Piperidine-containing phosphonates as immunоcorrectors

A. Malmakova, N. Kystaubayeva, T. Zharkinbek, M. Myrzakhanov, M. Balabekova, V. Yu
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Abstract

The objective of Research is the target synthesis of azaheterocyclic systems as potential immunomodulators. Encouraging results had been obtained from the biotesting of structures combining the piperidine cycle and the phosphonate fragment in the molecule (where, R=alkoxyalkyl or arylalkyl, A=OH, Ph, fluorophenyl, heteterocyclic moiety, etc). Target piperidine-containing phosphonates (PP) are synthesized quite simply either by nucleophilic addition via the ketone group of piperidone or under the Kabachnik-Fields reaction conditions.The objective of Research is the target synthesis of azaheterocyclic systems as potential immunomodulators. Encouraging results had been obtained from the biotesting of structures combining the piperidine cycle and the phosphonate fragment in the molecule (where, R=alkoxyalkyl or arylalkyl, A=OH, Ph, fluorophenyl, heteterocyclic moiety, etc). Target piperidine-containing phosphonates (PP) are synthesized quite simply either by nucleophilic addition via the ketone group of piperidone or under the Kabachnik-Fields reaction conditions.
含哌啶膦酸盐作为免疫校正剂
研究的目的是靶合成氮杂环系统作为潜在的免疫调节剂。从结合哌啶循环和分子中膦酸盐片段的结构(其中,R=烷氧烷基或芳基烷基,A=OH, Ph,氟苯基,杂环部分等)的生物测试中获得了令人鼓舞的结果。目标含哌啶膦酸盐(PP)可以通过哌啶酮的酮基亲核加成或在卡巴尼克场反应条件下简单地合成。研究的目的是靶合成氮杂环系统作为潜在的免疫调节剂。从结合哌啶循环和分子中膦酸盐片段的结构(其中,R=烷氧烷基或芳基烷基,A=OH, Ph,氟苯基,杂环部分等)的生物测试中获得了令人鼓舞的结果。目标含哌啶膦酸盐(PP)可以通过哌啶酮的酮基亲核加成或在卡巴尼克场反应条件下简单地合成。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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