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15 ºÅ13C NMR (151 MHz, MeOD) ¦Ä 15.69, 15.91, 16.42, 16.62, 24.49, 26.12, 26.41, 30.53, 31.26, 32.01, 33.47, 38.86, 39.03, 60.03, 68.27, 70.43, 70.81, 71.04, 72.51, 72.60, 73.49, 76.69, 76.95, 77.11, 77.72, 77.76, 78.35, 100.19, 100.23, 124.34, 130.82, 154.72.
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1 .     poranic acid B
C32H58O17     ÏàËÆ¶È:81.2%
Journal of Asian Natural Products Research          2014          16          135-140
Resin glycosides from Porana duclouxii
Wen-Bing Ding, Dai-Gui Zhang, Chun-Jie Liu, Guan-Hua Li & You-Zhi Li
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
2 .     (24R)-24-O-¦Á-d-glucopyranosyl-27-nor-5¦Á-cholestane-3¦Â,4¦Â,5,6¦Á,7¦Â,8,14,15¦Á,24-nonaol
C32H56O14     ÏàËÆ¶È:75%
Steroids          2010          75          897-904
Highly hydroxylated steroids of the starfish Archaster typicus from the Vietnamese waters
Natalia V. Ivanchina, Alla A. Kicha, Trinh T.T. Huong, Anatoly I. Kalinovsky, Pavel S. Dmitrenok, Irina G. Agafonova, Pham Q. Long, Valentin A. Stonik
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
3 .     poranic acid A
C32H58O16     ÏàËÆ¶È:75%
Journal of Asian Natural Products Research          2014          16          135-140
Resin glycosides from Porana duclouxii
Wen-Bing Ding, Dai-Gui Zhang, Chun-Jie Liu, Guan-Hua Li & You-Zhi Li
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
4 .     compound 3
C125H209N9O69S     ÏàËÆ¶È:71.8%
Carbohydrate Research          2006          341          1341-1352
Synthesis of a novel glycosphingolipid from the millipede, Parafontaria laminata armigera, and the assembly of its carbohydrate moiety into multivalent structures
Noriyasu Hada, Yoshiko Sonoda, Tadahiro Takeda
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
5 .     3-O-[{¦Â¡úD-glucopyranosyl(1¡ú2)}{¦Â-D-glucopyranosyl(1¡ú2)-¦Á-L-rhamnopyranosyl(16)}-¦Â-D-glucopyranosyl]-olean-12-ene-28-oic-3¦Â-ol
C58H88O22     ÏàËÆ¶È:69.6%
Planta Medica          1986          52          381-383
Molluscicidal Saponins of Xeromphis spinosa
Om Prakash Sati, Dinesh Chandra Chaukiyal and Usha Rana
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
6 .     (20S)-1¦Â,3¦Â,16¦Â-trihydroxypregn-5-ene-20-carboxylic acid 22,16-lactone 1-O-[¦Á-L-rhamnopyranosyl-(1¡ú4)-O-¦Â-D-glucopyranoside]
    ÏàËÆ¶È:69.6%
Phytochemistry          2011          72          651-661
Steroidal glycosides from Ruscus ponticus
Assunta Napolitano, Tamar Muzashvili, Angela Perrone, Cosimo Pizza, Ether Kemertelidze, Sonia Piacente
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
7 .     marsdenoside I
C35H56O12     ÏàËÆ¶È:68.5%
Helvetica Chimica Acta          2005          Vol. 88          2675
Three New Polyoxypregnane Glycosides from Marsdenia tenacissima
Jun Deng, Zhixin Liao, and Daofeng Chen
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
8 .     notoginsenoside T4
C36H62O11     ÏàËÆ¶È:66.6%
Helvetica Chimica Acta          2004          Vol. 87          1270
Hydrolytic Reaction of Plant Extracts to Generate Molecular Diversity: New Dammarane Glycosides from the Mild Acid Hydrolysate of Root Saponins of Panax notoginseng
Rong-Wei Teng, Hai-Zhou Li, De-Zu Wang, and Chong-Ren Yang
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
9 .     vina-ginsenoside-R10
C36H62O10     ÏàËÆ¶È:66.6%
Chemical & Pharmaceutical Bulletin          1994          42          634-640
Saponins from Vietnamese Ginseng, Panax vietnamensis HA et GRUSHV. Collected in Central Vietnam. III
NGUYEN Minh Duc,Ryoji KASAI,Kazuhiro OHTANI,Aiko ITO,Thoi Nham NGUYEN,Kazuo YAMASAKI and Osamu TANAKA
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
10 .     proloquatifoligenin-I
C33H56O14     ÏàËÆ¶È:66.6%
Chemical & Pharmaceutical Bulletin          1988          36          1270-1274
A Sesquiterpene Glycoside, Loquatifolin A, from the Leaves of Eriobotrya japonica
HIROAKI YANAGISAWA,YUKIO OHSHIMA,YOSHIHITO OKADA,KUNIO TAKAHASHI and SHIOJI SHIBATA
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
11 .     chikusetsusaponin-L9a
C36H62O10     ÏàËÆ¶È:66.6%
Chemical & Pharmaceutical Bulletin          1977          25          2041-2047
New Dammarane Type Saponins of Leaves of Panax japonicus C.A. MEYER. (1). Chikusetsusaponins-L5, -L9a and -L10
SHOJI YAHARA,RYOJI KASAI and OSAMU TANAKA Release Date: 2008/03/31
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
12 .     adoligose A
C33H58O18     ÏàËÆ¶È:66.6%
Journal of Natural Products          1995          Vol 58          483-494
Adoligoses, Oligosaccharides of Rare Sugars from Adonis aleppica
Guido F. Pauli
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
13 .     20(S)-È˲ÎÔíÜÕ2Rh1
    ÏàËÆ¶È:66.6%
Chinese Traditional and Herbal Drugs          2009          40          360-363
ÒæÖǸ´·½ÌÀµÄ»¯Ñ§³É·ÖÑо¿(¢ó)
ËïÁ¬ÄÈ;Àîϼ;ÑîÓ±²©;ÕÔ¹ó¾û;³ÂÍòÉú
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
14 .     ginsenoside Rk3
C42H70O12     ÏàËÆ¶È:66.6%
Archives of Pharmacal Research          2002          25          428-432
Three new dammarane glycosides from heat processed ginseng
II Ho Park, Na Young Kim, Sang Beom Han, Jong Moon Kim and Sung Won Kwon, et al.
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
15 .     ginsenoside Rk3
    ÏàËÆ¶È:66.6%
Archives of Pharmacal Research          2002          25          837-841
Four new acetylated ginsenosides from processed ginseng (sun ginseng)
Il Ho Park, Sang Beom Han, Jong Moon Kim, Longzhu Piao and Sung Won Kwon, et al.
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
16 .     ginsenoside Rk3
    ÏàËÆ¶È:66.6%
Chinese Wild Plant Resources          2014          33          13-15
Chemical Constituents from the Flower Buds of Panax ginseng C£®A£®M ey£®
Pan Xiao-ling, Li Zhen-lin, Qian Shi-hui, Pu She-ban
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
17 .     notoginsenoside ST-1
C36H62O10     ÏàËÆ¶È:66.6%
Journal of Agricultural and Food Chemistry          2008          56          1751-1756
Dammarane-Type Glycosides from Steamed Notoginseng
Peng-Ying Liao, Dong Wang, Ying-Jun Zhang and Chong-Ren Yang
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
18 .     ginsenosides RK3
    ÏàËÆ¶È:66.6%
Chinese Herbal Medicines          2014          6          159-163
Saponins from Roots of Panax notoginseng
Li-feng Han,Kaunda Joseph Sakah,Li-li Liu,Agyemang Kojo,Tao Wang and Yi Zhang
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
19 .     3¦Â,6¦Á,12¦Â-dammar-E-20(22)-ene-3,6,12,25-tetraol
C36H60O8     ÏàËÆ¶È:66.6%
Chinese Traditional and Herbal Drugs          2015          46          169−173
A new triterpene natural product from stems and leaves of Panax ginseng
LI Ke-ke, YANG Xiu-wei
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
20 .     tenacigenin C
C35H58O13     ÏàËÆ¶È:65.7%
Chinese Chemical Letters          2005          16          487-490
Two New C21 Steroids from Marsdenia tenacissima
Jun DENG, Zhi Xin LIAO, Dao Feng CHEN
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
21 .     compound 4
C35H58O9     ÏàËÆ¶È:65.7%
Phytochemistry          1989          28          1197-1201
Triterpenoid saponins from Centipeda minima
Dipti Gupta,J. Singh
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
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