Organic extracts of the twigs and leaves of Aglaia odorata yielded eight in
secticidal cyclopentatetrahydrobenzofuran rocaglamide derivatives including
three congeners which proved to be new natural products. Moreover, four ne
w cyclopentatetrahydrobenzopyran aglain derivatives, as well as the known a
minopyrrolidine odorine and odorinol, syringaresinol and flavonoid derivati
ves were also isolated. Structure elucidation of the new compounds is descr
ibed and a rationale of the biosynthesis of the rocaglamide and aglain cong
eners is considered. The isolated rocaglamide derivatives exhibited strong
insecticidal activity towards neonate larvae of the polyphagous pest insect
Spodoptera littoralis when incorporated into artificial diet with LC50 val
ues varying from 1.0-8.0 ppm. The most active compounds showed LC50 values
between 1.0 and 1.1 ppm, comparable to those of the insecticide azadirachti
n, which was used as a positive control. The remaining compounds isolated f
rom A. odorata were inactive with regard to insecticidal activity. (C) 1999
Elsevier Science Ltd. All rights reserved.