A new class of leukotriene biosynthesis inhibitor: the development of MK-0591.

Journal of lipid mediators Pub Date : 1993-03-01
P Prasit, M Belley, M Blouin, C Brideau, C Chan, S Charleson, J F Evans, R Frenette, J Y Gauthier, J Guay
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引用次数: 0

Abstract

The evolution of MK-0591 (3-[1-(4-chlorobenzyl)-3-(t-butylthio)-5-(quinolin-2-ylmethoxy+ ++)indol-2-yl]- 2,2-dimethylpropanoic acid), 12, a potent, orally active leukotriene biosynthesis inhibitor is described. MK-0591 is currently undergoing clinical evaluation as a potential agent for the treatment of asthma and inflammatory bowel disease. It acts through a novel mechanism by a specific interaction with a membrane protein, 5-lipoxygenase activating protein (FLAP), which has been shown to be essential for LT synthesis in inflammatory cells. A brief comparison of its biological activity with that of its progenitors MK-886 and L-674,636 is described.

一类新的白三烯生物合成抑制剂:MK-0591的研制。
描述了有效的口服白三烯生物合成抑制剂MK-0591(3-[1-(4-氯苯基)-3-(t-丁基硫基)-5-(喹啉-2-基甲氧基++ +)吲哚-2-基]- 2,2-二甲基丙酸),12的进化过程。MK-0591目前正在进行临床评估,作为治疗哮喘和炎症性肠病的潜在药物。它通过与膜蛋白5-脂氧合酶激活蛋白(FLAP)的特异性相互作用的新机制起作用,该蛋白已被证明是炎症细胞中LT合成所必需的。对其生物活性与其祖细胞MK-886和L-674,636进行了简要比较。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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