Fruits of Aglaia elliptica and leaves of A. harmsiana yielded seven in
secticidal rocaglamide derivatives including five components which pro
ved to be new natural products. Structure elucidation of the new compo
unds is described. All rocaglamide derivatives isolated exhibited stro
ng insecticidal activity towards neonate larvae of the polyphagous pes
t insect Spodoptera littoralis when incorporated into an artificial di
et with LC50 values varying from 0.8-19.7 ppm. The known didesmethylro
caglamide was the most active compound encountered. Its LC50 (0.8 ppm)
and EC50 (0.05 ppm) were identical to those of azadirachtin which was
included as a positive control. (C) 1997 Elsevier Science Ltd. All ri
ghts reserved.