Synthesis of methyl α-sialosides N-substituted with large alkanoyl groups, and investigation of their inhibition of agglutination of erythrocytes by influenza A virus
- 30 April 1993
- journal article
- Published by Elsevier in Bioorganic & Medicinal Chemistry Letters
- Vol. 3 (4) , 747-752
- https://doi.org/10.1016/s0960-894x(01)81267-1
Abstract
No abstract availableKeywords
This publication has 19 references indexed in Scilit:
- Molecular recognition of bivalent sialosides by influenza virusJournal of the American Chemical Society, 1991
- Polyacrylamides bearing pendant .alpha.-sialoside groups strongly inhibit agglutination of erythrocytes by influenza virusJournal of the American Chemical Society, 1991
- Synthesis of protein conjugates and analogues of N-acetylneuraminic acidCanadian Journal of Chemistry, 1990
- Synthetic polymeric sialoside inhibitors of influenza virus receptor‐binding activityFEBS Letters, 1990
- Hemagglutinins from two influenza virus variants bind to sialic acid derivatives with millimolar dissociation constants: a 500-MHz proton nuclear magnetic resonance studyBiochemistry, 1989
- The neuraminidase of influenza virusProteins-Structure Function and Bioinformatics, 1989
- Structure of the influenza virus haemagglutinin complexed with its receptor, sialic acidNature, 1988
- Recognition of monovalent sialosides by influenza virus H3 hemagglutininVirology, 1987
- THE STRUCTURE AND FUNCTION OF THE HEMAGGLUTININ MEMBRANE GLYCOPROTEIN OF INFLUENZA VIRUSAnnual Review of Biochemistry, 1987
- Molecular Biological Background of the Species and Organ Specificity of Influenza A VirusesAngewandte Chemie International Edition in English, 1986