神经激肽B
神经激肽A
P物质
兴奋剂
化学
结合位点
速激肽受体
立体化学
内科学
药理学
受体
神经肽
生物
生物化学
医学
作者
Solange Lavielle,Gérard Chassaing,D. Lœuillet,Odile Convert,Y. Torrens,Beaujouan Jc,Monique Saffroy,François Petitet,Lena Bergström,J. Głowiński
标识
DOI:10.1111/j.1472-8206.1990.tb00493.x
摘要
Three types of binding sites for the mammalian tachykinins, ie Substance P (SP) Neurokinin A (NKA) and Neurokinin B (NKB), have been found in both the central and peripheral nervous systems. Substance P binds to the NK-1 subclass of binding site while NKA and NKB are less selective endogenous ligands, which preferentially interact with the NK-2 and NK-3 subclasses of binding sites, respectively. Complementary strategies, including 3-dimensional structure analysis by NMR spectroscopy and structure-activity relationship led to the design of selective agonists of these binding sites. [Pro9] SP, [Pro10] SP and the cyclic analogues [Cys3,6, Tyr8, Pro9] SP and [Cys3,6, Tyr8, Pro10] SP are selective NK-1 agonists. [Lys5] NKA(4-10) is a water soluble NK-2 potent agonist. Finally, [Pro7] NKB, which completely discriminates NK-2 and NK-3 binding sites, is a water-soluble NK-3 selective agonist.
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