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Synthesis, Bioactivity and Molecular Docking of Nereistoxin Derivatives Containing Phosphonate.
Yan, Qiaoli; Lu, Xiaogang; Zhang, Zixuan; Jin, Qian; Gao, Runli; Li, Liqin; Wang, Hongmei.
Afiliación
  • Yan Q; State Key Laboratory of NBC Protection for Civilian, Beijing 102205, China.
  • Lu X; State Key Laboratory of NBC Protection for Civilian, Beijing 102205, China.
  • Zhang Z; State Key Laboratory of NBC Protection for Civilian, Beijing 102205, China.
  • Jin Q; State Key Laboratory of NBC Protection for Civilian, Beijing 102205, China.
  • Gao R; State Key Laboratory of NBC Protection for Civilian, Beijing 102205, China.
  • Li L; State Key Laboratory of NBC Protection for Civilian, Beijing 102205, China.
  • Wang H; State Key Laboratory of NBC Protection for Civilian, Beijing 102205, China.
Molecules ; 28(12)2023 Jun 19.
Article en En | MEDLINE | ID: mdl-37375402
ABSTRACT
Novel nereistoxin derivatives containing phosphonate were synthesized and characterized via 31P, 1H and 13C NMR and HRMS. The anticholinesterase activity of the synthesized compounds was evaluated on human acetylcholinesterase (AChE) using the in vitro Ellman method. Most of the compounds exhibited good inhibition of acetylcholinesterase. All of these compounds were selected to assess their insecticidal activity (in vivo) against Mythimna separata Walker, Myzus persicae Sulzer and Rhopalosiphum padi. Most of the tested compounds displayed potent insecticidal activity against these three species. Compound 7f displayed good activity against all three insect species, showing LC50 values of 136.86 µg/mL for M. separata, 138.37 µg/mL for M. persicae and 131.64 µg/mL for R. padi. Compound 7b had the highest activity against M. persicae and R. padi, with LC50 values of 42.93 µg/mL and 58.19 µg/mL, respectively. Docking studies were performed to speculate the possible binding sites of the compounds and explain the reasons for the activity of the compounds. The results showed that the compounds had lower binding energies with AChE than with the acetylcholine receptor (AchR), suggesting that compounds are more easily bound with AChE.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Áfidos / Organofosfonatos / Insecticidas Límite: Animals / Humans Idioma: En Revista: Molecules Asunto de la revista: BIOLOGIA Año: 2023 Tipo del documento: Article País de afiliación: China

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Áfidos / Organofosfonatos / Insecticidas Límite: Animals / Humans Idioma: En Revista: Molecules Asunto de la revista: BIOLOGIA Año: 2023 Tipo del documento: Article País de afiliación: China