New insecticidal rocaglamide derivatives and related compounds from Aglaia oligophylla

被引:34
作者
Dreyer, M
Nugroho, BW
Bohnenstengel, FI
Ebel, R
Wray, V
Witte, L
Bringmann, G
Mühlbacher, J
Herold, M
Hung, PD
Kiet, LC
Proksch, P
机构
[1] Univ Dusseldorf, Inst Pharmazeut Biol, D-40225 Dusseldorf, Germany
[2] Gesell Biotechnol Forsch GmbH, D-38124 Braunschweig, Germany
[3] Tech Univ Braunschweig, Inst Pharmazeut Biol, D-38106 Braunschweig, Germany
[4] Univ Wurzburg, Inst Organ Chem, D-97074 Wurzburg, Germany
[5] Vietnam Natl Univ, Coll Nat Sci, Dept Chem, Ho Chi Minh, Vietnam
[6] Vietnam Natl Univ, Coll Nat Sci, Dept Bot, Ho Chi Minh, Vietnam
[7] Bogor Agr Univ, Dept Plant Pests & Dis, Fac Agr, Jl Raya Pajajaran Bogor 16144, Indonesia
来源
JOURNAL OF NATURAL PRODUCTS | 2001年 / 64卷 / 04期
关键词
D O I
10.1021/np000123x
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Organic-soluble extracts of the twigs of Aglaia oligophylla collected in Vietnam yielded four insecticidal cyclopentatetrahydrobenzofurans of the rocaglamide type including one new natural product (compound 4). Moreover, two cyclopentatetrahydrobenzopyran derivatives, belonging to the aglain and aglaforbesin types, respectively, were also isolated. The aglaforbesin derivative 6 proved likewise to be a new natural product. All isolated rocaglamide, aglain, and aglaforbesin derivatives have a characteristic methylenedioxy substituent linked to C-6 and C-7 or to C-7 and C-8, respectively. Structure elucidation of the new natural products and the determination of the absolute configuration of compound 1 by calculation of its CD spectrum with molecular dynamics simulation are described. All isolated rocaglamide derivatives exhibited strong insecticidal activity toward neonate larvae of the polyphageous pest insect Spodoptera littoralis when incorporated into an artificial diet, with LC50 values varying between 2.15 and 6.52 ppm.
引用
收藏
页码:415 / 420
页数:6
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