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血红素与 plakortin 和合成内过氧化物类似物的相互作用:血红素激活抗疟机制的新见解。

The interaction of heme with plakortin and a synthetic endoperoxide analogue: new insights into the heme-activated antimalarial mechanism.

机构信息

University of Naples "Federico II", Department of Pharmacy, Via D. Montesano 49, Napoli, 80131, Italy.

Italian Malaria Network - Centro Interuniversitario di Ricerca Sulla Malaria (CIRM) Department of Experimental Medicine and Biochemical Science, Via Del Giochetto, Perugia, Italy.

出版信息

Sci Rep. 2017 Apr 6;7:45485. doi: 10.1038/srep45485.

Abstract

In the present work we performed a combined experimental and computational study on the interaction of the natural antimalarial endoperoxide plakortin and its synthetic analogue 4a with heme. Obtained results indicate that the studied compounds produce reactive carbon radical species after being reductively activated by heme. In particular, similarly to artemisinin, the formation of radicals prone to inter-molecular reactions should represent the key event responsible for Plasmodium death. To our knowledge this is the first experimental investigation on the reductive activation of simple antimalarial endoperoxides (1,2-dioxanes) by heme and results were compared to the ones previously obtained from the reaction with FeCl. The obtained experimental data and the calculated molecular interaction models represent crucial tools for the rational optimization of our promising class of low-cost synthetic antimalarial endoperoxides.

摘要

在本工作中,我们对天然抗疟内过氧化物 plakortin 及其合成类似物 4a 与血红素的相互作用进行了组合实验和计算研究。结果表明,研究的化合物在被血红素还原激活后产生反应性碳自由基。特别是与青蒿素类似,易于发生分子间反应的自由基的形成应该是导致疟原虫死亡的关键事件。据我们所知,这是首次对血红素还原激活简单抗疟内过氧化物(1,2-二氧杂环己烷)的实验研究,并将结果与之前用 FeCl 反应得到的结果进行了比较。获得的实验数据和计算的分子相互作用模型是合理优化我们有前途的低成本合成抗疟内过氧化物类药物的关键工具。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6dff/5382535/1da5c18363db/srep45485-f1.jpg

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