甲基磺草酮
化学
生物测定
双加氧酶
稗属
体外
铅化合物
拟南芥
立体化学
对接(动物)
IC50型
高粱
抑制性突触后电位
生物信息学
生物化学
EC50型
生物活性
生物活性化合物
结构-活动关系
体外毒理学
HEK 293细胞
棘科
天然产物
生物
作者
Tengfei Ma,Siyi Yang,Ying Hui Bian,Tiansong Li,Yi Zhang,Yongfeng Yao,Bowen Ye,Ying Fu,Fei Ye
标识
DOI:10.1021/acs.jafc.5c17631
摘要
4-Hydroxyphenylpyruvate dioxygenase (HPPD) is an attractive target for the development of bleaching herbicides. To develop novel HPPD inhibitors, 40 diketonitrile derivatives were designed by active-fragment splicing, synthesized, and characterized. In vitro inhibitory assays against Echinochloa crus-galli HPPD (EcHPPD) showed that compound III-2 exhibited the strongest activity, with a half-maximal inhibitory concentration (IC50) of 0.132 μM, outperforming mesotrione (0.277 μM). Preliminary bioassays demonstrated that compound III-2 had excellent herbicidal activity against E. crus-galli and Arabidopsis thaliana (AT) at a dose of 150 g a.i./ha. Crop safety evaluations revealed that compound III-2 was safer than the commercial herbicides mesotrione and isoxaflutole in sorghum and soybean. Molecular docking and molecular dynamics simulations revealed stable binding to HPPD, while electrostatic potential and density functional theory analyses demonstrated favorable electronic properties underlying its high activity. Compound III-2 represents a promising lead for developing novel HPPD-inhibiting diketonitrile herbicides.
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