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苯并咪唑 - 嘧啶杂化物:合成与药用特性

Benzimidazole-Pyrimidine Hybrids: Synthesis and Medicinal Properties.

作者信息

Marinescu Maria, Zalaru Christina

机构信息

Department of Inorganic Chemistry, Organic Chemistry, Biochemistry and Catalysis, Faculty of Chemistry, University of Bucharest, Soseaua Panduri, 030018 Bucharest, Romania.

出版信息

Pharmaceuticals (Basel). 2025 Aug 19;18(8):1225. doi: 10.3390/ph18081225.

Abstract

: Heterocyclic compounds represent a key class of compounds in medicinal chemistry. Both benzimidazoles and pyrimidines are essential heterocycles in medicinal chemistry, with various therapeutic properties. Recent literature presents a series of hybrid heterocyclic compounds, as their medicinal properties are generally improved compared to those of single heterocyclic rings. : A literature search was conducted across relevant scientific literature from peer-reviewed sources, using keywords, including "benzimidazole", "pyrimidine", "Biginelli", "benzimidazole-pyrimidine hybrids", "anticancer", "antiviral", "antimicrobial", and "anti-inflammatory". : In this review, benzimidazole-pyrimidine hybrids are reported as anticancer, antimicrobial, antiviral, anti-inflammatory, analgesic, antiulcer, antidepressant, anti-Alzheimer's, or antioxidant agents, with activities even better than those of existing drugs. The IC values for these anticancer hybrids are in the nanomolar range, which signifies potent anticancer agents. It can be mentioned here that the anticancer hybrid Abemaciclib, as a CDK4/6 inhibitor for the treatment of certain types of breast cancer, was approved in 2017. The antimicrobial activity of these hybrids proved especially potent against a broad variety of infections, with MIC values in the range of µM or even nM. Moreover, these hybrids exhibited good antiviral properties against SARS-CoV-2, HIV-1, and the hepatitis C virus. The hybrids also functioned as JAK3 inhibitors, COX-1 inhibitors, and MAO-A inhibitors. : This review presents synthesis methods of benzimidazole-pyrimidine hybrids, their medicinal properties, and SAR studies reported in the last 20 years. For almost every therapeutic activity, SAR studies have revealed the essential presence of a substituent on the aromatic rings or between the two benzimidazole and pyrimidine nuclei.

摘要

杂环化合物是药物化学中的一类关键化合物。苯并咪唑和嘧啶都是药物化学中必不可少的杂环,具有多种治疗特性。近期文献报道了一系列杂环化合物,因为它们的药用特性通常比单个杂环有所改善。

通过使用包括“苯并咪唑”“嘧啶”“贝西利”“苯并咪唑 - 嘧啶杂化物”“抗癌”“抗病毒”“抗菌”和“抗炎”等关键词,对同行评审来源的相关科学文献进行了检索。

在本综述中,苯并咪唑 - 嘧啶杂化物被报道为具有抗癌、抗菌、抗病毒、抗炎、止痛、抗溃疡、抗抑郁、抗阿尔茨海默病或抗氧化作用的药物,其活性甚至优于现有药物。这些抗癌杂化物的半数抑制浓度(IC)值处于纳摩尔范围,这表明它们是强效抗癌剂。在此可以提及,抗癌杂化物阿贝西利作为一种用于治疗某些类型乳腺癌的细胞周期蛋白依赖性激酶4/6(CDK4/6)抑制剂,于2017年获得批准。这些杂化物的抗菌活性对多种感染特别有效,最低抑菌浓度(MIC)值在微摩尔甚至纳摩尔范围内。此外,这些杂化物对严重急性呼吸综合征冠状病毒2(SARS-CoV-2)、人类免疫缺陷病毒1型(HIV-1)和丙型肝炎病毒表现出良好的抗病毒特性。这些杂化物还可作为Janus激酶3(JAK3)抑制剂、环氧化酶-1(COX-1)抑制剂和单胺氧化酶A(MAO-A)抑制剂发挥作用。

本综述介绍了苯并咪唑 - 嘧啶杂化物的合成方法、它们的药用特性以及过去20年报道的构效关系(SAR)研究。对于几乎每种治疗活性,SAR研究都揭示了芳环上或两个苯并咪唑和嘧啶核之间必须存在取代基。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/78eb/12389660/b49ddfad6bf4/pharmaceuticals-18-01225-g001.jpg

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