Abstract

The invasion of Spodoptera frugiperda has imposed a serious impact on global food security. Matrine is a botanical pesticide with a broad spectrum of insecticidal activity which was recommended for controlling Spodoptera frugiperda. In order to discover effective insecticide for Spodoptera frugiperda, two matrine derivatives modified with carbon disulfide and nitrogen-containing groups were systhesized. And their inhibition activities on Sf9 cell were evaluated. The structural configuration of compounds were characterized by IR, HPLC, MS, NMR and XRD, with yields of 52% and 65%, respectively. The IC50 of the two newly synthesized compounds on Sf9 cell reduced to 0.648 mmol/L and 1.13 mmol/L, respectively, compared with that of matrine (5.330 mmol/L). In addition, microscopic observation of Sf9 cell treated with the compounds showed that the number of adherent cells decreased, the cells shrunk, vacuolated and apoptotic bodies appeared. The two newly synthesized compounds exhibited better inhibitory effect on Sf9 cell than that of the parent matrine, suggesting that the positive effect of the introduction of 1-pyrrolidinecarbodithioate and diethylcarbamodithioate groups to matrine. The morphological observation of Sf9 cell induced by derivatives indicated that apoptosis induction may be a mechanism that inhibits insect cell proliferation and exerts insecticidal effect.

Highlights

  • The invasion of Spodoptera frugiperda has imposed a serious impact on global food security

  • The amine reacted with carbon disulfide to synthesize intermediate compounds (1-pyrrolidinecarbodithioic acid, diethylcarbamodithioic acid)

  • Experiments showed that carbon disulfide could react with sophocarpine at the first step, but the yields were low

Read more

Summary

Introduction

The invasion of Spodoptera frugiperda has imposed a serious impact on global food security. Matrine is a botanical pesticide with a broad spectrum of insecticidal activity which was recommended for controlling Spodoptera frugiperda. In order to discover effective insecticide for Spodoptera frugiperda, two matrine derivatives modified with carbon disulfide and nitrogen-containing groups were systhesized. Their inhibition activities on Sf9 cell were evaluated. Studies on the insecticidal activities of natural compounds and their derivatives against S. frugiperda have been reported, such as botanical essential oils and sesquiterpenoids. According to the special insecticidal mechanism of pyridalyl against lepidopterous larvae, 1,1-dichloropropene derivatives bearing structurally diverse substituted heterocycle rings that replace the pyridine ring of pyridalyl have been designed and synthesized, and the compounds displayed significant insecticidal activity against prodenia litura and diamondback moths[20]. Research on the insecticidal mechanism is of great significance to the development of insecticides

Objectives
Methods
Results
Conclusion
Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call