新型9-烷基胺取代嘧啶-[2,1-f]-嘌呤的合成及初步药理评价。

A Drabczyńska, M Pawłowski, M Gorczyca, D Malec, J Modzelewski
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引用次数: 0

摘要

制备了n9 -烷基胺甲基-、烷基哌嗪-、烷基哌啶取代1,3-二甲基-(六氢嘧啶)-和(四氢嘧啶)-[2,1-f]-两个系列嘌呤,并对它们的理化性质和药理学性质进行了描述。在中枢神经系统测试中最活跃的是含有苯基哌嗪烷基取代基的化合物,即1,3-二甲基-2,4-二氧基-9-[N1N4-(苯基)-哌嗪丙基]- 1,3,6,7,8,9 -六氢嘧啶-[2,1-f]嘌呤6a及其丁基和异丁基同源物9和12。这些化合物显著抑制自发性运动和安非他命活性,并表现出镇静、镇痛和降体温的特性。
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Synthesis and preliminary pharmacological assessment of novel 9-alkylamino substituted pyrimidino-[2,1-f]-purines.

Two series of N9-alkylaminomethyl-, alkylpiperazino-, alkylpiperidino-substituted 1,3-dimethyl-(hexahydropyrimidino)- and (tetrahydropyrimidono)-[2,1-f]-purines were prepared and their physicochemical and pharmacological properties were described. The most active in central nervous system tests were the compounds with phenylpiperazinealkyl substituent i.e. 1,3-dimethyl-2,4-dioxo-9-[N1N4-(phenyl)-piperazinopropyl]-1, 3,6,7,8,9- hexahydropyrimidino-[2,1-f] purine 6a and its butyl and isobutyl homologs 9 and 12. The compounds depressed statistically significantly spontaneous locomotor and amphetamine activity and showed sedative, analgetic and hypothermizing properties.

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