4.6 Article

A Potential Lead for Insect Growth Regulator: Design, Synthesis, and Biological Activity Evaluation of Novel Hexacyclic Pyrazolamide Derivatives

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MOLECULES
卷 28, 期 9, 页码 -

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MDPI
DOI: 10.3390/molecules28093741

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insect growth regulators; pyrazolamide; ecdysone receptor; chitinase; molecular docking; dual-target IGRs

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In this study, hexacyclic pyrazolamide derivatives were designed and synthesized as novel insect growth regulators targeting Ecdysone receptor (EcR) and chitinase. The insecticidal activity was improved by inserting an additional methylene spacer between the substituted phenyl ring and the amide bond. Compound 6j showed promising insecticidal activities against Plutella xylostella and Spodoptera frugiperda and targeted both EcR and OfChtI. This research provides valuable clues for the development of new dual-target insect growth regulators.
Ecdysone receptor (EcR) and chitinase play a critical role in the molting stage of insect pests. Each of them is considered a promising target for the development of novel insect growth regulators (IGRs). In the present paper, a total of 24 (23 novel) hexacyclic pyrazolamide derivatives were designed and synthesized by reducing the heptacycle and inserting small flexible linkers on the basis of the previously discovered dual-target compound D-27 acting simultaneously on EcR and Ostrinia furnacalis chitinase (OfChtI). Their insecticidal activities against Plutella xylostella, Spodoptera frugiperda, and Ostrinia furnacalis larvae were evaluated. The results revealed that the insecticidal activity was not significantly enhanced when the heptacycle on the pyrazole ring was reduced to a hexacycle. However, the insertion of an additional methylene spacer between the substituted phenyl ring and the amide bond can improve the insecticidal activity. Among the derivatives, the most potent compound, 6j, exhibited promising insecticidal activities against P. xylostella and S. frugiperda. Further protein binding assays and molecular docking indicated that 6j could target both EcR and OfChtI, and is a potential lead compound for IGRs. The present work provides valuable clues for the development of new dual-target IGRs.

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