Cyclooxygenase 2 inhibitors: discovery, selectivity and the future

被引:182
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
相关论文
共 54 条
[41]   Dynamics of prostaglandin H synthases - Studies with prostaglandin H synthase 2 Y355F unmask mechanisms of time-dependent inhibition and allosteric activation [J].
So, OY ;
Scarafia, LE ;
Mak, AY ;
Callan, OH ;
Swinney, DC .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (10) :5801-5807
[42]  
Talley JJ, 1999, MED RES REV, V19, P199, DOI 10.1002/(SICI)1098-1128(199905)19:3<199::AID-MED1>3.0.CO
[43]  
2-7
[44]  
Talley JJ, 1999, PROGR MED CHEM, V36, P201, DOI 10.1016/S0079-6468(08)70048-1
[45]   ASPIRIN USE AND REDUCED RISK OF FATAL COLON CANCER [J].
THUN, MJ ;
NAMBOODIRI, MM ;
HEATH, CW .
NEW ENGLAND JOURNAL OF MEDICINE, 1991, 325 (23) :1593-1596
[46]   Cyclooxygenase regulates angiogenesis induced by colon cancer cells [J].
Tsujii, M ;
Kawano, S ;
Tsuji, S ;
Sawaoka, H ;
Hori, M ;
DuBois, RN .
CELL, 1998, 93 (05) :705-716
[47]   INHIBITION OF PROSTAGLANDIN SYNTHESIS AS A MECHANISM OF ACTION FOR ASPIRIN-LIKE DRUGS [J].
VANE, JR .
NATURE-NEW BIOLOGY, 1971, 231 (25) :232-&
[48]   Cyclooxygenases 1 and 2 [J].
Vane, JR ;
Bakhle, YS ;
Botting, RM .
ANNUAL REVIEW OF PHARMACOLOGY AND TOXICOLOGY, 1998, 38 :97-120
[49]  
VANE JR, 1990, STROKE, V21, P12
[50]  
Vane JR, 1996, SCAND J RHEUMATOL, P9