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首页> 外文期刊>Industrial Crops and Products >Natural products-based pesticides: Design, synthesis and pesticidal activities of novel fraxinellone derivatives containing N-phenylpyrazole moiety
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Natural products-based pesticides: Design, synthesis and pesticidal activities of novel fraxinellone derivatives containing N-phenylpyrazole moiety

机译:基于天然产品的杀虫剂:含N-苯基吡唑部分的新型法肾上腺酮衍生物的设计,合成和杀虫活性

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摘要

Fraxinellone, a degraded limonoid, has been mainly isolated from some renewable plants in Meliaceae and Rutaceae. In a continuous effort to discover new natural products-based pesticides, two series of fraxinellone derivatives containing N-phenylpyrazole moiety were designed, synthesized and evaluated for their pesticidal activities against Mythimna separata Walker and Plutella xylostella Linnaeus. Two structures of compounds 7g and 8k were unambiguously determined by X-ray diffraction further. The bioassay showed that over half of the target compounds exhibited better insecticidal activity against M. separata than the precursor fraxinellone. Among all the target compounds, the compounds 7g-i and 8g-j exhibited more potent insecticidal activity than toosendanin, a commercial botanical pesticide. Furthermore, the compound 8g displayed more promising larvicidal activity with the LC50 value of 0.31 mu mol mL(-1) than the toosendanin against P. xylostella. The structure activity relationship (SAR) revealed that introduction of polyhalogenated phenylpyrazole ring on furyl-ring of fraxinellone could lead more potent compounds both against M. separata and P. xylostella than that of monohalogenated phenylpyrazole ring or electron-donating groups substituted phenylpyrazole ring.
机译:Fraxinellone是一种降解的皂苷,主要是从Meliaceae和Rutaceae的一些可再生植物中分离出来。在持续努力寻找基于新的天然产物的农药,设计了两种含有N-苯基吡唑部分的Fraxinellone衍生物,综合和评估其针对神肢分层助行器和Plutella Xylostella Linnaeus的杀虫活动。通过进一步通过X射线衍射明确地确定化合物7G和8K的两个结构。生物测定表明,超过一半的目标化合物对M.分区的杀虫活性表现出比前体Fraxinerlone的杀虫剂活性。在所有靶化合物中,化合物7G-1和8G-J表现出比ToOSendanin,商业植物农药更有效的杀虫活性。此外,化合物8g显示比对木龙蛋白蛋白蛋白蛋白的LC50值为0.31μmml(-1)的LC50值更高的幼稚活性。结构活性关系(SAR)揭示了呋喃啉骨笼上的多卤代苯吡唑环的引入可以引导与M. Sextaata和P. Xylostella相比的更有效的化合物比单卤化苯吡唑环或电子给苯吡唑环的苯吡唑环。

著录项

  • 来源
    《Industrial Crops and Products》 |2018年第2018期|共8页
  • 作者单位

    Zhengzhou Univ Sch Pharmaceut Sci 100 KeXue Ave Zhengzhou 450001 Henan Peoples R China;

    Zhengzhou Univ Sch Pharmaceut Sci 100 KeXue Ave Zhengzhou 450001 Henan Peoples R China;

    Zhengzhou Univ Sch Pharmaceut Sci 100 KeXue Ave Zhengzhou 450001 Henan Peoples R China;

    Zhengzhou Univ Sch Pharmaceut Sci 100 KeXue Ave Zhengzhou 450001 Henan Peoples R China;

    Zhengzhou Univ Sch Pharmaceut Sci 100 KeXue Ave Zhengzhou 450001 Henan Peoples R China;

    Zhengzhou Univ Sch Pharmaceut Sci 100 KeXue Ave Zhengzhou 450001 Henan Peoples R China;

    Zhengzhou Univ Sch Pharmaceut Sci 100 KeXue Ave Zhengzhou 450001 Henan Peoples R China;

    Hebei Agr Univ Coll Sci &

    Technol Huanghua 061100 Peoples R China;

    Zhengzhou Univ Sch Pharmaceut Sci 100 KeXue Ave Zhengzhou 450001 Henan Peoples R China;

  • 收录信息
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 农作物;
  • 关键词

    Natural products-based pesticide; Fraxinellone; Pesticidal activity; Pyrazole ring; Structure-activity relationship;

    机译:基于天然产品的农药;Fraxinellone;杀虫活性;吡唑环;结构 - 活动关系;

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