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IR 5790的合成、除草活性及作用方式

Synthesis, herbicidal activity, and mode of action of IR 5790.

作者信息

Dayan F E, Meazza G, Bettarini F, Signorini E, Piccardi P, Romagni J G, Duke S O

机构信息

Natural Products Utilization Research Unit, Agricultural Research Service, U.S. Department of Agriculture, P.O. Box 8048, University, Mississippi 38677, USA.

出版信息

J Agric Food Chem. 2001 May;49(5):2302-7. doi: 10.1021/jf001393o.

Abstract

IR 5790, an arylthiadiazolone herbicide structurally related to oxadiargyl and oxadiazon, was synthesized. The herbicidal activity and mode of action of IR 5790 were investigated. This herbicide has broad-spectrum pre-emergence activity against both dicotyledonous and monocotyledonous weeds. The phenotypic responses of susceptible plants, such as interruption of growth and light-dependent development of necrotic areas on the foliage, are consistent with those observed with protoporphyrinogen oxidase-inhibiting herbicides. Tissues exposed to IR 5790 in darkness accumulated protoporphyrin IX, which led to a photodynamic loss of membrane integrity upon exposure to light. Consistent with these physiological symptoms, IR 5790 strongly inhibited protoporphyrinogen oxidase, with an I(50) value of 3 nM. The presence of a sulfur atom did not significantly alter the molecular properties of the thiadiazolone ring, relative to the oxadiazolone ring of oxadiargyl, which explains why IR 5790 has the same mode of action as this herbicide.

摘要

合成了IR 5790,一种与恶唑禾草灵和恶草酮结构相关的芳基噻二唑啉酮类除草剂。对IR 5790的除草活性和作用方式进行了研究。这种除草剂对双子叶和单子叶杂草均具有广谱芽前活性。敏感植物的表型反应,如生长中断和叶片上坏死区域的光依赖性发育,与原卟啉原氧化酶抑制性除草剂所观察到的一致。在黑暗中暴露于IR 5790的组织积累了原卟啉IX,这导致在光照下膜完整性发生光动力丧失。与这些生理症状一致,IR 5790强烈抑制原卟啉原氧化酶,I(50)值为3 nM。相对于恶唑禾草灵的恶二唑酮环,硫原子的存在并未显著改变噻二唑啉酮环的分子性质,这解释了为什么IR 5790与这种除草剂具有相同的作用方式。

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