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jiyannangxj: ½ð±Ò+2, ¹ÄÀøÓ¦Öú 2014-01-13 23:10:20
±Ë°¶»¨¿ªlj: ½ð±Ò+8, ¡ïÓаïÖú, лл£¡ 2014-01-14 01:17:15
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1 .     22¦Á-hydroxyolean-12-en-3¦Â-yl-¦Â-D-galactopyra-noside
C36H60O7     ÏàËÆ¶È:69.4%
Chemical & Pharmaceutical Bulletin          2010          58          1093-1095
Two New Aristolochic Acid Derivatives from the Roots of Aristolochia fangchi and Their Cytotoxicities
Yu Cai and Tian-Ge Cai
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     Oleanolic acid 3-O-¦Â-D-galactopyranoside
C36H58O8     ÏàËÆ¶È:63.8%
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
3 .     sigmoiside A
C36H60O7     ÏàËÆ¶È:63.8%
Journal of Natural Products          1991          Vol 54          1288
Two New Triterpenoid Saponins from Erythrina sigmoidea
J. Kouam, A. Ephrem Nkengfack, Z. Tanee Fomum, Rosa Ubillas, Michael S. Tempesta, Mich¨¨le Meyer
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     oleanolic acid-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
5 .     gamboukokoenside B
C35H54O10     ÏàËÆ¶È:62.8%
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
6 .     echinocystic acid
    ÏàËÆ¶È:61.7%
China Journal of Chinese Materia Medica          2004          29          1108-1109
Èý·Öµ¤»¯Ñ§³É·ÖµÄÑо¿
»ÆÑ§Ê¯, Û¬ áÔ, ·¶Àö»ª, â×ʯɽ , ÁºÏþÌì
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     termiarjunoside II
C36H56O12     ÏàËÆ¶È:61.7%
Zeitschrift f¨¹r Naturforschung B          2006          61b          1282-1286
Two New Oleanane Triterpene Glycosides from the Bark of Terminalia arjuna
Asif Ali, Mohammed Ali, and Mohd S. Alam
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     ¦Â-amyrin
    ÏàËÆ¶È:61.7%
Journal of Shenyang Pharmaceutical University          2008          25          639-641
Chemical constituents of the fruits of Caesalpinia minax Hance
WU Zhao-hua, WANGLi-bo, GAO Hui-yuan, SUN Bo-hang, HUANGJian, WU Li-jun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     erythrodiol
    ÏàËÆ¶È:61.7%
Natural Product Communications          2007          2          835-840
Coumestoside A, Coumestoside B and Erythrodiside A,Three Glycosides from Cylicodiscus gabunensis(Mimmosaceae)
Jacques Kouam, Pierre Tane, Meli Lanang Alain, Xavier Siwe Noundou,Muhammad Iqbal Choudhary and Zacharias Tanee Fomum
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     calenduloside E
    ÏàËÆ¶È:61.7%
Chemistry of Natural Compounds          2012          48          258-261
A new triterpenoid saponin and other saponins from Salicornia europaea
Min Yin, Xiangyun Wang, Ming Wang, Yu Chen and Yunfa Dong, et al.
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     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
12 .     prosapogenin
C36H58O8     ÏàËÆ¶È:61.1%
Journal of Asian Natural Products Research          2001          3          213-217
Eclalbatin, a Triterpene Saponin from Eclipta Alba
R. K. UPADHYAY, M. B. PANDEY, R. N. JHA and V. B. PANDEY
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
13 .     chikusetsusaponin-IV a
C42H66O14     ÏàËÆ¶È:61.1%
China Journal of Chinese Materia Medica          2007          32          1138-1141
Studies on Chemical Constituents of Alternan theraphilox eroid es (Martl) Griseb
LUO Xiaoru, LI Bin, NIAN Jinxing, DONG Junxing
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
14 .     chikusetsusaponin-IVa
C42H66O14     ÏàËÆ¶È:61.1%
Chinese Pharmaceutical Journal          2007          42          1138-1141
Studies on Chemical Constituents of Alternan theraphilox eroid es
LUO Xiao-ru, LI Bin, NIAN Jin-xing, DONG Jun-xing
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
15 .     hederagenin-3-O-¦Â-glucuronopyranoside
    ÏàËÆ¶È:61.1%
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
16 .     glinoside A
C35H58O9     ÏàËÆ¶È:60%
Planta Medica          2000          66          368-371
Structure and Antiprotozoal Activity of Triterpenoid Saponins from Glinus oppositifolius
Fanta Traore,Robert Faure,Evelyne Ollivier,Monique Gasquet,Nadine Azas,Laurent Debrauwer,Arouna Keita,Pierre Timon-David,Guy Balansard
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
17 .     oleanolic acid-3-O-¦Á-D-xylopyranoside
    ÏàËÆ¶È:60%
Journal of China Pharmaceutical University          2002          33          101-103
Studies on the Constituents of Patrinia scabiosaefolia Fisch
LI Yan Fang; LI Ming Hui; LOU Feng Chang; TANG Yu Ping
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
18 .     16¦Á-hydroxy-olean-12-en-28oicacid-3-O-¦Á-L-arabinopyranoside
C35H56O8     ÏàËÆ¶È:60%
Journal of Anhui Agricultural Sciences          2012          40          745-747
Study on the Chemical Constitutes of C. robustum root
MA Yang-min et al
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
19 .     quillaic acid
    ÏàËÆ¶È:58.8%
China Journal of Chinese Materia Medica          2006          31          1640-1641
˿ʯÖñÈýÝÆ³É·ÖµÄÑо¿
ÂÞ½¨¹â, ÕÅ ½à, ¿×ÁîÒå
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
20 .     oleanic acid
C30H48O3     ÏàËÆ¶È:58.8%
China Journal of Chinese Materia Medica          2005          30          1926-1932
Studies on triterpenoid constituents from Rabdosia japonica var. galaucocalyx
Wang Fudong, DING Lan, WANG Hanqing
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
21 .     maniladiol
    ÏàËÆ¶È:58.8%
Journal of Natural Products          1991          Vol 54          1288
Two New Triterpenoid Saponins from Erythrina sigmoidea
J. Kouam, A. Ephrem Nkengfack, Z. Tanee Fomum, Rosa Ubillas, Michael S. Tempesta, Mich¨¨le Meyer
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
22 .     Olean-12-oxo-4-hydroxy-3,28-dioic acid
C30H48O6     ÏàËÆ¶È:58.8%
Journal of Natural Products          2010          73          1743-1750
Synthesis and Biological Evaluation of Oleanolic Acid Derivatives As Inhibitors of Protein Tyrosine Phosphatase 1B
Shan Qian, Haijiao Li, Yin Chen, Weiyu Zhang, Shengyong Yang, and Yong Wu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
23 .     methyl 3¦Â,21¦Á-dihydroxyolean-12-en-28-oate
    ÏàËÆ¶È:58.8%
Korean Journal of Pharmacognosy          1987          18(3)          151-167
13C NMR Spectroscopy of Amyrins
Kang, Sam-Sik
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
24 .     quillaic acid
    ÏàËÆ¶È:58.8%
Chemical & Pharmaceutical Bulletin          2010          58          412-414
Triterpenoid Saponins from Gypsophila altissima L.
Qing Chen, Jian-Guang Luo and Ling-Yi Kong
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
25 .     Æë¶Õ¹ûËá
    ÏàËÆ¶È:58.8%
Chinese Traditional and Herbal Drugs          2009          40          1723-1725
Ì«°×¶Å¾éµÄ»¯Ñ§³É·ÖÑо¿
ÁõÐÛ;¸ß½¨µÂ;ÕÔÀÚ
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
26 .     oleanlic acid
C30H48O3     ÏàËÆ¶È:58.8%
Chinese Journal of Natural Medicines          2005          3          181-183
Chemical Constituents of Nauclea officinalis
XUAN Wei-Dong; CHEN Hai-Sheng); YUAN Zhi-Xian; ZHU Ping
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
27 .     erigeronol
C32H52O5     ÏàËÆ¶È:58.8%
Chinese Chemical Letters          2010          21          834-837
A new derivative of triterpene with anti-melanoma B16 activity from Conyza canadensis
Ming Ming Yan; Ting You Li; Da Qing Zhao; Shuai Shao; Sheng Nan Bi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
28 .     oleanolic acid
    ÏàËÆ¶È:58.8%
Modern Chinese Medicine          2007          9(12)          11-13
Studies on the chemical Constituents of Ampelopsis grossedentata
He Guixia, Pei Gang, Du Fanglu, OU Yangwen, Li Bin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
29 .     oleanolic acid
    ÏàËÆ¶È:58.8%
Chinese Journal of Medicinal Chemistry          2010          20          125-128
Isolation and identification of the Chemical constituents from Swertia yunnanensis Burk.
YU Ying, WANG Shi-sheng*, DING Feng-uan, ZHU Jing-bo, ZHAO Wei-jie
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
30 .     oleanolic acid
    ÏàËÆ¶È:58.8%
Journal of Chinese Medicinal Materials          2012          35          404-406
Study on the Chemical Constituent from the Dichloromethane Extract.
of the Pine Needles of Cedrus deodara
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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1 .     22¦Á-hydroxyolean-12-en-3¦Â-yl-¦Â-D-galactopyra-noside
C36H60O7     ÏàËÆ¶È:69.4%
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