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ÈܼÁ£ºDMSO 170.4, 170.2, 169.4, 169.2, 146.2, 136.0, 134.7, 114.0, 78.3, 73.1, 69.5, 69.1, 68.9, 67.8, 67.2, 47.0, 44.8, 43.2, 39.7, 37.7, 27.8, 25.9, 21.3, 21.1, 20.9, 20.7, 15.6, 13.3 [ Last edited by karl2100 on 2013-3-14 at 22:44 ] |
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²éѯ½á¹û£º¹²²éµ½12¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . 10,13-Deacetylabeobaccatin IV C28H40O12 ÏàËÆ¶È:71.4% Phytochemistry 1995 39 869-870 A rearranged taxane from the Himalayan yew Sunil K. Chattopadhyay, Ram P. Sharma, Giovanni Appendino, Pierluigi Gariboldi Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . taxumairol O C28H42O13 ÏàËÆ¶È:65.5% Journal of Natural Products 2000 63 720-722 New Taxanes with an Opened Oxetane Ring from the Roots of Taxus mairei Ya-Ching Shen, Kuang-Liang Lo,Ching-Yeu Chen,Yao-Haur Kuo,and Meng-Chieh Hung Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . taxa-4(20),11-diene-2¦Á,5¦Á,10¦Âtriacetoxy-14¦Â,2-methybutyrate ÏàËÆ¶È:58.0% Chinese Traditional and Herbal Drugs 2007 38 979-982 Chemical constituents in heartwood of Taxus yunnanensis CHEN Xue-ying; LIANG Jing-yu Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . per-O-acetylated'4'-O-(¦Á-D-Mannopyranosyl)glucosinalbin C36H44NO23S2K ÏàËÆ¶È:55.5% European Journal of Organic Chemistry 2010 3657-3664 Glucosinolate Chemistry: Synthesis of O-Glycosylated Derivatives of Glucosinalbin David Gueyrard, Renato Iori, Arnaud Tatibouët and Patrick Rollin Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . N-(octa-O-acetyllactobionyl)-2-methyl-2-hydroxylaminopropanamide ÏàËÆ¶È:55.5% Journal of Medicinal Chemistry 2010 53 4849-4861 Amphiphilic Amide Nitrones: A New Class of Protective Agents Acting as Modifiers of Mitochondrial Metabolism Gr¨¦gory Durand, Burkhard Poeggeler, St¨¦phanie Ortial, Ange Polidori, Frederick A. Villamena, Jutta Böker, R¨¹diger Hardeland, Miguel A. Pappolla and Bernard Pucci Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . per-O-acetylated'4'-O-(¦Á-L-Rhamnopyranosyl)glucosinalbin C34H42NO21S2K ÏàËÆ¶È:53.5% European Journal of Organic Chemistry 2010 3657-3664 Glucosinolate Chemistry: Synthesis of O-Glycosylated Derivatives of Glucosinalbin David Gueyrard, Renato Iori, Arnaud Tatibouët and Patrick Rollin Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . per-O-acetylated'4'-O-(¦Â-D-galactopyranosyl)glucosinalbin C36H44NO23S2K ÏàËÆ¶È:53.5% European Journal of Organic Chemistry 2010 3657-3664 Glucosinolate Chemistry: Synthesis of O-Glycosylated Derivatives of Glucosinalbin David Gueyrard, Renato Iori, Arnaud Tatibouët and Patrick Rollin Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . 10-O-acetylpatrinoside-aglycone-11-O-[4''-O-acetyl-¦Á-L-rhamnopyranosyl-(1¡ú2)-¦Â-D-glucopyranoside] C31H48O17 ÏàËÆ¶È:53.3% Journal of Natural Products 2009 72 1798-1803 Iridoid Glycosides from the Leaves of Sambucus ebulus Valerio Pieri, Stefan Schwaiger, Ernst P. Ellmerer, and Hermann Stuppner Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . trans-5-[2-(2-amino-6-chloropurin-7-yl)ethyl]-2-D-ribo-(1',2',3',4'-tetraacetoxybutyl)-1,3-dioxane C23H30ClN5O10 ÏàËÆ¶È:51.8% Journal of Heterocyclic Chemistry 2001 38 45-51 Synthesis of 5-[2-(guanin-9-yl)- and 5-[2-(2-aminopurin-9-yl)ethyl]-2-D-ribo-(1,2',3',4'-tetrahydroxybutyl)-1,3-dioxane Dae-Kee Kim, Young-Woo Kim and Namkyu Lee Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . compound 13 ÏàËÆ¶È:51.7% Bioorganic & Medicinal Chemistry Letters 2011 21 6319-6321 Biological evaluation of glycosyl-isoindigo derivatives against the pathogenic agents of tropical diseases (malaria, Chagas disease, leishmaniasis and human African trypanosomiasis) Fadoua Bouchikhi, Fabrice Anizon, Reto Brun, Pascale Moreau Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . 10-O-acetylpatrinoside-aglycone-11-O-[4''-O-acetyl-¦Á-L-rhamnopyranosyl-(1¡ú2)-¦Â-D-ribohexo-3-ulopyranoside] C31H46O17 ÏàËÆ¶È:50% Journal of Natural Products 2009 72 1798-1803 Iridoid Glycosides from the Leaves of Sambucus ebulus Valerio Pieri, Stefan Schwaiger, Ernst P. Ellmerer, and Hermann Stuppner Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . renillin C C28H40O9 ÏàËÆ¶È:50% Journal of Natural Products 2005 68 511-516 Isolation and Structure Elucidation of Feeding Deterrent Diterpenoids from the Sea Pansy, Renilla reniformis Todd Barsby, and Julia Kubanek Structure 13C NMR ̼Æ×Ä£Äâͼ |

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