Background: A substantial amount of empirical research indicates that the development of novel pesticides through the intermediate derivatization method can significantly enhance the success rate of new pesticide creation while reducing research and development costs. In response to this demand, a series of novel derivatives containing pyrazole imidazo[5,1-b]thiazole were synthesized by the intermediate derivatization method to modify the imine skeleton, which was found to have good antifungal activity in a previous work, and subjecting it to intramolecular nucleophilic substitution reaction.
Results: These compounds showed good performance in antifungal activity tests. Compounds 4f and 18f [median effective concentration (EC) values 0.98 and 0.95 mg L, respectively] had comparable activity against Sclerotinia sclerotiorum to that of the commercial pesticide boscalid (EC = 0.82 mg L). In vivo testing showed that compound 18f had a good protective effect on rape leaves at 40 mg L concentration. Scanning (SEM) and transmission electron microscopy (TEM) revealed that compound 18f exerted a notable detrimental effect on the integrity of the fungal cell membrane, and thus antifungal activity. Subsequent leakage of cell content, relative conductivity tests, cell membrane permeability assays and reactive oxygen species (ROS) assays showed similar results. Moreover, we evaluated the lower toxicity of compound 18f to aquatic organisms compared to the positive control boscalid through acute toxicity experiments on zebrafish.
Conclusions: In this study, we designed a novel imidazo[5,1-b]thiazole derivative containing a pyrazole ring using the intermediate derivatization method and subsequently evaluated its antifungal activity. The highly efficient and low toxicity compound 18f may become a new candidate antifungal pesticide. This study provides a certain reference value for the development of novel fungicides based on imidazo[5,1-b]thiazole derivatives. © 2025 Society of Chemical Industry.
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http://dx.doi.org/10.1002/ps.8739 | DOI Listing |
J Am Soc Mass Spectrom
March 2025
Immunity, Inflammation, and Disease Laboratory, National Institute of Environmental Health Sciences, National Institutes of Health, Research Triangle Park, North Carolina 27709, United States.
The analysis of small carboxyl-containing metabolites (CCMs), such as tricarboxylic acid (TCA) cycle intermediates, provides highly useful information about the metabolic state of cells. However, their detection using liquid chromatography-electrospray ionization-tandem mass spectrometry (LC-ESI-MS/MS) methods can face sensitivity and specificity challenges given their low ionization efficiency and the presence of isomers. Ion mobility spectrometry (IMS), such as trapped ion mobility spectrometry (TIMS), provides additional specificity, but further signal loss can occur during the mobility separation process.
View Article and Find Full Text PDFPest Manag Sci
March 2025
College of Materials and Chemistry and School of Plant Protection, Anhui Agricultural University, Hefei, China.
Background: A substantial amount of empirical research indicates that the development of novel pesticides through the intermediate derivatization method can significantly enhance the success rate of new pesticide creation while reducing research and development costs. In response to this demand, a series of novel derivatives containing pyrazole imidazo[5,1-b]thiazole were synthesized by the intermediate derivatization method to modify the imine skeleton, which was found to have good antifungal activity in a previous work, and subjecting it to intramolecular nucleophilic substitution reaction.
Results: These compounds showed good performance in antifungal activity tests.
Acc Chem Res
February 2025
Center of Basic Molecular Science (CBMS), Department of Chemistry, Tsinghua University, Beijing 100084, China.
ConspectusPyridine is a crucial heterocyclic compound in organic chemistry. Typically, the pyridine motif behaves as an N-nucleophile and an electron-deficient aromatic ring. Transforming the pyridine ring into an electron-rich system that exhibits reactivity contrary to classical expectations could unveil new opportunities in pyridine chemistry.
View Article and Find Full Text PDFOrg Lett
March 2025
Department of Applied Chemistry, Faculty of Science and Technology, Keio University, 3-14-1 Hiyoshi, Kohoku-ku, Yokohama 223-8522, Japan.
Direct C-N bond formation from nitroarenes is a valuable synthetic tool for quick access to aniline derivatives. Transformation via nitroso intermediates could be useful due to their unique properties, but the generation of nitrosoarenes in situ from nitroarenes is challenging due to the tendency for various side reactions. Herein we report the photoinduced reductive [4 + 2] cycloaddition of nitroarenes.
View Article and Find Full Text PDFRapid Commun Mass Spectrom
May 2025
Key Laboratory of Advanced Mass Spectrometry and Molecular Analysis of Zhejiang Province, School of Materials Science and Chemical Engineering, Ningbo University, Ningbo, Zhejiang, China.
Rationale: Dimethylbipyridine (DMDP) serves as a versatile industrial intermediate, with methyl substitutions at distinct positions tailored for varied applications, including the synthesis of DNA reagents and proton receptors. However, the pronounced structural and chemical similarities among its isomers underscore the critical need for an effective method to achieve their quantification and precise identification.
Methods: This study developed a straightforward, swift, and effective approach for the identification and quantification of two dimethylbipyridine positional isomers, namely, 6,6'-dimethyl-2,2'-bipyridine and 4,4'-dimethyl-2,2'-bipyridine based on the analysis of ion mobility spectrometry (IMS) of their cyclodextrin complex ion in gas phase.
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