Cyclooxygenase 2 inhibitors: discovery, selectivity and the future

被引:181
作者
Marnett, LJ
Kalgutkar, AS
机构
[1] Vanderbilt Univ, Sch Med, Mem Lab Canc Res,Dept Biochem, Ctr Mol Toxicol, Nashville, TN 37232 USA
[2] Vanderbilt Univ, Sch Med, Mem Lab Canc Res,Dept Chem, Ctr Mol Toxicol, Nashville, TN 37232 USA
[3] Vanderbilt Univ, Sch Med, Vanderbilt Canc Ctr, Nashville, TN 37232 USA
关键词
D O I
10.1016/S0165-6147(99)01385-1
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The recent marketing of two selective cyclooxygenase 2 (COX-2) inhibitors climaxes the first phase of an exciting and fast-paced effort to exploit a novel molecular target for nonsteroidal anti-inflammatory drugs (NSAIDs). Much has been written in the lay and scientific press about the potential of COX-2 inhibitors as anti-inflammatory and analgesic agents that lack the gastrointestinal side-effects of traditional NSAIDs. Although research on COX-2 inhibitors has focussed mainly on inflammation and pain, experimental and epidemiological data suggest that COX-2 inhibitors could be used in the treatment or prevention of a broader range of diseases. In this review, some key points and unresolved issues related to the discovery of COX-2 inhibitors, the kinetic and structural basis for their selectivity, and possible complications in their development and use will be discussed.
引用
收藏
页码:465 / 469
页数:7
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