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yteamoy: ½ð±Ò+20, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸, ºÜºÃ£¬ºÜ¸øÁ¦£¡Ð»Ð»£¡ 2012-10-19 17:15:42
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1 . Soyasapogenol E
  ÏàËÆ¶È:76.6%
Phytochemistry     1998     49     709-717
Bioactive polar triterpenoids from Melilotus messanensis
Francisco A. Mac¨ªas, Ana M. Simonet, Juan Carlos G. Galindo, Pedro C. Pacheco, Jose A. S¨¢nchez
Structure   13C NMR̼Æ×Ä£Äâͼ
2 . olean-18-en-3-one
  ÏàËÆ¶È:73.3%
Chemical & Pharmaceutical Bulletin     2002     50(9)     1273-1275
Fern Constituents: Triterpenoids from Adiantum capillus-veneris
Takahisa NAKANE,Yoshiko MAEDA, Hideharu EBIHARA,Yoko ARAI,Kazuo MASUDA,Akihito TAKANO, Hiroyuki AGETA,Kenji SHIOJIMA,Shao-Qing CAI,and Osama Bashir ABDEL-HALIM
Structure   13C NMR̼Æ×Ä£Äâͼ
3 . Abrisapogenol F
  ÏàËÆ¶È:73.3%
Chemistry of Natural Compounds     1992     28     1-23
13C NMR SPECTROSCOPY OF OLEANANE DERIVATIVES
A. I. Kalinovskii
Structure   13C NMR̼Æ×Ä£Äâͼ
4 . soyasapogenol E
  ÏàËÆ¶È:73.3%
Journal of Natural Products     1988     Vol 51     335
Melilotigenin, a New Sapogenin from Melilotus officinalis
Sam Sik Kang, Won Sick Woo
Structure   13C NMR̼Æ×Ä£Äâͼ
5 . soyasapogenol E
  ÏàËÆ¶È:73.3%
Journal of Natural Products     1991     Vol 54     830
Constituents of Leguminous Plants, XIII. New Triterpenoid Saponins from Wistaria brachybotrys
Takao Konoshima, Mutsuo Kozuka, Mitsumasa Haruna, Kazuo Ito
Structure   13C NMR̼Æ×Ä£Äâͼ
6 . Soyasapogenol E
  ÏàËÆ¶È:73.3%
Korean Journal of Pharmacognosy     2008     39(3)     186-193
Phytochemical Studies on Astragalus Root (3);Triterpenoids and Sterols
Jung, Hye-Sil; Lee, Eun-Ju; Lee, Je-Hyun; Kim, Ju-Sun; Kang, Sam-Sik
Structure   13C NMR̼Æ×Ä£Äâͼ
7 . camelliagenone
C30H48O4   ÏàËÆ¶È:73.3%
Chemical & Pharmaceutical Bulletin     2011     59(6)     778-782
New Triterpenes from Barringtonia asiatica
Consolacion Yasa㸠RAGASA, Dinah Lorenzana ESPINELI, and Chien-Chang SHEN
Structure   13C NMR̼Æ×Ä£Äâͼ
8 . ¦Â-amyrenone
C30H48O   ÏàËÆ¶È:73.3%
Chinese Journal of Natural Medicines     2010     8     270-273
Chemical Constituents from the Roots of Dysoxylum densiflorum
LI Chang-Song; YU Hong-Wei; LI Guo-You; ZHANG Guo-Lin
Structure   13C NMR̼Æ×Ä£Äâͼ
9 . ¦Â-amyrone
  ÏàËÆ¶È:73.3%
Chinese Journal of Natural Medicines     2010     8     244-246
A New Benzoic Acid Derivative from Eclipta prostrata
SUN Zhi-Hua; ZHANG Chao-Feng; ZHANG Mian
Structure   13C NMR̼Æ×Ä£Äâͼ
10 . 21¦Â,28-dihydroxy-3-oxo-olean-12,20(30)-diene
C29H44O3   ÏàËÆ¶È:72.4%
Tetrahedron     2001     57     8413-8424
Immunosuppressive terpenoids from extracts of Tripterygium wilfordii
Hongquan Duan, Yoshihisa Takaishi, Hiroshi Momota, Yasukazu Ohmoto, Takao Taki, Motoo Tori, Shigeru Takaoka, Yongfeng Jia, Duan Li
Structure   13C NMR̼Æ×Ä£Äâͼ
11 . 29-hydroxy-12-oleanene-3,22-dione
C30H46O3   ÏàËÆ¶È:70%
Journal of Natural Products     2008     71(11)     1829-1832
Triterpenoids and Aromatics from Derris laxiflora
Hsi-Lin Chiu, Jyh-Horng Wu, Yu-Tang Tung, Tzong-Huei Lee, Shin-Chang Chien, and Yueh-Hsiung Kuo
Structure   13C NMR̼Æ×Ä£Äâͼ
12 . sumaresinolic acid
  ÏàËÆ¶È:70%
Journal of Natural Products     2006     69(5)     807-810
Triterpenoids from the Resin of Styrax tonkinensis and Their Antiproliferative and Differentiation Effects in Human Leukemia HL-60 Cells
Feng Wang, Huiming Hua, Yuehu Pei, Duo Chen, and Yongkui Jing
Structure   13C NMR̼Æ×Ä£Äâͼ
13 . abrisapogenol F
C30H48O2   ÏàËÆ¶È:70%
Chemical & Pharmaceutical Bulletin     1989     37     846-848
NEW TRITERPENOID SAPOGENOLS FROM ABRUS CANTONIENSIS (I)
Takashi TAKESHITA,Shuichi HAMADA and Toshihiro NOHARA
Structure   13C NMR̼Æ×Ä£Äâͼ
14 . ¦Â-amyrone
  ÏàËÆ¶È:70%
Acta Botanica Sinica     2001     43     426-430
The Chemical Constituents of Amoora yunnanensis
LUO Xiao-Dong, WU Shao-Hua, MA Yun-Bao, WU Da-Gang
Structure   13C NMR̼Æ×Ä£Äâͼ
15 . ST-F 1
  ÏàËÆ¶È:67.7%
Chemistry of Natural Compounds     1997     33     316-319
TRITERPENE GLYCOSIDES OF Hedera taurica XVI. STRUCTURES OF GLYCOSIDES St-A, St-B 1, St-B 2, St-C,St-D1, St-D2, St-E, St-F 1, AND St-F 2 FROM THE STEMS OF CRIMEAN IVY
V. I. GriShkovets, S. V. Godin, O. Ya. Tsvetkov,A. S. Shamhkov, and V. Ya. Chirva
Structure   13C NMR̼Æ×Ä£Äâͼ
16 . methyl 3-epi-sumaresinolate
C31H50O4   ÏàËÆ¶È:67.7%
Journal of Natural Products     1992     Vol 55     963
Triterpenes from Miconia stenostachya
Wilfred R. Chan, Veronica Sheppard, Kathleen A. Medford, Winston F. Tinto, William F. Reynolds, Stewart McLean
Structure   13C NMR̼Æ×Ä£Äâͼ
17 . 3-Oxo-12-en-28-(2'-nitro-vinyl)-olean
C31H47NO3   ÏàËÆ¶È:67.7%
Journal of Asian Natural Products Research     2012     14     355-363
Synthesis and biological evaluation of oleanolic acid derivatives as antitumor agents
Lei Chen,Jian-Bo Wu,Fan Lei,Shan Qian,Li Hai and Yong Wu
Structure   13C NMR̼Æ×Ä£Äâͼ
18 . 2,3-seco-3-oxoolean-12-en-2-oic acid
C30H48O3   ÏàËÆ¶È:66.6%
Chemical & Pharmaceutical Bulletin     2003     51(1)     89-91
New Triterpenoids from Gentiana lutea
Yoshitaka TORIUMI, Rie KAKUDA, Masafumi KIKUCHI, Yasunori YAOITA, and Masao KIKUCHI
Structure   13C NMR̼Æ×Ä£Äâͼ
19 . 3¦Á,21¦Â-dihydroxy-olean-12-ene
  ÏàËÆ¶È:66.6%
Phytochemistry     2008     69     1057-1064
21¦Â-Hydroxy-oleanane-type triterpenes from Hippocratea excelsa
David C¨¢ceres-Castillo, Gonzalo J. Mena-R
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