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Synthesis, antifungal evaluation, two-dimensional quantitative structure-activity relationship and molecular docking studies of isoxazole derivatives as potential fungicides.
Tripathi, Kailashpati; Kaushik, Parshant; Yadav, Dinesh Kumar; Kumar, Rakesh; Misra, Sameer Ranjan; Godara, Rajni; Bashyal, Bishnu Maya; Rana, Virendra Singh; Kumar, Rajesh; Yadav, Jagdish; Shakil, Najam Akhtar.
Afiliação
  • Tripathi K; Division of Agricultural Chemicals, ICAR-Indian Agricultural Research Institute, New Delhi, India.
  • Kaushik P; ICAR-National Research Centre on Seed Spices, Ajmer, India.
  • Yadav DK; The Graduate School, ICAR-Indian Agricultural Research Institute, New Delhi, India.
  • Kumar R; Division of Agricultural Chemicals, ICAR-Indian Agricultural Research Institute, New Delhi, India.
  • Misra SR; ICAR-Indian Institute of Soil Science, Bhopal, India.
  • Godara R; ICAR-Central Inland Fishries Research Institute, Guwahati, India.
  • Bashyal BM; Division of Agricultural Chemicals, ICAR-Indian Agricultural Research Institute, New Delhi, India.
  • Rana VS; Division of Agricultural Chemicals, ICAR-Indian Agricultural Research Institute, New Delhi, India.
  • Kumar R; Division of Plant Pathology, ICAR-Indian Agricultural Research Institute, New Delhi, India.
  • Yadav J; Division of Agricultural Chemicals, ICAR-Indian Agricultural Research Institute, New Delhi, India.
  • Shakil NA; Division of Agricultural Chemicals, ICAR-Indian Agricultural Research Institute, New Delhi, India.
Pest Manag Sci ; 2024 May 01.
Article em En | MEDLINE | ID: mdl-38690722
ABSTRACT

BACKGROUND:

Sheath blight and bakanae disease, prominent among emerging rice ailments, exert a profound impact on rice productivity, causing severe impediments to crop yield. Excessive use of older fungicides may lead to the development of resistance in the pathogen. Indeed, a pressing and immediate need exists for novel, low-toxicity and highly selective fungicides that can effectively combat resistant fungal strains.

RESULTS:

A series of 20 isoxazole derivatives were synthesized using alkoxy/halo acetophenones and N,N-dimethylformamidedimethylacetal. These compounds were characterized by various spectroscopic techniques, namely 1H nuclear magnetic resonance (NMR), 13C NMR and liquid chromatography-high-resolution mass spectrometry, and were evaluated for their fungicidal activity against Rhizoctonia solani and Fusarium fujikuroi. Compound 5n (5-(2-chlorophenyl) isoxazole) exhibited highest activity (effective dose for 50% inhibition [ED50] = 4.43 µg mL-1) against R. solani, while 5p (5-(2,4-dichloro-2-hydroxylphenyl) isoxazole) exhibited highest activity (ED50 = 6.7 µg mL-1) against F. fujikuroi. Two-dimensional quantitative structural-activity relationship (QSAR) analysis, particularly multiple linear regression (MLR) (Model 1), highlighted chi6chain and DistTopo as the key descriptors influencing fungicidal activity. Molecular docking studies revealed the potential of these isoxazole derivatives as novel fungicides targeting sterol 14α-demethylase enzyme, suggesting their importance as crucial intermediates for the development of novel and effective fungicides.

CONCLUSION:

All test compounds were effective in inhibiting both fungi, according to the QSAR model, with various descriptors, such as structural, molecular shape analysis, electronic and thermodynamic, playing an important role. Molecular docking studies confirmed that these compounds can potentially replace commercially available fungicides and help control fungal pathogens in rice crops effectively. © 2024 Society of Chemical Industry.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article