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sumey1: ½ð±Ò+15, ¡ï¡ï¡ïºÜÓаïÖú 2013-03-18 13:02:12
1 .     3-O-¦Â-D-xylopyranosyl-(1¡ú3)[¦Á-L-rhamnopyranosyl(1¡ú2)]-¦Á-L-arabinopyranosyl hederagenin
C46H74O16     ÏàËÆ¶È:91.4%
Phytochemistry          1995          40          891-897
Hederagenin glycosides from Pometia eximia
Lalith Jayasinghe, Hiroyasu Shimada, Noriyuki Hara, Yoshinori Fujimoto
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     rarasaponin I
C48H76O17     ÏàËÆ¶È:89.5%
Phytochemistry          2009          70          1166-1172
Oleanane-type triterpene oligoglycosides with pancreatic lipase inhibitory activity from the pericarps of Sapindus rarak
Toshio Morikawa, Yuanyuan Xie, Yasunobu Asao, Masaki Okamoto, Chihiro Yamashita, Osamu Muraoka, Hisashi Matsuda, Yutana Pongpiriyadacha, Dan Yuan, Masayuki Yoshikawa
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     clematoside S
    ÏàËÆ¶È:89.3%
Journal of Asian Natural Products Research          2009          11          332-338
Triterpenoid saponins from the stems of Clematis parviloba
Li-Hua Yan, Li-Zhen Xu, Jia Lin, Shi-Lin Yang and Yu-Lin Feng
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     clematoside S
    ÏàËÆ¶È:89.3%
Natural Product Research and Development          1997          9(2)          12-16
STUDIES ON THE CHEMICAL CONSTITUENTS OF CLEMATIS INTRICAT A BUNGE(¢ò)
Song Zhihong; Zhang Jianlan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     compound N-IV(b)
    ÏàËÆ¶È:87.2%
Acta Pharmaceutica Sinica          1996          31          689-694
STUDIES ON THE CHEMICAL CONSTITUENTS OF SEED FROM NIGELLA GLANDULIFERA
HF Hao; LJ Ren; YW Chen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     3-O-¦Â-D-apiosyl(1¡ú3)[¦Á-L-rhamnopyranosyl(1¡ú2)]-¦Â-D-glucopyranosyl hederagenin
C47H76O17     ÏàËÆ¶È:87.2%
Phytochemistry          1995          40          891-897
Hederagenin glycosides from Pometia eximia
Lalith Jayasinghe, Hiroyasu Shimada, Noriyuki Hara, Yoshinori Fujimoto
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     3-O-¦Â-Dxylopyranosyl(1¡ú3)[¦Á-L-rhamnopyranosyl(1¡ú2)]-¦Â-D-glucopyranosyl hederagenin
C47H76O17     ÏàËÆ¶È:87.2%
Phytochemistry          1995          40          891-897
Hederagenin glycosides from Pometia eximia
Lalith Jayasinghe, Hiroyasu Shimada, Noriyuki Hara, Yoshinori Fujimoto
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     glycoside A2
    ÏàËÆ¶È:87.2%
Chemistry of Natural Compounds          2011          Vol. 47, No. 2          313-315
TRITERPENE GLYCOSIDES FROM Clematis.I. GLYCOSIDES FROM THE ROOTS OF Clematis vitalba
G. P. Zaitsev,D. A. Panov, and V. Ya. Chirva
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     Hederagenin 3-O-¦Á-L-Arabinopyranosyl-(1¡ú3)-¦Á-L-rhamnopyranosyl-(1¡ú2)-¦Á-L-arabinopyranoside
    ÏàËÆ¶È:87.2%
Chemistry of Natural Compounds          2012          47          935-939
A new hederagenin glycoside from Nephelium lappaceum
Wen-Juan Liang, Qing-Yun Ma, He-Zhong Jiang, Jun Zhou and Jie Pang, et al.
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     Hederagenin 3-O-(2,4-O-Di-acetyl-¦Á-L-arabinopyranoside)-(1¡ú3)-¦Á-L-rhamnopyranosyl-(1¡ú2)-¦Á-L-arabinopyranoside
C50H78O18     ÏàËÆ¶È:86%
Journal of Agricultural and Food Chemistry          2003          51          4916-4919
Molluscicidal Saponins from Sapindus mukorossi, Inhibitory Agents of Golden Apple Snails, Pomacea canaliculata
Hui-Chi Huang, Sin-Chung Liao, Fang-Rong Chang, Yao-Haur Kuo, and Yang-Chang Wu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     parvilobaside A
C48H76O17     ÏàËÆ¶È:85.4%
Journal of Asian Natural Products Research          2009          11          332-338
Triterpenoid saponins from the stems of Clematis parviloba
Li-Hua Yan, Li-Zhen Xu, Jia Lin, Shi-Lin Yang and Yu-Lin Feng
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     compound 9
    ÏàËÆ¶È:85.1%
Chemical & Pharmaceutical Bulletin          1989          37          311-314
Saponins from Roots of Kalopanax septemlobus (THUNB.) KOIDZ., Ciqiu : Structures of Kalopanax-saponins C, D, E and F
Chun-Jie SHAO,Ryoji KASAI,Jing-Da XU and Osamu TANAKA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
13 .     3-O-[¦Â-D-xylopyranosyl-(1¡ú3)-¦Á-L-rhamnopyranosyl-(1¡ú2)-¦Á-L-arabinpyranosyl]-hederagenin
    ÏàËÆ¶È:85.1%
China Journal of Chinese Materia Medica          2005          30          981-983
Studies on chemical constituents in the seeds of Nigella glandulifera
LIU Yuming, YANG Junshan, LIU Qinghua
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
14 .     hederagenin-3-O-(4-O-acetyl-¦Â-D-xylopyranosyl)-(1¡ú3)-¦Á-L-rhamnopyranosyl-(1¡ú2)-¦Á-L-arabinopyranoside.
C48H77O17     ÏàËÆ¶È:85.1%
Phytochemistry          1998          48          885-888
Saponins from Gliricidia sepium
Keisuke Kojima, Xiao-Bing Zhu, Yukio Ogihara
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
15 .     3-O-¦Á-L-arabinofuranosyl(1¡ú3)[¦Á-L-rhamnopyranosyl (1¡ú2)-¦Â-L-arabinopyranosyl hederagenin
C46H74O16     ÏàËÆ¶È:85.1%
Phytochemistry          1995          40          891-897
Hederagenin glycosides from Pometia eximia
Lalith Jayasinghe, Hiroyasu Shimada, Noriyuki Hara, Yoshinori Fujimoto
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
16 .     3-O-¦Â-D-galactopyranosyl(1¡ú3)[¦Á-L-rhamnopyranosyl(1¡ú2)]-¦Â-D-glucopyranosyl hederagenin
C48H78O18     ÏàËÆ¶È:85.1%
Phytochemistry          1995          40          891-897
Hederagenin glycosides from Pometia eximia
Lalith Jayasinghe, Hiroyasu Shimada, Noriyuki Hara, Yoshinori Fujimoto
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
17 .     hederagenin-3-O-(3,4-di-O-acetyl ¦Â-D-xylopyranosyl)-(1¡ú3)-¦Á-L-rhamnopyranosyl-(1¡ú2)-¦Á-L-arabinopyranoside
C50H78O18     ÏàËÆ¶È:84.3%
Phytochemistry          1998          48          885-888
Saponins from Gliricidia sepium
Keisuke Kojima, Xiao-Bing Zhu, Yukio Ogihara
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
18 .     hederagenin 3-O-(2-O-acetyl-¦Â-D-xylopyranosyl)-(1¡ú3)-¦Á-L-rhamnopyranosyl-(1¡ú2)-¦Á-L-arabinopyranoside
C48H76O17     ÏàËÆ¶È:83.3%
Chemical & Pharmaceutical Bulletin          2001          49(9)          1195-1197
Acetylated Triterpene Saponins from the Thai Medicinal Plant, Sapindus emarginatus
Tripetch KANCHANAPOOM,a,b Ryoji KASAI,a and Kazuo YAMASAKI
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
19 .     Hederagenin 3-O-(4-O-Acetyl-¦Á-L-arabinopyranosyl)-(1¡ú3)-¦Á-L-rhamnopyranosyl-(1¡ú2)-¦Á-L-arabinopyranoside
    ÏàËÆ¶È:83.3%
Chemistry of Natural Compounds          2012          47          935-939
A new hederagenin glycoside from Nephelium lappaceum
Wen-Juan Liang, Qing-Yun Ma, He-Zhong Jiang, Jun Zhou and Jie Pang, et al.
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
20 .     caryocaroside II-24
C61H90O28     ÏàËÆ¶È:82.9%
Phytochemistry          2006          67          2096-2102
Triterpenoid saponins from the stem bark of Caryocar villosum
Abdulmagid Alabdul Magid, Laurence Voutquenne-Nazabadioko, Isabelle Renimel,Dominique Harakat, Christian Moretti, Catherine Lavaud
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
21 .     CP9a
    ÏàËÆ¶È:82.9%
Chemical & Pharmaceutical Bulletin          1982          30          859-865
Studies on the Constituents of Clematis Species. IV. On the Saponins of the Root of Clematis chinensis OSBECK. IV
HARUHISA KIZU and TSUYOSHI TOMIMORI
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
22 .     compound 3
    ÏàËÆ¶È:82.9%
Chemistry of Natural Compounds          2005          41          194-199
TRITERPENE GLYCOSIDES FROM Kalopanax septemlobum.1. GLYCOSIDES A, B, C, F, G1, G2, I2, H, AND J FROM LEAVES OF Kalopanax septemlobum VAR. maximowichiiINTRODUCED TO CRIMEA
V. I. Grishkovets, D. A. Panov,V. V. Kachala, and A. S. Shashkov
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
23 .     hederagenin-3-O-¦Â-D-xylopyranosyl(1¡ú3)-¦Á-L-rhamnopyranosyl(1¡ú2)-¦Á-L-arabinopyranoside
C46H74O16     ÏàËÆ¶È:82.9%
China Journal of Chinese Materia Medica          2008          33          38-42
Triterpenoid saponins from flower bud of Jasminum officianle var. grandiflorum
ZHAO Guiqin, DONG Junxiang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
24 .     hederagenin 3-O-¦Â-D-glucopyranosyl(1¡ú3)-¦Á-L-rhamnopyranosyl(1¡ú2)-¦Á-L-arabinopyranoside
C47H76O17     ÏàËÆ¶È:82.9%
Acta Pharmaceutica Sinica          2000          Vol 35          756-759
TRITERPENE SAPONINS FROM PULSATILLA CERNUA
ZHANG Qing-wen; YE Wen-cai; CHE Chun-tao; ZHAO Shou-xun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
25 .     3-O-¦Á-L-arabinofuranosyi-(1¡ú3) [~-L-rhamnopyranosyl(1¡ú2])-¦Â-D-xylopyranosyl hederagenin
C46H74O16     ÏàËÆ¶È:82.9%
Phytochemistry          1995          40          891-897
Hederagenin glycosides from Pometia eximia
Lalith Jayasinghe, Hiroyasu Shimada, Noriyuki Hara, Yoshinori Fujimoto
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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