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-Reference-Cited by-同舟云学术

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

Published:1997-01-01 Issue:4 Volume:119 Page:681-690
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Kim Choung U.¹,Lew Willard¹,Williams Matthew A.¹,Liu Hongtao¹,Zhang Lijun¹,Swaminathan S.¹,Bischofberger Norbert¹,Chen Ming S.¹,Mendel Dirk B.¹,Tai Chun Y.¹,Laver W. Graeme¹,Stevens Raymond C.¹

Affiliation:

1. Contribution from Gilead Sciences Inc., 353 Lakeside Drive, Foster City, California 94404, John Curtin School of Medical Research, The Australian National University, Canberra 260, Australia, and Department of Chemistry, University of California, Berkeley, California 94720

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja963036t

Reference53 articles.

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2. (a) Couch, R. B.; Six, H. R. InAntiviral Chemotherapy: New Directionfor Clinical Application and Research; Mills J., Corey L., Eds.; Elsevier Science Publishing: Oxford, 1986; pp 50−56.

3. Emergence and Apparent Transmission of Rimantadine-Resistant Influenza A Virus in Families

4. Binding of influenza virus hemagglutinin to analogs of its cell-surface receptor, sialic acid: analysis by proton nuclear magnetic resonance spectroscopy and x-ray crystallography

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