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拓扑异构酶的天然产物抑制剂:综述与对接研究

Natural Product Inhibitors of Topoisomerases: Review and Docking Study.

作者信息

Scotti Luciana, Bezerra Mendonca Francisco Jaime, Ribeiro Frederico Favaro, Tavares Josean Fechine, da Silva Marcelo Sobral, Barbosa Filho Jose Maria, Scotti Marcus Tullius

机构信息

Federal University of Paraíba, Campus I, Joao Pessoa-PB. Brazil.

State University of Paraíba, Biological Science Department, Laboratory of Synthesis and Drug Delivery, 58070-450, Joao Pessoa-PB. Brazil.

出版信息

Curr Protein Pept Sci. 2018;19(3):275-291. doi: 10.2174/1389203718666170111114442.

Abstract

Since ancient times, natural products have been used in treating various diseases effectively and safely. Nowadays, these natural compounds are submitted to sophisticated methodologies from isolation, computing, analytical, and even serving as pharmacophore suggestions for synthesis. The substances extracted from marine species, plants, and microorganisms present activities beneficial to our health, including protection against malignant tumors. The topoisomerase enzymes play an important role in DNA metabolism, and searching for enzyme inhibitors is an important target in the search for new anticancer drugs. This review discusses this problem, reporting research involving alkaloids, terpenes, flavonoids, xanthones, coumarins, acetogenins, and in addition, includes a docking study with our Brazilian diterpenes to topoisomerases I and II. The better compound, the trachylobane 1, forms one hydrogen bond when submitted to docking with Topo I (with the ASP533 residue) and two with residues in Topo II (THR213 and TYR188). The difference observed in the energy of formation can be attributed to hydrogen-bond interactions. The difference observed in the energy of formation can be attributed to hydrogen-bond interactions.

摘要

自古以来,天然产物就被有效地、安全地用于治疗各种疾病。如今,这些天然化合物要经过从分离、计算、分析等复杂方法,甚至还要作为合成药效团的建议。从海洋物种、植物和微生物中提取的物质具有对我们健康有益的活性,包括预防恶性肿瘤。拓扑异构酶在DNA代谢中起重要作用,寻找酶抑制剂是寻找新型抗癌药物的一个重要靶点。本综述讨论了这个问题,报告了涉及生物碱、萜类、黄酮类、呫吨酮类、香豆素类、产乙酸素类的研究,此外,还包括一项关于我们巴西二萜与拓扑异构酶I和II对接的研究。效果更好的化合物trachylobane 1,与拓扑异构酶I对接时(与ASP533残基)形成一个氢键,与拓扑异构酶II中的残基(THR213和TYR188)形成两个氢键。观察到的形成能量差异可归因于氢键相互作用。观察到的形成能量差异可归因于氢键相互作用。

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