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shaoyan415гæ (СÓÐÃûÆø)
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[ÇóÖú]
GS3---CÆ×ÇóÖú ÒÑÓÐ2È˲ÎÓë
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| 13C NMR (126 MHz, Pyr) ¦Ä 16.60,16.65,17.37,19.65,19.70,19.78,20.20,20.33,22.49,23.47,27.86,28.71,28.95,33.07,35.36,36.92,38.97,39.25,39.27,47.44,48.58,49.78,49.93,50.08,52.17,52.64,54.64,56.92,69.34,72.25,77.47,79.73,141.76154.48,160.37,161.32,199.71,199.90 |
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1 . ganodermacetal C33H50O7 ÏàËÆ¶È:63.1% Phytochemistry Letters 2012 5 576-580 Toxic lanostane triterpenes from the basidiomycete Ganoderma amboinense Sheng-Xiang Yang, Zhao-Cheng Yu, Qiang-Qiang Lu, Wen-Quan Shi, Hartmut Laatsch, Jin-Ming Gao Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . Ganodermacetal ÏàËÆ¶È:63.1% Molecules 2014 19 17478-17535 A Comprehensive Review of the Structure Elucidation and Biological Activity of Triterpenoids from Ganoderma spp. Qing Xia, Huazheng Zhang, Xuefei Sun, Haijuan Zhao, Lingfang Wu, Dan Zhu, Guanghui Yang, Yanyan Shao, Xiaoxue Zhang, Xin Mao, Lanzhen Zhang and Gaimei She Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . 21¦Â, 22¦Á-O-diangeloyl camelliagenin D C40H60O8 ÏàËÆ¶È:61.5% Phytochemistry 2002 59 825-832 Triterpenoid saponins and acylated prosapogenins from Harpullia austro-caledonica Laurence Voutquenne, C¨¦cile Kokougan, Catherine Lavaud,Isabelle Pouny, Marc Litaudon Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . 21¦Â,22¦Á-O-diangeloyl-protoaesciyenin C40H6208 ÏàËÆ¶È:60.5% Phytochemistry 1998 48 1229-1232 Harpuloside a triterpenoid saponin from Harpullia ramiflora C. Dizes, F. Gerald, C. Lavaud, R. Ellas, R. Faure, G. Massiot, G. Balansard Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . Cumingianoside R C37H64O10 ÏàËÆ¶È:60.5% Phytochemistry 2011 72 2205-2211 Triterpenes and a triterpene glucoside from Dysoxylum cumingianum Shin-ichiro Kurimoto, Yoshiki Kashiwada, Kuo-Hsiung Lee, Yoshihisa Takaishi Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . 11¦Á,12¦Á-epoxy-3-O-¦Â-D-xylopyranosylolean-28,13¦Â-olide C35H54O8 ÏàËÆ¶È:60.5% Journal of Asian Natural Products Research 2012 14 333-341 New triterpenoid saponins from Patrinia scabiosifolia Liang Gao,Lin Zhang,Li-Ming Wang,Jiang-Yun Liu,Pei-Lie Cai and Shi-Lin Yang Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . 3¦Â-hydroxyurs-12,19-dien-28-¦Â-D-glucopyranoside ÏàËÆ¶È:60.5% Chinese Traditional and Herbal Drugs 2010 41 1048-1052 Chemical constituents of charred Sanguisorbae Radix(¢ò) XIA Hong-min; ZHONG Ying; SUN Jing-yong; SUN Li-li; AN Kun; WANG Ju Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . compound K C36H62NaO8 ÏàËÆ¶È:60.5% Natural Product Research and Development 2014 26 1552-1556,1567 Chenmical Constituents of Enzymatic Hydrolysate of Total Ginsenoside Extract of Panax quinquefolium JIN Jian-ming, LI You-hua, ZHANG Hai-lun, LIANG Chao-ning, TANG Shuang yan Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 9 . 22-angeloyl-21-epoxyangeloylbarringto-genol C C40H62O8 ÏàËÆ¶È:60% Planta Medica 2005 71 1068-1070 Two New Triterpenes from the Husks of Xanthoceras sorbifolia Zhan-Lin Li , Xian Li , Lin-Hao Li , Ning Li , Ming Yu , Da-Li Meng Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 10 . sutherlandioside B C36H60O10 ÏàËÆ¶È:57.8% Journal of Natural Products 2008 71(10) 1749-1753 Cycloartane Glycosides from Sutherlandia frutescens Xiang Fu, Xing-Cong Li, Troy J. Smillie, Paulo Carvalho, Wilfred Mabusela, James Syce, Quinton Johnson, William Folk, Mitchell A. Avery, and Ikhlas A. Khan Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |
2Â¥2015-03-16 18:44:29
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1 . ganodermacetal C33H50O7 ÏàËÆ¶È:63.1% Phytochemistry Letters 2012 5 576-580 Toxic lanostane triterpenes from the basidiomycete Ganoderma amboinense Sheng-Xiang Yang, Zhao-Cheng Yu, Qiang-Qiang Lu, Wen-Quan Shi, Hartmut Laatsch, Jin-Ming Gao Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 2 . Ganodermacetal ÏàËÆ¶È:63.1% Molecules 2014 19 17478-17535 A Comprehensive Review of the Structure Elucidation and Biological Activity of Triterpenoids from Ganoderma spp. Qing Xia, Huazheng Zhang, Xuefei Sun, Haijuan Zhao, Lingfang Wu, Dan Zhu, Guanghui Yang, Yanyan Shao, Xiaoxue Zhang, Xin Mao, Lanzhen Zhang and Gaimei She Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 3 . 21¦Â, 22¦Á-O-diangeloyl camelliagenin D C40H60O8 ÏàËÆ¶È:61.5% Phytochemistry 2002 59 825-832 Triterpenoid saponins and acylated prosapogenins from Harpullia austro-caledonica Laurence Voutquenne, C¨¦cile Kokougan, Catherine Lavaud,Isabelle Pouny, Marc Litaudon Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 4 . 21¦Â,22¦Á-O-diangeloyl-protoaesciyenin C40H6208 ÏàËÆ¶È:60.5% Phytochemistry 1998 48 1229-1232 Harpuloside a triterpenoid saponin from Harpullia ramiflora C. Dizes, F. Gerald, C. Lavaud, R. Ellas, R. Faure, G. Massiot, G. Balansard Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 5 . Cumingianoside R C37H64O10 ÏàËÆ¶È:60.5% Phytochemistry 2011 72 2205-2211 Triterpenes and a triterpene glucoside from Dysoxylum cumingianum Shin-ichiro Kurimoto, Yoshiki Kashiwada, Kuo-Hsiung Lee, Yoshihisa Takaishi Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 6 . 11¦Á,12¦Á-epoxy-3-O-¦Â-D-xylopyranosylolean-28,13¦Â-olide C35H54O8 ÏàËÆ¶È:60.5% Journal of Asian Natural Products Research 2012 14 333-341 New triterpenoid saponins from Patrinia scabiosifolia Liang Gao,Lin Zhang,Li-Ming Wang,Jiang-Yun Liu,Pei-Lie Cai and Shi-Lin Yang Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 7 . 3¦Â-hydroxyurs-12,19-dien-28-¦Â-D-glucopyranoside ÏàËÆ¶È:60.5% Chinese Traditional and Herbal Drugs 2010 41 1048-1052 Chemical constituents of charred Sanguisorbae Radix(¢ò) XIA Hong-min; ZHONG Ying; SUN Jing-yong; SUN Li-li; AN Kun; WANG Ju Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 8 . compound K C36H62NaO8 ÏàËÆ¶È:60.5% Natural Product Research and Development 2014 26 1552-1556,1567 Chenmical Constituents of Enzymatic Hydrolysate of Total Ginsenoside Extract of Panax quinquefolium JIN Jian-ming, LI You-hua, ZHANG Hai-lun, LIANG Chao-ning, TANG Shuang yan Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 9 . 22-angeloyl-21-epoxyangeloylbarringto-genol C C40H62O8 ÏàËÆ¶È:60% Planta Medica 2005 71 1068-1070 Two New Triterpenes from the Husks of Xanthoceras sorbifolia Zhan-Lin Li , Xian Li , Lin-Hao Li , Ning Li , Ming Yu , Da-Li Meng Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 10 . datiscoside C ÏàËÆ¶È:60% Journal of the Chemical Society, Perkin Transactions 1 1983 1333-1347 New cytotoxic principles from Datisca glomerata Hiroshi Sasamori, K. Sambi Reddy, Michael P. Kirkup, Jeffrey Shabanowitz, David G. Lynn, Sidney M. Hecht, Kwamena A. Woode, Robert F. Bryan, James Campbell, William S. Lynn, Ernst Egert and George M. Sheldrick Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 11 . cumingianoside C ÏàËÆ¶È:58.5% Chemical & Pharmaceutical Bulletin 1997 45 202-206 Antitumor Agents. 169. Dysoxylum cumingianum. V. Cumingianosides P and Q, New Cytotoxic Triterpene Glucosides with an Apotirucallane-Type Skeleton from Dysoxylum cumingianum Toshihiro FUJIOKA,Akio SAKURAI,Kunihide MIHASHI,Yoshiki KASHIWADA,Ih-Sheng CHEN and Kuo-Hsiung LEE Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 12 . sutherlandioside B C36H60O10 ÏàËÆ¶È:57.8% Journal of Natural Products 2008 71(10) 1749-1753 Cycloartane Glycosides from Sutherlandia frutescens Xiang Fu, Xing-Cong Li, Troy J. Smillie, Paulo Carvalho, Wilfred Mabusela, James Syce, Quinton Johnson, William Folk, Mitchell A. Avery, and Ikhlas A. Khan Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 13 . compound K ÏàËÆ¶È:57.8% Chemical & Pharmaceutical Bulletin 1982 30 2393-2398 Studies on the Saponins of Ginseng. IV. On the Structure and Enzymatic Hydrolysis of Ginsenoside-Ra1 HARUYO KOIZUMI,SHUICHI SANADA,YOSHITERU IDA and JUNZO SHOJI Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 14 . 3¦Â-O-(2-deoxy-¦Á-L-arabinohexopyranosyl)-20(29)-lupen-28-oic acid C37H60O7 ÏàËÆ¶È:57.8% Chemistry of Natural Compounds 2006 42 706-709 SYNTHESIS OF METHYL ESTERS OF BETULINIC ACID 2-DEOXY-a-GLYCOSIDES AND 28-OXO-19,28-EPOXYOLEANANE O. B. Flekhter, N. I. Medvedeva, E. V. Tret'yakova,F. Z. Galin, and G. A. Tolstikov Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 15 . compound 63 ÏàËÆ¶È:57.8% Chemistry of Natural Compounds 1992 28 1-23 13C NMR SPECTROSCOPY OF OLEANANE DERIVATIVES A. I. Kalinovskii Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 16 . compound 7 ÏàËÆ¶È:57.8% Chemistry of Natural Compounds 1985 21 605-612 13C NMR SPECTRA OF A NUMBER OF PENTA- AND HEXACYCLIC TRITERPENOIDS DERIVED FROM GLYCYRRHETIC ACID G. A. Tolstikov, L. M. Khalilov, L. A. Baltina, R. M. Kondratenko, A. A. Panasenko, and E. V. Vasil'eva Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 17 . compound SU1 ÏàËÆ¶È:57.8% 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 Structure & 13C NMR ̼Æ×Ä£Äâͼ 18 . cumingianoside M C38H62O11 ÏàËÆ¶È:57.8% Chemical & Pharmaceutical Bulletin 1997 45 68-74 Antitumor Agents. 168. Dysoxylum cumingianum. IV. The Structures of Cumingianosides G-O, New Triterpene Glucosides with a 14, 18-Cycloapotirucallane-Type Skeleton from Dysoxylum cumingianum, and Their Cytotoxicity against Human Cancer Cell Lines Toshihiro FUJIOKA,Akio SAKURAI,Kunihide MIHASHI,Yoshiki KASHIWADA,Ih-Sheng CHEN and Kuo-Hsiung LEE Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 19 . derivative of methyl tormentate C35H54O7 ÏàËÆ¶È:57.8% Phytochemistry 1998 48 171-174 Cecropioic acid, a pentacyclic triterpene from Musanga cecropioides D. Lontsi, B. L. Sondengam, M. T. Martin, B. Bodo Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |

3Â¥2015-03-16 18:46:07













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