Huang Huazhang, Dickhaut Joachim, Weisel Martin, Mao Lixin, Rankl Nancy, Takeda Haruka, Stam Lynn F, Peacock Quinn M, Höffken Hans Wolfgang
BASF Corporation, Global Insecticide Discovery/ Early Biology, Research Triangle Park, Research Triangle Park, NC, USA.
BASF SE, Global Insecticide Discovery/ Chemistry at Ludwigshafen, Ludwigshafen am Rhein, Germany.
Pest Manag Sci. 2025 May;81(5):2535-2552. doi: 10.1002/ps.8108. Epub 2024 Apr 10.
Many piercing-sucking insects have developed resistance or cross-resistance to many insecticides targeting insect neural nicotinic acetylcholine receptor (nAChR). Here we are aiming to present the discovery of a novel mesoionic insecticide, fenmezoditiaz, by BASF through structure-based drug design (SBDD) approaches. It has recently been added to the Insecticide Resistance Action Committee mode of classification (IRAC 4E). It is being developed for plant protection against piercing-sucking pests, especially rice hopper complex.
The soluble acetylcholine binding protein (AChBP) from the sea slug Aplysia californica was modified using site-directed mutagenesis and based on putative aphid nAChR subunit sequences to create soluble insect-like AChBPs. Among them, insect-like β1 AChBP and native aphid membrane preparation showed the highest correlated biochemical affinity toward structurally diverse ligands. This mutant AChBP was used to understand how insect nAChRs structurally interact with mesoionics, which was then utilized to design novel mesoionics including fenmezoditiaz. It is an excellent systemic insecticide with diverse application methods and has a broad insecticidal spectrum, especially against piercing/sucking insects. It lacks cross-resistance for neonicotinoid resistant plant hoppers. Field-collected brown plant hopper populations from Asian countries showed high susceptibility.
Fenmezoditiaz is a systemic insecticide with a broad spectrum, lack of cross-resistance and it could be an additional tool for integrated pest management and insecticide resistance management, especially for the rice hopper complex. © 2024 The Authors. Pest Management Science published by John Wiley & Sons Ltd on behalf of Society of Chemical Industry.
许多刺吸式昆虫已对多种针对昆虫神经烟碱型乙酰胆碱受体(nAChR)的杀虫剂产生抗性或交叉抗性。在此,我们旨在介绍巴斯夫公司通过基于结构的药物设计(SBDD)方法发现的一种新型中离子型杀虫剂——芬美唑地嗪。它最近已被添加到杀虫剂抗性行动委员会的分类模式(IRAC 4E)中。它正在被开发用于植物保护,以防治刺吸式害虫,尤其是稻飞虱复合体。
利用定点突变技术,基于假定的蚜虫nAChR亚基序列对海兔加利福尼亚海兔的可溶性乙酰胆碱结合蛋白(AChBP)进行修饰,以创建可溶性昆虫样AChBP。其中,昆虫样β1 AChBP与天然蚜虫膜制剂对结构多样的配体表现出最高的相关生化亲和力。这种突变型AChBP被用于了解昆虫nAChR如何与中离子型化合物在结构上相互作用,进而用于设计包括芬美唑地嗪在内的新型中离子型化合物。它是一种优秀的内吸性杀虫剂,具有多种施用方法,杀虫谱广,尤其对刺吸式昆虫有效。它对新烟碱类抗性稻飞虱没有交叉抗性。从亚洲国家田间采集的褐飞虱种群对其表现出高度敏感性。
芬美唑地嗪是一种内吸性杀虫剂,具有广谱性、无交叉抗性,它可能是害虫综合治理和杀虫剂抗性治理的又一工具,尤其适用于稻飞虱复合体。© 2024作者。《害虫管理科学》由约翰·威利父子有限公司代表化学工业协会出版。