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Acyclic tethers mimicking subunits of polysaccharide ligands: selectin antagonists.

ABSTRACT: We report on the design and synthesis of molecules having E- and P-selectins blocking activity both in vitro and in vivo. The GlcNAc component of the selectin ligand sialyl Lewis(X) was replaced by an acyclic tether that links two saccharide units. The minimization of intramolecular dipole-dipole interactions and the gauche effect would be at the origin of the conformational bias imposed by this acyclic tether. The stereoselective synthesis of these molecules, their biochemical and biological evaluations using surface plasmon resonance spectroscopy (SPR), and in vivo assays are described. Because the structure of our analogues differs from the most potent E-selectin antagonists reported, our acyclic analogues offer new opportunities for chemical diversity.

SUBMITTER: Calosso M

PROVIDER: S-EPMC4160748 | biostudies-literature | 2014 Sep

REPOSITORIES: biostudies-literature

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Acyclic tethers mimicking subunits of polysaccharide ligands: selectin antagonists.

Calosso Mickael M Tambutet Guillaume G Charpentier Daniel D St-Pierre Gabrielle G Vaillancourt Marc M Bencheqroun Mohammed M Gratton Jean-Philippe JP Prévost Michel M Guindon Yvan Y

ACS medicinal chemistry letters 20140716 9

We report on the design and synthesis of molecules having E- and P-selectins blocking activity both in vitro and in vivo. The GlcNAc component of the selectin ligand sialyl Lewis(X) was replaced by an acyclic tether that links two saccharide units. The minimization of intramolecular dipole-dipole interactions and the gauche effect would be at the origin of the conformational bias imposed by this acyclic tether. The stereoselective synthesis of these molecules, their biochemical and biological ev ...[more]

PMID: 25221666

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