Design of Multi-Binding-Site Inhibitors, Ligand Efficiency, and Consensus Screening of Avian Influenza H5N1 Wild-Type Neuraminidase and of the Oseltamivir-Resistant H274Y Variant
Author:
Affiliation:
1. Institute of Chemistry, University of Tartu, Jakobi 2-319, Tartu 51014, Estonia
Publisher
American Chemical Society (ACS)
Subject
Library and Information Sciences,Computer Science Applications,General Chemical Engineering,General Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/ci800242z
Reference36 articles.
1. World Health Organization. Cumulative Number of Confirmed Human Cases of Avian Influenza A/(H5N1) Reported to WHO, 18 Mar 2008, 2008.
2. World Health Organization. Influenza A (H5N1) in Hong Kong Special Administrative Region of China, 19 Feb 2003, 2003.
3. 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 Activity
4. Rational design of potent sialidase-based inhibitors of influenza virus replication
5. Selection of Influenza Virus Mutants in Experimentally Infected Volunteers Treated with Oseltamivir
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