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Synthesis and evaluation of selective anticholinergics phencynonate hydrochloride

机译:选择性抗胆碱药芬非那酯盐酸盐的合成与评价

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series of alkyl amines, substituted amino-ethers and esters were synthesized. Preliminary pharmacological resutls showed that most of them exhibited potnet icentral anticholinergic activities. Those with a substituted cycloamine show higher bioactivities than those with a substituted chain amine. In ethers or esters, when the substituted groups are phenyl, cyclopentyl or cyclohexyl, then the compounds show greater activity. In some stereosiomers and optical isomers, exist significantly differnet anticholinergic activity. Through many years chemical and biological work, Phencynonate hydrochloride, a selective anticholinergiecs, was found. It had been approved by the authority for the protection of motion diseases.
机译:合成了一系列烷基胺,取代的氨基醚和酯。初步药理学结果表明,它们大多数表现出potnet icentral抗胆碱能活性。具有取代的环胺的那些显示出比具有取代的链胺的那些更高的生物活性。在醚或酯中,当取代的基团是苯基,环戊基或环己基时,则化合物显示出更大的活性。在某些立体异构体和旋光异构体中,存在明显不同的抗胆碱能活性。经过多年的化学和生物学研究,人们发现了盐酸苯磺酸壬酯(一种选择性的抗胆碱药)。它已得到运动疾病保护当局的批准。

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