51. Design, synthesis and aphicidal activity of N-terminal modified insect kinin analogs
- Author
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Dunlun Song, Yun Ling, Xiaoqing Wu, Chuanliang Zhang, Xinling Yang, and Qu Yanyan
- Subjects
Insecticides ,Physiology ,Stereochemistry ,Peptidomimetic ,media_common.quotation_subject ,Aphis glycines ,Kinins ,Insect ,Kinin ,Biology ,Biochemistry ,Pentapeptide repeat ,Cellular and Molecular Neuroscience ,chemistry.chemical_compound ,Endocrinology ,chemistry ,Design synthesis ,Aphids ,Drug Design ,Animals ,Insect Proteins ,Peptidomimetics ,Lead compound ,media_common - Abstract
The insect kinins are a class of multifunctional insect neuropeptides present in a diverse variety of insects. Insect kinin analogs showed multiple bioactivities, especially, the aphicidal activity. To find a biostable and bioactive insecticide candidate with simplified structure, a series of N-terminal modified insect kinin analogs was designed and synthesized based on the lead compound [Aib]-Phe-Phe-[Aib]-Trp-Gly-NH 2 . Their aphicidal activity against the soybean aphid Aphis glycines was evaluated. The results showed that all the analogs maintained the aphicidal activity. In particular, the aphicidal activity of the pentapeptide analog X Phe-Phe-[Aib]-Trp-Gly-NH 2 (LC 50 = 0.045 mmol/L) was similar to the lead compound (LC 50 = 0.048 mmol/L). This indicated that the N-terminal protective group may not play an important role in the activity and the analogs structure could be simplified to pentapeptide analogs while retaining good aphicidal activity. The core pentapeptide analog X can be used as the lead compound for further chemical modifications to discover potential insecticides.
- Published
- 2015