N-hydroxyurea and hydroxamic acid inhibitors of cyclooxygenase and 5-lipoxygenase

被引:38
|
作者
Connolly, PJ [1 ]
Wetter, SK [1 ]
Beers, KN [1 ]
Hamel, SC [1 ]
Chen, RHK [1 ]
Wachter, MP [1 ]
Ansell, J [1 ]
Singer, MM [1 ]
Steber, M [1 ]
Ritchie, DM [1 ]
Argentieri, DC [1 ]
机构
[1] RW Johnson Pharmaceut Res Inst, Raritan, NJ 08869 USA
关键词
D O I
10.1016/S0960-894X(99)00117-1
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Two series of compounds (1 and 2) having structural features of the dual COX/5-LO inhibitor tepoxalin and the 5-LO inhibitor ABT-761 were prepared. Many of these hybrid compounds are potent COX and 5-LO inhibitors; two compounds (la and 2t) inhibit eicosanoid biosynthesis in an ex vivo assay. (C) 1999 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:979 / 984
页数:6
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