1. Academic Validation
  2. Design, synthesis, and biological activities of arecoline derivatives containing 1,3,4-oxadiazole structure

Design, synthesis, and biological activities of arecoline derivatives containing 1,3,4-oxadiazole structure

  • Bioorg Chem. 2024 Aug 8:151:107708. doi: 10.1016/j.bioorg.2024.107708.
Taiqing Li 1 Sijia Liu 1 Xin Guo 1 Xingxing He 1 Aidang Lu 2 Qingmin Wang 3 Ziwen Wang 4
Affiliations

Affiliations

  • 1 Tianjin Key Laboratory of Structure and Performance for Functional Molecules, College of Chemistry, Tianjin Normal University, Tianjin 300387, China.
  • 2 School of Chemical Engineering and Technology, Hebei University of Technology, Hebei Collaborative Innovation Center of Modern Marine Chemical Technology, Tianjin 300130, China.
  • 3 State Key Laboratory of Elemento-Organic Chemistry, Research Institute of Elemento-Organic Chemistry, College of Chemistry, Collaborative Innovation Center of Chemical Science and Engineering (Tianjin), Nankai University, Tianjin 300071, China.
  • 4 Tianjin Key Laboratory of Structure and Performance for Functional Molecules, College of Chemistry, Tianjin Normal University, Tianjin 300387, China. Electronic address: hxxywzw@tjnu.edu.cn.
Abstract

Pesticides play an important role in the development of agriculture, as they can prevent and control crop diseases and pests, improve crop yield and quality. However, the abuse and improper use of pesticides can lead to negative impacts such as environmental pollution and pest resistance issues. There is an urgent need to develop green, safe, and efficient pesticides. In this work, natural product arecoline was selected as parent structure, a series of arecoline derivatives were designed, synthesized, and systematically investigated Antiviral activities against tobacco mosaic virus (TMV). These compounds were found to have good to excellent anti-TMV activities for the first time. The Antiviral activities of 4a, 4 h, 4 l, 4p, 6a, 6c, and 6f are higher than that of ningnanmycin. Compounds 4 h (EC50 value 146 µg/mL) and 4p (EC50 value 161 µg/mL) with simple structures and excellent activities emerged as new Antiviral candidates. We chose 4 h to further investigate the Antiviral mechanism, which revealed that it can cause virus fragmentation by acting on the viral coat protein (CP). We further validated this result through molecular docking. These compounds also displayed broad-spectrum fungicidal activities against 8 plant pathogenic fungi. This work lays the theoretical foundation for the application of arecoline derivatives in the agricultural field.

Keywords

Anti-TMV activity; Antifungal activity; Arecoline; Mode of action; Natural product.

Figures
Products
  • Cat. No.
    Product Name
    Description
    Target
    Research Area
  • HY-162807
    Anti-tobacco Mosaic Virus Compound
    TMV