The development of COX2 inhibitors

被引:363
|
作者
Flower, RJ [1 ]
机构
[1] Queen Mary Univ London, William Harvey Res Inst, Dept Biochem Pharmacol, London EC1M 6BQ, England
关键词
D O I
10.1038/nrd1034
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Aspirin, arguably the world's favourite drug, has been around since the late nineteenth century, but it wasn't until the late 1970s that its ability to inhibit prostaglandin production by the cyclooxygenase enzyme was identified as the basis of its therapeutic action. Early hints of a second form of the cyclooxygenase that was differentially sensitive to other aspirin-like drugs ultimately ushered in an exciting era of drug discovery, culminating in the introduction of an entirely new generation of anti-inflammatories. This article reviews the story of this discovery and looks at the future of cyclooxygenase pharmacology.
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页码:179 / 191
页数:13
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