Four New Triterpenes from Fungus of Fomes officinalis

被引:25
作者
Wu, Xia [1 ,2 ,3 ]
Yang, Jun-Shan [1 ,2 ]
Yan, Ming [4 ]
机构
[1] Chinese Acad Med Sci, Inst Med Plant Dev, Beijing 100193, Peoples R China
[2] Peking Union Med Coll, Beijing 100193, Peoples R China
[3] Captial Med Univ, Sch Tradit Chinese Med, Beijing 100069, Peoples R China
[4] Xinjiang Inst Mat Med, Xinjiang 830002, Peoples R China
基金
中国国家自然科学基金;
关键词
Fomes officinalis; polyporaceace; lanostane-type triterpene; triterpene lactone; ACID;
D O I
10.1248/cpb.57.195
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
In the previous work we reported five lanostane-type triterpenes from the CHCl3 soluble fraction of Fomes officinalis. In further study on the isolation of constituents from the CHCl3 soluble fraction, four new triterpenes, fomefficinic acids F (1), 6 (2) and fomefficinols A (3), B (4), together with seven known compounds officinalic acid (5), fomlactone A (6), fomlactone B (7), fomlactone C (8), laricinolic acid (9), ergosterol (10), ergota-7,22,dien-3 beta-ol (11) were isolated. The structures of new compounds were determined by spectroscopic analyses and chemical methods including NMR spectroscopic techniques (C-13, H-1, heteronuclear multiple quantum coherence (HMQC), heteronuclear multiple bonding correlation (HMBC), correlation spectroscopy (COSY) and nuclear Overhauser effect spectroscopy (NOESY)).
引用
收藏
页码:195 / 197
页数:3
相关论文
共 12 条
[1]   METABOLIC INTERMEDIATES IN BIOLOGICAL OXIDATION OF LANOSTEROL TO EBURICOIC ACID [J].
ANDERSON, CG ;
EPSTEIN, WW .
PHYTOCHEMISTRY, 1971, 10 (11) :2713-&
[2]   MINOR TRITERPENOIDS OF FOMES-OFFICINALIS [J].
ANDERSON, CG ;
VANLEAR, G ;
EPSTEIN, WW .
PHYTOCHEMISTRY, 1972, 11 (09) :2847-&
[3]  
BERNHARD E, 2000, J CHEM SOC P1, P2307
[4]   STRUCTURE AND STEREOCHEMISTRY OF OFFICINALIC ACID, A NOVEL TRITERPENE FROM FOMES-OFFICINALIS [J].
EPSTEIN, WW ;
SWEAT, FW ;
VANLEAR, G ;
LOVELL, FM ;
GABE, EJ .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1979, 101 (10) :2748-2750
[5]   Fomlactones A-C, novel triterpene lactones from Fomes cajanderi [J].
He, J ;
Feng, XZ ;
Lu, Y ;
Zhao, B .
JOURNAL OF NATURAL PRODUCTS, 2003, 66 (09) :1249-1251
[6]  
He J., 2000, NAT PROD RES DEV, V12, P33, DOI [10.16333/j.1001, DOI 10.16333/J.1001]
[7]  
Jiangsu New Medical College, 1977, DICT CHIN MAT MED, P1188
[8]  
Overholts L.O., 1953, POLYPORACEAE US ALAS, P48
[9]  
SAKURAI N, 1990, HETEROCYCLES, V30, P897
[10]  
Shen Yun-xiu, 2002, Zhongguo Zhongyao Zazhi, V27, P674