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甲苯磺菌胺衍生物的合成及其对稻瘟病的活性:聚酮合酶活性、黑色素生物合成与稻瘟病之间的关系

Synthesis and activities of tolprocarb derivatives against : relationships among the activities for polyketide synthase, melanin biosynthesis, and rice blast.

作者信息

Banba Shinichi, Hamada Takahiro, Araki Natsuko, Ebihara Koichi

机构信息

Agrochemicals Research Center, Mitsui Chemicals Agro, Inc., Mobara, Chiba 297-0017, Japan.

Research & Development Division, Mitsui Chemicals Agro, Inc., Chuo-ku, Tokyo 103-0027, Japan.

出版信息

J Pestic Sci. 2017 May 20;42(2):25-31. doi: 10.1584/jpestics.D16-100.

Abstract

The target site of tolprocarb has been reported to be polyketide synthase (PKS). Here, we evaluated the activities for PKS and melanin biosynthesis as well as the control efficacy of rice blast using a series of tolprocarb derivatives. A comparison of the inhibitory activities of PKS and melanin biosynthesis revealed a linear relationship ( =0.90), confirming PKS as the target site of tolprocarb. A compound beyond this relationship was metabolized by to an inactive compound. The control efficacy of rice blast was explained using the melting point and either the inhibitory activity of PKS or melanin biosynthesis. Structure-activity analysis revealed that both end parts of tolprocarb preferred hydrophobic groups, and the chirality of the substituent in the middle part significantly influenced the activities. These relationships will provide useful information for the development of novel PKS inhibitors.

摘要

据报道,甲苯磺菌胺的作用靶点是聚酮合酶(PKS)。在此,我们使用一系列甲苯磺菌胺衍生物评估了PKS和黑色素生物合成的活性以及对稻瘟病的防治效果。PKS和黑色素生物合成抑制活性的比较显示出线性关系(=0.90),证实PKS是甲苯磺菌胺的作用靶点。超出这种关系的一种化合物被代谢为无活性的化合物。使用熔点以及PKS或黑色素生物合成的抑制活性来解释稻瘟病的防治效果。构效分析表明,甲苯磺菌胺的两个末端部分都偏好疏水基团,中间部分取代基的手性显著影响活性。这些关系将为新型PKS抑制剂的开发提供有用信息。

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