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Synthesis and Potent Antimalarial Activity of Kalihinol B

机译:卡利胆酚B的合成及其有效的抗疟活性

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摘要

Of the 50+ kalihinane diterpenoids reported to date, only five had been tested for antimalarial activity, in spite of the fact that kalihinol A is the most potent among the members of the larger family of antimalarial isocyanoterpenes. We have validated a strategy designed to access many of the kalihinanes with a 12-step enantioselective synthesis of kalihinol B, the tetrahydrofur-an isomer of kalihinol A (a tetrahydropyran). Kalihinol B shows similarly high potency against chloroquine-resistant Plasmodium falciparum.
机译:迄今为止,在50种以上的卡利西烷二萜类化合物中,尽管卡利西诺A在较大的抗疟异氰基萜烯家族中是最有效的,但仅对其中五种进行了抗疟活性测试。我们已经验证了一种设计用于通过12个步骤对映选择性合成卡利西诺尔B(卡利西诺尔A(四氢吡喃)的四氢呋喃-异构体)的对映选择性合成方法来访问许多卡利西烷的策略。 Kalihinol B对耐氯喹的恶性疟原虫表现出同样高的效力。

著录项

  • 来源
    《Journal of the American Chemical Society》 |2015年第15期|4912-4915|共4页
  • 作者单位

    Department of Chemistry, University of California, Irvine, 1102 Natural Sciences Ⅱ, Irvine, California 92697-2025, United States;

    Department of Cell Biology and Neuroscience, University of California, Riverside, 900 University Avenue, Riverside, California 92521, United States;

    Department of Cell Biology and Neuroscience, University of California, Riverside, 900 University Avenue, Riverside, California 92521, United States;

    Department of Chemistry, University of California, Irvine, 1102 Natural Sciences Ⅱ, Irvine, California 92697-2025, United States;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
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  • 入库时间 2022-08-18 03:09:38

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