BDBM50291609 CHEMBL3215458::CHEMBL410026::Sialyl Lewis X Analog

SMILES C[C@@H]1O[C@@H](O[C@@H]2[C@H](NC(=O)c3ccc4ccccc4c3)[C@H](OCCCc3cccc(CCCO)c3)O[C@@H](CO)[C@H]2O[C@@H]2O[C@@H](CO)[C@H](O)[C@H](O[C@@]3(C[C@@H](O)[C@@H](NC(C)=O)[C@@H](O3)[C@H](O)[C@H](O)CO)C([O-])=O)[C@@H]2O)[C@@H](O)[C@@H](O)[C@@H]1O

InChI Key InChIKey=GZXDJFFCWNYDPO-UHFFFAOYSA-M

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 = 50291609   

TargetE-selectin(Human)
TBA

Curated by ChEMBL
LigandPNGBDBM50291609(Sialyl Lewis X Analog | CHEMBL410026 | CHEMBL32154...)
Affinity DataIC50: 2.00E+5nMAssay Description:Compound was evaluated for its inhibitory activity against adhesion of HL-60(human promyelocytic leukemia cells) to recombinant human soluble E-selec...More data for this Ligand-Target Pair
In Depth
Date in BDB:
9/28/2012
Entry Details Article