肽多溴三烯拮抗剂的设计策略。

Journal of lipid mediators Pub Date : 1993-03-01
A von Sprecher, A Beck, M Gerspacher, A Sallmann, G P Anderson, N Subramanian, U Niederhauser, M A Bray
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引用次数: 0

摘要

近二十年来在SRS-A和肽二烯(pLT)拮抗剂领域的研究为设计有效的pLT拮抗剂提供了信息,这些拮抗剂具有以下部分或全部结构元素:(1)亲脂锚,适合LTD4受体的亲脂口袋;(2)模拟LTD4的四烯体系的中心亲脂性单元;(3)一个或两个酸性基团,作为LTD4的二十烷骨架中的半胱氨酸-甘氨酸单元和/或羧基的模拟物;(4)连接这些元件的垫片。缺乏第二极性结合基团的强效pLT拮抗剂通过与受体其他区域更强的相互作用来补偿。pLT拮抗剂的鉴定是基于先导物优化、pLT类似物的制备和对pLT受体的了解。
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Strategies in the design of peptidoleukotriene antagonists.

The research of the last two decades in the field of SRS-A and peptidoleukotriene (pLT) antagonists has provided information for the design of potent pLT antagonists, which share some or all of the following structural elements: (1) a lipophilic anchor, which fits into the lipophilic pocket of the LTD4 receptor; (2) a central lipophilic unit mimicking the tetraene system of LTD4; (3) one or two acidic groups, as mimics of the cysteinyl-glycine unit and/or the carboxylic group in the eicosanoid backbone of LTD4; (4) spacers connecting these elements. Potent pLT antagonists lacking a second polar binding group compensate by stronger interaction in other regions of the receptor. Identification of pLT antagonists is based on lead optimisation, preparation of pLT analogs and on the knowledge of the pLT receptor.

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