咪唑的绿色合成与生物活性的最新发展趋势

Irum Jamil, Faisal Nawaz, Maryam Shafiq, Muqdssa Rashid, Areeba Akram, Aleeza Siddique, Shanza Taimur, Tehreem Zahra
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引用次数: 0

摘要

咪唑是一种五元平面杂环,由 3C、2N 和 N(第 1 位和第 3 位)组成。嘌呤、组胺、组氨酸和核酸只是含有咪唑环的几种重要天然化合物。咪唑环是一种芳香族化学物质,具有极性和可电离性,可改善铅分子的药代动力学特性,因此被用作优化弱溶性铅化合物溶解度和生物利用度特性的一种疗法。咪唑衍生物在药物化学中占有特殊地位。在发现新药的过程中,一项重要的合成技术就是整合咪唑核。由于咪唑类药物疗效显著,药物化学家们受到启发,创造出了许多创新的化疗药物。本综述总结了近年来咪唑衍生物的不同合成方法及其作为抗艾滋病毒、抗癌、抗病毒、抗真菌、抗糖尿病、抗抑郁、抗氧化和抗结核药物的潜在活性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A Recent Trends on Green Synthesis and Bioactivity of Imidazole
Imidazole is a five-membered, planar heterocyclic ring made up of 3C, 2N, and N in the 1st and 3rd places. Purine, histamine, histidine, and nucleic acid are only a few significant natural compounds that contain the imidazole ring. It is utilised as a cure to optimize the solubility and bioavailability properties of proposed weakly soluble lead compounds since it is an aromatic chemical that is polar and ionizable and so improves the pharmacokinetic features of lead molecules. Derivatives of imidazole have a special place in medicinal chemistry. An essential synthesis technique in the process of discovering new drugs is the integration of the imidazole nucleus. Due to the remarkable therapeutic efficacy of medications related to imidazole, medicinal chemists have been inspired to create numerous innovative chemotherapy agents. This review summarized the work that has been done in recent years about different synthetic approaches of imidazole derivatives and their potential activity as anti-HIV, anticancer, anticovid, antifungal, antidiabetic, antidepressant, antioxidant, and antituberculosis.
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