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The existing agricultural insecticides have developed drug resistance from long-term use. Isoxazoline derivatives are new insecticides discovered in the 21st century. Because of their unique insecticidal mechanism, high selectivity, safety, and no significant cross resistance with the existing pesticides on the market, they have become a hot spot in the field of pesticide research. Herein, a series of novel isoxazoline derivatives containing ether and oxime-ether structures were designed and synthesized by a scaffold-hopping strategy using the pesticide fluralaner as a template structure. Through the investigation of insecticidal activity and the systematic structure-activity relationship, a series of compounds with high insecticidal activities were found, and compounds , , and with LC values of 0.00008-0.00036 mg/L against diamondback moth emerged as novel insecticide candidates. These compounds also exhibited broad spectrum fungicidal activities against 14 plant fungi. The current work provides a reference for the design of new isoxazoline compounds based on the scaffold-hopping strategy.
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http://dx.doi.org/10.1021/acs.jafc.2c08161 | DOI Listing |
Eur J Pharm Sci
September 2025
Department of Organic Chemistry, University of Debrecen, P.O. Box 400, H-4002 Debrecen, Hungary. Electronic address:
Platinum-group metal half-sandwich complexes are considered to be potential replacements of the clinically widely used platins which have several side effects and tend to cause resistance to develop. In our previous works, we used a range of 2-pyridyl-substituted N- and C-glycosyl heterocycles as N,N-chelating ligands to prepare ruthenium(II), osmium(II), iridium(III) and rhodium(III) polyhapto arene/arenyl half-sandwich complexes. Some of these complexes, particularly with the C-glucopyranosyl isoxazole derived ligand in its O-perbenzoylated form, exhibited greater anticancer efficiency than cisplatin and had minimal or negligible effects on non-transformed fibroblasts.
View Article and Find Full Text PDFJ Agric Food Chem
September 2025
School of Pharmaceutical Sciences Guizhou University, Guiyang 550025 P. R. China.
Insecticide misuse has caused pest resistance, stressing the need for novel pesticides. The isoxazoline structure offers broad-spectrum effectiveness, mammalian safety, and no cross-resistance. Developing efficient insecticides with this scaffold remains challenging.
View Article and Find Full Text PDFSe Pu
September 2025
School of Chemistry and Chemical Engineering,Henan University of Technology,Zhengzhou 450001,China.
Isoxazoline drugs (ISOs) are a class of five-membered heterocyclic compounds containing N and O atoms. They can inhibit -aminobutyric acid gated chloride channels and are widely used in the treatment of parasitic diseases in poultry. The intake of animal-derived foods by humans is an important way to come into contact with ISOs.
View Article and Find Full Text PDFRSC Adv
August 2025
Laboratory of Applied Physics, Department of Physics, Faculty of Sciences of Sfax, University of Sfax Sfax Tunisia.
The mechanistic pathway of the (3 + 2) cycloaddition (32CA) between azomethine ylide 1 and dimethyl acetylenedicarboxylate 2, affording 4-isoxazoline derivatives, was elucidated Density Functional Theory (DFT) calculations employing the B3LYP-D3 functional and the 6-311++G(d,p) basis set in 1,4-dioxane. Reactivity insights derived from Conceptual DFT (CDFT) demonstrated that compound 1 behaves as an ambiphilic species with significant nucleophilic and electrophilic tendencies, whereas compound 2 functions predominantly as an electrophile. These electronic features reveal a marked polarity in the cycloaddition and align with a forward electron density flux (FEDF) governing the reaction process.
View Article and Find Full Text PDFACS Pharmacol Transl Sci
August 2025
LAQV/REQUIMTE, Laboratory of Pharmacology, Department of Drug Sciences, Faculty of Pharmacy, University of Porto, Porto 4050-313, Portugal.
Isoxazole-derived compounds possess various bioactivities including anticancer, immunomodulatory, antimicrobial, anti-inflammatory, or antipsychotic effects with successful implementation in clinical practice. Treatment of hematological malignancies with isoxazole derivatives represents a promising area of research. The present study aimed to synthesize 11 novel 3,5-diaryl-4,5-dihydroisoxazole compounds and assess their antiproliferative effects using cell viability assay in a panel of nine cancer types including breast (MCF-7), colon (HCT-116), cervical (HeLa), lung (A549), ovarian cancer (A2780), glioblastoma (U87), hepatocellular carcinoma (HepG2), and leukemia (Jurkat and HL-60) cells as well as two noncancerous cell lines (Bj-5ta and MCF-10A).
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