Insecticidal constituents from rhizomes of Zingiber cassumunar and Kaempferia rotunda

被引:41
作者
Nugroho, BW
Schwarz, B
Wray, V
Proksch, P
机构
[1] UNIV WURZBURG,JULIUS VON SACHS INST BIOWISSENSCH,LEHRSTUHL PHARMAZEUT BIOL,D-97082 WURZBURG,GERMANY
[2] GESELL BIOTECHNOL FORSCH MBH,D-38124 BRAUNSCHWEIG,GERMANY
[3] BOGOR AGR UNIV,FAC AGR,DEPT PLANT PESTS & DIS,BOGOR,INDONESIA
关键词
Kaempferia rotunda; Zingiber cassumunar; zingiberaceae; rhizomes; insecticidal constituents; Spodoptera littoralis;
D O I
10.1016/0031-9422(95)00454-8
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Rhizomes from 18 different species of the Zingiberaceae were screened for insecticidal constituents against neonate larvae of the pest insect, Spodoptera littoralis. Extracts from rhizomes of Kaempferia rotunda and Zingiber cassumunar, when incorporated into artificial diets, displayed significant insecticidal activity in chronic feeding bioassays at concentrations of 2500 ppm and 1250 ppm, respectively. Bioassay-guided isolation afforded two phenyl-butanoids from rhizomes of Z. cassumunar which had LC(50) values against neonate larvae of 121 and 127 ppm, respectively, in the chronic feeding bioassay. Both compounds were also active in the residue-contact bioassay (LC(50) values of 0.5 and 3.6 mu g cm(-2), respectively). The presence of oxygenated substituents (-OH or -OAc groups) in the side-chain nullified insecticidal activity. Rhizomes of K. rotunda yielded two active metabolites: benzyl benzoate and the cyclohexane derivative, crotepoxide. Compared to the bioactive phenylbutanoids from Z. cassumunar, crotepoxide was less active in the chronic feeding bioassay (LC(50), 1450 ppm) and was inactive in the residue-contact bioassay. Benzyl benzoate, however, exhibited insecticidal activity only when applied topically (LC(50), 5.6 mu g cm(-2)) suggesting detoxification in the larval gut when applied orally.
引用
收藏
页码:129 / 132
页数:4
相关论文
共 14 条
[1]  
Brucher H., 1977, Tropische Nutzpflanzen: Ursprung, Evolution und Domestikation
[2]  
BUNYAPRAPHATSAR.N, 1990, EC MED PLANT RES, V4, P141
[3]   QUANTITATIVE STRUCTURE-ACTIVITY-RELATIONSHIPS AND CARMINATIVE ACTIVITY [J].
EVANS, BK ;
JAMES, KC ;
LUSCOMBE, DK .
JOURNAL OF PHARMACEUTICAL SCIENCES, 1978, 67 (02) :277-278
[4]  
Grainge M, 1988, HDB PLANTS PEST CONT
[5]  
HAGINIWA J, 1963, YAKUGAKU ZASSHI, V83, P624
[6]   TUMOR INHIBITORS .45. CROTEPOXIDE, A NOVEL CYCLOHEXANE DIEPOXIDE TUMOR INHIBITOR FROM CROTON MACROSTACHYS [J].
KUPCHAN, SM ;
HEMINGWAY, RJ ;
SMITH, RM .
JOURNAL OF ORGANIC CHEMISTRY, 1969, 34 (12) :3898-+
[7]  
KUROYANAGI M, 1980, CHEM PHARM BULL, V28, P2948
[8]   INSECTICIDAL CONSTITUENTS FROM 4 SPECIES OF THE ZINGIBERACEAE [J].
PANDJI, C ;
GRIMM, C ;
WRAY, V ;
WITTE, L ;
PROKSCH, P .
PHYTOCHEMISTRY, 1993, 34 (02) :415-419
[9]  
Purseglove J., 1972, Tropical Crops: Dicotyledons. Land on Long Man
[10]  
ROSE MFS, 1977, INTRO PHYTOPHARMACY, P159