首页> 外文期刊>Pesticide Biochemistry and Physiology >Study of the in vivo antiviral activity against TMV treated with novel 1-(t-butyl)-5-amino-4-pyrazole derivatives containing a 1,3,4-oxadiazole sulfide moiety
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Study of the in vivo antiviral activity against TMV treated with novel 1-(t-butyl)-5-amino-4-pyrazole derivatives containing a 1,3,4-oxadiazole sulfide moiety

机译:用新型1-(叔丁基)-5-氨基-4-吡唑衍生物治疗含有1,3,4-二唑硫醚的TMV的体内抗病毒活性研究

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摘要

A series of new 1-tert-butyl-5-amino-4-pyrazole bioxadiazole sulfide derivatives containing a 1,3,4-oxadiazole moiety were designed and synthesized. The bioactivity results showed that some title compounds exhibited excellent protective activity against TMV and certain insecticidal activity. Among the tested compounds, the EC50 values of 5d, 5j, 5k and 5l were 165.8, 163.2, 159.7 and 193.1 mg/L, respectively, which are better than the EC50 value of ningnanmycin (271.3 mg/L). The chlorophyll contents and the defense enzyme activities of the tobacco leaves after treatment with 5j were significantly increased, which indicated that this series of title compounds may induce the systemic acquired resistance of host to defend against diseases. Further in vivo protective activity research on 5j using TMV with a GFP gene tag found that it can effectively inhibit the spread of TMV in inoculated tobacco. A morphological study with TEM revealed that title compound 5h can cause a distinct break of the rod-shaped TMV. Moreover, the insecticidal activity revealed that the fatality rates of 5a, 5b and 5m against aphidoidea were 85%, 83% and 87%, respectively, which indicated that the title compounds can effectively block the common carrier of plant viruses, thereby effectively reducing the TMV infection risk of tobacco. This series of synergistic effects provide key information for the research and development of antiviral agents.
机译:设计并合成了一系列含1,3,4-恶二唑部分的新型1-叔丁基-5-氨基-4-吡唑-二唑硫醚衍生物。生物活性结果表明,部分目标化合物对TMV具有良好的保护活性和一定的杀虫活性。在受试化合物中,5d、5j、5k和5l的EC50值分别为165.8、163.2、159.7和193.1 mg/L,优于宁南霉素(271.3 mg/L)的EC50值。5j处理后烟叶叶绿素含量和防御酶活性显著提高,表明该系列化合物可能诱导寄主系统获得性抗病性。进一步利用带有GFP基因标签的TMV对5j的体内保护活性研究发现,它能有效抑制TMV在接种烟草中的传播。TEM形态学研究表明,标题化合物5h可导致杆状TMV明显断裂。此外,杀虫活性显示,5a、5b和5m对蚜总科的致死率分别为85%、83%和87%,这表明标题化合物能有效阻断植物病毒的共同载体,从而有效降低烟草感染TMV的风险。这一系列协同效应为抗病毒药物的研究和开发提供了关键信息。

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  • 作者单位

    Guizhou Univ State Key Lab Breeding Base Green Pesticide &

    Agr Key Lab Green Pesticide &

    Agr Bioengn Minist Educ Ctr R&

    D Fine Chem Guiyang 550025 Peoples R China;

    Guizhou Univ State Key Lab Breeding Base Green Pesticide &

    Agr Key Lab Green Pesticide &

    Agr Bioengn Minist Educ Ctr R&

    D Fine Chem Guiyang 550025 Peoples R China;

    Guizhou Univ State Key Lab Breeding Base Green Pesticide &

    Agr Key Lab Green Pesticide &

    Agr Bioengn Minist Educ Ctr R&

    D Fine Chem Guiyang 550025 Peoples R China;

    Guizhou Univ State Key Lab Breeding Base Green Pesticide &

    Agr Key Lab Green Pesticide &

    Agr Bioengn Minist Educ Ctr R&

    D Fine Chem Guiyang 550025 Peoples R China;

    Guizhou Univ State Key Lab Breeding Base Green Pesticide &

    Agr Key Lab Green Pesticide &

    Agr Bioengn Minist Educ Ctr R&

    D Fine Chem Guiyang 550025 Peoples R China;

  • 收录信息
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 植物保护;
  • 关键词

    1; 3; 4-oxadiazole sulfide; Tobacco mosaic virus; Defense enzyme activity; Green fluorescent protein; Insecticidal activity;

    机译:1;3;4-氧代唑硫化物;烟叶病毒;防御酶活性;绿色荧光蛋白;杀虫活性;

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