null

SMILES CCC1CC(C[C@@H](O[C@@H]2O[C@@H](CO)[C@H](O)C(O[C@@H](CC3CCCCC3)C(=O)O[Na])C2NC(C)=O)[C@@H]1O[C@@H]1OC(C)[C@@H](O)[C@H](O)C1O)C(=O)NCCNC(=O)CCOCCOCCNC(=O)c1cn(nn1)C(COS(=O)(=O)O[Na])(COS(=O)(=O)O[Na])COS(=O)(=O)O[Na]

InChI Key

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

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 1 hit for monomerid = 528669   

TargetE-selectin(Homo sapiens (Human))TBA
LigandPNGBDBM528669(US11197877, Compound 46)copy SMILES
Affinity DataIC50: 192nMAssay Description:The inhibition assay to screen for and characterize glycomimetic antagonists of E-selectin is a competitive binding assay, which allows the determina...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2JM2DT8US Patent