Synthesis and activity of C2-substituted analogs of influenza neuraminidase inhibitor GS 4071-Reference-Cited by-同舟云学术

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Synthesis and activity of C2-substituted analogs of influenza neuraminidase inhibitor GS 4071

Published:1997-07 Issue:14 Volume:7 Page:1847-1850
ISSN:0960-894X
Container-title:Bioorganic & Medicinal Chemistry Letters
language:en
Short-container-title:Bioorganic & Medicinal Chemistry Letters

Author:

Zhang Lijun,Williams Matthew A.,Mendel Dirk B.,Escarpe Paul A.,Kim Choung U.

Publisher

Elsevier BV

Subject

Organic Chemistry,Clinical Biochemistry,Drug Discovery,Pharmaceutical Science,Molecular Biology,Molecular Medicine,Biochemistry

Reference6 articles.

1. Impact of influenza epidemics on mortality in the United States from October 1972 to May 1985.

2. 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

3. New Potent, Orally Active Neuraminidase Inhibitors as Anti-Influenza Agents: In Vitro and In Vivo Activity of GS 4071 and Analogs;Kim,1996

4. Synthesis of (-)-2-Chloroshikimic Acid

5. Synthesis of 2-methyl-1-cyclopentene-1-carboxylate esters. Reaction of cuprates with .beta.-substituted cyclopentenecarboxylates

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1. Synthetic Advancement of Neuraminidase Inhibitor “Tamiflu”;ChemistrySelect;2020-05-27

2. Applications of Artificial Intelligence and Machine Learning in Viral Biology;Global Virology III: Virology in the 21st Century;2019

3. Production and Synthetic Modifications of Shikimic Acid;Chemical Reviews;2018-10-11

4. Total Syntheses of Biologically Active Compounds around Marine Natural Products;Journal of Synthetic Organic Chemistry, Japan;2016

5. Quantitative structure–activity relationship study of influenza virus neuraminidase A/PR/8/34 (H1N1) inhibitors by genetic algorithm feature selection and support vector regression;Chemometrics and Intelligent Laboratory Systems;2013-08

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