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13C NMR (101 MHz, MeOD) ¦Ä 171.33, 171.03, 138.18, 137.71, 134.91, 134.66, 79.57, 78.24, 72.52, 72.06, 71.42, 69.11, 68.46, 56.88, 49.25, 49.17, 40.58, 40.39, 39.80, 37.95, 36.78, 33.98, 33.89, 33.63, 33.25, 30.56, 30.36, 30.24, 29.01, 28.82, 28.47, 28.02, 25.84, 25.39, 25.27, 24.62, 24.48, 23.03, 22.91, 22.32, 22.06, 20.02, 19.67, 19.39, 19.18, 19.09, 19.05.
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1 .     3-O-¦Â-glucuronyl-olean-12-en-28-oic acid 28-(O-¦Á-rhamnopyranosyl-( 1¡ú2 )-a-arabinopyranosyl) ester
C47H74O17     ÏàËÆ¶È:59.5%
Planta Medica          1998          64          50-53
Triterpenoid Saponins from Aster auriculatus
Chang Zeng Wang and De Quan Yu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     pinnatoxin F
C45H67NO9     ÏàËÆ¶È:59.5%
Journal of Agricultural and Food Chemistry          2010          58          6532-6542
Isolation, Structural Determination and Acute Toxicity of Pinnatoxins E, F and G
Andrew I. Selwood, Christopher O. Miles, Alistair L. Wilkins, Roel van Ginkel, Rex Munday, Frode Rise and Paul McNabb
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     (25R)-26-tert-butyidiphenylsilyloxy-3¦Á-(2-azido-3,4,-6-tri-O-benzyl-2-deoxy-¦Â-D-glucopyranosyloxy)-5¦Â-cholestan-7¦Á-yl acetate
    ÏàËÆ¶È:59.1%
Bioorganic & Medicinal Chemistry          1997          5          2251-2265
Synthesis of pavoninin-1, a shark repellent substance, and its structural analogues toward mechanistic studies on their membrane perturbation
Yuki Ohnishi, Kazuo Tachibana
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     ¦Á-L-rhanmnopyranosyl-(1¡ú2)-[¦Â-D-xylofuranosyl-(1¡ú6)]-[¦Â-D-glucopyranose
    ÏàËÆ¶È:58%
Archives of Pharmacal Research          1996          19          429-431
A novel cycloartane glycoside from Thalictrum uchiyamai
Young-Hee Choi, Nan Gyeong Kim and Ihn Ran Lee
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     stigmast-5-en-3¦Â-ol-3-O-¦Â-D-(2'-n-triacontanoyl) glucopyranoside
C65H118O7     ÏàËÆ¶È:57.4%
Journal of Asian Natural Products Research          2012          14          301-307
New steroidal glycoside ester and aliphatic acid from the fruits of Lycium chinense
Woo-Suk Jung,Ill-Min Chung,Mohd Ali and Ateeque Ahmad
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     1-O-octadecyl-2-(4-(¦Á-tocopheroxy)-4-oxobutanoyl)-snglycero-3-phospho-(S)-glycerol
C57H102O12PNa     ÏàËÆ¶È:57.4%
Bioorganic & Medicinal Chemistry          2012          20          3972-3978
Synthesis of tocopheryl succinate phospholipid conjugates and monitoring of phospholipase A2 activity
Palle J. Pedersen, H¨¦l¨¨ne M.-F. Viart, Fredrik Melander, Thomas L. Andresen, Robert Madsen, Mads H. Clausen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     compound 28
C51H82O21     ÏàËÆ¶È:56%
Chemistry of Natural Compounds          2005          41          117-140
STRUCTURAL STUDIES AND BIOLOGICAL ACTIVITY OF PLANT TRITERPENOIDS FROM THE Thalictrum GENUS
V. I. Lutskii, A. S. Gromova,E. A. Khamidullina, and N. L. Owen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     1¦Á,3¦Â,23-trihydroxy-olean-12-en-29-oate-23-O-¦Á[3,4-diacetylrhamnopyranosyl] -29-O-¦Á-rhamnopyranoside
C46H72O15     ÏàËÆ¶È:55.3%
Phytochemistry          2003                   81-88
Antimicrobial activity of pentacyclic triterpenes isolated from African Combretaceae
David R. Katerere, Alexander I. Gray, Robert J. Nash, Roger D. Waigh
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     bodinitin A
C47H76O17     ÏàËÆ¶È:55.3%
Journal of Natural Products          1996          59          1043-1046
Four New Triterpene Glycosides from Schefflera bodinieri Roots
Min Zhu, Shiling Yang, J. David Phillipson, and Norman G. Bowery
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     macrophyllosaponin D
C46H78O17     ÏàËÆ¶È:55.3%
Journal of Natural Products          1996          59          1019-1023
Four Novel Cycloartane Glycosides from Astragalus oleifolius
I¨²hsan Çalış, Murat Zor, İclal Saracoğlu, Aşkın Işımer, and Heinz R¨¹egger
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     3-O-[¦Á-L-rhamnopyranosyl-(1¡ú2)-¦Â-D-xylopyranosyl-(1¡ú2)-¦Â-D-glucuronopyranosyl]-3¦Â,22¦Á-dihydroxyolean-13-en-11-one
C47H74O17     ÏàËÆ¶È:55.3%
Zeitschrift f¨¹r Naturforschung B          2004          59b          124-128
A New Triterpenoid Saponin from Ononis spinosa and Two New Flavonoid Glycosides from Ononis vaginalis
Kamel H. Shaker, Katja Dockendorff, Mirko Bernhardt, and Karlheinz Seifert
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     compound 1
C61H110O7     ÏàËÆ¶È:55.3%
Archives of Pharmacal Research          2007          30          172-176
Isolation of constituents and anti-complement activity from Acer okamotoanum
WenYi Jin, Byung-Sun Min, JongPill Lee, Phuong Thien Thuong and Hyeong-Kyu Lee, et al.
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
13 .     3-O-{¦Á-L-rhamnopyranosyl-(1¡ú4)-[¦Á-L-arabinopyranosyl-(1¡ú2)]-¦Â-D-glucopyranosyl}-3¦Â,6¦Á,16¦Â,24(R),25-pentahydroxycycloartane
C47H80O18     ÏàËÆ¶È:55.3%
Phytochemistry          2012          73          119-126
Cycloartane glycosides from Astragalus stereocalyx Bornm.
Funda Nuray Yalçın, Sonia Piacente, Angela Perrone, Anna Capasso, Hayri Duman, İhsan Çalış
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
14 .     Ilexsaponin D
C47H72O19     ÏàËÆ¶È:55.3%
Journal of Asian Natural Products Research          2012          14          1169-1174
Three new triterpenoid saponins from Ilex pubescens
Ling Li, Yu-Xin He, Mei-Ling Gou & Chun Dai
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
15 .     caryocaroside IV-6
    ÏàËÆ¶È:55.1%
Journal of Natural Products          2006          69(2)          196-205
Triterpenoid Saponins from the Fruits of Caryocar glabrum
Abdulmagid Alabdul Magid, Laurence Voutquenne, Christian Moretti, Christophe Long, and Catherine Lavaud
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
16 .     caryocaroside IV-5
    ÏàËÆ¶È:54.1%
Journal of Natural Products          2006          69(2)          196-205
Triterpenoid Saponins from the Fruits of Caryocar glabrum
Abdulmagid Alabdul Magid, Laurence Voutquenne, Christian Moretti, Christophe Long, and Catherine Lavaud
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
17 .     3-O-[¦Á-L-rhamnopyranosyl-(1¡ú2)-¦Â-Dgalactopyranosyl-(1¡ú2)-¦Â-D-glucuronopyranosyl]-3¦Â,16¦Â,22¦Á-trihydroxy-olean-12-ene
C48H78O18     ÏàËÆ¶È:54.1%
Journal of Natural Products          2007          70          979-983
Oleanane Saponins from Stylosanthes erecta
Marinella De Leo,Rokia Sanogo, Nunziatina De Tommasi, and Alessandra Braca
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
18 .     acacioside A
C48H77NO17     ÏàËÆ¶È:54.1%
Journal of Natural Products          2002          65          170-174
Bioactive Saponins from Acacia tenuifolia from the Suriname Rainforest1
Youngwan Seo,Jeannine Hoch, Maged Abdel-Kader, S. Malone, I. Derveld, Hermus Adams,M. C. M. Werkhoven, Jan H. Wisse, Stephen W. Mamber,r James M. Dalton,r and David G. I. Kingston
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
19 .     3-O-[¦Á-L-arabinopyranosyl-(1¡ú2)-¦Á-L-arabinopyranosyl-(1¡ú6)-2-acetamido-2-deoxy-¦Â-D-glucopyranosyl]echinocystic acid
C48H77NO17     ÏàËÆ¶È:54.1%
Journal of Natural Products          2002          65          170-174
Bioactive Saponins from Acacia tenuifolia from the Suriname Rainforest1
Youngwan Seo,Jeannine Hoch, Maged Abdel-Kader, S. Malone, I. Derveld, Hermus Adams,M. C. M. Werkhoven, Jan H. Wisse, Stephen W. Mamber,r James M. Dalton,r and David G. I. Kingston
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
20 .     tauroside I
    ÏàËÆ¶È:54.1%
Chemistry of Natural Compounds          1992          28          593-596
TRITERPENE GLYCOSIDES OF Hedera taurica X. STRUCTURES OF COMPOUNDS F 4, I, AND J FROM THE LEAVES OF CRIMEAN IVY
V. I. Grishkovets, N. V. Tolkacheva,A. S. Shashkov, and V. Ya. Chirva
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
21 .     3¦Á-hydroxy-urs-12-ene-23,28-dioic acid 28-O-[¦Á-L-rhamnopyranosyl(1¡ú4)-O-¦Â-D-glucopyranosyl(1¡ú6)]-¦Â-D-glucopyranoside
    ÏàËÆ¶È:54.1%
Phytochemistry          1992          31          227-231
Triterpenoids and their glycosides from the bark ofSchefflera octophylla
T.V. Sung, C. Lavaud, A. Porzel, W. Steglich, G. Adam
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
22 .     Bifinoside B
C48H76O18     ÏàËÆ¶È:54.1%
Chemical & Pharmaceutical Bulletin          2011          59          1417-1420
Oleanolic Triterpene Saponins from the Roots of Panax bipinnatifidus
Nguyen Huu TUNG, Tran Hong QUANG, Nguyen Thi Thanh NGAN, Chau Van MINH, Bui Kim ANH, Pham Quoc LONG, Nguyen Manh CUONG, and Young Ho KIM
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
23 .     3-O-[¦Á-L-arabinopyranosyl-(1¡ú2)-O-3-acetoxy-¦Á-L-arabinopyranosyl]-6-O-¦Â-D-glucopyranosyl-3¦Â,6¦Á,16¦Â,24(S),25-pentahydroxycycloartane
C48H80O19     ÏàËÆ¶È:54.1%
Phytochemistry          2010          71          956-963
Triterpene glycosides from Astragalus icmadophilus
İbrahim Horo, Erdal Bedir, Angela Perrone, Fevzi Özgökçe, Sonia Piacente, Özgen Alankuş-Çalışkan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
24 .     3-O-[O-(¦Á-L-Rhamnopyranosyl)-(1¡ú2)-O-(¦Â-D-glucopyra-nosyl)-(1¡ú2)-(¦Â-glucuronopyranosyl)]-3¦Â,22¦Â,24-trihydroxy-olean-12-ene
C48H78O18     ÏàËÆ¶È:54.1%
Russian Chemical Bulletin          2001          50          1107-1112
Secondary metabolites of Astragalus danicus Retz. and A. inopinatus Boriss.
A. S. Gromova, V. I. Lutsky, J. G. Cannon, D. Li and N. L. Owen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
25 .     compound 6
C57H82O16     ÏàËÆ¶È:54%
Journal of Natural Products          2006          69(2)          240-246
Triterpenoid Saponins from Campsiandra guayanensis
Alessandra Braca, Ayman F. Abdel-Razik, Jeannette Mendez, and Nunziatina De Tommasi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
26 .     2-cyano-3-hydroxy-N-{3-[6-({5-[(3aS,4S,6aR)-2-oxohexahydro-1H-thieno[3,4-d]imidazol-4-yl]pentanoyl}amino)hexyl]aminocarbonyl}propyl-12-oxooleana-2,9(11)-dien-28-amide
C51H78N6O6S     ÏàËÆ¶È:54%
Journal of Medicinal Chemistry          2004          47          4923-4932
Design, Synthesis, and Biological Evaluation of Biotin Conjugates of 2-Cyano-3,12-dioxooleana-1,9(11)-dien-28-oic Acid for the Isolation of the Protein Targets
Tadashi Honda, Tomasz Janosik, Yukiko Honda, Jie Han, Karen T. Liby, Charlotte R. Williams, Robin D. Couch, Amy C. Anderson, Michael B. Sporn, and Gordon W. Gribble
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
27 .     amaroxocane B
C54H82Na3O20S4     ÏàËÆ¶È:53.8%
Journal of Natural Products          2009          72          259-264
Amaroxocanes A and B: Sulfated Dimeric Sterols Defend the Caribbean Coral Reef Sponge Phorbas amaranthus from Fish Predators
Brandon I. Morinaka, Joseph R. Pawlik, and Tadeusz F. Molinski
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
28 .     cincholic acid 3¦Â-O-¦Â-D-glucopyranosyl-(1¡ú4)-¦Â-D-fucopyranosyl-28-O-¦Â-D-glucopyranosyl ester
C48H76O19     ÏàËÆ¶È:53.1%
Chemical & Pharmaceutical Bulletin          2004          52(10)          1258-1261
New Oleanan-Type Triterpene and Cincholic Acid Glycosides from Peruvian ¡°Uña de Gato¡± (Uncaria tomentosa)
Mariko KITAJIMA,Ken-ichiro HASHIMOTO, Manuel SANDOVAL,Norio AIMI,andHiromitsu TAKAYAMA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
29 .     3-sulfate ester of 3¦Â,23-dihydroxyolean-12-en-28-oic acid 28-O-¦Â-D-glucopyranosyl-(1¡ú6)-¦Â-D-glucopyranoside
C42H68O17S     ÏàËÆ¶È:53.1%
Journal of Natural Products          2008          71(6)          1000-1004
Antiproliferative Oleanane Saponins from Meryta denhamii
Giuseppina Cioffi, Fabrizio Dal Piaz, Antonio Vassallo, Fabio Venturella,Paolo De Caprariis, Francesco De Simone, and Nunziatina De Tommasi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
30 .     compound 9
C47H76O16     ÏàËÆ¶È:53.1%
Journal of Natural Products          2006          69(2)          240-246
Triterpenoid Saponins from Campsiandra guayanensis
Alessandra Braca, Ayman F. Abdel-Razik, Jeannette Mendez, and Nunziatina De Tommasi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
31 .     guaiacin B
    ÏàËÆ¶È:53.1%
Phytochemistry          1999          51          1049-1053
Triterpenoid saponins from Fagonia indica
Kamel H. Shaker, Mirko Bernhardt, M. Hani A. Elgamal, Karlheinz Seifert
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
32 .     Bidenoside B
C46H72O18     ÏàËÆ¶È:53.1%
Zeitschrift f¨¹r Naturforschung B          2004          59b          821-824
Triterpene Saponins from Knautia integrifolia var. bidens
Özgen Alankuş-Çalışkan, Safiye Emirdağ, Erdal Bedir, Sibel Avunduk, and H¨¹seyin Anıl
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
33 .     bryoniaoside B
C42H70O13     ÏàËÆ¶È:53.1%
Chemical & Pharmaceutical Bulletin          2010          58          747-751
Cucurbitane-Type Triterpenes with Anti-proliferative Effects on U937 Cells from an Egyptian Natural Medicine, Bryonia cretica: Structures of New Triterpene Glycosides, Bryoniaosides A and B
Hisashi Matsuda, Souichi Nakashima, Osama Bashir Abdel-Halim, Toshio Morikawa and Masayuki Yoshikawa
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
34 .     pseudoginsenoside RT1
    ÏàËÆ¶È:53.1%
Bioorganic & Medicinal Chemistry Letters          2010          20          7110-7115
Oleanane-type triterpenoids from Panax stipuleanatus and their anticancer activities
Chun Liang, Yan Ding, Huu Tung Nguyen, Jeong-Ah Kim, Hye-Jin Boo, Hee-Kyoung Kang, Mahn Cuong Nguyen, Young Ho Kim
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
35 .     2-cyano-N-[6-({5-[(3aS,4S,6aR)-2-oxohexahydro-1H-thieno[3,4-d]imidazol-4-yl]pentanoyl}amino)hexyl]-3,12-dioxooleana-1,9(11)-dien-28-amide
C47H69N5O5S     ÏàËÆ¶È:53.1%
Journal of Medicinal Chemistry          2004          47          4923-4932
Design, Synthesis, and Biological Evaluation of Biotin Conjugates of 2-Cyano-3,12-dioxooleana-1,9(11)-dien-28-oic Acid for the Isolation of the Protein Targets
Tadashi Honda, Tomasz Janosik, Yukiko Honda, Jie Han, Karen T. Liby, Charlotte R. Williams, Robin D. Couch, Amy C. Anderson, Michael B. Sporn, and Gordon W. Gribble
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
36 .     2-cyano-3-hydroxy-N-[6-({5-[(3aS,4S,6aR)-2-oxohexahydro-1H-thieno[3,4-d]imidazol-4-yl]pentanoyl}amino)hex-yl]-12-oxooleana-2,9(11)-dien-28-amide
C47H71N5O5S     ÏàËÆ¶È:53.1%
Journal of Medicinal Chemistry          2004          47          4923-4932
Design, Synthesis, and Biological Evaluation of Biotin Conjugates of 2-Cyano-3,12-dioxooleana-1,9(11)-dien-28-oic Acid for the Isolation of the Protein Targets
Tadashi Honda, Tomasz Janosik, Yukiko Honda, Jie Han, Karen T. Liby, Charlotte R. Williams, Robin D. Couch, Amy C. Anderson, Michael B. Sporn, and Gordon W. Gribble
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
37 .     3-O-¦Â-arabinopyranosyl-(1¡ú3)-[¦Â-galactopyranosyl-(1¡ú2)]-¦Â-glucuronopyranosyl gypsogenin
C47H72O19     ÏàËÆ¶È:53.1%
Phytochemistry Letters          2012          5          752-755
Triterpenoids in Gypsophila trichotoma Wend.
Maya Yotova, Ilina Krasteva, Kristina Jenett-Siems, Petranka Zdraveva, Stefan Nikolov
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
38 .     ¨¢cido 3-O-¦Â-D-glicopiranosil-28-O-¦Â-glicopiranosilcinch¨®lico
    ÏàËÆ¶È:53.1%
Qu¨ªmica Nova          2008          31          755-758
Chemical constituents of the roots of Guettarda pohliana M¨¹ll. Arg. (Rubiaceae)
Oliveira, Paulo Roberto Neves de; Testa, Gl¨¢ucio; Sena, Simone Bortolotti de; Costa, Willian Ferreira da; Sarragiotto, Maria Helena; Santin, Silvana Maria de Oliveira; Souza, Maria Conceição de
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
39 .     3-O-¦Â-D-xylopyranosyl(1¡ú3)-¦Â-D-glucopyranosylursolicacid 28-O-methylester
    ÏàËÆ¶È:53.1%
Chemistry and Industry of Forest Products          2008          28          92-94
Lipophilic Components from the Bark of Quercus pannosa Hand. -Mazz.
LI Qin, SHEN Yue-mao, LI Ping
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
40 .     3-O-[¦Á-L-arabinopyranosyl-(1¡ú2)-¦Â-D-xylopyranosyl]-3¦Â,6¦Á,16¦Â,20(S),24(R),25-hexahydroxycycloartane
C40H68O14     ÏàËÆ¶È:53.1%
Phytochemistry          2012          73          119-126
Cycloartane glycosides from Astragalus stereocalyx Bornm.
Funda Nuray Yalçın, Sonia Piacente, Angela Perrone, Anna Capasso, Hayri Duman, İhsan Çalış
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
41 .     3-O-[¦Á-L-arabinopyranosyl-(1¡ú2)-¦Â-D-glucopyranosyl]-3¦Â,6¦Á,16¦Â,20(S),24(R),25-hexahydroxycycloartane
C41H70O15     ÏàËÆ¶È:53.1%
Phytochemistry          2012          73          119-126
Cycloartane glycosides from Astragalus stereocalyx Bornm.
Funda Nuray Yalçın, Sonia Piacente, Angela Perrone, Anna Capasso, Hayri Duman, İhsan Çalış
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
42 .     3-O-[¦Á-L-arabinopyranosyl-(1¡ú2)-¦Â-D-glucopyranosyl]-24-O-¦Â-D-glucopyranosyl-3¦Â,6¦Á,16¦Â,24(R),25-pentahydroxycycloartane
C47H80O19     ÏàËÆ¶È:53.1%
Phytochemistry          2012          73          119-126
Cycloartane glycosides from Astragalus stereocalyx Bornm.
Funda Nuray Yalçın, Sonia Piacente, Angela Perrone, Anna Capasso, Hayri Duman, İhsan Çalış
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
43 .     ¦Â-Sitosteryl linoleate
    ÏàËÆ¶È:53.1%
Zeitschrift f¨¹r Naturforschung C          2012          67          172-180
Anti-Helicobacter pylori Activity of the Methanolic Extract of Geum iranicum and its Main Compounds
Somayeh Shahani, Hamid R. Monsef-Esfahani, Soodabeh Saeidnia, Parastoo Saniee, Farideh Siavoshi, Alireza Foroumadi, Nasrin Samadi, and Ahmad R. Gohari
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
44 .     indicasaponin C
C47H76O20S     ÏàËÆ¶È:53.1%
Zeitschrift f¨¹r Naturforschung C          2000          55          520-523
Sulfonated Triterpenoid Saponins from Fagonia indica
K. H. Shaker, M. Bernhardt, M. H. A. Elgamal, and K. Seifert
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
45 .     compound 8
C52H84O17     ÏàËÆ¶È:52.9%
Journal of Natural Products          2006          69(2)          240-246
Triterpenoid Saponins from Campsiandra guayanensis
Alessandra Braca, Ayman F. Abdel-Razik, Jeannette Mendez, and Nunziatina De Tommasi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
46 .     3-sulfate ester of 3¦Â,23-dihydroxyolean-12-en-28-oic acid 28-O-¦Á-L-rhamnopyranosyl-(1¡ú4)-¦Â-D-glucopyranosyl-(1¡ú6)-¦Â-D-glucopyranoside
C48H78O21S     ÏàËÆ¶È:52.0%
Journal of Natural Products          2008          71(6)          1000-1004
Antiproliferative Oleanane Saponins from Meryta denhamii
Giuseppina Cioffi, Fabrizio Dal Piaz, Antonio Vassallo, Fabio Venturella,Paolo De Caprariis, Francesco De Simone, and Nunziatina De Tommasi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
47 .     albiziatrioside A
C48H77NO16     ÏàËÆ¶È:52.0%
Journal of Natural Products          2002          65          170-174
Bioactive Saponins from Acacia tenuifolia from the Suriname Rainforest1
Youngwan Seo,Jeannine Hoch, Maged Abdel-Kader, S. Malone, I. Derveld, Hermus Adams,M. C. M. Werkhoven, Jan H. Wisse, Stephen W. Mamber,r James M. Dalton,r and David G. I. Kingston
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
48 .     3-O-[¦Á-L-arabinopyranosyl-(1¡ú2)-¦Á-L-arabinopyranosyl-(1¡ú6)-2-acetamido-2-deoxy-¦Â-D-glucopyranosyl]oleanolic acid
C30H48O3     ÏàËÆ¶È:52.0%
Journal of Natural Products          2002          65          170-174
Bioactive Saponins from Acacia tenuifolia from the Suriname Rainforest1
Youngwan Seo,Jeannine Hoch, Maged Abdel-Kader, S. Malone, I. Derveld, Hermus Adams,M. C. M. Werkhoven, Jan H. Wisse, Stephen W. Mamber,r James M. Dalton,r and David G. I. Kingston
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
49 .     compound 9
    ÏàËÆ¶È:52.0%
Journal of Natural Products          2002          65          1560-1567
Acylated Triterpenoid Saponins from the Stem Bark of Foetidia africana
Marie-Laure Crublet,Isabelle Pouny, Cl¨¦ment Delaude, and Catherine Lavaud
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
50 .     albiziatrioside A
C48H77NO16     ÏàËÆ¶È:52.0%
Journal of Natural Products          2001          64          536-539
Two Bioactive Saponins from Albizia subdimidiata from the Suriname Rainforest1
Maged Abdel-Kader,Jeannine Hoch, John M. Berger, Randy Evans, James S. Miller, Jan H.Wisse,Stephen W. Mamber, James M.Dalton,and David G. I. Kingston
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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1 .     ¦Á-L-rhanmnopyranosyl-(1¡ú2)-[¦Â-D-xylofuranosyl-(1¡ú6)]-[¦Â-D-glucopyranose
    ÏàËÆ¶È:58%
Archives of Pharmacal Research          1996          19          429-431
A novel cycloartane glycoside from Thalictrum uchiyamai
Young-Hee Choi, Nan Gyeong Kim and Ihn Ran Lee
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     stigmast-5-en-3¦Â-ol-3-O-¦Â-D-(2'-n-triacontanoyl) glucopyranoside
C65H118O7     ÏàËÆ¶È:57.4%
Journal of Asian Natural Products Research          2012          14          301-307
New steroidal glycoside ester and aliphatic acid from the fruits of Lycium chinense
Woo-Suk Jung,Ill-Min Chung,Mohd Ali and Ateeque Ahmad
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     1-O-octadecyl-2-(4-(¦Á-tocopheroxy)-4-oxobutanoyl)-snglycero-3-phospho-(S)-glycerol
C57H102O12PNa     ÏàËÆ¶È:57.4%
Bioorganic & Medicinal Chemistry          2012          20          3972-3978
Synthesis of tocopheryl succinate phospholipid conjugates and monitoring of phospholipase A2 activity
Palle J. Pedersen, H¨¦l¨¨ne M.-F. Viart, Fredrik Melander, Thomas L. Andresen, Robert Madsen, Mads H. Clausen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     pinnatoxin F
C45H67NO9     ÏàËÆ¶È:57.4%
Journal of Agricultural and Food Chemistry          2010          58          6532-6542
Isolation, Structural Determination and Acute Toxicity of Pinnatoxins E, F and G
Andrew I. Selwood, Christopher O. Miles, Alistair L. Wilkins, Roel van Ginkel, Rex Munday, Frode Rise and Paul McNabb
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     (25R)-26-tert-butyidiphenylsilyloxy-3¦Á-(2-azido-3,4,-6-tri-O-benzyl-2-deoxy-¦Â-D-glucopyranosyloxy)-5¦Â-cholestan-7¦Á-yl acetate
    ÏàËÆ¶È:57.1%
Bioorganic & Medicinal Chemistry          1997          5          2251-2265
Synthesis of pavoninin-1, a shark repellent substance, and its structural analogues toward mechanistic studies on their membrane perturbation
Yuki Ohnishi, Kazuo Tachibana
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     compound 28
C51H82O21     ÏàËÆ¶È:56%
Chemistry of Natural Compounds          2005          41          117-140
STRUCTURAL STUDIES AND BIOLOGICAL ACTIVITY OF PLANT TRITERPENOIDS FROM THE Thalictrum GENUS
V. I. Lutskii, A. S. Gromova,E. A. Khamidullina, and N. L. Owen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     bodinitin A
C47H76O17     ÏàËÆ¶È:55.3%
Journal of Natural Products          1996          59          1043-1046
Four New Triterpene Glycosides from Schefflera bodinieri Roots
Min Zhu, Shiling Yang, J. David Phillipson, and Norman G. Bowery
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     compound 1
C61H110O7     ÏàËÆ¶È:55.3%
Archives of Pharmacal Research          2007          30          172-176
Isolation of constituents and anti-complement activity from Acer okamotoanum
WenYi Jin, Byung-Sun Min, JongPill Lee, Phuong Thien Thuong and Hyeong-Kyu Lee, et al.
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     Ilexsaponin D
C47H72O19     ÏàËÆ¶È:55.3%
Journal of Asian Natural Products Research          2012          14          1169-1174
Three new triterpenoid saponins from Ilex pubescens
Ling Li, Yu-Xin He, Mei-Ling Gou & Chun Dai
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     acacioside A
C48H77NO17     ÏàËÆ¶È:54.1%
Journal of Natural Products          2002          65          170-174
Bioactive Saponins from Acacia tenuifolia from the Suriname Rainforest1
Youngwan Seo,Jeannine Hoch, Maged Abdel-Kader, S. Malone, I. Derveld, Hermus Adams,M. C. M. Werkhoven, Jan H. Wisse, Stephen W. Mamber,r James M. Dalton,r and David G. I. Kingston
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     3-O-[¦Á-L-arabinopyranosyl-(1¡ú2)-O-3-acetoxy-¦Á-L-arabinopyranosyl]-6-O-¦Â-D-glucopyranosyl-3¦Â,6¦Á,16¦Â,24(S),25-pentahydroxycycloartane
C48H80O19     ÏàËÆ¶È:54.1%
Phytochemistry          2010          71          956-963
Triterpene glycosides from Astragalus icmadophilus
İbrahim Horo, Erdal Bedir, Angela Perrone, Fevzi Özgökçe, Sonia Piacente, Özgen Alankuş-Çalışkan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     2-cyano-3-hydroxy-N-{3-[6-({5-[(3aS,4S,6aR)-2-oxohexahydro-1H-thieno[3,4-d]imidazol-4-yl]pentanoyl}amino)hexyl]aminocarbonyl}propyl-12-oxooleana-2,9(11)-dien-28-amide
C51H78N6O6S     ÏàËÆ¶È:54%
Journal of Medicinal Chemistry          2004          47          4923-4932
Design, Synthesis, and Biological Evaluation of Biotin Conjugates of 2-Cyano-3,12-dioxooleana-1,9(11)-dien-28-oic Acid for the Isolation of the Protein Targets
Tadashi Honda, Tomasz Janosik, Yukiko Honda, Jie Han, Karen T. Liby, Charlotte R. Williams, Robin D. Couch, Amy C. Anderson, Michael B. Sporn, and Gordon W. Gribble
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
13 .     macrophyllosaponin D
C46H78O17     ÏàËÆ¶È:53.1%
Journal of Natural Products          1996          59          1019-1023
Four Novel Cycloartane Glycosides from Astragalus oleifolius
I¨²hsan Çalış, Murat Zor, İclal Saracoğlu, Aşkın Işımer, and Heinz R¨¹egger
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
14 .     3-O-¦Â-glucuronyl-olean-12-en-28-oic acid 28-(O-¦Á-rhamnopyranosyl-( 1¡ú2 )-a-arabinopyranosyl) ester
C47H74O17     ÏàËÆ¶È:53.1%
Planta Medica          1998          64          50-53
Triterpenoid Saponins from Aster auriculatus
Chang Zeng Wang and De Quan Yu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
15 .     3-O-[¦Á-L-rhamnopyranosyl-(1¡ú2)-¦Â-D-xylopyranosyl-(1¡ú2)-¦Â-D-glucuronopyranosyl]-3¦Â,22¦Á-dihydroxyolean-13-en-11-one
C47H74O17     ÏàËÆ¶È:53.1%
Zeitschrift f¨¹r Naturforschung B          2004          59b          124-128
A New Triterpenoid Saponin from Ononis spinosa and Two New Flavonoid Glycosides from Ononis vaginalis
Kamel H. Shaker, Katja Dockendorff, Mirko Bernhardt, and Karlheinz Seifert
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
16 .     Bidenoside B
C46H72O18     ÏàËÆ¶È:53.1%
Zeitschrift f¨¹r Naturforschung B          2004          59b          821-824
Triterpene Saponins from Knautia integrifolia var. bidens
Özgen Alankuş-Çalışkan, Safiye Emirdağ, Erdal Bedir, Sibel Avunduk, and H¨¹seyin Anıl
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
17 .     2-cyano-N-[6-({5-[(3aS,4S,6aR)-2-oxohexahydro-1H-thieno[3,4-d]imidazol-4-yl]pentanoyl}amino)hexyl]-3,12-dioxooleana-1,9(11)-dien-28-amide
C47H69N5O5S     ÏàËÆ¶È:53.1%
Journal of Medicinal Chemistry          2004          47          4923-4932
Design, Synthesis, and Biological Evaluation of Biotin Conjugates of 2-Cyano-3,12-dioxooleana-1,9(11)-dien-28-oic Acid for the Isolation of the Protein Targets
Tadashi Honda, Tomasz Janosik, Yukiko Honda, Jie Han, Karen T. Liby, Charlotte R. Williams, Robin D. Couch, Amy C. Anderson, Michael B. Sporn, and Gordon W. Gribble
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
18 .     2-cyano-3-hydroxy-N-[6-({5-[(3aS,4S,6aR)-2-oxohexahydro-1H-thieno[3,4-d]imidazol-4-yl]pentanoyl}amino)hex-yl]-12-oxooleana-2,9(11)-dien-28-amide
C47H71N5O5S     ÏàËÆ¶È:53.1%
Journal of Medicinal Chemistry          2004          47          4923-4932
Design, Synthesis, and Biological Evaluation of Biotin Conjugates of 2-Cyano-3,12-dioxooleana-1,9(11)-dien-28-oic Acid for the Isolation of the Protein Targets
Tadashi Honda, Tomasz Janosik, Yukiko Honda, Jie Han, Karen T. Liby, Charlotte R. Williams, Robin D. Couch, Amy C. Anderson, Michael B. Sporn, and Gordon W. Gribble
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
19 .     3-O-¦Â-D-xylopyranosyl(1¡ú3)-¦Â-D-glucopyranosylursolicacid 28-O-methylester
    ÏàËÆ¶È:53.1%
Chemistry and Industry of Forest Products          2008          28          92-94
Lipophilic Components from the Bark of Quercus pannosa Hand. -Mazz.
LI Qin, SHEN Yue-mao, LI Ping
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
20 .     3-O-[¦Á-L-arabinopyranosyl-(1¡ú2)-¦Â-D-glucopyranosyl]-24-O-¦Â-D-glucopyranosyl-3¦Â,6¦Á,16¦Â,24(R),25-pentahydroxycycloartane
C47H80O19     ÏàËÆ¶È:53.1%
Phytochemistry          2012          73          119-126
Cycloartane glycosides from Astragalus stereocalyx Bornm.
Funda Nuray Yalçın, Sonia Piacente, Angela Perrone, Anna Capasso, Hayri Duman, İhsan Çalış
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
21 .     3-O-{¦Á-L-rhamnopyranosyl-(1¡ú4)-[¦Á-L-arabinopyranosyl-(1¡ú2)]-¦Â-D-glucopyranosyl}-3¦Â,6¦Á,16¦Â,24(R),25-pentahydroxycycloartane
C47H80O18     ÏàËÆ¶È:53.1%
Phytochemistry          2012          73          119-126
Cycloartane glycosides from Astragalus stereocalyx Bornm.
Funda Nuray Yalçın, Sonia Piacente, Angela Perrone, Anna Capasso, Hayri Duman, İhsan Çalış
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
22 .     ¦Â-Sitosteryl linoleate
    ÏàËÆ¶È:53.1%
Zeitschrift f¨¹r Naturforschung C          2012          67          172-180
Anti-Helicobacter pylori Activity of the Methanolic Extract of Geum iranicum and its Main Compounds
Somayeh Shahani, Hamid R. Monsef-Esfahani, Soodabeh Saeidnia, Parastoo Saniee, Farideh Siavoshi, Alireza Foroumadi, Nasrin Samadi, and Ahmad R. Gohari
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
23 .     3-O-[¦Á-L-rhamnopyranosyl-(1¡ú2)-¦Â-Dgalactopyranosyl-(1¡ú2)-¦Â-D-glucuronopyranosyl]-3¦Â,16¦Â,22¦Á-trihydroxy-olean-12-ene
C48H78O18     ÏàËÆ¶È:52.0%
Journal of Natural Products          2007          70          979-983
Oleanane Saponins from Stylosanthes erecta
Marinella De Leo,Rokia Sanogo, Nunziatina De Tommasi, and Alessandra Braca
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
24 .     3-O-[¦Á-L-arabinopyranosyl-(1¡ú2)-¦Á-L-arabinopyranosyl-(1¡ú6)-2-acetamido-2-deoxy-¦Â-D-glucopyranosyl]echinocystic acid
C48H77NO17     ÏàËÆ¶È:52.0%
Journal of Natural Products          2002          65          170-174
Bioactive Saponins from Acacia tenuifolia from the Suriname Rainforest1
Youngwan Seo,Jeannine Hoch, Maged Abdel-Kader, S. Malone, I. Derveld, Hermus Adams,M. C. M. Werkhoven, Jan H. Wisse, Stephen W. Mamber,r James M. Dalton,r and David G. I. Kingston
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
25 .     castaraleside H methyl ester
C47H76O17     ÏàËÆ¶È:52.0%
Chemical & Pharmaceutical Bulletin          1994          42          314-317
Isolation and Characterization of Saponins from Castanospermum australe CUNN. et FRASER
Waseemuddin AHMED,Khan USMANGHANI,Iqbal AHMAD,Viqar Uddin AHMAD and Toshio MIYASE
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
26 .     tauroside I
    ÏàËÆ¶È:52.0%
Chemistry of Natural Compounds          1992          28          593-596
TRITERPENE GLYCOSIDES OF Hedera taurica X. STRUCTURES OF COMPOUNDS F 4, I, AND J FROM THE LEAVES OF CRIMEAN IVY
V. I. Grishkovets, N. V. Tolkacheva,A. S. Shashkov, and V. Ya. Chirva
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
27 .     Arvensoside C
C48H74O18     ÏàËÆ¶È:52.0%
Zeitschrift f¨¹r Naturforschung B          2006          61b          1170-1173
Triterpene Saponins from Calendula arvensis
Hasan Kırmızıbekmez, Carla Bassarello, Sonia Piacente, Cosimo Pizza, and İhsan Çalış
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
28 .     Bifinoside B
C48H76O18     ÏàËÆ¶È:52.0%
Chemical & Pharmaceutical Bulletin          2011          59          1417-1420
Oleanolic Triterpene Saponins from the Roots of Panax bipinnatifidus
Nguyen Huu TUNG, Tran Hong QUANG, Nguyen Thi Thanh NGAN, Chau Van MINH, Bui Kim ANH, Pham Quoc LONG, Nguyen Manh CUONG, and Young Ho KIM
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
29 .     compound
    ÏàËÆ¶È:52.0%
Bioorganic & Medicinal Chemistry          1997          5          2251-2265
Synthesis of pavoninin-1, a shark repellent substance, and its structural analogues toward mechanistic studies on their membrane perturbation
Yuki Ohnishi, Kazuo Tachibana
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
30 .     3-O-[O-(¦Á-L-Rhamnopyranosyl)-(1¡ú2)-O-(¦Â-D-glucopyra-nosyl)-(1¡ú2)-(¦Â-glucuronopyranosyl)]-3¦Â,22¦Â,24-trihydroxy-olean-12-ene
C48H78O18     ÏàËÆ¶È:52.0%
Russian Chemical Bulletin          2001          50          1107-1112
Secondary metabolites of Astragalus danicus Retz. and A. inopinatus Boriss.
A. S. Gromova, V. I. Lutsky, J. G. Cannon, D. Li and N. L. Owen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
31 .     compound 6
C57H82O16     ÏàËÆ¶È:52%
Journal of Natural Products          2006          69(2)          240-246
Triterpenoid Saponins from Campsiandra guayanensis
Alessandra Braca, Ayman F. Abdel-Razik, Jeannette Mendez, and Nunziatina De Tommasi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
32 .     amaroxocane B
C54H82Na3O20S4     ÏàËÆ¶È:51.9%
Journal of Natural Products          2009          72          259-264
Amaroxocanes A and B: Sulfated Dimeric Sterols Defend the Caribbean Coral Reef Sponge Phorbas amaranthus from Fish Predators
Brandon I. Morinaka, Joseph R. Pawlik, and Tadeusz F. Molinski
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
33 .     atriplicosaponin B
C42H70O14S     ÏàËÆ¶È:51.0%
Chemical & Pharmaceutical Bulletin          2005          53(9)          1126-1130
Two New Saponins from Zygophyllum atriplicoides
Viqar Uddin AHMAD,Shazia IQBAL,Farzana KOUSAR,Sadia BADER,Saima ARSHAD,and Rasool Bakhsh TAREEN
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
34 .     1¦Á,3¦Â,23-trihydroxy-olean-12-en-29-oate-23-O-¦Á[3,4-diacetylrhamnopyranosyl] -29-O-¦Á-rhamnopyranoside
C46H72O15     ÏàËÆ¶È:51.0%
Phytochemistry          2003                   81-88
Antimicrobial activity of pentacyclic triterpenes isolated from African Combretaceae
David R. Katerere, Alexander I. Gray, Robert J. Nash, Roger D. Waigh
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
35 .     3-sulfate ester of 3¦Â,23-dihydroxyolean-12-en-28-oic acid 28-O-¦Â-D-glucopyranosyl-(1¡ú6)-¦Â-D-glucopyranoside
C42H68O17S     ÏàËÆ¶È:51.0%
Journal of Natural Products          2008          71(6)          1000-1004
Antiproliferative Oleanane Saponins from Meryta denhamii
Giuseppina Cioffi, Fabrizio Dal Piaz, Antonio Vassallo, Fabio Venturella,Paolo De Caprariis, Francesco De Simone, and Nunziatina De Tommasi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
36 .     compound 9
C47H76O16     ÏàËÆ¶È:51.0%
Journal of Natural Products          2006          69(2)          240-246
Triterpenoid Saponins from Campsiandra guayanensis
Alessandra Braca, Ayman F. Abdel-Razik, Jeannette Mendez, and Nunziatina De Tommasi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
37 .     guaiacin B
C47H76O17     ÏàËÆ¶È:51.0%
Planta Medica          1989          55          307-308
Guaiacin A and B from the Leaves of Guaiacum officinale
Viqar Uddin Ahmad, Shaista Perveen, and Shaheen Bano
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
38 .     3-O-[¦Â-D-glucuronopyranosyl-(1¡ú2)-¦Â-D-xylopyranosyl]-25-O-¦Â-D-glucopyranosyl-3¦Â,6¦Á,16¦Â,24(S),25-pentahydroxy-cycloartane
C47H78O20     ÏàËÆ¶È:51.0%
Phytochemistry          2009          70          628-634
Cycloartane-type glycosides from Astragalus amblolepis
Emre Polat, Ozgen Caliskan-Alankus, Angela Perrone, Sonia Piacente, Erdal Bedir
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
39 .     24,25-O-¦Â-D-Diglucopyranosyl-6¦Á-hydroxycycloart-3-one
C42H70O14     ÏàËÆ¶È:51.0%
Phytochemistry Letters          2009          2          123-125
SU3, an oxocycloartane diglucoside from Sutherlandia humilis
Denise K. Olivier, Carl F. Albrecht, Ben-Erik van Wyk, Fanie R. van Heerden
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
40 .     guaiacin B
    ÏàËÆ¶È:51.0%
Phytochemistry          1999          51          1049-1053
Triterpenoid saponins from Fagonia indica
Kamel H. Shaker, Mirko Bernhardt, M. Hani A. Elgamal, Karlheinz Seifert
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
41 .     compound 8
C48H76O19     ÏàËÆ¶È:51.0%
Phytochemistry          1997          45          1035-1040
Triterpenes and quinovic acid glycosides from Uncaria tomentosa
R. Aquino, N. De Tommasi, F. De Simone, C. Pizza
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
42 .     leonticin E prosapogenin
    ÏàËÆ¶È:51.0%
Phytochemistry          1997          44          497-504
Leonticins D-H, five triterpene saponins from Leontice kiangnanensis
Min Chen, Wei Wei Wu, Daniel Nanz, Otto Sticher
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
43 .     28-O-[¦Á-L-rhamnopyranosyl(1¡ú4)-O-¦Â-D-glucopyranosyl (1¡ú6)-]-¦Â-D-glucopyranoside of 3¦Â-hydroxy-isopolygalic-13(14)-ene-28-acid
C47H76O17     ÏàËÆ¶È:51.0%
Phytochemistry          1996          43          1313-1318
Triterpene glycosides from Schefflera bodinieri roots
Min Zhu, Shiling Yang, J. David Phillipson, Pam M. Greengrass, Norman G. Bowery
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
44 .     3-O-[¦Á-L-rhamnopyranosyl (1¡ú3)-¦Â-D-glucuronopyranosyl]-3¦Â-hydroxyolean-12-en-28-oic acid
    ÏàËÆ¶È:51.0%
Journal of Natural Products          1990          Vol 53          466
A New Saponin from Deeringia amaranthoides
O. P. Sati, S. Bahuguna, S. Uniyal, J. Sakakibara, T. Kaiya, A. Nakamura
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
45 .     bryoniaoside B
C42H70O13     ÏàËÆ¶È:51.0%
Chemical & Pharmaceutical Bulletin          2010          58          747-751
Cucurbitane-Type Triterpenes with Anti-proliferative Effects on U937 Cells from an Egyptian Natural Medicine, Bryonia cretica: Structures of New Triterpene Glycosides, Bryoniaosides A and B
Hisashi Matsuda, Souichi Nakashima, Osama Bashir Abdel-Halim, Toshio Morikawa and Masayuki Yoshikawa
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
46 .     3-O-[O-(¦Á-L-Rhamnopyranosyl)-(1¡ú2)-O-(¦Â-D-xylopyra-nosyl)-(1¡ú2)-(¦Â-glucuronopyranosyl)]-3¦Â,22¦Â,24-trihydroxy-olean-12-ene
C47H76O17     ÏàËÆ¶È:51.0%
Russian Chemical Bulletin          2001          50          1107-1112
Secondary metabolites of Astragalus danicus Retz. and A. inopinatus Boriss.
A. S. Gromova, V. I. Lutsky, J. G. Cannon, D. Li and N. L. Owen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
47 .     A90720A
C45H72N10O16S     ÏàËÆ¶È:51.0%
Tetrahedron          1996          52          395-404
A90720A, a serine protease inhibitor isolated from a terrestrial blue-green alga Microchaete loktakensis
Rosanne Bonjouklian, Tim A. Smitka, Ann H. Hunt, John L. Occolowitz, Thomas J. Perun Jr., Lawrence Doolin, Stephanie Stevenson, Lisa Knauss, Ranmali Wijayaratne, Stanley Szewczyk, Gregory M.L. Patterson
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
48 .     GK-IV
    ÏàËÆ¶È:51.0%
The Journal of Antibiotics          1991          44          541-545
STRUCTURE ELUCIDATION OF GLYCOSIDIC ANTIBIOTICS GLYKENINS FROM Basidiomycetes sp. III. STRUCTURE OF GLYKENIN IV
FUMIKO NISHIDA, YUJI MORI, CHIHARU SONOBE, MAKOTO SUZUKI, VITHAYA MEEVOOTISOM, TIMOTHY W. FLEGEL, YODHATHAI THEBTARANONTH, SUTHUM INTARARUANGSORN
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
49 .     3-O-¦Â-arabinopyranosyl-(1¡ú3)-[¦Â-galactopyranosyl-(1¡ú2)]-¦Â-glucuronopyranosyl gypsogenin
C47H72O19     ÏàËÆ¶È:51.0%
Phytochemistry Letters          2012          5          752-755
Triterpenoids in Gypsophila trichotoma Wend.
Maya Yotova, Ilina Krasteva, Kristina Jenett-Siems, Petranka Zdraveva, Stefan Nikolov
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
50 .     ¨¢cido 3-O-¦Â-D-glicopiranosil-28-O-¦Â-glicopiranosilcinch¨®lico
    ÏàËÆ¶È:51.0%
Qu¨ªmica Nova          2008          31          755-758
Chemical constituents of the roots of Guettarda pohliana M¨¹ll. Arg. (Rubiaceae)
Oliveira, Paulo Roberto Neves de; Testa, Gl¨¢ucio; Sena, Simone Bortolotti de; Costa, Willian Ferreira da; Sarragiotto, Maria Helena; Santin, Silvana Maria de Oliveira; Souza, Maria Conceição de
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
51 .     momordin IIc
    ÏàËÆ¶È:51.0%
Modern Chinese Medicine          2013          15          936-939
Triterpene Saponins from the Aerial Parts of Agriophyllum squarrosum
LIU Zi-chun, LI Ying-hua, QU Jun-ye, LI Yu-shan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
52 .     oleanolic acid 3-O- [¦Á-L-arabinopyranosyl-(1¡ú3)-¦Â-D-glucuronopyranosyl]-28-O-¦Â-D-glucopyranoside
    ÏàËÆ¶È:51.0%
Modern Chinese Medicine          2013          15          936-939
Triterpene Saponins from the Aerial Parts of Agriophyllum squarrosum
LIU Zi-chun, LI Ying-hua, QU Jun-ye, LI Yu-shan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
53 .     oleanolic acid 3-O- [¦Â-D-glucopyranosyl-(1¡ú3)-¦Á-L-arabinopyranosyl]-28-O-¦Â-D-glucopyranoside
    ÏàËÆ¶È:51.0%
Modern Chinese Medicine          2013          15          936-939
Triterpene Saponins from the Aerial Parts of Agriophyllum squarrosum
LIU Zi-chun, LI Ying-hua, QU Jun-ye, LI Yu-shan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
54 .     3-O-[¦Á-L-arabinopyranosyl-(1¡ú2)-¦Â-D-xylopyranosyl]-3¦Â,6¦Á,16¦Â,20(S),24(R),25-hexahydroxycycloartane
C40H68O14     ÏàËÆ¶È:51.0%
Phytochemistry          2012          73          119-126
Cycloartane glycosides from Astragalus stereocalyx Bornm.
Funda Nuray Yalçın, Sonia Piacente, Angela Perrone, Anna Capasso, Hayri Duman, İhsan Çalış
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
55 .     3-O-[¦Á-L-arabinopyranosyl-(1¡ú2)-¦Â-D-glucopyranosyl]-3¦Â,6¦Á,16¦Â,20(S),24(R),25-hexahydroxycycloartane
C41H70O15     ÏàËÆ¶È:51.0%
Phytochemistry          2012          73          119-126
Cycloartane glycosides from Astragalus stereocalyx Bornm.
Funda Nuray Yalçın, Sonia Piacente, Angela Perrone, Anna Capasso, Hayri Duman, İhsan Çalış
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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2Â¥: Originally posted by jiangtao2956 at 2014-12-11 15:28:21

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21.4,30.4,37.4,73.2,73.7,125.6,126.6,139.6,140.2,168.2

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13C NMR (101 MHz, MeOD)19.0,19.1,19.2,19.4,19.7,20.0,22.1,22.3,22.9,23.0,24.5,24.6,25.3,25.4,25.8,28.0,28.5,28.8,29.0,30.2,
30.4,30.6,33.3,33.6,33.9,34.0,36.8,38.0,39.8,40.4,40.6,49.2,49.3,56.9,68.5,69.1,71.4,72.1,72.5,78.2,
79.6,134.7,134.9,137.7,138.2,171.0,171.3
4Â¥2014-12-11 16:02:23
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