Cytotoxic constituents from Podocarpus fasciculus

被引:38
作者
Kuo, Yu-Jen [1 ,2 ]
Hwang, Shy-Yuan [3 ]
Wu, Ming-Der [4 ]
Liao, Chia-Ching [1 ]
Liang, Yu-Han [1 ]
Kuo, Yao-Haur [1 ,5 ]
Ho, Hsiu-O [2 ]
机构
[1] Natl Res Inst Chinese Med, Taipei 112, Taiwan
[2] Taipei Med Univ, Sch Pharm, Taipei 110, Taiwan
[3] Endem Species Res Inst, Div Botany, Nantou 552, Taiwan
[4] Food Ind Res & Dev Inst, Hsinchu 300, Taiwan
[5] Chinese Med Univ, Grad Inst Integrated MEd, Taichung 404, Taiwan
关键词
podocarpus fasciculus; Podocarpaceae; 16-hydroxy communic acid; cytotoxic activity;
D O I
10.1248/cpb.56.585
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
A new diterpene, 16-hydroxy communic acid (1), along with thirty one known compounds including live norditerpenes (2-6), twenty two flavonoids containing four billavonoids (7-10), nine monoflavonoids (11-19) and nine flavanoid glycosides (20-28), as well as four phenolic constituents (29-32) were isolated from the 95% ethanolic extract of Podocarpus fascieulus. The structure of 1 was elucidated using spectral methods. Of these isolates, nagilactone C (2) showed the most significant inhibitory effects against DLD cells (human colon carcinoma) (ED50= 2.57 mu g/ml) and compounds 7, 8, 10, 11, and 12 had moderate cytotoxic activity against human KB (human oral epithelium carcinoma), Hela (human cervical carcinoma), Hepa (human hepatoma), DLD (colon carcinoma), and A-549 (human lung carcinoma) tumor cell lines. Preliminary structure-activity relationship studies of the isolated diterpenoids and biflavonoids are discussed.
引用
收藏
页码:585 / 588
页数:4
相关论文
共 36 条
[1]   ANTIFUNGAL STRESS COMPOUNDS FROM ADZUKI BEAN, VIGNA-ANGULARIS, TREATED WITH CEPHALOSPORIUM-GREGATUM TYPE-B [J].
ABE, N ;
SATO, H ;
SAKAMURA, S .
AGRICULTURAL AND BIOLOGICAL CHEMISTRY, 1987, 51 (02) :349-353
[2]  
AHMED AH, 2007, J NAT PRODUCTS, V70, P293
[3]   STRUCTURAL DETERMINATION OF C-GLYCOSYLFLAVONES BY MASS-SPECTROMETRY OF THEIR PERMETHYL ETHERS [J].
BOUILLANT, ML ;
FAVREBONVIN, J ;
CHOPIN, J .
PHYTOCHEMISTRY, 1975, 14 (10) :2267-2274
[4]  
BROWN KS, 1974, BIOCHEM SYST ECOL, V2, P11
[5]   CHEMISTRY OF THE PODOCARPACEAE .65. PHENOLIC DITERPENOIDS OF SOME PODOCARPS [J].
CAMBIE, RC ;
COX, RE ;
CROFT, KD ;
SIDWELL, D .
PHYTOCHEMISTRY, 1983, 22 (05) :1163-1166
[6]   Separation and identification of phenolic compounds in olive oil by coupling high-performance liquid chromatography with postcolumn solid-phase extraction to nuclear magnetic resonance spectroscopy (LC-SPE-NMR) [J].
Christophoridou, S ;
Dais, P ;
Tseng, LH ;
Spraul, M .
JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 2005, 53 (12) :4667-4679
[7]   Nitrification inhibitors from the roots of Leucaena leucocephala [J].
Erickson, AJ ;
Ramsewak, RS ;
Smucker, AJ ;
Nair, MG .
JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 2000, 48 (12) :6174-6177
[8]   DITERPENOID ACIDS FROM THE LEAVES OF ARMAND PINE [J].
FANG, JM ;
LANG, CI ;
CHEN, WL ;
CHENG, YS .
PHYTOCHEMISTRY, 1991, 30 (08) :2793-2795
[9]   Stable isotope labeling pattern of resveratrol and related natural stilbenes [J].
Fronza, G ;
Fuganti, C ;
Serra, S ;
Cisero, M ;
Koziet, J .
JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 2002, 50 (10) :2748-2754
[10]   STRUCTURES OF PODOLACTONE-A AND PODOLACTONE-B, INHIBITORS OF EXPANSION AND DIVISION OF PLANT CELLS [J].
GALBRAIT.MN ;
HORN, DHS ;
SASSE, JM ;
ADAMSON, D .
JOURNAL OF THE CHEMICAL SOCIETY D-CHEMICAL COMMUNICATIONS, 1970, (03) :170-&