Prasit P, Belley M, Blouin M, Brideau C, Chan C, Charleson S, Evans J F, Frenette R, Gauthier J Y, Guay J
Merck Frosst Centre for Therapeutic Research, Pointe Claire-Dorval, Québec, Canada.
J Lipid Mediat. 1993 Mar-Apr;6(1-3):239-44.
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.
描述了强效口服活性白三烯生物合成抑制剂MK-0591(3-[1-(4-氯苄基)-3-(叔丁硫基)-5-(喹啉-2-基甲氧基)吲哚-2-基]-2,2-二甲基丙酸),即化合物12的研发过程。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。它通过与一种膜蛋白——5-脂氧合酶激活蛋白(FLAP)特异性相互作用的新机制发挥作用,该蛋白已被证明对炎症细胞中白三烯的合成至关重要。文中还简要比较了它与其前身MK-886和L-674,636的生物活性。