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ÈܼÁ£ºßÁठ13C NMR: 16.16,16.18,16.92,17.95,19.61,21.26,22.02,22.12,24.26,25.58,28.52,29.11,32.36,33.78,35.89,37.71,39.58,39.68,41.82,42.05,42.08,46.02,47.42,47.47,47.55,55.53,62.78,72.24,72.50,72.95,78.35,126.04,129.86,136.37,143.70,168.40,171.03 |
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txdydsw: ½ð±Ò+15, ¡ïÓаïÖú 2014-05-21 10:14:27
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txdydsw: ½ð±Ò+15, ¡ïÓаïÖú 2014-05-21 10:14:27
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1 . Isoracemosol A C37H60O8 ÏàËÆ¶È:75.6% Journal of Natural Products 2009 72 791-795 Oleanane-Type Isomeric Triterpenoids from Barringtonia racemosa P. Mangala Gowri, S. V. S. Radhakrishnan, S. Jeelani Basha, A. V. S. Sarma, and J. Madhusudana Rao Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 2 . 21,22-di-O-angeloyl R1-barrigenol ÏàËÆ¶È:75% Chemical & Pharmaceutical Bulletin 1985 33 127-134 Studies on the Constituents of Xanthoceras sorbifolia BUNGE. III. Minor Prosapogenins from the Fruits of Xanthoceras sorbifolia BUNGE YINGJIE CHEN,TADAHIRO TAKEDA and YUKIO OGIHARA Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 3 . hippocaesculin C40H62O8 ÏàËÆ¶È:75% Journal of Natural Products 1986 Vol 49 650 Antitumor Agents, 82. Cytotoxic Sapogenols from Aesculus hippocastanum Takao Konoshima, Kuo-Hsiung Lee Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 4 . 21,22-O-di-angeloyl-R1-barri-genol ÏàËÆ¶È:75% Journal of Shenyang Pharmaceutical University 2005 22 189-192 Chemical constituents of the carpohore of Xanthoceras sorbifolia Bunge LI Wei, LI Xian, LI Zhan-lin, ZHANG Peng, XU Jing, WANG Yi Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 5 . 28-O-¦Â-D-Glucopyranosyl 21-O-angeloyl-R1 barrigenol C41H66O12 ÏàËÆ¶È:73.1% Chemistry of Natural Compounds 2014 50 100-102 Triterpenoid Saponins from the Carpophore of Xanthoceras sorbifolia Wei Li, Xian Li Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 6 . aesculioside IIb C52H82O22 ÏàËÆ¶È:72.9% Phytochemistry 2006 67 784-794 Triterpenoid saponins from the fruits of Aesculus pavia Zhizhen Zhang, Shiyou Li, Shanmin Zhang, David Gorenstein Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 7 . aesculioside IId C46H72O17 ÏàËÆ¶È:72.9% Phytochemistry 2006 67 784-794 Triterpenoid saponins from the fruits of Aesculus pavia Zhizhen Zhang, Shiyou Li, Shanmin Zhang, David Gorenstein Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 8 . 21-O-angeloyl-R1-barrigenol ÏàËÆ¶È:72.9% Journal of Shenyang Pharmaceutical University 2005 22 187-188 Chemical constituents of the carpohore of Xanthoceras sorbifolia Bunge LI Wei, LI Xian, LI Zhan-lin, ZHANG Peng, XU Jing, WANG Yi Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 9 . 21,22-di-O-angeloyl-R1-barrigenol C40H62O8 ÏàËÆ¶È:71.7% Chemical & Pharmaceutical Bulletin 1984 32 3378-3383 Studies on the Constituents of Xanthoceras sorbifolia BUNGE. II. Major Sapogenol and a Prosapogenin from the Fruits of Xanthoceras sorbifolia BUNGE YINGJIE CHEN,TADAHIRO TAKEDA,YUKIO OGIHARA and YOICHI IITAKA Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 10 . Peracetylated 3-O-¦Â-D-glucopyranosyl-oleanolic acid ÏàËÆ¶È:71.4% Journal of the Brazilian Chemical Society 2001 12 32-36 Steroidal and Triterpenoidal Glucosides from Passiflora alata Fl¨¢vio H. Reginatto, Carla Kauffmann, Jan Schripsema, Dominique Guillaume, Grace Gosmann and Eloir P. Schenkel Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 11 . Olean-12-ene-3¦Â,15¦Á,16¦Á,28-tetrol-21-(2-methylbutanoic acid)-22-angelic acid C40H64O8 ÏàËÆ¶È:71.0% Phytochemical Analysis 1995 6 157-163 Prosapogenins from Dodonaea attenuata Andrew Y. T. Han, Leon Van Gorkom, Ian J. McFarlane and Kevin D. Barrow Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 12 . Racemosol A C30H60O8 ÏàËÆ¶È:70.2% Journal of Natural Products 2009 72 791-795 Oleanane-Type Isomeric Triterpenoids from Barringtonia racemosa P. Mangala Gowri, S. V. S. Radhakrishnan, S. Jeelani Basha, A. V. S. Sarma, and J. Madhusudana Rao Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 13 . aesculioside IIc C52H82O21 ÏàËÆ¶È:70.2% Phytochemistry 2006 67 784-794 Triterpenoid saponins from the fruits of Aesculus pavia Zhizhen Zhang, Shiyou Li, Shanmin Zhang, David Gorenstein Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 14 . 2¦Á,3¦Â,21¦Â-trihydroxyolean-12-en-28-oic acid 28-O-¦Â-D-glucopyranoside C36H58O10 ÏàËÆ¶È:70.2% Planta Medica 2009 75 522-527 Antimicrobial Pentacyclic Triterpenoids from Terminalia superba Turibio Kuiate Tabopda, Joseph Ngoupayo, Sheraz A. Khan Tanoli, Anne-Claire Mitaine-Offer,Bonaventure Tchaleu Ngadjui, Muhammad Shaiq Ali, Bang Luu, Marie-Aleth Lacaille-Dubois Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 15 . 2¦Á,3¦Â,29-trihydroxyolean-12-en-28-oic acid 28-O-¦Â-D-glucopyranoside C36H58O10 ÏàËÆ¶È:70.2% Planta Medica 2009 75 522-527 Antimicrobial Pentacyclic Triterpenoids from Terminalia superba Turibio Kuiate Tabopda, Joseph Ngoupayo, Sheraz A. Khan Tanoli, Anne-Claire Mitaine-Offer,Bonaventure Tchaleu Ngadjui, Muhammad Shaiq Ali, Bang Luu, Marie-Aleth Lacaille-Dubois Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 16 . 22-O-angeloylcamelliagenin B C35H54O5 ÏàËÆ¶È:70.2% Chemical & Pharmaceutical Bulletin 1996 44 1899-1907 Bioactive Saponins and Glycosides. V. Acylated Polyhydroxyolean-12-ene Triterpene Oligoglycosides, Camelliasaponins A1, A2, B1, B2, C1, and C11, from the Seeds of Camellia japonica L. : Structures and Inhibitory Activity on Alcohol Absorption Masayuki YOSHIKAWA,Toshiyuki MURAKAMI,Satoshi YOSHIZUMI,Nobutoshi MURAKAMI,Johji YAMAHARA and Hisashi MATSUDA Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 17 . compound 2 ÏàËÆ¶È:70.2% Chinese Chemical Letters 2006 17 211-214 A New Triterpenoid Spaonin Isolated from the Seeds of Aesculus assamica Griff Hong Wei LIU, Xin Sheng YAO, Nai Li WANG, Guo Ping CAI Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 18 . barringtogenol-C21-angelate ÏàËÆ¶È:70.2% Journal of Natural Products 1986 Vol 49 650 Antitumor Agents, 82. Cytotoxic Sapogenols from Aesculus hippocastanum Takao Konoshima, Kuo-Hsiung Lee Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 19 . Saniculagenin N C35H56O7 ÏàËÆ¶È:70.2% Journal of Natural Products 1997 60 1170-1173 Saniculoside N from Sanicula europaea L. Nazlı Arda, Nezhun Gören, Avni Kuru, Thitima Pengsuparp, John M. Pezzuto, Sheng-Xiang Qiu, and Geoffrey A. Cordell Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 20 . aesculioside IVa C57H90O23 ÏàËÆ¶È:70% Phytochemistry 2006 67 784-794 Triterpenoid saponins from the fruits of Aesculus pavia Zhizhen Zhang, Shiyou Li, Shanmin Zhang, David Gorenstein Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 21 . aesculioside IVb C57H90O23 ÏàËÆ¶È:70% Phytochemistry 2006 67 784-794 Triterpenoid saponins from the fruits of Aesculus pavia Zhizhen Zhang, Shiyou Li, Shanmin Zhang, David Gorenstein Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 22 . aesculioside IVc C57H90O22 ÏàËÆ¶È:70% Phytochemistry 2006 67 784-794 Triterpenoid saponins from the fruits of Aesculus pavia Zhizhen Zhang, Shiyou Li, Shanmin Zhang, David Gorenstein Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 23 . 22¦Á-O-[(2Z)-3,7-dimethyl-2,6-octadienoyl]-A1-barrigenol C40H64O6 ÏàËÆ¶È:70% Journal of Natural Products 2006 69 1680-1686 Cytotoxic Oxygenated Triterpenoid Saponins from Symplocos chinensis Guangmiao Fu, Yue Liu, Shishan Yu, Xiangzhong Huang, Youcai Hu, Xiaoguang Chen, and Furong Zhang Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 24 . pittoviridagenin C40H62O8 ÏàËÆ¶È:70% Journal of Natural Products 2002 65 65-68 A New Triterpene Saponin from Pittosporum viridiflorum from the Madagascar Rainforest1 Youngwan Seo,John M. Berger, Jeannine Hoch, Kim M. Neddermann, Isia Bursuker,Steven W. Mamber, and David G. I. Kingston Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 25 . 21,22-diangeloyl-24-hydroxy-R1-barrigenol C40H62O9 ÏàËÆ¶È:70% 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 26 . aesculioside IIa C52H82O22 ÏàËÆ¶È:67.5% Phytochemistry 2006 67 784-794 Triterpenoid saponins from the fruits of Aesculus pavia Zhizhen Zhang, Shiyou Li, Shanmin Zhang, David Gorenstein Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 27 . 22-O-tigloylcamelliagenin B C35H54O5 ÏàËÆ¶È:67.5% Chemical & Pharmaceutical Bulletin 1996 44 1899-1907 Bioactive Saponins and Glycosides. V. Acylated Polyhydroxyolean-12-ene Triterpene Oligoglycosides, Camelliasaponins A1, A2, B1, B2, C1, and C2, from the Seeds of Camellia japonica L. : Structures and Inhibitory Activity on Alcohol Absorption Masayuki YOSHIKAWA,Toshiyuki MURAKAMI,Satoshi YOSHIZUMI,Nobutoshi MURAKAMI,Johji YAMAHARA and Hisashi MATSUDA Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 28 . 22-O-angeloylcamelliagenin C C35H54O6 ÏàËÆ¶È:67.5% Chemical & Pharmaceutical Bulletin 1996 44 1899-1907 Bioactive Saponins and Glycosides. V. Acylated Polyhydroxyolean-12-ene Triterpene Oligoglycosides, Camelliasaponins A1, A2, B1, B2, C1, and C3, from the Seeds of Camellia japonica L. : Structures and Inhibitory Activity on Alcohol Absorption Masayuki YOSHIKAWA,Toshiyuki MURAKAMI,Satoshi YOSHIZUMI,Nobutoshi MURAKAMI,Johji YAMAHARA and Hisashi MATSUDA Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 29 . ¦Á-L-Rhamnopyranosyl oleanolate C36H58O7 ÏàËÆ¶È:67.5% Molecules 2008 13 1472-1486 Facile Synthesis of Oleanolic Acid Monoglycosides and Diglycosides Yu Sha, Mao-Cai Yan, Jiao Liu, Yang Liu and Mao-Sheng Cheng Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 30 . compound IId ÏàËÆ¶È:67.5% Acta Pharmaceutica Sinica 1990 Vol 25 515-521 NEW TRITERPENOIDAL SAPOGENINS FROM THE ROOTS OF GLYCYRRHIZA YUNNANENSIS L Zeng; RY Zhang; P Wei; D Wang; CY Gao and ZC Lou Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |

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