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Éñµñ¸çľ³æ (ÕýʽдÊÖ)
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΢Æ×ÇóÖú ÒÑÓÐ1È˲ÎÓë
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| 13C NMR (151 MHz, D2O) ¦Ä 176.08, 175.31, 175.13, 170.71, 109.44, 109.16, 107.81, 107.30, 103.32, 103.06, 102.52, 100.64, 99.97, 99.27, 98.85, 97.13, 96.03, 92.07, 84.51, 84.14, 83.71, 83.19, 82.45, 81.23, 80.46, 79.97, 79.70, 79.11, 79.01, 78.25, 77.72, 76.94, 76.70, 76.44, 76.05, 75.50, 75.24, 74.95, 74.49, 74.22, 74.12, 73.77, 73.61, 73.20, 72.71, 72.63, 72.47, 72.24, 72.15, 71.81, 71.18, 70.72, 70.63, 70.42, 70.15, 69.90, 69.72, 69.43, 69.21, 68.83, 68.51, 68.17, 67.83, 63.19, 61.45, 61.12, 60.93, 59.93, 57.34, 52.75, 30.19, 30.15, 16.68, 16.40. |
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13C NMR (151 MHz, D2O) ¦Ä 16.40,16.68, 30.15, 30.19, 52.75, 57.34, 59.93, 60.93, 61.12,61.45,63.19, 67.83, 68.17, 68.51, 68.83,69.21,69.43, 69.72,69.90,70.15, 70.42,70.63, 70.72, 71.18, 71.81, 72.15,72.24, 72.47, 72.63, 72.71, 73.20, 73.61,73.77,74.12,74.22,74.49,74.95,75.24, 75.50, 76.05,76.44, 76.70,76.94,77.72, 78.25, 79.01, 79.11, 79.70, 79.97, 80.46, 81.23, 82.45, 83.19, 83.71, 84.14, 84.51,92.07, 96.03, 97.13,98.85,99.27,99.97,100.64, 102.52, 103.06, 103.32,107.30, 107.81, 109.16,109.44,170.71, 175.13, 175.31,176.08. |
3Â¥2014-06-25 13:00:06
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²éѯģʽ£ºÄ£ºý²éѯ ̼Æ×Êý¾ÝÊäÈ룺 °´´ÓСµ½´ó˳ÐòÊäÈ룬Êý×Ö¼äÓÃÓ¢Îİë½Ç¶ººÅ(,)·Ö¸ôÀýÈ磺 21.4,30.4,37.4,73.2,73.7,125.6,126.6,139.6,140.2,168.2 ÈܼÁÑ¡Ï Æ¥ÅäÈݲ (Êý×Ö¸ñʽ£¬¿É×ÔÐÐÉ趨) ÏàËÆ¶È£º %(ÏàËÆ¶È>=50%) ²éѯ½á¹û£º¹²²éµ½239¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . compound S3:7 ÏàËÆ¶È:71.6% Archives of Biochemistry and Biophysics 1990 278 297-311 Isolation and structural analysis of three new disialylated oligosaccharides from human milk Gunnar Grönberg, Peter Lipniunas, Torgny Lundgren, Frank Lindh, Bo Nilsson Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . HPS4-2A ÏàËÆ¶È:70.2% Fitoterapia 2013 89 20-32 Structure and antioxidant activity study of sulfated acetamido-polysaccharide from Radix Hedysari Zilong Dang, Demei Feng, Xiaohua Liu, Tao Yang, Long Guo, Jin Liang, Jiandi Liang, Fangdi Hu, Fang Cui, Shilan Feng Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . OS1 ÏàËÆ¶È:64.5% Chemistry-A European Journal 2012 18 3729-3735 Characterization of the Core Oligosaccharide and the O-Antigen Biological Repeating Unit from Halomonas stevensii Lipopolysaccharide: The First Case of O-Antigen Linked to the Inner Core Dr. Giuseppina Pieretti, Sara Carillo, Dr. Buko Lindner, Kwang Kyu Kim, Keun Chul Lee, Jung-Sook Lee, Prof. Dr. Rosa Lanzetta, Prof. Dr. Michelangelo Parrilli and Prof. Dr. Maria Michela Corsaro Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . compound 10 C70H119N7O45 ÏàËÆ¶È:63.5% Tetrahedron Letters 2005 46 4201-4204 Synthesis of a N-glycan nonasaccharide of the bisecting type with additional core-fucose Ralf Schuberth, Carlo Unverzagt Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . lipooligosaccharide ÏàËÆ¶È:62.3% Carbohydrate Research 2012 357 75-82 Structure of the lipopolysaccharide isolated from the novel species Uruburuella suis Alba Silipo, Luisa Sturiale, Cristina De Castro, Rosa Lanzetta, Michelangelo Parrilli, Domenico Garozzo, Antonio Molinaro Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . hupehensis saponin G ÏàËÆ¶È:62.1% Carbohydrate Research 2012 353 49-56 Structure revision of hupehensis saponin F and G and characterization of new trace triterpenoid saponins from Anemone hupehensis by tandem electrospray ionization mass spectrometry Fu Li, Xin Liu, Minghai Tang, Bin Chen, Lisheng Ding, Lijuan Chen, Mingkui Wang Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . CSP-III ÏàËÆ¶È:62.1% Shoyakugaku Zasshi 1990 44 29-37 Further Studies on the Structure of Polysaccharides from the Bark of Melia azadirachta (VII) KUROKAWA YUMI, TAKEDA TADAHIRO,OGIHARA YUKIO Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . GP-3 ÏàËÆ¶È:60.8% Chemical & Pharmaceutical Bulletin 2006 54(3) 287-291 Biologically Active Glycosides from Asteroidea, 42.1) Isolation and Structure of a New Biologically Active Ganglioside Molecular Species from the Starfish Asterina pectinifera Ryuichi HIGUCHI,Shinichi INOUE,Kouji INAGAKI,Maki SAKAI,Tomofumi MIYAMOTO,Tetsuya KOMORI,Masanori INAGAKI,and Ryuichi ISOBE Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . orchidastroside C C77H126O43 ÏàËÆ¶È:59.7% Journal of Natural Products 2010 73 7-11 Steroidal Saponins from Chlorophytum orchidastrum Debabrata Acharya, Anne-Claire Mitaine-Offer, Nutan Kaushik, Tomofumi Miyamoto, Thomas Paululat, Jean-François Mirjolet, Olivier Duchamp and Marie-Aleth Lacaille-Dubois Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . 23-hydroxy-3¦Â-[(O-¦Á-L-rhamnopyranosyl-(1¡ú2)-O-[O-¦Â-D-glucopyranosyl-(1¡ú4)-¦Â-D-glucopyranosyl-(1¡ú4)]-¦Á-L-arabinopyranosyl)oxy]lup-20(29)-en-28-oic acid 28-O-¦Á-L-rhamnopyranosyl-(1¡ú4)-O-¦Â-D-glucopyranosyl-(1¡ú6)-¦Â-D-glucopyranosyl ester C71H116O36 ÏàËÆ¶È:59.4% Journal of Natural Products 2001 64 1226-1229 New Bisdesmosidic Triterpene Saponins from the Roots of Pulsatilla chinensis Yoshihiro Mimaki,Akihito Yokosuka, Minpei Kuroda, Mari Hamanaka, Chiseko Sakuma, and Yutaka Sashida Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . Batatin V C132H212O42 ÏàËÆ¶È:59.2% Phytochemistry 2011 72 773-780 Batatins III¨CVI, glycolipid ester-type dimers from Ipomoea batatas Daniel Rosas-Ram¨ªrez, Edgar Escalante-S¨¢nchez, Rogelio Pereda-Miranda Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . Hederagenin 3-O-¦Â-D-glucopyranosyl(1¡ú3)-¦Á-L-rhamnopyranosyl(1¡ú2)[¦Á-L-rhamnopyranosyl(1¡ú2)-¦Â-D-glucopyranosyl(1¡ú4)]-¦Á-L-arabinopyranosyl-28-O-¦Á-L-rhamnopyranosyl(1¡ú4)-¦Â-D-glucopyranosyl(1¡ú6)-¦Â-D-glucopyranosyl ester ÏàËÆ¶È:58.4% Molecules 2012 17 5520-5531 Saponins with Neuroprotective Effects from the Roots of Pulsatilla cernua Jian-Yu Liu, Ying-Li Guan, Li-Bo Zou, Yi-Xia Gong, Hui-Ming Hua, Yong-Nan Xu, Hui Zhang, Zong-Gui Yu and Wen-Hao Fan Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . orchidastroside B C72H118O39 ÏàËÆ¶È:58.1% Journal of Natural Products 2010 73 7-11 Steroidal Saponins from Chlorophytum orchidastrum Debabrata Acharya, Anne-Claire Mitaine-Offer, Nutan Kaushik, Tomofumi Miyamoto, Thomas Paululat, Jean-François Mirjolet, Olivier Duchamp and Marie-Aleth Lacaille-Dubois Structure 13C NMR ̼Æ×Ä£Äâͼ |

4Â¥2014-06-25 13:07:05














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