Efficacy of orally administered T-705 pyrazine analog on lethal West Nile virus infection in rodents

被引:103
作者
Morrey, John D. [1 ]
Taro, Brandon S. [1 ]
Siddharthan, Venkatraman [1 ]
Wang, Hong [1 ]
Smee, Donald F. [1 ]
Christensen, Andrew J. [1 ]
Furuta, Yousuke [2 ]
机构
[1] Utah State Univ, Inst Antiviral Res, Logan, UT 84322 USA
[2] Toyama Chem Co Ltd, Tokyo, Japan
关键词
T-705; West Nile virus; Hamsters; Mice; 6-Fluoro-3-hydroxy-2-pyrazinecarboxamide;
D O I
10.1016/j.antiviral.2008.07.009
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
We describe herein that a pyrazine derivative, T-705 (6-fluoro-3-hydroxy-2-pyrazinecarboxamide), is protective for a lethal West Nile virus infection in rodents. Oral T-705 at 200 mg/kg administered twice daily beginning 4 h after subcutaneous (s.c.) viral challenge protected mice and hamsters against WNV-induced mortality, and reduced viral protein expression and viral RNA in brains. The minimal effective oral dose was between 20 and 65 mg/kg when administered twice a day beginning I day after viral s.c. challenge of mice. Treatment could be delayed out to 2 days after viral challenge to still achieve efficacy in mice. Further development of this compound should be considered for treatment of WNV. (C) 2008 Published by Elsevier B.V.
引用
收藏
页码:377 / 379
页数:3
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