Targeting Cytosolic Phospholipase A2α for Novel Anti-Inflammatory Agents

被引:22
作者
Soubhye, Jalal [1 ]
van Antwerpen, Pierre [1 ]
Dufrasne, Francois [2 ]
机构
[1] Univ Libre Bruxelles, Fac Pharm, Dept Pharmacognosy Bioanal & Drug Discovery, Blvd Triomphe, B-1050 Brussels, Belgium
[2] Univ Libre Bruxelles, Fac Pharm, Microbiol Bioorgan & Macromol Chem, Campus Plaine,Blvd Triomphe, B-1050 Brussels, Belgium
关键词
Cytosolic phospholipase A2 alpha; inflammation; anti-inflammatory; cPLA2 alpha inhibitors; structure-activity relationship; arachidonic acid; ARACHIDONIC-ACID RELEASE; PROSTAGLANDIN E-2; C2; DOMAIN; METABOLIC STABILITY; 1-(5-CARBOXYINDOL-1-YL)PROPAN-2-ONE INHIBITORS; ANTISENSE OLIGONUCLEOTIDE; PYRROLIDINE INHIBITORS; BIOLOGICAL EVALUATION; INTESTINAL POLYPOSIS; RHEUMATOID-ARTHRITIS;
D O I
10.2174/0929867325666180117103919
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Group IV cytosolic phospholipase A2 (cPLA2 alpha) plays a critical role in inflammatory processes. It produces arachidonic acid which is the main source of the pro-inflammatory eicosanoids mediators that are important in innate immune system. In some cases, these proinflammatory mediators cause damages to the host tissues and therefore promote autoimmune diseases. Consequently, development of potent inhibitors against cPLA2 alpha could improve the therapy of inflammatory diseases. In the last two decades, intense efforts have been done to find potent cPLA2 alpha inhibitors. Several scaffolds have been developed with the use of structure-activity relationship (SAR) studies, and potent inhibitors have been obtained. The poor absorption of these compounds from intestine was the main challenge for clinical application. This review illustrates the search for cPLA2 alpha inhibitors, their SAR studies and biological effects.
引用
收藏
页码:2418 / 2447
页数:30
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