BDBM50654256 CHEMBL6133033

SMILES O=C(O)[C@H]1O[C@@H](Oc2ccc([N+](=O)[O-])cc2)[C@H](O)[C@@H](O)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O[C@@H]2O[C@@H](C(=O)O)[C@@H](O[C@H]3O[C@H](CO)[C@@H](O[C@@H]4O[C@@H](C(=O)O)[C@@H](O[C@H]5O[C@H](CO)[C@@H](O[C@@H]6O[C@@H](C(=O)O)[C@@H](O[C@H]7O[C@H](CO)[C@@H](O[C@@H]8O[C@@H](C(=O)O)[C@@H](O[C@H]9O[C@H](CO)[C@@H](O[C@@H]%10O[C@@H](C(=O)O)[C@@H](O[C@H]%11O[C@H](CO)[C@@H](O[C@@H]%12O[C@@H](C(=O)O)[C@@H](O[C@H]%13O[C@H](CO)[C@@H](O[C@@H]%14O[C@@H](C(=O)O)[C@@H](O[C@H]%15O[C@H](CO)[C@@H](O[C@@H]%16O[C@H](C(=O)O)[C@@H](O[C@H]%17O[C@H](CO)[C@@H](O)[C@H](O)[C@H]%17NS(=O)(=O)O)[C@H](O)[C@H]%16O)[C@H](O)[C@H]%15NS(=O)(=O)O)[C@H](O)[C@H]%14OS(=O)(=O)O)[C@H](O)[C@H]%13NS(=O)(=O)O)[C@H](O)[C@H]%12OS(=O)(=O)O)[C@H](O)[C@H]%11NS(=O)(=O)O)[C@H](O)[C@H]%10OS(=O)(=O)O)[C@H](O)[C@H]9NS(=O)(=O)O)[C@H](O)[C@H]8OS(=O)(=O)O)[C@H](O)[C@H]7NS(=O)(=O)O)[C@H](O)[C@H]6OS(=O)(=O)O)[C@H](O)[C@H]5NS(=O)(=O)O)[C@H](O)[C@H]4OS(=O)(=O)O)[C@H](O)[C@H]3NS(=O)(=O)O)[C@H](O)[C@H]2OS(=O)(=O)O)[C@H](O)[C@H]1NS(=O)(=O)O

InChI Key

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
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   Substructure
Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 1 hit for monomerid = 50654256   

TargetHigh mobility group protein B1(Human)
China Pharmaceutical University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50654256BDBM50654256(CHEMBL6133033)
Affinity DataKd:  187nMAssay Description:Agonist activity against S1P1 receptor by cell based FRET assayMore data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/4/2026
Entry Details PubMed