BDBM50586766 CHEMBL5079023

SMILES [H][C@]12OC(=O)C(=C)[C@]1([H])[C@@H](C\C(CC(O)=O)=C\CC\C(C)=C\2)OC(=O)C(\C)=C\C

InChI Key InChIKey=LHSDRJQBPKZSPG-UHFFFAOYSA-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 = 50586766   

TargetTyrosine-protein phosphatase non-receptor type 1(Human)
Tohoku Medical and Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50586766(CHEMBL5079023)
Affinity DataIC50: 2.40E+4nMAssay Description:Inhibition of human recombinant PTP1B using pNPP as substrate assessed as reduction in p-nitrophenol release incubated for 30 mins by absorbance base...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/7/2023
Entry Details Article
PubMed
TargetTyrosine-protein phosphatase non-receptor type 2(Human)
Tohoku Medical and Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50586766(CHEMBL5079023)
Affinity DataIC50: 2.80E+4nMAssay Description:Inhibition of human recombinant TCPTP using pNPP as substrate assessed as reduction in p-nitrophenol release incubated for 30 mins by absorbance base...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/7/2023
Entry Details Article
PubMed
TargetMaltase-glucoamylase(Human)
Tohoku Medical and Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50586766(CHEMBL5079023)
Affinity DataIC50: 2.80E+4nMAssay Description:Inhibition of alpha-glucosidase (unknown origin) using p-nitrophenyl-alpha-D-glucopyranoside as substrate incubated for 50 mins by microplate reader ...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/7/2023
Entry Details Article
PubMed