A comprehensive review on the synthesis of substituted piperazine and its novel bio-medicinal applications

Muhammad Rizwan , Sobia Noreen , Sadia Asim , Zohaib Liaqat , Musrat Shaheen , Hina Ibrahim
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Abstract

Piperazine is two nitrogen containing heterocyclic compound. The fundamental activity of the piperazine is due to the 1,4-position of nitrogen atoms and their substitutions. The SN1 reaction is followed by the others alkylation and substitution reactions. Substituted piperazine derivatives hold an important position for the development of crucial drugs. They exhibit a broad spectrum of biological activities e.g. antitubercular, antibacterial, anti-inflammatory, anticancer, antiviral, antidiabetic and antimalarial. Immense numbers of biological activities displayed by disubstituted piperazine derivatives are due to the presence of two nitrogen atoms in the ring. Keeping in mind their biological activity profile, a series of novel 1,4-substituted piperazine synthesized derivatives were collected. All the prepared derivatives are expected to show different biological activities particularly enzyme inhibition activities against α-Amylase.

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取代哌嗪的合成及其新型生物医学应用综述
哌嗪是一种含氮杂环化合物。哌嗪的基本活性来自于氮原子的 1,4-位及其取代。SN1 反应之后是其他的烷基化和取代反应。取代的哌嗪衍生物在关键药物的开发中占有重要地位。它们具有广泛的生物活性,如抗结核、抗菌、消炎、抗癌、抗病毒、抗糖尿病和抗疟。二取代哌嗪衍生物之所以具有如此多的生物活性,是因为环中含有两个氮原子。考虑到它们的生物活性特征,我们收集了一系列新型 1,4-取代哌嗪合成衍生物。所有制备的衍生物都有望显示出不同的生物活性,尤其是对α-淀粉酶的酶抑制活性。
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