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ÀÏʵÈËsdu3375: ½ð±Ò+25 2015-05-12 17:33:39
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²éѯ½á¹û£º¹²²éµ½1327¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×Ä£Äâͼ 19 . dudinoside F C47H74O18 ÏàËÆ¶È:68.0% |

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