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Design synthesis docking and antimicrobial evaluation of some novel pyrazolo15-a pyrimidines and their corresponding cycloalkane ring-fused derivatives as purine analogs

机译:设计合成对接和抗菌评估一些新型的吡唑并15-a嘧啶及其相应的环烷环稠合衍生物作为嘌呤类似物

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摘要

BackgroundOver the years, pyrazolopyrimidine derivatives have been recognized as having antimicrobial activities. Recently, we reported different synthetic methods to prepare pyrazolopyrimidine derivatives as anticancer and antimicrobial agents. The studies showed that our previously reported 5-aminopyrazoles >2 act as a building block for the preparation of a variety of interesting pyrazolopyrimidines as purine analogs.
机译:背景技术多年来,吡唑并嘧啶衍生物被认为具有抗菌活性。最近,我们报道了制备吡唑并嘧啶衍生物作为抗癌和抗菌剂的不同合成方法。研究表明,我们先前报道的5-氨基吡唑> 2 可作为构建各种有趣的吡唑并嘧啶类嘌呤类似物的基础。

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