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CÆ×Êý¾Ý12.92,13.50,15.05,15.83,16.32,18.43,18.48,19.30,21.12,21.21,27.77,28.54,28.80,29.09,33.17,33.19,33.58,33.61,35.83,35.92,39.63,39.84,42.25,42.28,50.49,55.77,55.95,57.29,58.90,58.96,59.09,78.15,78.71,80.03,82.05,85.49,85.77,122.39,124.46,138.70,138.75
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Ò©Îﻯѧli: ½ð±Ò+10, ¡ï¡ï¡ïºÜÓаïÖú 2015-05-15 20:07:11
1 .     scoparianoside C
C41H64O13     ÏàËÆ¶È:60.9%
Chemical & Pharmaceutical Bulletin          1997          45          1300-1305
Medicinal Foodstuffs. VII. On the Saponin Constituents with Glucose and Alcohol Absorption-Inhibitory Activity from a Food Garnish "Tonburi", the Fruit of Japanese Kochia scoparia (L.) SCHRAD. : Structures of Scoparianosides A, B, and C
Masayuki YOSHIKAWA,Hiromi SHIMADA,Toshio MORIKAWA,Satoshi YOSHIZUMI,Narumi MATSUMURA,Toshiyuki MURAKAMI,Hisashi MATSUDA,Kazuyuki HORI and Johji YAMAHARA
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
2 .     3¦Â-Urs-12-en-3-yl palmitate
    ÏàËÆ¶È:60.9%
Pharmaceutical Chemistry Journal          2014          48          531−535
CYTOTOXIC TRITERPENE FROM Barringtonia asiatica
Consolacion Y. Ragasa, Dinah L. Espineli, and Chien-Chang Shen
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
3 .     3¦Â-acetoxy-11¦Á[2',3'-epoxyferulyloxy]-olean-13(18)-ene
C42H60O7     ÏàËÆ¶È:59.5%
Natural Product Research          2001          15          339-344
A New Oleanane Triterpenoid from Gordonia ceylanica
H. M. T. B. Herath; P. S. Athukoralage; Joanne F. Jamie
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
4 .     compound A
    ÏàËÆ¶È:58.6%
Yakugaku Zasshi          1983          103          43-48
The Principles of Tetragonia tetragonoides Having an Antiulcerogenic Activity. I. Isolation and Identification of Sterylglucoside Mixture (Compound A)
EMI OKUYAMA, MIKIO YAMAZAKI
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
5 .     ¦Á-amyrin caprylate
    ÏàËÆ¶È:58.5%
Acta Pharmaceutica Sinica          1992          27          589-594
STUDIES ON THE CHEMICAL CONSTITUENTS OF CYNANCHUM THESIOIDES
HQ Yuan; CX Zuo
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
6 .     8¦Â,17-epoxy-11,15-epoxy-15-hydroxy-12-labden-16-al
C20H30O4     ÏàËÆ¶È:58.5%
Tetrahedron          2002          58          2725-2728
A norbislabdane and other labdanes from Aframomum sulcatum
Apollinaire Tsopmo, Godfred A Ayimele, Pierre Tane, Johnson Foyere Ayafor, Joseph D Connolly, Olov Sterner
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
7 .     22-angeloyl-21-epoxyangeloylbarringto-genol C
C40H62O8     ÏàËÆ¶È:56.0%
Planta Medica          2005          71          1068-1070
Two New Triterpenes from the Husks of Xanthoceras sorbifolia
Zhan-Lin Li , Xian Li , Lin-Hao Li , Ning Li , Ming Yu , Da-Li Meng
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
8 .     scoparianoside B
C41H64O13     ÏàËÆ¶È:56.0%
Chemical & Pharmaceutical Bulletin          1997          45          1300-1305
Medicinal Foodstuffs. VII. On the Saponin Constituents with Glucose and Alcohol Absorption-Inhibitory Activity from a Food Garnish "Tonburi", the Fruit of Japanese Kochia scoparia (L.) SCHRAD. : Structures of Scoparianosides A, B, and C
Masayuki YOSHIKAWA,Hiromi SHIMADA,Toshio MORIKAWA,Satoshi YOSHIZUMI,Narumi MATSUMURA,Toshiyuki MURAKAMI,Hisashi MATSUDA,Kazuyuki HORI and Johji YAMAHARA
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
9 .     24¦Î-hydroperoxy-24-vinyl-lathosterol
C29H48O3     ÏàËÆ¶È:56.0%
Planta Medica          2011          77          922-928
Cytotoxic Triterpenoids and Steroids from the Bark of Melia azedarach
Shi-BiaoWu, Qiu-Ying Bao,Wen-XuanWang, Yun Zhao, Gang Xia,Zheng Zhao, Huaqiang Zeng, Jin-Feng Hu
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
10 .     acacigenin-B
C40H60O7     ÏàËÆ¶È:56.0%
Phytochemistry          1979          18          463-466
Structure of acacigenin-B, a novel triterpene ester isolated from Acacia concinna
A. S. R. Anjaneyulu, M. Bapuji, L. Ramachandra Row, A. Sree
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
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