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The major problems in basmati rice are sheath blight and bakanae diseases caused by Rhizoctonia solani and Fusarium fujikuroi, which significantly lower the productivity of basmati rice. However, the excessive use of fungicides can result in pathogen resistance, environmental overload and mammalian toxicity. Therefore, there is a need for new fungicides with novel modes of action, low toxicity and minimal residue. To address this, 20 pyrazole derivatives from alkoxy/halo acetophenones and N,N-dimethylformamide dimethyl acetal are synthesized and characterized by various techniques, namely, H NMR, C NMR and LC-HRMS, expressing fungicidal activity against R. solani and F. fujikuroi. Compound 5r (3-(5-fluoro-2-hydroxylphenyl) pyrazole) exhibited the highest activity (ED = 2.75 µg mL) against both R. solani and F. fujikuroi. 2D-quantitative structure-activity relationship (2D-QSAR) analysis, particularly MLR (Model 1), with a strong correlation coefficient (r) of 0.973, a cross-validated correlation coefficient (q) of 0.84, and an of 0.93, highlighted AI descriptors T_2_F_6, T_2_Cl_7, T_T_O_4 and DeltaAlphaA, the key descriptors influencing fungicidal activity. Molecular docking studies revealed the potential of these pyrazole derivatives as novel fungicides as succinate dehydrogenase inhibitors (SDHI), suggesting valuable reference for design of effective fungicides.
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http://dx.doi.org/10.1002/cbdv.202501550 | DOI Listing |
Bioorg Chem
September 2025
Post Graduate and Research Department of Botany, A.V.V.M. Sri Pushpam College (Affiliated to Bharathidasan University), Poondi 613 503, Thanjavur, India. Electronic address:
The research employed zirconyl oxychloride as a catalyst in a reaction involving pyrazole aldehyde, (thio)urea, and acetyl acetone to establish an aqueous approach for synthesizing 3,4-dihydropyrimidinone derivatives (compounds 4a-j) with potential claims as antidiabetic agents. FT-IR, HR-MS, H NMR and C NMR were employed to analyze the synthesized compounds. The HOMO-LUMO analysis was performed to evaluate the stability of the synthesized derivatives.
View Article and Find Full Text PDFAnal Methods
September 2025
Department of Pharmaceutical Chemistry, College of Pharmacy, King Saud University, P.O. Box 2457, Riyadh 11451, Saudi Arabia.
Avapritinib (Ayvakit™) is a highly selective inhibitor of the platelet-derived growth factor receptor alpha (PDGFRA), including D842V mutations. Avapritinib (APB) is authorized in the United States for individuals with metastatic or unresectable gastrointestinal stromal tumors (GISTs). APB is considered the exclusive therapy for adults with indolent systemic mastocytosis.
View Article and Find Full Text PDFCurr Med Chem
September 2025
Laboratory of Molecular Basis of Action of physiologically active compounds, Engelhardt Institute of Molecular Biology, Russian Academy of Sciences, 119991, Moscow, Russia.
Introduction: Chemotherapy remains essential despite advances in immunotherapy, radiotherapy, and biological therapy. However, the wide range of chemical drugs is limited by a narrow therapeutic index, low selectivity, and the development of resistance. In this regard, new high-efficiency drugs are in extremely high demand.
View Article and Find Full Text PDFbioRxiv
August 2025
Department of Chemistry, University of Alberta, Edmonton, AB T6G 2G2, Canada.
Genetically-encoded libraries of peptide-derived macrocycles containing electrophile 'warheads' (cGELs) can be used to identify potent and selective covalent ligands for protein targets. Such cGELs are synthesized either by incorporation of unnatural amino acids that display mild electrophiles on their side chains or by chemical post-translational modification (cPTM) of mRNA or phage-displayed peptide libraries. Here we investigate fundamental barriers to the synthesis of cGELs.
View Article and Find Full Text PDFCurr Top Med Chem
September 2025
Department of Pharmaceutical Chemistry, Faculty of Pharmacy, Trakya University, Edirne, Turkiye.