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含氮杂环在抗胃癌药物中的研究进展与展望:综述

Research Progress and Prospect of Nitrogen-containing Heterocycle in Anti-gastric Cancer Drugs: A Review.

作者信息

Li Yang, Jiang Lizhi, Qu Junfeng, Peng Xiaoyu, Wu Kaiyue, Chen Miaojia, Peng Yuanyuan, Cao Xuan

机构信息

Institute of Pharmacy and Pharmacology, Hunan Province, Cooperative Innovation Center for Molecular Target New Drug Study, College of Pharmacy, Hengyang Medical School, University of South China, Hengyang, 421001, China.

Department of Pharmacy, Ezhou Central Hospital, Ezhou, Hubei, China.

出版信息

Curr Med Chem. 2024 Apr 24. doi: 10.2174/0109298673296147240405113328.

Abstract

Gastric cancer was the fifth most common cancer, and its drug treatment mainly included chemotherapy, targeted therapy, and immunotherapy. With the rise of immunotherapy in gastric cancer, small-molecule anti-gastric cancer drugs still have irreplaceable places because of many advantages, such as high stability and mass-productivity, high efficiency, and low cost. At present, the small-molecule anti-gastric cancer drugs in the clinic are constrained by their side effects. So, developing more novel anti-gastric cancer drugs with better efficacy and fewer side effects is urgently needed. Nitrogen-containing heterocycle molecules have attracted much attention from researchers due to their high biocompatibility, activity, and bioavailability, and they even could act with a unique mechanism. This review summarized various types of nitrogen-containing heterocycle antigastric cancer lead compounds from 2017 to 2022 in the last five years. Compared with monocyclic nitrogen-containing heterocycle and bicyclic nitrogen-containing heterocycle, the thick nitrogen-containing heterocycle applied as the skeleton not only showed high efficiency and low toxicity but also, interestingly, may have had some unique mechanism such as inhibition of aurora A and B kinases, etc. We propose two prospective and valuable strategies to develop more efficient candidates for anti-gastric cancer. One strategy was further optimized for some lead compounds mentioned in this review. The other strategy involved utilizing the "pseudo-natural products" concept proposed by Professor Wilhelm Waldmann, combining different nitrogen-containing heterocycle fragments in two and three-dimensional spaces to obtain new thick nitrogen-containing heterocycle skeletons. The strategy will contribute to the expansion of the thick nitrogenous heterocycle's framework, and it was expected that more novel mechanisms and more effective antigastric drugs could be found. These two strategies are expected to help researchers develop more anti-gastric cancer drugs with better potency and lower side effects.

摘要

胃癌是第五大常见癌症,其药物治疗主要包括化疗、靶向治疗和免疫治疗。随着免疫疗法在胃癌治疗中的兴起,小分子抗胃癌药物因其诸多优势,如高稳定性、可大规模生产、高效且低成本等,仍具有不可替代的地位。目前,临床中的小分子抗胃癌药物受到副作用的限制。因此,迫切需要研发出疗效更好、副作用更少的新型抗胃癌药物。含氮杂环分子因其高生物相容性、活性和生物利用度而备受研究人员关注,甚至可能具有独特的作用机制。本综述总结了过去五年(2017年至2022年)各类含氮杂环抗胃癌先导化合物。与单环含氮杂环和双环含氮杂环相比,用作骨架的稠合含氮杂环不仅显示出高效低毒,而且有趣的是,可能具有一些独特的机制,如抑制极光激酶A和B等。我们提出了两种具有前瞻性和价值的策略来开发更高效的抗胃癌候选药物。一种策略是对本综述中提到的一些先导化合物进行进一步优化。另一种策略是利用威廉·瓦尔德曼教授提出的“伪天然产物”概念,在二维和三维空间中组合不同的含氮杂环片段以获得新的稠合含氮杂环骨架。该策略将有助于扩展稠合含氮杂环的框架,有望发现更多新颖的机制和更有效的抗胃癌药物。这两种策略有望帮助研究人员开发出效力更强、副作用更低的更多抗胃癌药物。

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