4,4′-dibromobenzylic acid β- and γ-aminoalkyl ester hydrochlorides and their biological properties
作者:O. L. Mndzhoyan、A. A. Gamburyan、L. S. Papoyan、Dzh A. Gerasimyan、R. M. Srapionyan、L. A. Grigoryan、A. A. Bagdasaryan、D. A. Melkonyan、L. K. Durgaryan、A. V. Akopyan
DOI:10.1007/bf00772107
日期:1991.4
Pharmacological investigations showed that benzylic acid ~-diethylaminoethyl ester hydrochloride, amizyl, has cholinolytic and gangliolytic properties [8]. To study the changes in the cholinolytic action of amizyl, when two bromine atoms are introduced into its acid part at the 4,4'-positions of the phenyl groups, and also on altering the aminoalkanol chain, we synthesized the $and y-aminoalkyl esters of 4,4'-dibromobenzylic
药理研究表明,苄酸~-二乙氨基乙酯盐酸盐,酰胺基,具有胆碱溶解和神经节溶解特性[8]。为了研究脒基的胆碱分解作用的变化,当在苯基的 4,4'-位处将两个溴原子引入其酸部分时,以及改变氨基烷醇链时,我们合成了 $ 和 y-氨基烷基4,4'-二溴苄酸 (IIIa-k) 的酯: