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作为原卟啉原IX氧化酶抑制型除草剂的四氢邻苯二甲酰亚胺苯甲酸酯类化合物

Tetrahydrophthalimidobenzoates as protoporphyrinogen IX oxidase inhibiting herbicides.

作者信息

Chen Lin, Zhang Yong, Yu Haibo, Cui Dongliang, Li Bin

机构信息

State Key Laboratory of the Discovery and Development of Novel Pesticide, Shenyang Sinochem Agrochemicals R&D Co., Ltd, Shenyang 110021, China.

State Key Laboratory of the Discovery and Development of Novel Pesticide, Shenyang Sinochem Agrochemicals R&D Co., Ltd, Shenyang 110021, China.

出版信息

Pestic Biochem Physiol. 2017 Jun;139:40-45. doi: 10.1016/j.pestbp.2017.04.007. Epub 2017 Apr 21.

Abstract

Tetrahydrophthalimidobenzoates are a class of protoporphyrinogen oxidase herbicides acting on the protoporphyrinogen oxidase enzyme. After the discovery of compound 1, a series of novel tetrahydrophthalimidobenzoate derivatives were designed and synthesized, and some synthesized compounds exhibited good herbicidal activity in controlling broadleaf weeds. The structure activity relationship of the synthesized compounds was also determined. Substitution of a fluorine atom at the 4-position of benzene ring resulted in better herbicidal activity than that with non-substitution. Among the conjunctional groups, methylene group with more methyl substitutions was the best. Consequently, compound 9 was found as the best of all in the synthesized compounds, and it is worthy of being developed not only because of its good herbicidal activity against broadleaf weeds with selectivity for maize, but also for its low toxicity to mammals.

摘要

四氢邻苯二甲酰亚胺苯甲酸酯是一类作用于原卟啉原氧化酶的除草剂。在发现化合物1后,设计并合成了一系列新型四氢邻苯二甲酰亚胺苯甲酸酯衍生物,一些合成化合物在防治阔叶杂草方面表现出良好的除草活性。还确定了合成化合物的构效关系。苯环4位上取代氟原子比未取代时具有更好的除草活性。在连接基团中,甲基取代较多的亚甲基是最好的。因此,化合物9被发现是所有合成化合物中最好的,它不仅因其对阔叶杂草具有良好的除草活性且对玉米具有选择性,还因其对哺乳动物毒性低而值得开发。

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