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Design, Synthesis and Bioactivities of Novel Pyridyl Containing Pyrazole Oxime Ether Derivatives.
He, Jie; Zhou, Beibei; Wang, Xinjuan; Chen, Qi; Jiang, Xiaoqian; Kong, Ting; Yao, Long; Zhao, Yingying; Chen, Rong; Xu, Ying; Dai, Hong.
Afiliación
  • He J; College of Chemistry and Chemical Engineering, Nantong University, Nantong 226019, China.
  • Zhou B; College of Chemistry and Chemical Engineering, Nantong University, Nantong 226019, China.
  • Wang X; College of Chemistry and Chemical Engineering, Nantong University, Nantong 226019, China.
  • Chen Q; College of Chemistry and Chemical Engineering, Nantong University, Nantong 226019, China.
  • Jiang X; College of Chemistry and Chemical Engineering, Nantong University, Nantong 226019, China.
  • Kong T; College of Chemistry and Chemical Engineering, Nantong University, Nantong 226019, China.
  • Yao L; Analysis and Testing Center, Nantong University, Nantong 226019, China.
  • Zhao Y; College of Chemistry and Chemical Engineering, Nantong University, Nantong 226019, China.
  • Chen R; College of Chemistry and Chemical Engineering, Nantong University, Nantong 226019, China.
  • Xu Y; College of Chemistry and Chemical Engineering, Nantong University, Nantong 226019, China.
  • Dai H; College of Chemistry and Chemical Engineering, Nantong University, Nantong 226019, China.
Molecules ; 29(12)2024 Jun 11.
Article en En | MEDLINE | ID: mdl-38930832
ABSTRACT
In this research, with an aim to develop novel pyrazole oxime ether derivatives possessing potential biological activity, thirty-two pyrazole oxime ethers, including a substituted pyridine ring, have been synthesized and structurally identified through 1H NMR, 13C NMR, and HRMS. Bioassay data indicated that most of these compounds owned strong insecticidal properties against Mythimna separata, Tetranychus cinnabarinus, Plutella xylostella, and Aphis medicaginis at a dosage of 500 µg/mL, and some title compounds were active towards Nilaparvata lugens at 500 µg/mL. Furthermore, some of the designed compounds had potent insecticidal effects against M. separata, T. cinnabarinus, or A. medicaginis at 100 µg/mL, with the mortalities of compounds 8a, 8c, 8d, 8e, 8f, 8g, 8o, 8s, 8v, 8x, and 8z against A. medicaginis, in particular, all reaching 100%. Even when the dosage was lowered to 20 µg/mL, compound 8s also expressed 50% insecticidal activity against M. separata, and compounds 8a, 8e, 8f, 8o, 8v, and 8x displayed more than 60% inhibition rates against A. medicaginis. The current results provided a significant basis for the rational design of biologically active pyrazole oxime ethers in future.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Oximas / Pirazoles / Diseño de Fármacos / Insecticidas Límite: Animals Idioma: En Revista: Molecules Asunto de la revista: BIOLOGIA Año: 2024 Tipo del documento: Article País de afiliación: China

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Oximas / Pirazoles / Diseño de Fármacos / Insecticidas Límite: Animals Idioma: En Revista: Molecules Asunto de la revista: BIOLOGIA Año: 2024 Tipo del documento: Article País de afiliación: China
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