A Comprehensive Review of the Current Knowledge of Chlorfenapyr: Synthesis, Mode of Action, Resistance, and Environmental Toxicology

• Published in: Molecules (Basel, Switzerland) Vol. 28; no. 22; p. 7673
• Main Authors: Huang, Ping, Yan, Xiyue, Yu, Bo, He, Xuan, Lu, Lidan, Ren, Yuanhang
• Format: Journal Article
• Language: English
• Published: Basel MDPI AG 01.11.2023
• Subjects: Acids; Agricultural chemicals industry; Amino acids; Antibiotics; Carcinogens; chlorfenapyr; environmental toxicology; Hydrocarbons; Insecticides; Lead compounds; Mediation; Metabolism; Metabolites; mode of action; Natural products; Permethrin; Pesticides; Phosphorylation; Phytotoxicity; Raw materials; Researchers; resistance; synthesis; Toxicity; Toxicology; United States; China
• ISSN: 1420-3049; 1420-3049
• DOI: 10.3390/molecules28227673

Creating new insecticide lead compounds based on the design and modification of natural products is a novel process, of which chlorfenapyr is a typical successful example. Chlorfenapyr is an arylpyrrole derivative that has high biological activity, a wide insecticidal spectrum, and a unique mode of action. For decades, a series of chlorfenapyr derivatives were designed and synthesized continuously, of which many highly active insecticidal compounds were discovered sequentially. However, due to the widespread application of chlorfenapyr and its degradation properties, some adverse effects, including pest resistance and environmental toxicity, occurred. In this review, a brief history of the discovery and development of chlorfenapyr is first introduced. Then, the synthesis, structural modification, structure activity relationship, and action mechanism of arylpyrroles are summarized. However, challenges and limitations still exist, especially in regard to the connection with pest resistance and environmental toxicology, which is discussed at the end of this review. This comprehensive summary of chlorfenapyr further promotes its progress and sensible application for pest management.