Different Antiviral Potencies of BV-araU and Related Nucleoside Analogues against Herpes Simplex Virus Type 1 in Human Cell Lines and Vero Cells

Author:

Machida Haruhiko1,Nishitani Makiko1,Suzutani Tatsuo2,Hayashi Kozaburo3

Affiliation:

1. Biology Laboratory, R & D Division; Yamasa Shoyu Co., Ltd.; Choshi Chiba 288 Japan

2. Division of Microbiology; Asahikawa Medical College; Asahikawa Hokkaido 078-11 Japan

3. Public Health Research Institute of Kobe City; Kobe Hyogo 650 Japan

Publisher

Wiley

Subject

Virology,Immunology,Microbiology

Reference18 articles.

1. Role of viral ribonucleotide reductase in the increase of dTTP pool size in herpes simplex virus-infected Vero cells;Daikoku;J. Gen. Virol.,1991

2. Comparative efficacy of antiherpes drugs in different cell lines;De Clercq;Antimicrob. Agents Chemother.,1982

3. Structure-activity analysis of antagonism of the feedback inhibition of thymidine kinase;Fischer;Biochem. Pharmacol.,1988

4. Antiviral activities of some newer 2′-fluoro-5-substituted arabinosylpyrimidine nucleosides,1985

5. Influence of cells and virus multiplicity on the inhibition of herpesviruses with acycloguanosine;Harmenberg;Intervirology,1980

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