Antifeedant activity of plant extracts and of new natural diglyceride compounds isolated from Ajuga pseudoiva leaves against Spodoptera littoralis larvae

被引:39
作者
Ben Jannet, H
H-Skhiri, F
Mighri, Z [1 ]
Simmonds, MSJ
Blaney, WM
机构
[1] Univ Ctr, Fac Sci Monastir, Lab Chim Subst Nat & Synthese Organ, Monastir 5000, Tunisia
[2] Univ Ctr, Ecole Super Hort, Lab Biol Vegetale & Bot, Chott Meriem, Sousse, Tunisia
[3] Royal Bot Gardens, Jodrell Lab, Richmond, Surrey, England
[4] Univ London Birkbeck Coll, Dept Biol, London, England
关键词
antifeedant; plant extracts; Ajuga pseudoiva; new natural diglycerides; Spodoptera littoralis;
D O I
10.1016/S0926-6690(01)00086-3
中图分类号
S2 [农业工程];
学科分类号
0828 ;
摘要
Antifeedant activity of 215 natural extracts prepared from a range of medicinal plants growing in Tunisia, against larvae of Egyptian cotton leafworm. Spodoptera littoralis (Lepidoptera) has been studied. Feeding inhibition occurs with 35 extracts, of which 18 have been prepared from leaves. We also found potent antifeedant activity of petroleum ether, methylene chloride, acetone and methanol extracts of Olea europea stem barks. An active mixture of three new 1,3-diglyceride homologous compounds, ivaides A-C (I-III), was isolated from acetone extract of Ajuga pseudoiva leaves by chromatographic techniques guided by bioassay-positive responses. The behavioral response of Spodoptera littoralis larvae to these new natural compounds showed that significant activity might be associated with the presence in each of two beta -hydroxy-alkanoic moieties. This conclusion is reinforced by previous work showing the existence of 3-hydroxy-alkanoic acids and their derivatives in some biological systems and their production by micro-organisms. (C) 2001 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:213 / 222
页数:10
相关论文
共 14 条
[1]   INSECT ANTIFEEDANT ACTIVITY OF CLERODANE DITERPENOIDS AGAINST LARVAE OF SPODOPTERA-LITTORALIS (BOISD) (LEPIDOPTERA) [J].
BELLES, X ;
CAMPS, F ;
COLL, J ;
PIULACHS, MD .
JOURNAL OF CHEMICAL ECOLOGY, 1985, 11 (10) :1439-1445
[2]   Responses of Spodoptera littoralis larvae to Tunisian plant extracts and to neo-clerodane diterpenoids isolated from Ajuga pseudoiva leaves [J].
Ben Jannet, H ;
Harzallah-Skhiri, F ;
Mighri, Z ;
Simmonds, MSJ ;
Blaney, WM .
FITOTERAPIA, 2000, 71 (02) :105-112
[3]  
BLANEY WM, 1988, ENTOMOL EXP APPL, V46, P267, DOI 10.1007/BF00364198
[4]   NEO-CLERODANE DITERPENOIDS FROM AJUGA-CHAMAEPITYS [J].
CAMPS, F ;
COLL, J ;
DARGALLO, O .
PHYTOCHEMISTRY, 1984, 23 (11) :2577-2579
[5]   CLERODANE DITERPENOIDS FROM TEUCRIUM AND AJUGA PLANTS [J].
CAMPS, F ;
COLL, J ;
DARGALLO, O ;
RIUS, J ;
MIRAVITLLES, C .
PHYTOCHEMISTRY, 1987, 26 (05) :1475-1479
[6]   INSECT ALLELOCHEMICALS FROM AJUGA PLANTS [J].
CAMPS, F ;
COLL, J .
PHYTOCHEMISTRY, 1993, 32 (06) :1361-1370
[7]  
Chaari A., 1998, J SOC CHIM TUN, V4, P257
[8]   Ethyl (R)-3-hydroxy-4-phenylthiobutyrate: Synthesis by the bakers' yeast reduction and use as a precursor of enantiomerically pure beta-lactam [J].
Hayakawa, R ;
Shimizu, M ;
Fujisawa, T .
TETRAHEDRON LETTERS, 1996, 37 (42) :7533-7536
[9]   An efficient synthesis of (R)-3-hydroxytetradecanoic acid [J].
Huang, GF ;
Hollingsworth, RI .
TETRAHEDRON-ASYMMETRY, 1998, 9 (23) :4113-4115
[10]  
IMAI S, 1970, J AM CHEM SOC, V92, P7510