Ueda Y, Melchiorre C, Lippert B, Belleau B, Chona S, Triggle D J
Farmaco Sci. 1978 Jul;33(7):479-95.
The synthesis and alpha-adrenoreceptor blocking activity of several substituted analogs of the prototype alpha-blocker N,N'-bis-(5-aminopentyl)cystamine (APC) are described. The three optical forms of the analog carrying methyl groups on the carbons alpha- to the sulfurs were synthesized and shown to be equipotent and somewhat less active than APC. The omega, omega'-bis-guanidino analog of APC was less active. Significant improvement in potency was observed only with APC analogs carrying benzyl and substituted benzyl groups on the terminal nitrogens. Linking the terminal nitrogens of APC with a p.xyledenyl group so as to give the 26-membered analog caused a sharp drop in activity. The significance of these results as regards the alpha-receptor topography is discussed.
本文描述了原型α-阻滞剂N,N'-双-(5-氨基戊基)胱胺(APC)的几种取代类似物的合成及其α-肾上腺素受体阻断活性。合成了硫原子α位碳原子上带有甲基的类似物的三种旋光形式,结果表明它们与APC等效,但活性略低于APC。APC的ω,ω'-双胍基类似物活性较低。仅在末端氮原子上带有苄基和取代苄基的APC类似物中观察到活性有显著提高。将APC的末端氮原子与对二甲苯撑基连接形成26元类似物,导致活性急剧下降。讨论了这些结果对于α受体拓扑结构的意义。