NOVEL INHIBITOR OF PHOSPHOLIPASE-A2 WITH TOPICAL ANTIINFLAMMATORY ACTIVITY

被引:30
作者
TRAMPOSCH, KM
STEINER, SA
STANLEY, PL
NETTLETON, DO
FRANSON, RC
LEWIN, AH
CARROLL, FI
机构
[1] RES TRIANGLE INST, DEPT CHEM & LIFE SCI, RES TRIANGLE PK, NC 27709 USA
[2] VIRGINIA COMMONWEALTH UNIV, DEPT BIOCHEM & MOLEC BIOPHYS, RICHMOND, VA 23298 USA
关键词
D O I
10.1016/0006-291X(92)91554-4
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
Activation of a phospholipase A2 (PLA2) is a key step in the production of precursors for the biosynthesis of lipid mediators of inflammation. Inhibition of this enzyme could result in the suppression of three important classes of inflammatory lipids, prostaglandins, leukotrienes and platelet activating factor (PAF), and offers an attractive therapeutic approach to design novel agents for the treatment of inflammation and tissue injury. In this report we describe a novel compound, BMS-181162 4(3′-carboxyphenyl)-3,7-dimethyl-9(2″,6″6″-trimethyl-1″-cyclohexenyl),2Z,4E,6E,8E-nonatetraenoic acid which specifically inhibits a 14 kD human PLA2 and effectively blocks phorbol ester induced skin inflammation in mice. BMS-181162 is the first reported specific inhibitor of PLA2 and its specificity may make it a useful tool in the dissection of the role of PLA2 in the inflammatory process. © 1992.
引用
收藏
页码:272 / 279
页数:8
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