BDBM50626571 CHEMBL5429017

SMILES [H][C@@]12O[C@H](Cn3cc(CO[C@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@@H]4O)nn3)[C@@H](O[C@@]3([H])O[C@H](Cn4cc(CO[C@H]5O[C@H](CO)[C@@H](O)[C@H](O)[C@@H]5O)nn4)[C@@H](O[C@@]4([H])O[C@H](Cn5cc(CO[C@H]6O[C@H](CO)[C@@H](O)[C@H](O)[C@@H]6O)nn5)[C@@H](O[C@@]5([H])O[C@H](Cn6cc(CO[C@H]7O[C@H](CO)[C@@H](O)[C@H](O)[C@@H]7O)nn6)[C@@H](O[C@@]6([H])O[C@H](Cn7cc(CO[C@H]8O[C@H](CO)[C@@H](O)[C@H](O)[C@@H]8O)nn7)[C@@H](O[C@@]7([H])O[C@H](Cn8cc(CO[C@H]9O[C@H](CO)[C@@H](O)[C@H](O)[C@@H]9O)nn8)[C@@H](O[C@@]8([H])O[C@H](Cn9cc(CO[C@H]%10O[C@H](CO)[C@@H](O)[C@H](O)[C@@H]%10O)nn9)[C@@H](O[C@@]9([H])O[C@H](Cn%10cc(CO[C@H]%11O[C@H](CO)[C@@H](O)[C@H](O)[C@@H]%11O)nn%10)[C@@H](O1)[C@H](O)[C@H]9O)[C@H](O)[C@H]8O)[C@H](O)[C@H]7O)[C@H](O)[C@H]6O)[C@H](O)[C@H]5O)[C@H](O)[C@H]4O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O

InChI Key InChIKey=ISHZJQKMMZNHFW-UHFFFAOYSA-N

Data  1 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 1 hit for monomerid = 50626571   

TargetPlatelet-derived growth factor receptor alpha/beta(Mouse)
Quaid-I-Azam University

Curated by ChEMBL
LigandPNGBDBM50626571(CHEMBL5429017)
Affinity DataIC50: 3.20E+4nMAssay Description:Inhibition of Saccharomyces cerevisiae alpha-glucosidase using p-nitrophenyl-alpha-D-glucopyranoside as substrate incubated for 15 mins by UV-visible...More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/18/2024
Entry Details
PubMed