Novel α- and β-Amino Acid Inhibitors of Influenza Virus Neuraminidase
Author:
Affiliation:
1. Discovery Research, Pharmaceutical Products Division, Abbott Laboratories, Abbott Park, Illinois 60064-6217,1 and
2. John Curtin School of Medical Research, Australian National University, Canberra 2601, Australia2
Abstract
Publisher
American Society for Microbiology
Subject
Infectious Diseases,Pharmacology (medical),Pharmacology
Link
https://journals.asm.org/doi/pdf/10.1128/AAC.45.9.2563-2570.2001
Reference32 articles.
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2. BCX-1812 (RWJ-270201): discovery of a novel, highly potent, orally active, and selective influenza neuraminidase inhibitor through structure-based drug design.;Babu Y. S.;J. Med. Chem.,2000
3. Brunger A. T. X-PLOR Version 3.1. A system for X-ray crystallography and NMR. 1992 Yale University Press New Haven Conn
4. Influenza B virus neuraminidase can synthesize its own inhibitor.;Burmeister W. P.;Structure,1993
5. Evidence for a sialosyl cation transition state complex in the reaction of sialidase from influenza virus.;Chong A. K. J.;Eur. J. Biochem.,1992
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