Preparation and Anti-Tobacco Mosaic Virus Activities of Crocetin Diesters

J Agric Food Chem. 2021 Nov 17;69(45):13637-13643. doi: 10.1021/acs.jafc.1c03884. Epub 2021 Nov 3.

Abstract

The development of antiviral agents with an original structure and noticeable effect is always in great need. Natural products are important lead compounds in the development of new pesticides. Crocin-1 and crocin-2 were effectively isolated from Gardeniae fructus and found to have higher anti-tobacco mosaic virus (TMV) activity levels than ribavirin. A series of the crocetin diester derivatives were synthesized with separated crocetin-1 as material and evaluated for their anti-TMV activities. They could be dissolved in common organic solvents as dichloromethane, ethyl acetate, tetrahydrofuran, and methanol. Compounds 5, 9, 13, 14, and 15 displayed higher activities in vivo than ribavirin. Compound 14 with significantly higher antiviral activities than lead compounds (crocin-1 and crocin-2) emerged as a new antiviral candidate.

Keywords: anti-TMV activity; crocetin diesters; extraction; natural product; solubility; synthesis.

MeSH terms

  • Antiviral Agents / pharmacology
  • Carotenoids
  • Drug Design
  • Ribavirin
  • Structure-Activity Relationship
  • Tobacco Mosaic Virus*
  • Vitamin A / analogs & derivatives

Substances

  • Antiviral Agents
  • trans-sodium crocetinate
  • Vitamin A
  • Carotenoids
  • Ribavirin