REGIOSPECIFIC AND ENANTIOSELECTIVE METABOLISM OF 8,9-EPOXYEICOSATRIENOIC ACID BY CYCLOOXYGENASE

被引:38
作者
ZHANG, JY
PRAKASH, C
YAMASHITA, K
BLAIR, IA
机构
[1] VANDERBILT UNIV, DEPT CHEM, NASHVILLE, TN 37232 USA
[2] VANDERBILT UNIV, DEPT PHARMACOL, NASHVILLE, TN 37232 USA
[3] VANDERBILT UNIV, CTR MOLEC TOXICOL, NASHVILLE, TN 37232 USA
关键词
D O I
10.1016/0006-291X(92)91619-2
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
8(S),9(R)-epoxyeicosatrienoic acid, a major product of the renal cortex, was found to be a substrate for cyclooxygenase from human platelets and ram seminal vesicles. 11(R)-hydroxy-8(S),9(R)-epoxyeicosatrienoic acid was the sole metabolic product. The 8(R),9(S)-enantiomer formed both C-11 and C-15 hydroxylated metabolites. These novel findings suggest that the cyclooxygenase-dependent renal vasoconstrictor activity of 8(S),9(R)-epoxyeicosatrienoic acid may be due to the 11(R)-hydroxy metabolite. © 1992.
引用
收藏
页码:138 / 143
页数:6
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