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首页> 外文期刊>J.Chem.Soc., Perkin Transaction 1 >Further evidence for the participation of primary carbon-centered free radicals in the antimalarial action of the qinghaosu (artemisinin) series of compounds
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Further evidence for the participation of primary carbon-centered free radicals in the antimalarial action of the qinghaosu (artemisinin) series of compounds

机译:碳中心自由基参与青蒿素(青蒿素)系列化合物抗疟作用的进一步证据

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摘要

Friedel–Crafts alkylation of 1,3-dimethoxybenzene with O-acetyldihydroqinghaosu gave a pair of 11-epimers ofn12-(2,4-dimethoxyphenyl)deoxoqinghaosu 2 and 2u0001. The antimalarial activity of 11β-epimer 2 was comparable withnthat of artemether. Compound 2 reacted smoothly with ferrous ions or -cysteine and catalytic amounts of ferrousnions to give a series of products derived from the previously postulated C-centered free radical, in particular thenprimary C-centered free radical. However, 11α-epimer 2u0001 was almost inert to ferrous ions and also showed lownantimalarial activity. The identification of free radical mediated products and the correlation between chemicalnreactivity and bio-activity once again provided evidence for the key role of primary carbon-centered free radicalsnin the antimalarial activity of the qinghaosu series of compounds.
机译:用O-乙酰基二氢青蒿素将1,3-二甲氧基苯进行Friedel-Crafts烷基化反应得到n11-(2,4-二甲氧基苯基)deoxoqinghaosu 2和2u0001的11个端基。 11β-epimer2的抗疟活性与蒿甲醚相当。化合物2与亚铁离子或β-半胱氨酸和催化量的亚铁离子平稳反应,得到一系列衍生自先前假定的C-中心自由基,特别是随后的伯C-中心自由基的产物。然而,11α-受体2u0001对亚铁离子几乎是惰性的,并且还显示出低的动物活性。自由基介导产物的鉴定以及化学反应性和生物活性之间的相关性再次为主要碳中心自由基在青蒿素系列化合物的抗疟活性中的关键作用提供了证据。

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  • 来源
    《J.Chem.Soc., Perkin Transaction 1》 |2001年第6期|p.605-609|共5页
  • 作者单位

    aState Key Laboratory of Bio-organic & Natural Products Chemistry,Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, 354 Fenglin Road,Shanghai 200032, China. E-mail: ylwu@pub.sioc.ac.cnbShanghai Institute of Materia Medica, Shanghai Institute for Biological Sciences,Chinese Academy of Sciences, 294 Taiyuan Road, Shanghai 200031, China.E-mail: yli@mail.shcnc.ac.cn;

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