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- Title
Sialylexoenitols as precursors for new analogues of sialidase inhibitors.
- Authors
Richichi, Barbara; Lunghi, Carlotta; Papakyriakou, Athanasios; Francesconi, Oscar; Nativi, Cristina
- Abstract
Sialic acids are involved in a plethora of important biological events; among these the most known certainly is the binding of N-acetylneuraminic acid (Neu5Ac) with influenza virus sialidase. Considering Neu5Ac as the template that led to the structure-based development of the two potent antiviral agents zanamivir and oseltamivir, we developed the synthesis of the sialylexoenitol, a new class of sialyl derivative that was used as precursor in powerful hetero-Diels--Alder reactions to form the corresponding spiroketals. Docking calculations employing the crystallographic structure of influenza virus sialidase indicate that these scaffolds could probably interact with most of the active site residues that stabilize Neu5Ac. In addition, their reduced polar nature with respect to Neu5Ac derivatives might provide inhibitors with increased bioavailability.
- Subjects
CHEMICAL precursors; NEURAMINIDASE; SIALIC acids; PLETHORA (Pathology); INFLUENZA viruses; DIELS-Alder reaction; CRYSTAL structure
- Publication
Pure & Applied Chemistry, 2013, Vol 85, Issue 9, p1803
- ISSN
0033-4545
- Publication type
Article
- DOI
10.1351/PAC-CON-12-11-08