CYCLIC ARYL HYDROXAMIC ACIDS - SYNTHESIS AND INHIBITION OF 5-LIPOXYGENASE

被引:10
|
作者
MISRA, RN
BOTTI, CM
HASLANGER, MF
ENGEBRECHT, JR
MAHONEY, EM
CIOSEK, CP
机构
[1] Bristol-Myers Squibb, Pharmaceutical Research Institute, Princeton, NJ 08543-4000
关键词
D O I
10.1016/S0960-894X(01)80811-8
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Cyclic aryl hydroxamic acids 11 were prepared and found to be significantly less potent in inhibiting 5-lipoxygenase than their acyclic analogs 8. This finding provides support to the hypothesis that hydroxamic acids may be inhibiting 5-LO by a mechanism other than simple iron (III) binding.
引用
收藏
页码:295 / 298
页数:4
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