New bioactive flavonoids and stilbenes in cube resin insecticide

被引:83
作者
Fang, NB [1 ]
Casida, JE [1 ]
机构
[1] Univ Calif Berkeley, Environm Chem & Toxicol Lab, Dept Environm Sci Policy & Management, Berkeley, CA 94720 USA
来源
JOURNAL OF NATURAL PRODUCTS | 1999年 / 62卷 / 02期
关键词
D O I
10.1021/np980119+
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Fractionation of cube resin from Lonchocarpus utilus and L. urucu roots led to the isolation and identification of 11 minor flavonoids and stilbenes containing the gem-dimethylpyran moiety or a dihydrodiol derivative thereof The eight new compounds were as follows: the isoflavonoid cis-4",5"-dihydro-4",5"-dihydroxylonchocarpusone (2); four (2S)-6-(gamma,gamma-dimethylallyl)-6",6"-dimethylpyran[2",3": 7,8]flavanones with substituents of 5-hydroxy-3',4'-dimethoxy (3), 5,3'-dihydroxy-4'-methoxy (4), 5,4'dihydroxy-3 '-methoxy (5), and 3',4'-dimethoxy (6); and three 6", 6"-dimethylpyran[2'', 3":3',4']stilbenes with 4-hydroxy-5'-methoxy (9), 3,5'-dimethoxy-4-hydroxy (10) and 3,4,5-trimethoxy (11) substitution patterns. Structure-activity relationships for inhibition of NADH:ubiquinone oxidoreductase activity (bovine heart electron transport particles) and phorbol ester-induced ornithine decarboxylase activity (cultured MCF-7 cells) generally parallel those for cytotoxicity (MCF-7 and Hepa 1clc7 cells).
引用
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页码:205 / 210
页数:6
相关论文
共 18 条
[1]   BIOSYNTHESIS OF THE A/B/C/D-RING SYSTEM OF THE ROTENOID AMORPHIGENIN BY AMORPHA-FRUTICOSA SEEDLINGS [J].
BHANDARI, P ;
CROMBIE, L ;
DANIELS, P ;
HOLDEN, I ;
VANBRUGGEN, N ;
WHITING, DA .
JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1, 1992, (07) :839-849
[2]   BIOSYNTHESIS OF ROTENOIDS - CHALCONE, ISOFLAVONE, AND ROTENOID STAGES IN FORMATION OF AMORPHIGENIN BY AMORPHA-FRUTICOSA SEEDLINGS [J].
CROMBIE, L ;
DEWICK, PM ;
WHITING, DA .
JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1, 1973, (12) :1285-1294
[3]   Anticancer action of cube insecticide:: Correlation for rotenoid constituents between inhibition of NADH:ubiquinone oxidoreductase and induced ornithine decarboxylase activities [J].
Fang, NB ;
Casida, JE .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (07) :3380-3384
[4]   Anomalous structure-activity relationships of 13-homo-13-oxarotenoids and 13-homo-13-oxadehydrorotenoids [J].
Fang, NB ;
Rowlands, JC ;
Casida, JE .
CHEMICAL RESEARCH IN TOXICOLOGY, 1997, 10 (08) :853-858
[5]   ROTENOIDS MEDIATE POTENT CANCER CHEMOPREVENTIVE ACTIVITY THROUGH TRANSCRIPTIONAL REGULATION OF ORNITHINE DECARBOXYLASE [J].
GERHAUSER, C ;
MAR, W ;
LEE, SK ;
SUH, N ;
LUO, YD ;
KOSMEDER, J ;
LUYENGI, L ;
FONG, HHS ;
KINGHORN, AD ;
MORIARTY, RM ;
MEHTA, RG ;
CONSTANTINOU, A ;
MOON, RC ;
PEZZUTO, JM .
NATURE MEDICINE, 1995, 1 (03) :260-266
[6]   RESOLUTION AND ASSIGNMENT OF ABSOLUTE-CONFIGURATION TO THE (+)-CIS AND (-)-CIS AND TRANS 3,4-DIOL METABOLITES OF THE ANTI-JUVENILE HORMONE PRECOCENE-I [J].
HALPIN, RA ;
ELNAGGAR, SF ;
MCCOMBE, KM ;
VYAS, KP ;
BOYD, DR ;
JERINA, DM .
TETRAHEDRON LETTERS, 1982, 23 (16) :1655-1658
[7]   Cancer chemopreventive activity of resveratrol, a natural product derived from grapes [J].
Jang, MS ;
Cai, EN ;
Udeani, GO ;
Slowing, KV ;
Thomas, CF ;
Beecher, CWW ;
Fong, HHS ;
Farnsworth, NR ;
Kinghorn, AD ;
Mehta, RG ;
Moon, RC ;
Pezzuto, JM .
SCIENCE, 1997, 275 (5297) :218-220
[8]   LONCHOCARPENE, A STILBENE, AND LONCHOCARPUSONE, AN ISOFLAVONE - 2 NEW PYRANOPOLYPHENOLS FROM LONCHOCARPUS-NICOU ROOTS [J].
KAOUADJI, M ;
AGBAN, A ;
MARIOTTE, AM .
JOURNAL OF NATURAL PRODUCTS, 1986, 49 (02) :281-285
[9]  
LAMARTINIERE CA, 1995, P SOC EXP BIOL MED, V208, P120
[10]   FLAVONOIDS FROM ARTOCARPUS-HETEROPHYLLUS [J].
LIN, CN ;
LU, CM ;
HUANG, PL .
PHYTOCHEMISTRY, 1995, 39 (06) :1447-1451