部分
EC50型
立体化学
芳基
茄丝核菌
化学
琥珀酸脱氢酶
体外
生物化学
酶
生物
有机化学
烷基
植物
作者
Aigui Zhang,Jian Yang,Tao Ke,Taiping Hou,Hong Jin
摘要
BACKGROUND: Succinate dehydrogenase inhibitors (SDHIs) emerging in fungicide markets are widely used in crop protection. Currently, the structural modification focusing on a structurally diverse 'core' moiety (aryl) of SDHIs is being gradually identified as one of the innovative strategies for developing novel, highly effective and low resistant fungicides. RESULTS: = 7.63 mg/L). Furthermore, in vitro inhibitory activity against fungal SDH showed the inhibitory ability of compound IIc was equivalent with that of compound SCU2028, and molecular dynamics simulation of the SDH-compound IIc complex suggested that compound IIc could strongly bind to and interact with the binding site of SDH. CONCLUSION: Novel aromatic carboxamides without a pyrazol group have potential as a class of SDHIs, and the strategy of replacing the pyrazol group with another aryl in the 'core' moiety might offer an alternative option in discovery of SDHI fungicides. © 2023 Society of Chemical Industry.
科研通智能强力驱动
Strongly Powered by AbleSci AI