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青蒿素可抑制克氏锥虫和布氏罗得西亚锥虫的体外生长。

Artemisinins inhibit Trypanosoma cruzi and Trypanosoma brucei rhodesiense in vitro growth.

作者信息

Mishina Yuliya V, Krishna Sanjeev, Haynes Richard K, Meade John C

机构信息

Department of Microbiology, University of Mississippi Medical Center, Jackson, MI 39216, USA.

出版信息

Antimicrob Agents Chemother. 2007 May;51(5):1852-4. doi: 10.1128/AAC.01544-06. Epub 2007 Mar 5.

DOI:10.1128/AAC.01544-06
PMID:17339374
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1855540/
Abstract

Artemisinin compounds inhibit in vitro growth of cultured Trypanosoma cruzi and Trypanosoma brucei rhodesiense at concentrations in the low micromolar range. Artemisinin also inhibits calcium-dependent ATPase activity in T. cruzi membranes, suggesting a mode of action via membrane pumps. Artemisinins merit further investigation as chemotherapeutic options for these pathogens.

摘要

青蒿素类化合物在低微摩尔浓度范围内可抑制培养的克氏锥虫和布氏罗得西亚锥虫的体外生长。青蒿素还可抑制克氏锥虫膜中钙依赖性ATP酶的活性,提示其作用方式可能是通过膜泵。青蒿素作为这些病原体的化疗选择值得进一步研究。

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本文引用的文献

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Artemisone--a highly active antimalarial drug of the artemisinin class.青蒿甲醚——一种活性很高的青蒿素类抗疟药物。
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A single amino acid residue can determine the sensitivity of SERCAs to artemisinins.单个氨基酸残基可决定肌浆网钙ATP酶对青蒿素的敏感性。
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Artemisinins.青蒿素类
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Structure-activity relationships of the antimalarial agent artemisinin. 8. design, synthesis, and CoMFA studies toward the development of artemisinin-based drugs against leishmaniasis and malaria.抗疟药物青蒿素的构效关系。8. 基于青蒿素开发抗利什曼病和疟疾药物的设计、合成及比较分子力场分析研究
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