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1 .     yunganogenin E
C30H44O5     ÏàËÆ¶È:73.3%
Phytochemistry          1992          31          1747-1752
Oleanane glycosides from Glycyrrhiza yunnanensis roots
Kazuhiro Ohtani, Katsuki Ogawa, Ryoji Kasai, Chong-Ren Yang, Kazuo Yamasaki, Jun Zhou, Osamu Tanaka
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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2 .     cycloartan-23E-ene-1¦Á,2¦Á,3¦Â,25-tetrol
C30H50O4     ÏàËÆ¶È:70%
Journal of Natural Products          2008          71(1)          81-86
Cycloartane-Type Triterpenoids from the Resinous Exudates of Commiphora opobalsamum
Tao Shen, Hui-Qing Yuan, Wen-Zhu Wan, Xiao-Ling Wang, Xiao-Ning Wang, Mei Ji, and Hong-Xiang Lou
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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3 .     macedonic acid
     ÏàËÆ¶È:70%
Acta Pharmaceutica Sinica          1993          28          116-121
STUDIES ON THE TRITERPENOIDS FROM ROOTS OF GLYCYRRHIZA SQUAMULOSA FROANCH
H Liang and RY Zhang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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4 .     1¦Â,22¦Â-dihydroxyolean-11,13(18)-diene
C30H48O2     ÏàËÆ¶È:70%
Phytochemistry          1998          48          693-697
Saikosaponins from Taverniera aegyptiaca
H. A. Hassanean
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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5 .     ursolic acid
     ÏàËÆ¶È:70%
Chinese Traditional and Herbal Drugs          1999          30(3)          161-164
Studies on the Chemical Constituents of Shady Jerusalemsage (Phlomis umbrosa)(¢ñ)
Liu Shiwang; Fu Hongzheng and Lin Wenhan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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6 .     pomolic acid
C30H48O4     ÏàËÆ¶È:70%
Natural Product Research and Development          2001          13(2)          11-13
THE STUDIES OF CHEMICAL COMPONENTS OF CLAUSENA DUNNIANA
CUI Shu ya;CHENG Dong liang; TIAN Jun; WU Feng e
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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7 .     compound 10a
     ÏàËÆ¶È:70%
Natural Medicines          1999          53          166-172
Studies on Index Compounds for HPLC Analysis of Glycyrrhiza macedonica
SHIBANO MAKIO,NUKUI HISASHI, et al.
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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8 .     19¦Á-hydroxylursolic acid
     ÏàËÆ¶È:70%
Journal of Chinese Medicinal Materials          2011          34          1540-1544
Study on the Triterpenoids from the Fruits of Ligustrum lucidum
FENG Jing, FENG Zhi-yi, WANG Jun-ming, CUI Ying
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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9 .     20¦Â,28-epoxy-28¦Á-methoxytaraxasteran-3¦Â-ol
C31H52O3     ÏàËÆ¶È:67.7%
Journal of Natural Products          2006          69          1164-1167
Taraxasterane- and Ursane-Type Triterpenes from Nerium oleander and Their Biological Activities
Ming Zhao, Shujun Zhang, Liwei Fu, Na Li, Jiao Bai, Junichi Sakai, Liyan Wang, Wanxia Tang, Toshiaki Hasegawa, Hirotsugu Ogura, Takao Kataoka, Seiko Oka, Miwa Kiuch, Katutoshi Hirose, and Masayoshi Ando
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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10 .     21-dehydro-macedonic acid methyl ester
C31H46O4     ÏàËÆ¶È:67.7%
Acta Pharmaceutica Sinica          1990          Vol 25          795-797
ISOLATION AND IDENTIFICATION OF YIBEINOSIDE A
DM Xu; S Arihara; N Shoji; XW Yang; EX Huang and CS Li
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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11 .     1¦Â,2¦Â,3¦Â,19¦Á-tetrahydroxy-urs-12-ene-28-oate
C31H50O6     ÏàËÆ¶È:67.7%
Pharmaceutical Biology          1999          37          314-317
Two New Triterpenoids from Centipeda minima
Rai N., Siddiqui I.R., Singh J.
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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12 .     3¦Â-hydroperoxy-7¦Â,25-epoxy-D:B-friedoolean-5-ene
C30H48O3     ÏàËÆ¶È:66.6%
Journal of Natural Products          2009          72          1045-1048
Triterpenoids and a Lignan from the Aerial Parts of Maytenus apurimacensis
Nabil E. J. Vazdekis, Haydee Ch¨¢vez, Ana Est¨¦vez-Braun, and Ángel G. Ravelo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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13 .     gamboukokoensein A
C30H48O7     ÏàËÆ¶È:66.6%
Phytochemistry          2003                   845-849
Pentacyclic triterpenoid and saponins from Gambeya boukokoensis
Jean Wandji, François Tillequin, Dulcie A. Mulholland, Jovita Chi Shirri,Nole Tsabang, ElisabethSeguin, Philippe Verite, Francine Libotb, Z.T. Fomum
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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14 .     6¦Â-hydroxybetulin
C30H50O3     ÏàËÆ¶È:66.6%
Journal of Natural Products          2005          68          1018-1021
Lupane Triterpenoids from Maytenus Species
Marvin J. Nez, Carolina P. Reyes, Ignacio A. Jimnez, Laila Moujir, and Isabel L. Bazzocchi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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15 .     argenteanol D
C30H50O3     ÏàËÆ¶È:66.6%
Journal of Natural Products          1997          60          81-85
Argenteanones C-E and Argenteanols B-E, Cytotoxic Cycloartanes from Aglaia argentea
K. Mohamad, M.-T. Martin, E. Leroy, C. Temp¨ºte, T. S¨¦venet, K. Awang, and M. Païs
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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16 .     pomolic acid
C36H46O4     ÏàËÆ¶È:66.6%
Chemical & Pharmaceutical Bulletin          1992          40          1990-1992
Triterpenoid Saponins of Aquifoliaceous Plants. V. Ilexosides XV-XIX from the Barks of Ilex crenata THUNB.
Chieko HATA,Miho KAKUNO,Kazuko YOSHIKAWA and Shigenobu ARIHARA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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17 .     pomolic acid
C30H48O4     ÏàËÆ¶È:66.6%
Chemical & Pharmaceutical Bulletin          1992          40          3138-3141
Triterpenoid Saponins of Aquifoliaceous Plants. VIII. Ilexosides XXIX-XXXII from the Leaves of Ilex rotunda THUNB.
Kayoko AMIMOTO,Kazuko YOSHIKAWA and Shigenobu ARIHARA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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18 .     compound 2a
C30H46O6     ÏàËÆ¶È:66.6%
Chemical & Pharmaceutical Bulletin          1992          40          3138-3141
Triterpenoid Saponins of Aquifoliaceous Plants. VIII. Ilexosides XXIX-XXXII from the Leaves of Ilex rotunda THUNB.
Kayoko AMIMOTO,Kazuko YOSHIKAWA and Shigenobu ARIHARA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------


19 .     compound 11
C30H50O5     ÏàËÆ¶È:66.6%
Chemical & Pharmaceutical Bulletin          1985          33          37-40
19¦Á-Hydroxyursane-Type Triterpene Glucosyl Esters from the Roots of Rubus suavissimus S. LEE
FENG GAO,FENGHUAI CHEN,TAKASHI TANAKA,RYOJI KASAI,TAKASHI SETO and OSAMU TANAKA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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20 .     cyclomacrogenin B
     ÏàËÆ¶È:66.6%
Chemistry of Natural Compounds          2009          45          55-60
TRITERPENE GLYCOSIDES FROM Astragalus AND THEIR GENINS.LXXX. CYCLOMACROSIDE D, A NEW BISDESMOSIDE
D. A. Iskenderov, I. M. Isaev, and M. I. Isaev
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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21 .     cyclomacrogenin B
     ÏàËÆ¶È:66.6%
Chemistry of Natural Compounds          2009          45          132-134
TRITERPENE GLYCOSIDES FROM Astragalus AND THEIR GENINS.LXXIX. STRUCTURE OF CYCLOMACROSIDE C
D. A. Iskenderov, I. M. Isaev, and M. I. Isaev
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2Â¥2013-11-22 17:02:31
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