结构和活性关系导致ICI D2138的发现,一个选择性的,有效的和口服活性的5-脂氧合酶抑制剂。

Journal of lipid mediators Pub Date : 1993-03-01
G C Crawley, T G Bird, P Bruneau, R I Dowell, P N Edwards, S J Foster, J M Girodeau, R M McMillan, E R Walker, D Waterson
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引用次数: 0

摘要

综述了(甲氧基烷基)噻唑和4-甲氧基四氢吡喃系列5-脂氧合酶抑制剂的结构和活性关系。4-甲氧基四氢吡喃系列的一个成员,6-([氟-5-(4-甲氧基-3,4,5,6-四氢- 2h -吡喃-4-基)苯氧基]甲基)-1-甲基喹啉-2- 1 (ICI D2138),正在进行临床评估。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Structure and activity relationships leading to the discovery of ICI D2138, a selective, potent and orally active inhibitor of 5-lipoxygenase.

Structure and activity relationships of (methoxyalkyl)thiazole and 4-methoxytetrahydropyran series of 5-lipoxygenase inhibitors are reviewed. One member of the 4-methoxytetrahydropyran series, 6-([fluoro-5-(4-methoxy-3,4,5,6-tetrahydro-2H-pyran-4-yl)phenoxy]methyl) -1- methylquinol-2-one (ICI D2138), is undergoing clinical evaluation.

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