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1 .     Arjunaside A
C36H56O10     ÏàËÆ¶È:80.5%
Planta Medica          2010          76          903-908
18,19-Secooleanane Type Triterpene Glycosyl Esters from the Bark of Terminalia arjuna
Wang, Wei; Ali, Zulfiqar; Li, Xing-Cong; Shen, Yunheng; Khan, Ikhlas A.
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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2 .     kakisaponin C
C36H58O10     ÏàËÆ¶È:77.7%
Chemical & Pharmaceutical Bulletin          2009          57          532-535
Three Minor Novel Triterpenoids from the Leaves of Diospyros kaki
Guang Chen, Zong-Quan Wang and Ji-Ming Jia
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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3 .     Arjunaside E
C38H62O11     ÏàËÆ¶È:72.9%
Planta Medica          2010          76          903-908
18,19-Secooleanane Type Triterpene Glycosyl Esters from the Bark of Terminalia arjuna
Wang, Wei; Ali, Zulfiqar; Li, Xing-Cong; Shen, Yunheng; Khan, Ikhlas A.
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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4 .     Arjunaside B
C36H56O11     ÏàËÆ¶È:72.2%
Planta Medica          2010          76          903-908
18,19-Secooleanane Type Triterpene Glycosyl Esters from the Bark of Terminalia arjuna
Wang, Wei; Ali, Zulfiqar; Li, Xing-Cong; Shen, Yunheng; Khan, Ikhlas A.
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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


5 .     Arjunaside C
C36H58O10     ÏàËÆ¶È:72.2%
Planta Medica          2010          76          903-908
18,19-Secooleanane Type Triterpene Glycosyl Esters from the Bark of Terminalia arjuna
Wang, Wei; Ali, Zulfiqar; Li, Xing-Cong; Shen, Yunheng; Khan, Ikhlas A.
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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6 .     24-epi-pinfaensin
     ÏàËÆ¶È:69.4%
Phytochemistry          1996          42          495-499
Triterpenes and triterpene glycosides from Paradrymonia macrophylla
Christian Terreaux, Marc P. Maillard, Mahabir P. Gupta, Kurt Hostettmann
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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


7 .     kakisaponin B
C36H58O10     ÏàËÆ¶È:69.4%
Chemical & Pharmaceutical Bulletin          2009          57          532-535
Three Minor Novel Triterpenoids from the Leaves of Diospyros kaki
Guang Chen, Zong-Quan Wang and Ji-Ming Jia
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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


8 .     swinhoeic acid
C30H46O5     ÏàËÆ¶È:67.6%
Chinese Traditional and Herbal Drugs          2008          39          978-981
ÈÕ±¾Â·±ßÇàµÄ»¯Ñ§³É·ÖÑо¿
ÕÔ¾§;¸ßÎÄÔ¶;¶ÎºêȪ;ëø½Ü;¸ßʯϲ¾Ã
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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9 .     kolokoside A
C36H58O10     ÏàËÆ¶È:66.6%
Journal of Natural Products          2007          70          378-382
Kolokosides A-D: Triterpenoid Glycosides from a Hawaiian Isolate of Xylaria sp.
Stephen T. Deyrup,James B. Gloer, Kerry O¡¯Donnell,and Donald T. Wicklow
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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10 .     glucosyl pinfaensate
C36H56O11     ÏàËÆ¶È:66.6%
Phytochemistry          1994          36          1469-1472
A triterpene from Rubus pinfaensis
David G. Durham, Xiaojun Liu, R. Michael E. Richards
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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11 .     Laevigin C
C36H56O11     ÏàËÆ¶È:66.6%
Bioorganic & Medicinal Chemistry          2013          23          3290-3297
Anti-inflammatory secondary metabolites from the leaves of Rosa laevigata
Min, Yan, Yan, Zhu, Hong-Jun, Zhang, Wei-Hua, Jiao, Bing-Nan, Han, Zhao-Xi, Liu, Feng, Qiu, Wan-Sheng, Chen, Hou-Wen, Lin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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12 .     geumonoid
C30H46O5     ÏàËÆ¶È:64.7%
Chemical & Pharmaceutical Bulletin          2000          48(9)          13647-1369
A New Anti-HIV Triterpene from Geum japonicum
Hong-Xi XU,Dong-Sheng MING,Hui Dong,and Paul Pui-Hay BUT
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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13 .     18,19-seco,2¦Á,3¦Á-dihydroxyl-19-oxo-urs-11,13(18)-dien-28-oic acid
C30H46O5     ÏàËÆ¶È:64.7%
Chinese Chemical Letters          2009          20          572-575
Two new triterpenes from Duchesnea indica
Wei Qiao, Zhi Yao, Wen Zhang, Hong Quan Duan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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14 .     2¦Á,3¦Á-dihydroxy-19-oxo-18,19-seco-urs-11,13(18)-dien-28-oic acid
C30H46O5     ÏàËÆ¶È:64.7%
Natural Product Research and Development          2005          17          404-408
Triterpene Acids from Toddalia asiatica
HUANG Ping*; KARAGIANIS Gloria; WEI Shan-xin; WATERMAN Peter G
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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15 .     2¦Á,3R,23-trihydroxy-19-oxo-18,19-seco-urs-11,13(18)-dien-28-oic acid
C30H46O6     ÏàËÆ¶È:64.7%
Journal of Natural Products          2011          74          732-738
Anti-inflammatory Triterpenes from the Leaves of Rosa laevigata
Na Zeng, Yang Shen, Ling-Zhi Li, Wei-Hua Jiao, Pin-Yi Gao, Shao-Jiang Song, Wan-Sheng Chen, and Hou-Wen Lin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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16 .     quadranoside VI
C36H56O11     ÏàËÆ¶È:63.8%
Chemical & Pharmaceutical Bulletin          2000          48(8)          1114-1120
Quadranosides VI-XI, Six New Triterpene Glucosides from the Seeds of Combretum quadrangulare
I Ketut ADNYANA,Yasuhiro TEZUKA, Suresh AWALE,Arjun Hari BANSKOTA, Kim Qui TRAN and Shigetoshi KADOTA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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17 .     Rosamultin
C36H58O10     ÏàËÆ¶È:63.8%
Acta Botanica Yunnanica          2008          30(1)          121-124
Triterpenoids from Saurauia napaulensis (Saurauiaceae)
WANGQiong,JU Peng,WANG Yi-Fen,LUO Shi-De
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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18 .     ilexoside XLIII
C36H58O11     ÏàËÆ¶È:63.8%
Chemical & Pharmaceutical Bulletin          1993          41          39-42
Triterpenoid Saponins of Aquifoliaceous Plants. XI.Ilexosides XLI-XLV from the Leaves of Ilex rotunda THUNB.
Kayoko AMIMOTO,Kazuko YOSHIKAWA and Shigenobu ARIHARA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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19 .     glucosyl tormentate
     ÏàËÆ¶È:63.8%
Acta Pharmaceutica Sinica          2008          Vol 43          504-508
Triterpene saponins from Adinandra nitida
WANG Ying; YE Wen-cai; YIN Zhi-qi; ZHAO Shou-xun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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20 .     glucosyl tormentate
     ÏàËÆ¶È:63.8%
Phytochemistry          1992          31          3642-3644
Oleanane and ursane glucosides from Rubus species
Zhou Xiao-Hong, Ryoji Kasai, Kazuhiro Ohtani, Osamu Tanaka, Nie Rui-Lin, Yang Chong-Ren, Zhou Jun, Kazuo Yamasaki
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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21 .     2¦Á,19¦Á-dihydroxy-3-oxo-12-ursen-28-oic acid ¦Â-D-glucopyranosyl ester
C36H56O10     ÏàËÆ¶È:63.8%
molecules          2011          16          4642-4651
Triterpenoids from the Roots of Sanguisorba tenuifolia var. Alba
Hai-Xue Kuang, Hong-Wei Li, Qiu-Hong Wang, Bing-You Yang, Zhi-Bin Wang and Yong-Gang Xia
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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22 .     28-(O-¦Â-D-Glucopyranosyl)-urs-12-ene-2¦Á,3¦Â,19¦Á-trihydroxy-28-oic acid
C36H58O10     ÏàËÆ¶È:63.8%
Natural Product Communications          2006          1          705-710
Smooth Muscle Relaxant Triterpenoid Glycosides fromRubus idaeus (Raspberry) Leaves
Janne Rojas Vera, Christopher G. Dacke, Gerald Blunden and Asmita V. Patel
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2Â¥2013-11-08 13:02:41
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