acid::CHEMBL523622

SMILES C[C@@H]1CC[C@@]2(CC[C@]3(C)C(=CC[C@@H]4[C@@]5(C)CC[C@H](O)[C@@](C)(CO)[C@@H]5CC[C@@]34C)[C@@H]2[C@H]1C)C(O)=O

InChI Key InChIKey=NZCULBURCGAPSF-PQWKYGPVSA-N

Data  3 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 3 hits for monomerid = 50250341   

TargetSterol O-acyltransferase 1(Rattus norvegicus)
Kayaku

Curated by ChEMBL
LigandPNGBDBM50250341(23-hydroxyursolic acid | CHEMBL523622)
Affinity DataIC50:  6.40E+4nMAssay Description:Inhibition of rat liver microsomal ACATMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTyrosine-protein phosphatase non-receptor type 1(Homo sapiens (Human))
University Of Copenhagen

Curated by ChEMBL
LigandPNGBDBM50250341(23-hydroxyursolic acid | CHEMBL523622)
Affinity DataIC50:  7.40E+3nMAssay Description:Inhibition of GST-tagged human PTP1B expressed in Escherichia coli using pNPP substrate assessed as reduction in p-nitrophenol releaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTyrosine-protein phosphatase non-receptor type 1(Homo sapiens (Human))
University Of Copenhagen

Curated by ChEMBL
LigandPNGBDBM50250341(23-hydroxyursolic acid | CHEMBL523622)
Affinity DataIC50:  7.40E+3nMAssay Description:Inhibition of human recombinant PTP1B using p-nitrophenyl phosphate as substrate assessed as p-nitrophenol release after 30 minsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed