BDBM50669055 CHEMBL6192808

SMILES O=C([C@H]1O[C@H](O[C@@H]2[C@@H](O)[C@H](O[C@H]3O[C@H](CNS(=O)(=O)[O-])[C@@H](O)C[C@H]3NS(=O)(=O)[O-])[C@@H](NS(=O)(=O)[O-])C[C@H]2NS(=O)(=O)[O-])[C@H](O)[C@@H](NS(=O)(=O)[O-])[C@@H]1O)N1CCc2ccccc21

InChI Key InChIKey=ILFDTWORRRQAAD-UHFFFAOYSA-I

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 = 50669055   

TargetHeparanase(Human)
Wayne State University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50669055BDBM50669055(CHEMBL6192808)
Affinity DataIC50: 2.39E+4nMAssay Description:Inhibition of N-terminal His-tagged recombinant human heparanase (36 to 543 residues) extracted from CHO cells using Biotin-heparin sulfate-Eu crypta...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed