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16.21,16.25,16.89,18.12,19.41,21.21,21.50,24.43,25.58,28.45,29.03,32.06,33.97,37.01,37.73,39.64,39.69,41.83,42.80,45.16,46.34,47.39,47.74,48.42,55.94,66.44,67.87,69.14,73.82,78.43,125.22,128.55,138.64,144.70,167.96
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txdydsw: ½ð±Ò+12, ¡ïÓаïÖú 2014-11-30 22:02:57
²éѯ½á¹û£º¹²²éµ½10961¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼)
1 .     22¦Á-µ±¹éõ£»ù-ÓñÈï´¼ A1
    ÏàËÆ¶È:82.8%
Chinese Traditional and Herbal Drugs          2011          42          1936-1938
Chemical constituents in roots of Camellia oleifera
TONG, Xiao-jing, CHEN, Zhong, LI, Xia, LI, Xiao-ran, XU, Qiong-ming, YANG, Shi-lin
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
2 .     A1-barrigenol
C30H50O5     ÏàËÆ¶È:80%
Phytochemistry          1990          29          2539-2543
Caffeine and theanine from cultured cells of Camellia sinensis
Tsutomu Furuya,Yutaka Orihara,Yumiko Tsuda
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
3 .     A1-barrigenol
C30H50O5     ÏàËÆ¶È:80%
The Open Natural Products Journal          2012          5          7-12
Complete Assignment of the 1H and 13C NMR Spectra of the Camelliagenin A and A1-Barrigenol from the seed of Barringtonia asiatica
Rymond J. Rumampuk,* Emma J. Pongoh Ponis Tarigan Anthony J. Herlt and Lewis N. Mander.
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
4 .     28-tigloylbarringtogenol C
    ÏàËÆ¶È:74.2%
Phytochemistry          1998          48          1411-1414
Triterpenoid saponins from Berneuxia thebetica
Ming-Kui Wang, Hong Cai, Shu-Lin Peng, Li-Sheng Ding, Feng-E Wu, Yao-Zu Chen
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
5 .     21¦Â,22¦Á-O-diangeloyl-protoaesciyenin
C40H6208     ÏàËÆ¶È:73.6%
Phytochemistry          1998          48          1229-1232
Harpuloside a triterpenoid saponin from Harpullia ramiflora
C. Dizes, F. Gerald, C. Lavaud, R. Ellas, R. Faure, G. Massiot, G. Balansard
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
6 .     aesculioside IIa
C52H82O22     ÏàËÆ¶È:71.4%
Phytochemistry          2006          67          784-794
Triterpenoid saponins from the fruits of Aesculus pavia
Zhizhen Zhang, Shiyou Li, Shanmin Zhang, David Gorenstein
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
7 .     aesculioside IIb
C52H82O22     ÏàËÆ¶È:71.4%
Phytochemistry          2006          67          784-794
Triterpenoid saponins from the fruits of Aesculus pavia
Zhizhen Zhang, Shiyou Li, Shanmin Zhang, David Gorenstein
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
8 .     aesculioside IId
C46H72O17     ÏàËÆ¶È:71.4%
Phytochemistry          2006          67          784-794
Triterpenoid saponins from the fruits of Aesculus pavia
Zhizhen Zhang, Shiyou Li, Shanmin Zhang, David Gorenstein
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
9 .     3,15,16-trihydroxy-18¦Â-olean-12-en-28-oic acid
    ÏàËÆ¶È:71.4%
Chemical & Pharmaceutical Bulletin          1988          36          5028-5030
13C NMR SPECTRAL STUDIES OF ENTAGENIC ACID TO ESTABLISH ITS STRUCTURE
Yoshihito Okada,Shoji Shibata,Osamu Kamo and Toru Okuyama
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
10 .     prosapogenin
    ÏàËÆ¶È:71.4%
Chemical & Pharmaceutical Bulletin          1987          35          524-529
New Triterpene Saponins from Ilex pubescens
KAZUYUKI HIDAKA,MIYOKO ITO,YOKO MATSUDA,HIROSHI KOHDA,KAZUO YAMASAKI,JOHJI YAMAHARA,TAKESHI CHISAKA,YOSHIYUKI KAWAKAMI,TADASHI SATO and KENGO KAGEI
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
11 .     ursolic
    ÏàËÆ¶È:71.4%
Chemistry of Natural Compounds          2005          41          200-204
TRITERPENE GLYCOSIDES FROM Cussonia paniculata.I. ISOLATION AND STRUCTURE DETERMINATION OF GLYCOSIDES A, B1, B2, C, D, G2, H1, AND H2 FROM LEAVES OF Cussonia paniculata
I. I. Dovgii, V. I. Grishkovets,V. V. Kachala, and A. S. Shashkov
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
12 .     Glycoside B 2
    ÏàËÆ¶È:71.4%
Chemistry of Natural Compounds          2000          36          173-176
TRITERPENE GLYCOSIDES OF Scheffleropsis angkae.I. STRUCTURE OF GLYCOSIDES L-B1, L-B2, L-H1, AND L-H 2
A. S. StolyarenkoJ V. I. Grishkovets, 1 N. N. Arnautov, S. V. Iksanova, and V. Ya. Chirva
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
13 .     2¦Á,3¦Á-dihydroxyurs-12-en-28-oic acid
C30H48O4     ÏàËÆ¶È:71.4%
China Journal of Chinese Materia Medica          2001          26          264-265
Lipid Chemical Constituents of Salvia sochifolia C. Y. Wu
WU Zhijun
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
14 .     barringtogenol-C21-angelate
    ÏàËÆ¶È:71.4%
Journal of Natural Products          1986          Vol 49          650
Antitumor Agents, 82. Cytotoxic Sapogenols from Aesculus hippocastanum
Takao Konoshima, Kuo-Hsiung Lee
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
15 .     2¦Á,3¦Á,23,24-tetrahydroxyurs-12-en-28-oic acid
    ÏàËÆ¶È:71.4%
Phytochemistry          1992          31          2801-2804
Triterpenoids from the fruit galls of Actinidia polygama
Yutaka Sashida, Kazunori Ogawa, Noriaki Mori, Tsuyoshi Yamanouchi
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
16 .     Saniculagenin N
C35H56O7     ÏàËÆ¶È:71.4%
Journal of Natural Products          1997          60          1170-1173
Saniculoside N from Sanicula europaea L.
Nazlı Arda, Nezhun Gören, Avni Kuru, Thitima Pengsuparp, John M. Pezzuto, Sheng-Xiang Qiu, and Geoffrey A. Cordell
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
17 .     3-epi-corosolic acid
C30H48O4     ÏàËÆ¶È:71.4%
Bioorganic & Medicinal Chemistry Letters          2007          17          5777-5782
Pentacyclic triterpenes. Part 5: Synthesis and SAR study of corosolic acid derivatives as inhibitors of glycogen phosphorylases
Xiaoan Wen, Jun Xia, Keguang Cheng, Liying Zhang, Pu Zhang, Jun Liu, Luyong Zhang, Peizhou Ni, Hongbin Sun
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
18 .     2¦Á,3¦Á-¶þôÇ»ùÐܹûËá
    ÏàËÆ¶È:71.4%
Chinese Traditional and Herbal Drugs          2010          41          544-546
ºÚ¹ûÏÙÀß»¨é±¹ûʵµÄ»¯Ñ§³É·Ö
ÓÚÃ÷;Àîϳ;ÕÅÀö;ÕÔÓàÇì
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
19 .     6¦Â-ôÇ»ù»ýÑ©²ÝËá
    ÏàËÆ¶È:71.4%
Modern Chinese Medicine          2008          10(3)          7-9
Chemical studies on the saponin compounds of Centella asiatica
Liu Yu, Zhao Yuqing
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
20 .     2¦Á,3¦Á-dihydroxyurs-12-en-28-oic acid
C30H48O4     ÏàËÆ¶È:71.4%
Journal of Shenyang Pharmaceutical University          2008          25          872-874
Constituents of the aerial part of Rabdosia rubescens
CAI Ming-lei, GAO Hui-yuan, HUANG Jian, SUN Bo-hang, SONG Xiao-mei, WU Li-jun
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
21 .     2¦Á,3¦Á,23,24-tetrahydroxyurs-12-en-28-oic acid
C30H48O6     ÏàËÆ¶È:71.4%
Academic Journal of Second Military Medical University          2011          32          749-753
Anti-tumor constituents from the roots of Actinidia valvata
XU Yi-xin, XIANG Zhao-bao, CHEN Xiao-jing, CHEN Hai-sheng
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
2Â¥2014-11-28 10:55:00
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