Pest management science · 2026
Discovery of natural product-derived pesticide candidates: synthesis, aphicidal activity, and toxicological evaluation of andrographolide derivatives.
СтатьяНазвание и аннотация: Перевод в очереди
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Zhang Wen, Song Xiao-Xia, Zhang Wen-Hui, Zhou Xin-Rui, Yuan Wei, Zhang Ji, Kong Wei-Bao, Liang Jun-Yu, Wu Fei
Аннотация
BACKGROUND: To address pest resistance, environmental concerns, and non-target toxicity associated with conventional pesticides, the natural product andrographolide was structurally optimized for the development of eco-friendly insecticides.
RESULTS: A series of andrographolide derivatives were designed and synthesized, among which compound 9i exhibited the strongest insecticidal activity against Myzus persicae Sulzer, with an LC50 value of 0.1248 mg mL-1, representing a 16-fold enhancement over the parent compound. In greenhouse pot experiments, 9i achieved a control efficacy 4.7 times greater than that of andrographolide. Structure-activity relationship analysis indicated that introducing aromatic substituents containing electron-withdrawing groups at the C3 position significantly improved insecticidal activity. Morphological observations by stereomicroscopy and scanning electron microscopy revealed severe damage to the insect body surface after treatment. Biochemical assays further showed that 9i markedly induced the activities of key antioxidant enzymes, including superoxide dismutase and catalase. Toxicological evaluation demonstrated favorable selectivity, with low toxicity toward non-target organisms, including honeybees, mammalian bEND.3 cells, zebrafish larvae, and representative microorganisms.
CONCLUSION: Structural optimization substantially enhances the insecticidal activity of andrographolide. Compound 9i represents a promising lead candidate for eco-friendly insecticide development and provides a valuable basis for future pesticide discovery. © 2026 Society of Chemical Industry.
RESULTS: A series of andrographolide derivatives were designed and synthesized, among which compound 9i exhibited the strongest insecticidal activity against Myzus persicae Sulzer, with an LC50 value of 0.1248 mg mL-1, representing a 16-fold enhancement over the parent compound. In greenhouse pot experiments, 9i achieved a control efficacy 4.7 times greater than that of andrographolide. Structure-activity relationship analysis indicated that introducing aromatic substituents containing electron-withdrawing groups at the C3 position significantly improved insecticidal activity. Morphological observations by stereomicroscopy and scanning electron microscopy revealed severe damage to the insect body surface after treatment. Biochemical assays further showed that 9i markedly induced the activities of key antioxidant enzymes, including superoxide dismutase and catalase. Toxicological evaluation demonstrated favorable selectivity, with low toxicity toward non-target organisms, including honeybees, mammalian bEND.3 cells, zebrafish larvae, and representative microorganisms.
CONCLUSION: Structural optimization substantially enhances the insecticidal activity of andrographolide. Compound 9i represents a promising lead candidate for eco-friendly insecticide development and provides a valuable basis for future pesticide discovery. © 2026 Society of Chemical Industry.