Experimental evaluation and structure-activity relationship analysis of bridged-ring terpenoid derivatives as novel repellent.

Cockroaches are urban pests that are very difficult to control. Using repellents is a green, safe and effective strategy for their control. In order to find novel cockroach repellents, the repellent activity of 45 bridged-ring terpenoid derivatives synthesized from β-pinene against was tested. The relationship between the molecular structure of these bridged-ring terpenoid derivatives and their repellent activity against was also analysed. The results show that some of the bridged-ring terpenoid derivatives exhibit good repellent activity against , and six compounds (RR = 60.44-87.32%) show higher repellent activity against than DEET (RR = 54.77%), making them promising for development as new cockroach repellents. Quantitative structure-activity relationship (QSAR) analysis revealed that the HOMO-1 energy, Kier and Hall index (order 2), Balaban index, and relative positive charged surface area of bridged-ring terpenoid derivatives have effects on repellent activity against . The present study may provide a theoretical basis for the high-value use of β-pinene and can be helpful to the development of novel repellents against .