Design of benzoic acid inhibitors of influenza neuraminidase containing a cyclic substitution for the N-acetyl grouping
- 1 July 1999
- journal article
- Published by Elsevier in Bioorganic & Medicinal Chemistry Letters
- Vol. 9 (14) , 1901-1906
- https://doi.org/10.1016/s0960-894x(99)00318-2
Abstract
No abstract availableKeywords
This publication has 11 references indexed in Scilit:
- Guanidinobenzoic acid inhibitors of influenza virus neuraminidase 1 1Edited by R. HuberJournal of Molecular Biology, 1997
- Influenza Neuraminidase Inhibitors Possessing a Novel Hydrophobic Interaction in the Enzyme Active Site: Design, Synthesis, and Structural Analysis of Carbocyclic Sialic Acid Analogues with Potent Anti-Influenza ActivityJournal of the American Chemical Society, 1997
- Safety and efficacy of the neuraminidase inhibitor GG167 in experimental human influenzaPublished by American Medical Association (AMA) ,1996
- Structure-Based Inhibitors of Influenza Virus Sialidase. A Benzoic Acid Lead with Novel InteractionJournal of Medicinal Chemistry, 1995
- Structures of Aromatic Inhibitors of Influenza Virus NeuraminidaseBiochemistry, 1995
- Rational design of potent sialidase-based inhibitors of influenza virus replicationNature, 1993
- Inhibition of sialidases from viral, bacterial and mammalian sources by analogues of 2-deoxy-2,3-didehydro-N-acetylneuraminic acid modified at the C-4 positionGlycoconjugate Journal, 1993
- The neuraminidase of influenza virusProteins-Structure Function and Bioinformatics, 1989
- Characterization of temperature sensitive influenza virus mutants defective in neuraminidaseVirology, 1974
- Inhibition of neuraminidase activity by derivatives of 2-deoxy-2,3-dehydro-N-acetylneuraminic acidVirology, 1974