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lmlfeixue: ½ð±Ò+10, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸, ¸Ðл»Ø¸´ 2013-01-03 19:29:32
1 .     rosamultin
C36H60O10     ÏàËÆ¶È:69.4%
Chinese Journal of Natural Medicines          2010          8          12-15
Triterpenoids from the Roots of Rose odorata var.gigantean
LIU Dai-Lin; ZHU Shan; MA Rong; ZHANG Jing-Ze; LI He-Yu; CHEN Hong
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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2 .     20(S),24(R)-epoxydammarane-12¦Á,3¦Â ,25-triol 3-o-(2',3',4',6' tetra-O-acetyl-¦Â-D-glucopyranoside)
C44H70O13     ÏàËÆ¶È:66.6%
Chemistry of Natural Compounds          1983          19          174-178
CATALYTIC REARRANGEMENT OF A 20(S),24(R)-EFOXYDAMMARANE-3¦Â,12¦Á,25-TRIOL (a-D-GLUCOSE 1,2-ORTHOACETATE). II.
N. S. Samoshina, V. L. Novikov, V. A. Denlsenko, and N. I. Uvarova
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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3 .     Ursolazuroside 1
C36H58O10     ÏàËÆ¶È:66.6%
Helvetica Chimica Acta          2010          93          457-465
Four New Triterpenes from Anchusa azurea var. azurea
Ayşe Kuru¨¹z¨¹m-Uz, Zuhal G¨¹venalp, Cavit Kazaz, Bekir Salih and L. Öm¨¹r Demirezer
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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4 .     kaji-ichigoside F1
C36H60O10     ÏàËÆ¶È:66.6%
Chinese Journal of Natural Medicines          2010          8          12-15
Triterpenoids from the Roots of Rose odorata var.gigantean
LIU Dai-Lin; ZHU Shan; MA Rong; ZHANG Jing-Ze; LI He-Yu; CHEN Hong
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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5 .     peracetylated 28-O-¦Â-D-glucopyranosylester of 20(S)-3¦Â,19¦Á,24-trihydroxyurs-12-ene-23,28-dioic acid
    ÏàËÆ¶È:63.8%
Natural Product Research          2002          16          401-406
Triterpenes and Saponins from Ilex psammophila
V. S. Pires; G. Gosmann; D. Guillaume; E. P. Schenkel
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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6 .     vitalboside-A
C36H58O8     ÏàËÆ¶È:63.8%
Fitoterapia          2001          72          140-145
A new oleanane glycoside from the stem bark of Albizia gummifera
G.M. Rukunga, P.G. Waterman
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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7 .     momorcharaside B
C36H60O9     ÏàËÆ¶È:63.8%
Acta Pharmaceutica Sinica          1990          Vol 25          898-903
STUDIES ON THE ACTIVE CONSTITUENTS OF MOMORDICA CHARANTIA L.
ZJ Zhu; ZC Zhong; ZY Luo and ZY Xiao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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8 .     24-deoxy-sericoside
C36H58O10     ÏàËÆ¶È:63.8%
Chinese Traditional and Herbal Drugs          2006          37          165-168
Triterpenoids from roots of Potentilla anserina
HONG Xia; CAI Guang-ming; XIAO Xiao-he
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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9 .     2¦Á,3¦Á,19¦Á,23-tetrahydroxy-urs-12-en-28-oic acid-3-O-¦Â-D-glucopyranosyl ester
C36H60O11     ÏàËÆ¶È:63.8%
Chinese Journal of Natural Medicines          2010          8          12-15
Triterpenoids from the Roots of Rose odorata var.gigantean
LIU Dai-Lin; ZHU Shan; MA Rong; ZHANG Jing-Ze; LI He-Yu; CHEN Hong
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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10 .     kajiichigoside F
    ÏàËÆ¶È:63.8%
Modern Chinese Medicine          2008          10(3)          10-12
Studies on the chemical constituents of Potentill anserine L.
Chu Liang, Wang Libo, Zhang Zhe, Gao Huiyuan, Huang Jian, Sun Bohang, Wu Lijun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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11 .     hederagenin-3-O-¦Â-glucuronopyranoside
    ÏàËÆ¶È:63.8%
Journal of Shenyang Pharmaceutical University          2005          22          181-182
Chemical constituents of the seeds of Acanthopanax senticosus(Rupr. et Maxim) Harms
ZHANG Jie, LI Wen, GAO Hui-Yuan, WU Bin, WU Li-jun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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12 .     Methyl ester of ocetylated 3-O-¦Â-D-glucuronopyranosy-oleanolic acid
    ÏàËÆ¶È:63.1%
Phytochemistry          1994          37          821-825
Triterpenoid saponins from Melanthera scandens
Andr¨¦ Penders, Cl¨¦ment Delaude
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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13 .     compound 7
C37H60O8     ÏàËÆ¶È:62.1%
Planta Medica          1998          64          189-191
Kalaic Acid, A New Ursane-Type Saponin from Musanga cecroploides
D. Lontsi, B. L. Sondengam, B. Bodo, and M. 1. Martin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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14 .     20-monoglucoside
    ÏàËÆ¶È:61.1%
Chemistry of Natural Compounds          1986          22          279-288
GLYCOSYLATION OF TRITERPENOIDS OF THE DAMMARANE SERIES.IV. ¦Â-D-GLUCOPYRANOSIDES OF BETULAFOLIENETRIOL AND ITS DERIVATIVES
L. N. Atopkina, V. A. Denisenko V. L. Novikov, and N. I. Uvarova
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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15 .     Oleanolic acid 3-O-¦Á-L-rhamnopyranoside
C36H58O7     ÏàËÆ¶È:61.1%
Molecules          2008          13          1472-1486
Facile Synthesis of Oleanolic Acid Monoglycosides and Diglycosides
Yu Sha, Mao-Cai Yan, Jiao Liu, Yang Liu and Mao-Sheng Cheng
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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16 .     ¦Â-D-galactopyranosyl oleanolate
C36H58O8     ÏàËÆ¶È:61.1%
Molecules          2008          13          1472-1486
Facile Synthesis of Oleanolic Acid Monoglycosides and Diglycosides
Yu Sha, Mao-Cai Yan, Jiao Liu, Yang Liu and Mao-Sheng Cheng
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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17 .     kaji-ichigoside F1
    ÏàËÆ¶È:61.1%
Acta Pharmaceutica Sinica          1996          31          844-848
NEW ELLAGIC GLYCOSIDES AND KNOWN TRITERPENOIDS FROM DUCHESNEA INDICA FOCKE
L Ye and JS Yang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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18 .     quillaic acid 3-O-{¦Â-D-galactopyranosyl-(1¡ú2)-¦Â-D-glucopyranosiduronic acid}
C42H64O16     ÏàËÆ¶È:61.1%
Phytochemistry          1998          48          175-180
Triterpenoid saponins from Quillaja saponaria
Shengjun Guo, Lennart Kenne, Lennart N. Lundgren, Bengt Rönnberg, Bo G. Sundquist
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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19 .     spinogenin C3 monoglucosyl ester
    ÏàËÆ¶È:61.1%
Phytochemistry          1997          46          1255-1259
3¦Á-hydroxy-oleanene type triterpene glycosyl esters from leaves of Acanthopanax spinosus
Masazumi Miyakoshi, Susumu Isoda, Hirotoshi Sato, Yasuaki Hirai, Junzo Shoji, Yoshiteru Ida
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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20 .     28-O-¦Â-D-glucopyranosyl-ester-oleanolic acid
    ÏàËÆ¶È:61.1%
Phytochemistry          1997          46          1267-1270
13C NMR analysis of monodesmosidic saponinis from Gomphrena macrocephala
Maria Cl¨¢udia Marx Young, Adriana Potomati, Edison Paulo Chu, Mitsue Haraguchi, Massao Yamamoto, Toshie Kawano
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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21 .     sericoside
    ÏàËÆ¶È:61.1%
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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22 .     28-O-¦Â-D-glucopyranosyl oleanolic acid peracetate
    ÏàËÆ¶È:61.1%
Phytochemistry          1994          37          1667-1670
Seco-glycosides of oleanolic acid fromBeta vulgaris
Georges Massiot, Marie-Genevieve Dijoux, Catherine Lavaud, Louisette Le Men-Olivier, Joseph D. Connolly, Douglas M. Sheeley
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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23 .     2¦Á,3¦Á,19¦Á-trihydroxy-ursa-12-en-28-oic acid-28-O-¦Â-D-glucopyranosyl ester
    ÏàËÆ¶È:61.1%
China Journal of Chinese Materia Medica          2010          35          3297-3301
Chemical constituents from Callicarpa nudiflora and their hemostatic acitivity
ZHANG Jie; LI Baoquan; FENG Feng; TANG Yuping; LIU Wenyuan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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24 .     Ursolazuroside 2
C36H56O11     ÏàËÆ¶È:61.1%
Helvetica Chimica Acta          2010          93          457-465
Four New Triterpenes from Anchusa azurea var. azurea
Ayşe Kuru¨¹z¨¹m-Uz, Zuhal G¨¹venalp, Cavit Kazaz, Bekir Salih and L. Öm¨¹r Demirezer
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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25 .     2-oxo-pomolic acid ¦Â-D-glucopyranosyl ester
    ÏàËÆ¶È:61.1%
Chinese Traditional and Herbal Drugs          2006          37          165-168
Triterpenoids from roots of Potentilla anserina
HONG Xia; CAI Guang-ming; XIAO Xiao-he
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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26 .     niga-ichigoside F1
C36H58O11     ÏàËÆ¶È:61.1%
Chinese Journal of Natural Medicines          2005          3          17-20
Isolation and Identification of Chemical Constituents from Rubus Parvifolius L.
DU Shu-Hu; FENG Fang; LIU Wen-Ying; RAO Jin-Hua; BAI Juan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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27 .     chikusetsusaponin I
    ÏàËÆ¶È:61.1%
Chinese Pharmaceutical Journal          2007          42          178-180
Studies on Triterpenoid Saponins from Achyranthese bidentata Bl
LI Juan, BI Zhi-ming, XIAO Ya-jie, LI Ping
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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28 .     kaji-ichigoside F1
    ÏàËÆ¶È:61.1%
Journal of China Pharmaceutical University          2002          33          184-187
Studies on the Constituents of Rosa multiflora Thunb
LI Yan Fang*; HU Li Hong; LOU Feng Chang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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29 .     rosamultin
    ÏàËÆ¶È:61.1%
Journal of China Pharmaceutical University          2002          33          184-187
Studies on the Constituents of Rosa multiflora Thunb
LI Yan Fang*; HU Li Hong; LOU Feng Chang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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30 .     Cycloccidentaliside II
C36H58O12     ÏàËÆ¶È:61.1%
Planta Medica          2012          78          821-827
Li, Shi-Fei; Di, Ying-Tong; Luo, Rong-Hua; Zheng, Yong-Tang; Wang, Yue-Hu; Fang, Xin; Zhang, Yu; Li, Ling; He, Hong-Ping; Li, Shun-Lin; Hao, Xiao-Jiang:
Cycloartane Triterpenoids from Cassia occidentalis
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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