Abstract
We have synthesized a panel of bivalent S-sialoside analogues, with modifications at the 4 position, as inhibitors of influenza virus. These first generation compounds show IC50 values ranging from low micromolar to high nanomolar in enzyme inhibition and plaque reduction assays with two intact viruses, Influenza H1N1 (A/California/07/2009) and H3N2 (A/Hongkong/8/68).
Original language | English (US) |
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Pages (from-to) | 636-643 |
Number of pages | 8 |
Journal | Bioorganic and Medicinal Chemistry Letters |
Volume | 24 |
Issue number | 2 |
DOIs | |
State | Published - Jan 15 2014 |
Externally published | Yes |
Keywords
- Bifunctional
- Glycoconjugates
- Influenza virus
- Inhibitors
- Sialic acid
ASJC Scopus subject areas
- Biochemistry
- Molecular Medicine
- Molecular Biology
- Pharmaceutical Science
- Drug Discovery
- Clinical Biochemistry
- Organic Chemistry