ABSTRACT
Cotton aphids, Aphis gosspyii and cotton jassids, Amrasca biguttula are destructive piercing sucking pests to many strategic crops, especially cotton, not only in Egypt but also all over the world. Using synthetic pesticides to control these pests led to several deleterious impacts. Natural pesticides can be used as a harmless alternative. Nine compounds were isolated from different fractions of Retama raetam using chromatographic techniques and identified by spectroscopic methods as eugenol (1), alpinumisoflavone (2), licoflavone C (3), ephedroidin (4), anagyrine (5), spartiene (6), genistein-8ß-C-glucoside (7), isoprunetin (8) and isoprunetin 7-O-ß-D-glucopyranoside (9). The methanol crude extract and its fractions (hexane, chloroform, ethyl acetate and butanol), as well as the isolated compounds were examined against A. gosspyii and A. biguttula as insecticides. The results showed that chloroform fraction was the most potent fraction against A. gosspyii and A. biguttula, with LC50 values of 65.66 and 64.43 ppm, respectively. As well, compounds 1, 5 and 6 were found to be more active, with LC50 values of 69.84, 25.49 and 27.22 ppm for A. gosspyii and 65.17, 24.07 and 24.78 ppm for A. biguttula, respectively. The most potent compounds (1, 5 and 6) exhibited AChE inhibition toward A. gosspyii compared with the control. So, it can be concluded that the isolated compounds eugenol 1, anagyrine 5 and spartiene 6 are the active principles due to their capability to inhibit AchE activity.
Subject(s)
Aphids , Insecticides , Animals , Chloroform , Eugenol , Molecular Structure , Plant Extracts/pharmacologyABSTRACT
The phytochemical investigation of Caralluma quadrangula aerial parts yielded six new pregnane glycosides, quadrangulosides A-F (1-6), in addition to nine known pregnane glycosides and three known flavone glycosides. Structures of isolated phyto-constituents were elucidated via spectroscopic 1D-, 2D-NMR and spectrometric ESI-MS spectra.
