Wirth K J, Schölkens B A, Wiemer G
Hoechst AG, Frankfurt am Main, Germany.
Eur J Pharmacol. 1994 Dec 15;288(1):R1-2. doi: 10.1016/0922-4106(94)90017-5.
WIN 64338 (phosphonium, [[4-[[2-[[bis(cyclohexylamino) methylene] amino]-3-(2-naphthalenyl) 1-oxopropyl]amino]-phenyl]- tributyl, chloride, monohydrochloride) is the first potent nonpeptide competitive bradykinin B2 receptor antagonist as shown in classical pharmacological preparations with no activity in the rabbit aorta stimulated by the bradykinin B1 receptor agonist des-Arg9-bradykinin. In primary cultured bovine aortic endothelial cells, both bradykinin and des-Arg9-bradykinin stimulate the production of intracellular cyclic GMP, an index for the production of nitric oxide. Surprisingly, WIN 64338 did not inhibit bradykinin but abolished the effect of des-Arg9-bradykinin suggesting that kinin receptor antagonists do not necessarily discriminate between kinin receptor subtypes in an identical way in different tissues and species.
WIN 64338(氯化三丁基[[4 - [[2 - [[双(环己基氨基)亚甲基]氨基]-3 -(2 - 萘基)-1 - 氧代丙基]氨基]苯基]鏻单盐酸盐)是第一种有效的非肽类缓激肽B2受体竞争性拮抗剂,在经典药理学制剂中显示出对缓激肽B1受体激动剂去 - Arg9 - 缓激肽刺激的兔主动脉无活性。在原代培养的牛主动脉内皮细胞中,缓激肽和去 - Arg9 - 缓激肽均刺激细胞内环鸟苷酸的产生,这是一氧化氮产生的一个指标。令人惊讶的是,WIN 64338不抑制缓激肽,但消除了去 - Arg9 - 缓激肽的作用,这表明激肽受体拮抗剂在不同组织和物种中不一定以相同方式区分激肽受体亚型。