Affiliations 

  • 1 Equipe de Chimie des Plantes et de Synthèse Organique et Bioorganique, URAC23, Faculty of Science, B.P. 1014, Geophysics, Natural Patrimony and Green Chemistry (GEOPAC) Research Center, Mohammed V University in Rabat, Agdal, Morocco
  • 2 Laboratory of Biodiversity, Ecology, and Genome (BioEcoGen), Faculty of Sciences, B.P. 1014, Biotechnologies Végétale et Microbienne, Biodiversité et Environnement (Biobio) Research Center, Mohammed V University in Rabat, Agdal, Morocco
  • 3 Chemical & Biochemical Sciences Green-Process Engineering (CBS) Mohammed VI Polytechnic University, Benguerir, Morocco
  • 4 Zoogeography Laboratory, University Paul-Valéry Montpellier 3, Montpellier, France
  • 5 X-ray Crystallography Unit, School of Physics, Universiti Sains Malaysia, Penang, Malaysia
  • 6 Laboratory of Analytical Chemistry and Bromatology, Faculty of Medicine and Pharmacy, Mohammed V University in Rabat, Agdal, Morocco
Pest Manag Sci, 2023 Dec;79(12):4847-4857.
PMID: 37500586 DOI: 10.1002/ps.7686

Abstract

BACKGROUND: Sphodroxia maroccana Ley is a pest of cork oak crops that damages the roots of seedlings and can severely impair cork oak regeneration. Since the banning of carbosulfan and chlorpyriphos, which were widely used against the larvae of Sphodroxia maroccana because of their harmful impact on the environment, until now there has been no pesticide against these pests. Therefore, it is particularly urgent to develop highly effective insecticidal molecules with novel scaffolds. Isoxazolines are a class of insecticides that act on γ-aminobutyric acid (GABA)-gated chloride channel allosteric modulators. In this work, a green synthesis of novel 3,5-disubstituted isoxazoline-sulfonamide derivatives was achieved in water via ultrasound-assisted four-component reactions, and their insecticidal activities against fourth-instar larvae of S. maroccana were evaluated.

RESULTS: Most of the tested compounds showed insecticidal activity compared to fluralaner as positive control and commercially available insecticide. Especially, the isoxazoline-secondary sulfonamides containing halogens (Br and Cl) on the phenyl group attached to the isoxazoline, 6g (LC50  = 0.31 mg/mL), 6j (LC50  = 0.38 mg/mL), 6k (LC50  = 0.18 mg/mL), 6L (LC50  = 0.49 mg/mL), 6m (LC50  = 0.24 mg/mL), 6q (LC50  = 0.46 mg/mL), exhibited much higher larvicidal activity than fluralaner (LC50  = 0.99 mg/mL).

CONCLUSION: Novel isoxazolines containing sulfonamide moieties were designed, synthesized and confirmed by two single-crystal structures of 4e and 6q. Their bioassay results showed significant larvicidal activity with significant morphological changes in vivo. These results will lay the foundation for the further discovery and development of isoxazoline-sulfonamide derivatives as novel crop protection larvicides of cork oak. © 2023 Society of Chemical Industry.

* Title and MeSH Headings from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.