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ÀÏʵÈËsdu3375: ½ð±Ò+25 2015-05-12 17:33:39
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1 .     1¦Á,3¦Â,23-trihydroxy-olean-12-en-29-oate-23-O-¦Á[3,4-diacetylrhamnopyranosyl] -29-O-¦Á-rhamnopyranoside
C46H72O15     ÏàËÆ¶È:69.5%
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    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
2 .     3-O-¦Â-D-xylopyranosyl-(1¡ú3)-¦Á-L-rhamnopyranosyl-(1¡ú2)-¦Â-D-xylopyranosyl-12¦Â,30-dihydroxy-olean-28,13¦Â-olide
C46H74O17     ÏàËÆ¶È:69.5%
Carbohydrate Research          2011          346          2881-2885
New triterpenoid saponins from Patrinia scabiosaefolia
Liang Gao, Lin Zhang, Nan Li, Jiang-Yun Liu, Pei-lie Cai, Shi-lin Yang
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
3 .     Quamoclin V
C49H84O24     ÏàËÆ¶È:69.3%
Chemical & Pharmaceutical Bulletin          2012          60          1083-1087
Three New Resin Glycosides and a New Tetrahydropyran Derivative from the Seeds of Quamoclit pennata
Masateru Ono, Yoshinari Takaki, Masamitsu Takatsuji, Kousuke Akiyama, Masafumi Okawa, Junei Kinjo, Hiroyuki Miyashita, Hitoshi Yoshimitsu, Toshihiro Nohara
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
4 .     glycoside(1a)
    ÏàËÆ¶È:68.8%
Chemical & Pharmaceutical Bulletin          2004          52(1)          142-145
Pregnane- and Furostane-Type Oligoglycosides from the Seeds of Allium tuberosum
Tsuyoshi IKEDA, Hidetsugu TSUMAGARI, Masafumi OKAWA, and Toshihiro NOHARA
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
5 .     23-hydroxyimberbic acid 3-O-¦Á-L-rhamnopyranosyl-23-O-¦Á-L-4-acetylrhamnopyranoside
C44H70O14     ÏàËÆ¶È:68.8%
Journal of Natural Products          1989          Vol 52          528
New Mono- and Bi-Desmosidic Triterpenoids Isolated from Combretum padoides Leaves
Colin B. Rogers
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
6 .     23-hydroxyimberbic acid 3-O-¦Á-L-rhamnopyranosyl-23-O-¦Á-L-rhamnoside
C42H68O13     ÏàËÆ¶È:68.8%
Journal of Natural Products          1989          Vol 52          528
New Mono- and Bi-Desmosidic Triterpenoids Isolated from Combretum padoides Leaves
Colin B. Rogers
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
7 .     l¦Á,3¦Â,23,29-tetrahydroxyolean-12-ene 3-O-¦Á-L-rhamnopyranosyl-23-O-¦Á-L-rhamnopyranoside
    ÏàËÆ¶È:68.8%
Journal of Natural Products          1989          Vol 52          528
New Mono- and Bi-Desmosidic Triterpenoids Isolated from Combretum padoides Leaves
Colin B. Rogers
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
8 .     11,12-di-O-iso-butyryl-8,9-anhydro-erythromycin A 6,9-hemiketal
C45H77NO14     ÏàËÆ¶È:68.8%
Bioorganic & Medicinal Chemistry Letters          2007          17          6340-6344
Design and synthesis via click chemistry of 8,9-anhydroerythromycin A 6,9-hemiketal analogues with anti-MRSA and -VRE activity
Akihiro Sugawara, Toshiaki Sunazuka, Tomoyasu Hirose, Kenichiro Nagai, Yukie Yamaguchi, Hideaki Hanaki, K. Barry Sharpless, Satoshi ¨­mura
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
9 .     stellatoside E
C42H66O14     ÏàËÆ¶È:68.8%
Heterocycles          2012          85          1377-1392
New Triterpenoid Saponins from Stenocereus eruca
Kazutaka Kakuta, Takeshi Koike, Kaoru Kinoshita, Satoru Ito, Kiyotaka Koyama, and Kunio Takahashi
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
10 .     roxithromycin
    ÏàËÆ¶È:68.8%
Magnetic Resonance in Chemistry          1990          28          846-855
Analysis of the 1H and 13C NMR spectra of the novel macrolide antibiotic roxithromycin. Structure and conformation in solution
Josyane Gharbi-Benarous, Marcel Delaforge, Isabelle Artaud and Jean-Pierre Girault
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
11 .     hauptsaponine S2
    ÏàËÆ¶È:68.8%
Pharmazie          1987          42          143-143
Steroidsaponine aus Dioscorea hispida L.
Ng. X. Cuong, D. Zeigan, Gabriele Voigt, und K. Hiller
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
12 .     Macaoside H
C45H74O17     ÏàËÆ¶È:68.8%
Journal of Natural Products          2014          77          1770-1783
Anti-Inflammatory Spirostanol and Furostanol Saponins from Solanum macaonense
Chia-Lin Lee, Tsong-Long Hwang, Juan-Cheng Yang, Hao-Ting Cheng, Wan-Jung He, Chiao-Ting Yen, Chao-Lin Kuo, Chao-Jung Chen, Wen-Yi Chang, and Yang-Chang Wu
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
13 .     Compound 6
C48H80O14     ÏàËÆ¶È:68.7%
Bioorganic & Medicinal Chemistry Letters          2009          19          2310-2314
Synthesis, cytotoxicity, and haemolytic activity of chacotrioside lupane-type neosaponins and their germanicane-type rearrangement products
Charles Gauthier, Jean Legault, Marianne Piochon, Serge Lavoie, Samuel Tremblay, Andr¨¦ Pichette
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
14 .     Compound 7
C48H80O15     ÏàËÆ¶È:68.7%
Bioorganic & Medicinal Chemistry Letters          2009          19          2310-2314
Synthesis, cytotoxicity, and haemolytic activity of chacotrioside lupane-type neosaponins and their germanicane-type rearrangement products
Charles Gauthier, Jean Legault, Marianne Piochon, Serge Lavoie, Samuel Tremblay, Andr¨¦ Pichette
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
15 .     stellatoside C
C48H76O18     ÏàËÆ¶È:68.7%
Heterocycles          2012          85          1377-1392
New Triterpenoid Saponins from Stenocereus eruca
Kazutaka Kakuta, Takeshi Koike, Kaoru Kinoshita, Satoru Ito, Kiyotaka Koyama, and Kunio Takahashi
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
16 .     kudinoside A
C47H74O18     ÏàËÆ¶È:68.0%
Phytochemistry          1996          43          443-445
Triterpenoid glycosides from Ilex kudincha
Ming-An Ouyang, Han-Qing Wang, Zi-Li Chen, Chong-Ren Yang
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
17 .     Kudinoside F
C47H74O18     ÏàËÆ¶È:68.0%
Phytochemistry          1996          41          871-877
Triterpenes and triterpenoid glycosides from the leaves of Ilex kudincha
Ming-An Ouyang, Chong-Ren Yang, Zi-Li Chen, Han-Qing Wang
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
18 .     (20S)-3¦Â,20,21-trihydroxydammar-24-ene 3-O-[¦Á-L-rhamnopyranosyl(1¡ú2)][¦Â-D-xylopyranosyl(1¡ú3)]-¦Â-D-glucopyranoside
    ÏàËÆ¶È:68.0%
Chinese Chemical Letters          2010          21          699-701
A new dammarane-type triterpene saponin from Gynostemma pentaphyllum
Lin Shi; Jia Qing Cao; Wei Li; Hong Zhao; Yu Qing Zhao
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
19 .     dudinoside F
C47H74O18     ÏàËÆ¶È:68.0%
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