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wei537113ͳæ (СÓÐÃûÆø)
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CÆ×£ºMEOD, 400MHZ 25.9, 35.5, 48.8, 61.2, 62.7, 70.3, 74.2, 74.6, 77, 77.8, 99.4, 115.4, 122.6, 124.5, 127.8, 128.4, 128.9, 129.5, 129.7, 129.8, 132.2, 133.3, 155.1, 166, 169.9, 206.2 |
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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£º¹²²éµ½411¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . tremulacin C27H28O11 ÏàËÆ¶È:96.1% Journal of Natural Products 2004 67 659-663 Isolation of Salicin Derivatives from Homalium cochinchinensis and Their Antiviral Activities Tsutomu Ishikawa, Kaori Nishigaya, Kazuko Takami, Hide Uchikoshi, Ih-Sheng Chen, and Ian-Lih Tsai Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . tremulacin C27H28O11 ÏàËÆ¶È:88.4% Journal of Natural Products 2006 69 1300-1304 Dovyalicin-Type Spermidine Alkaloids from Dovyalis Species Bonnie Rasmussen, Aimee-Justine Nkurunziza, Matthias Witt, Hellen A. Oketch-Rabah,Jerzy W. Jaroszewski and Dan Stærk Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . tremulacin ÏàËÆ¶È:88.4% Journal of Natural Products 1991 Vol 54 1447 Chaenomeloidin: A Phenolic Glucoside from Leaves of Salix chaenomeloides Mizuo Mizuno, Masaya Kato, Chiemi Misu, Munekazu Iinuma, Toshiyuki Tanaka Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . tremulacin ÏàËÆ¶È:84.6% Acta Pharmaceutica Sinica 1993 28 437-441 STUDIES ON THE CHEMICAL CONSTITUENTS OF POPULUS TOMENTOSA CARR M Lin and SZ Li Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . salicyl tremuloidin ÏàËÆ¶È:73.0% Journal of Natural Products 2004 67 659-663 Isolation of Salicin Derivatives from Homalium cochinchinensis and Their Antiviral Activities Tsutomu Ishikawa, Kaori Nishigaya, Kazuko Takami, Hide Uchikoshi, Ih-Sheng Chen, and Ian-Lih Tsai Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . cochinchiside B C27H28O12 ÏàËÆ¶È:73.0% Journal of Natural Products 2004 67 659-663 Isolation of Salicin Derivatives from Homalium cochinchinensis and Their Antiviral Activities Tsutomu Ishikawa, Kaori Nishigaya, Kazuko Takami, Hide Uchikoshi, Ih-Sheng Chen, and Ian-Lih Tsai Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . cochinchiside A C27H28O11 ÏàËÆ¶È:69.2% Journal of Natural Products 2004 67 659-663 Isolation of Salicin Derivatives from Homalium cochinchinensis and Their Antiviral Activities Tsutomu Ishikawa, Kaori Nishigaya, Kazuko Takami, Hide Uchikoshi, Ih-Sheng Chen, and Ian-Lih Tsai Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . tremulacinol epimer ÏàËÆ¶È:69.2% Journal of Natural Products 2004 67 659-663 Isolation of Salicin Derivatives from Homalium cochinchinensis and Their Antiviral Activities Tsutomu Ishikawa, Kaori Nishigaya, Kazuko Takami, Hide Uchikoshi, Ih-Sheng Chen, and Ian-Lih Tsai Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . tremulacinol C27H30O11 ÏàËÆ¶È:65.3% Journal of Natural Products 2004 67 659-663 Isolation of Salicin Derivatives from Homalium cochinchinensis and Their Antiviral Activities Tsutomu Ishikawa, Kaori Nishigaya, Kazuko Takami, Hide Uchikoshi, Ih-Sheng Chen, and Ian-Lih Tsai Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . demethylapollinin 7-O-¦Â‑D-glucopyranoside C27H26O10 ÏàËÆ¶È:62.9% Planta Medica 2011 77 1861-1864 Profiling of Phenolics from Tephrosia cinerea Maldini, Mariateresa; Montoro, Paola; Macchia, Mario; Pizza, Cosimo; Piacente, Sonia: Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . salicyloyltremuloidin ÏàËÆ¶È:61.5% Journal of Natural Products 1991 Vol 54 1447 Chaenomeloidin: A Phenolic Glucoside from Leaves of Salix chaenomeloides Mizuo Mizuno, Masaya Kato, Chiemi Misu, Munekazu Iinuma, Toshiyuki Tanaka Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . 2'-O-acetylsalicortin C22H26O11 ÏàËÆ¶È:61.5% Journal of Natural Products 1992 Vol 55 970 Phenolic Glycosides from Salix lasiandra Paul B. Reichardt, Howard M. Merken, Thomas P. Clausen, Jiejun Wu Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . 6-O-[(6''-O-allophanyl)-¦Â-D-glucopyranosyl]-2,5-dihydroxy-7-phenylphenalen-1-one ÏàËÆ¶È:61.5% Phytochemistry 2013 91 165-176 Biosynthesis of tetraoxygenated phenylphenalenones in Wachendorfia thyrsiflora Tobias Munde, Silke Brand, William Hidalgo, Ravi K. Maddula, Aleš Svatoš, Bernd Schneider Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . 6-O-[(6''-Oallophanyl)-¦Â-D-glucopyranosyl]-2,5-dihydroxy-7-phenylphenalen-1-one C27H24N2O11 ÏàËÆ¶È:59.2% Journal of Natural Products 2002 65 1122-1130 Phenylphenalenone-Related Compounds: Chemotaxonomic Markers of the Haemodoraceae from Xiphidium caeruleum Stefan Opitz, Dirk Hölscher, Neil J. Oldham, Stefan Bartram, and Bernd Schneider Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . (4S,5S)-4-(2-anilinocarbonylpyrrolidin-1-ylcarbonyl)-5-(1-naphthyl)-2-phenyl-4,5-dihydrooxazole C31H27N3O3 ÏàËÆ¶È:59.2% Heterocycles 2010 82 603-617 Diastereoselective Cyclization Reactions of Chiral Proline Auxiliary-Substituted N-Benzoyl-¦Á-dehydro(1-naphthyl)alaninamide Derivatives via Photoinduced Electron Transfer Yuhki Sato, Yuhta Haruyama, Tetsutaro Igarashi, and Tadamitsu Sakurai Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . Marinoid E C27H32O12 ÏàËÆ¶È:59.2% Magnetic Resonance in Chemistry 2008 46 638-642 Structure elucidation of five new iridoid glucosides from the leaves of Avicennia marina (pages 638¨C642) Yu Sun, Jie Ouyang, Zhiwei Deng, Qingshan Li and Wenhan Lin Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . lasiandrin C29H32O14 ÏàËÆ¶È:58.6% Journal of Natural Products 1992 Vol 55 970 Phenolic Glycosides from Salix lasiandra Paul B. Reichardt, Howard M. Merken, Thomas P. Clausen, Jiejun Wu Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . 5-(Methoxycarbonyl)pentyl 3,4-di-O-benzoyl-2-O-methyl-¦Á-L-fucopyranosyl-(1¡ú2)-4-O-methyl-¦Â-Dgalactopyranoside C35H46O14 ÏàËÆ¶È:58.0% Molecules 2012 17 9023-9042 Synthesis, Antigenicity Against Human Sera and Structure-Activity Relationships of Carbohydrate Moieties from Toxocara larvae and Their Analogues Akihiko Koizumi, Kimiaki Yamano, Takashi Tsuchiya, Frank Schweizer, Fumiyuki Kiuchi and Noriyasu Hada Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . 10-O-benzoyl-10-O-deacetyldaphylloside C24H28O12 ÏàËÆ¶È:57.6% Helvetica Chimica Acta 2006 Vol. 89 884 Study on the Chemical Constituents of Daphniphyllum angustifolium Haiyun Bai and Lihong Hu Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . eucomoside B C25H31NO11 ÏàËÆ¶È:57.6% Journal of Natural Products 2007 70 1312-1316 Iridoids from the Green Leaves of Eucommia ulmoides Chika Takamura,Tetsuya Hirata,Taro Ueda, Masateru Ono, Hiroyuki Miyashita, Tsuyoshi Ikeda, and Toshihiro Nohara Structure 13C NMR ̼Æ×Ä£Äâͼ |

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