摘要
背景:天然烯二炔类抗生素抗生素的首次报道可追溯到20世纪80年代后期;从那以后,人们对这个化合物家族的化学,生物学和潜在的医学应用有了很大的兴趣。烯二炔的生物活性与高度不饱和的己-1-烯-1,5-二炔体系的存在有关。该单元热诱导转变为苯σ-σ双基(Bergman旋光体化)是这些化合物的抗肿瘤性质的关键步骤:1,4-二芳基能够从DNA的脱氧核糖主链上抽取H-原子从而导致DNA链切割并最终导致细胞死亡。 方法:我们采用重点突出的高质量论文对同行评议的研究文献进行结构化的书目数据库搜索。描述了在理解和模拟与这些产品相关的靶向,激活和DNA切割过程中涉及的各种过程的研究工作。已经报道了许多非天然烯二炔在治疗许多感染性疾病中的潜力,除了它们在抗癌药物如抗菌活性,蛋白质降解活性中的作用之外 结果:由于这类化合物的作用方式有趣,烯二炔的独特分子结构已被用于合成许多非天然化合物以研究和提高其生物学性质。这篇评论纳入了76篇论文。它被分成段落,包括:碳氧 - 氮 - 和烯 - 烯二烯,聚合物和大环化合物。与合成化合物的生物学意义一起详细讨论了不同类别的化合物的合成方法 结论:综述总结了非天然烯二炔的合成和反应性的最新进展,特别关注碳 - 和烯 - 烯二炔家族中最有意思的成员的生物学性质。这次审查的结果证实非天然enediynes作为潜在的药物治疗癌症和许多传染病的重要性。
关键词: 抗生素,抗癌,抗肿瘤,bergman环化,碳烯和杂烯二烯,DNA切割
Current Medicinal Chemistry
Title:Synthesis and Biological Activity of Unnatural Enediynes
Volume: 24 Issue: 32
关键词: 抗生素,抗癌,抗肿瘤,bergman环化,碳烯和杂烯二烯,DNA切割
摘要: Background: The first reports of the natural enediyne anticancer antibiotics date back to the late 1980s; since then, a great deal of interest has been devoted to the chemistry, biology and potential medical applications of this family of compounds. The biological activity of enediynes is linked to the presence of a highly unsaturated hex-1-ene-1,5-diyne system. The thermally induced transformation of this unit into a benzene σ-σ diradical (the Bergman cycloaromatization) is the key step of the antitumor properties of such compounds: 1,4-diaryl radicals are able to abstract H-atoms from the deoxyribose backbone of DNA, thus leading to DNA strand cleavage and ultimately cell death.
Methods: We undertook a structured search of bibliographic databases for peer-reviewed research literature using focused and high quality papers. Research efforts addressed at understanding and mimicking the various processes involved in the targeting, activation and DNA cleavage associated with these products are described. The potential of a great number of non natural enediynes in the treatment of many infectious diseases, apart their role in anticancer drugs, such as antibacterial activity, protein degradation activity, has been reported
Results: Due to the interesting mode of action of this class of compounds, the unique molecular architecture of enediynes has been exploited towards the synthesis of many non natural compounds in order to study and enhance their biological properties. Seventy-six papers were included in this review. It is divided in paragraphs that include: Carbo- oxygen-nitrogen- and sulfur- enediynes, polymers and macrocycles. The synthetic approaches to the different classes of compounds are discussed in detail together with the biological implications of the synthesized compounds
Conclusion: The review summarizes the most recent advances in the synthesis and reactivity of non natural enediynes by focusing the attention particularly to the biological properties of the most interesting members of the family of carbo- and hetero- enediynes. The findings of this review confirm the importance of non natural enediynes as potential drugs in the treatment of cancer and many infectious diseases.
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Cite this article as:
Synthesis and Biological Activity of Unnatural Enediynes, Current Medicinal Chemistry 2017; 24 (32) . https://dx.doi.org/10.2174/0929867324666170425095719
DOI https://dx.doi.org/10.2174/0929867324666170425095719 |
Print ISSN 0929-8673 |
Publisher Name Bentham Science Publisher |
Online ISSN 1875-533X |
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