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xielitingгæ (ÖøÃûдÊÖ)
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[ÇóÖú]
̼Æ×ÇóÖú ÒÑÓÐ1È˲ÎÓë
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13C NMR (126 MHz, MeOD) ¦Ä 7.23,7.78,7.89,14.44,23.62,23.73, 24.84,26.09, 26.53,28.14,28.16,28.25,30.22,30.29,30.42,30.47,30.60,30.69,30.75,30.77,31.32,32.66,33.07,34.96,55.67, 61.56,70.90,102.16,102.37,105.65,109.09, 110.25,114.93,115.06, 115.15,122.80,129.00,129.04,129.10,130.80,130.86,130.92,131.22,132.60,155.20, 177.67,177.70,177.74 |
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xieliting: ½ð±Ò+15, ¡ïÓаïÖú 2015-06-09 09:12:16
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xieliting: ½ð±Ò+15, ¡ïÓаïÖú 2015-06-09 09:12:16
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²éѯ½á¹û£º¹²²éµ½35¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . 4-O-podophyllotoxinyl 12-[12'(octadec-Z-9'',12''-dienacyloxy)octadec-Z-9'-enacyloxy]octadec-Z-9-enoate C76H116O13 ÏàËÆ¶È:69.3% Lipids 2004 39 659-666 Synthesis, spectroscopic, and biological studies of novel estolides derived from anticancer active 4-O-podophyllotoxinyl 12-hydroxyl-octadec-Z-9-enoate Jamal Mustafa, Shabana I. Khan, Guoyi Ma, Larry A. Walker and Ikhlas A. Khan Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 2 . 4-O-podophyllotoxinyl 12-(eicosa-Z-5',8',11',14'-tetraenacyloxy)octadec-Z-9-enoate C60H84O11 ÏàËÆ¶È:68% Lipids 2004 39 659-666 Synthesis, spectroscopic, and biological studies of novel estolides derived from anticancer active 4-O-podophyllotoxinyl 12-hydroxyl-octadec-Z-9-enoate Jamal Mustafa, Shabana I. Khan, Guoyi Ma, Larry A. Walker and Ikhlas A. Khan Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 3 . PX12 ÏàËÆ¶È:66.6% Journal of the Chemical Society, Perkin Transactions 1 1996 2651-2656 Preparative transformation of natural phospholipids catalysed by phospholipase D from Streptomyces Paola D'Arrigo, Lorenzo de Ferra, Valentino Piergianni, Antonio Selva, Stefano Servi and Alberto Strini Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 4 . 4-O-podophyllotoxinyl 12-(octadec-Z-9',12'-dienacyloxy)octadec-Z-9-enoate C58H84O11 ÏàËÆ¶È:66.6% Lipids 2004 39 659-666 Synthesis, spectroscopic, and biological studies of novel estolides derived from anticancer active 4-O-podophyllotoxinyl 12-hydroxyl-octadec-Z-9-enoate Jamal Mustafa, Shabana I. Khan, Guoyi Ma, Larry A. Walker and Ikhlas A. Khan Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 5 . (2S)-1-O-Arachidoyl-2-O-palmitoyl-3-O-(¦Â-D-galactopyranosyl-6-1¦Á-D-galactopyranosyl)-glycerol C51H88O15 ÏàËÆ¶È:64.7% Journal of Applied Phycology 2013 25 951-960 Five new galactolipids from the freshwater microalga Porphyridium aerugineum and their nitric oxide inhibitory activity Arjun H. Banskota & Roumiana Stefanova & Sandra Sperker & Ronald Melanson & Jane A. Osborne & Stephen J. B. O¡¯Leary Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 6 . (2S)-1,2-O-diacylglyceryl ¦Â-D-galactopyranoside ÏàËÆ¶È:64.5% Bulletin of the Korean Chemical Society 1992 13 584-586 New Glyceroglycolipids from the Brown Alga Sargassum thunbergii Byeng-Wha Son*, Yong-Jin Cho, Nam-Kil Kim, Hong-Dae Choi Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 7 . 4-O-podophyllotoxinyl 12-(eicosanacyloxy)octadec-Z-9-enoate C60H92O11 ÏàËÆ¶È:64.5% Lipids 2004 39 659-666 Synthesis, spectroscopic, and biological studies of novel estolides derived from anticancer active 4-O-podophyllotoxinyl 12-hydroxyl-octadec-Z-9-enoate Jamal Mustafa, Shabana I. Khan, Guoyi Ma, Larry A. Walker and Ikhlas A. Khan Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 8 . 4-O-podophyllotoxinyl 12-(octadec-Z-9'-enacyloxy)octadec-Z-9-enoate C58H86O11 ÏàËÆ¶È:63.2% Lipids 2004 39 659-666 Synthesis, spectroscopic, and biological studies of novel estolides derived from anticancer active 4-O-podophyllotoxinyl 12-hydroxyl-octadec-Z-9-enoate Jamal Mustafa, Shabana I. Khan, Guoyi Ma, Larry A. Walker and Ikhlas A. Khan Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 9 . 4-O-podophyllotoxinyl 12-(octadec-Z-9',12',15'-trienacyloxy)octadec-Z-9-enoate C58H82O11 ÏàËÆ¶È:63.2% Lipids 2004 39 659-666 Synthesis, spectroscopic, and biological studies of novel estolides derived from anticancer active 4-O-podophyllotoxinyl 12-hydroxyl-octadec-Z-9-enoate Jamal Mustafa, Shabana I. Khan, Guoyi Ma, Larry A. Walker and Ikhlas A. Khan Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 10 . (2S)-1-O-eicosapentaenoyl-2-O-myristoyl-3-O-(¦Â-D-galactopyranosyl-6-1¦Á-D-galactopyranosyl)-glycero C49H82O15 ÏàËÆ¶È:63.2% Journal of Applied Phycology 2013 25 349-357 Mono- and digalactosyldiacylglycerols: potent nitric oxide inhibitors from the marine microalga Nannochloropsis granulata Arjun H. Banskota, Roumiana Stefanova, Pamela Gallant, Patrick J. McGinn Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 11 . crispin B C51H85NO12 ÏàËÆ¶È:62.7% Chemistry & Biodiversity 2007 Vol. 4 917 Two New Protease-Inhibiting Glycosphingolipids from Buddleja crispa Ijaz Ahmad, Itrat Anis, Itrat Fatima, Abdul Malik, Shafiullah Khan, Nighat Afza, Rasool Bakhsh Tareen, Muhammad Arif Lodhi, and M. Iqbal Choudhary Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 12 . (2S)-1-O-eicosapentaenoyl-2-O-palmitoyl-3-O-(¦Â-D-galactopyranosyl-6-1¦Á-D-galactopyranosyl)-glycerol C51H86O15 ÏàËÆ¶È:62.7% Journal of Applied Phycology 2013 25 349-357 Mono- and digalactosyldiacylglycerols: potent nitric oxide inhibitors from the marine microalga Nannochloropsis granulata Arjun H. Banskota, Roumiana Stefanova, Pamela Gallant, Patrick J. McGinn Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 13 . compound 2 C67H116O16 ÏàËÆ¶È:62.5% Phytochemistry 2008 69 2856-2861 Glycerogalactolipids from the fruit of Lycium barbarum Zengping Gao, Zulfiqar Ali, Ikhlas A. Khan Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 14 . belamcandone A Monoacetate C46H70O8 ÏàËÆ¶È:62.5% Phytochemistry 1995 38 703-709 Belamcandones A-D, dioxotetrahydrodibenzofurans from Belamcanda chinensis Katsura Seki, Kazuo Haga, Ryohei Kaneko Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 15 . belamcandone A Diacetate C48H72O9 ÏàËÆ¶È:62.5% Phytochemistry 1995 38 703-709 Belamcandones A-D, dioxotetrahydrodibenzofurans from Belamcanda chinensis Katsura Seki, Kazuo Haga, Ryohei Kaneko Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 16 . belamcandone A Diacetate C48H72O9 ÏàËÆ¶È:62.5% Phytochemistry 1995 38 703-709 Belamcandones A-D, dioxotetrahydrodibenzofurans from Belamcanda chinensis Katsura Seki, Kazuo Haga, Ryohei Kaneko Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 17 . Triacylglycerol(TAG) C59H106O6 ÏàËÆ¶È:62.5% Chemistry & Biodiversity 2011 Vol.8 1033-1051 Reinvestigation of Coenzyme Q10 Isolation from Sporidiobolus johnsonii David D. Dixson, Christopher N. Boddy, Robert P. Doyle Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 18 . 4-O-podophyllotoxinyl 12-[12'(12''-hydroxyl-octadec-Z-9''-enacyloxy)octadec-Z-9'-enacyloxy]octadec-Z-9-enoate C76H118O14 ÏàËÆ¶È:62.5% Lipids 2004 39 659-666 Synthesis, spectroscopic, and biological studies of novel estolides derived from anticancer active 4-O-podophyllotoxinyl 12-hydroxyl-octadec-Z-9-enoate Jamal Mustafa, Shabana I. Khan, Guoyi Ma, Larry A. Walker and Ikhlas A. Khan Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 19 . {1-[(12E,16E)-12,16-eicosadienoyl]-2-[(E,E)-7,11-octadecadienoyl]-3-stearoylglycerol} ÏàËÆ¶È:62.5% Chinese Traditional and Herbal Drugs 2013 44 24-30 Chemical constituents in aerial parts of Polygonum capitatum WANG Hong-ping, CAO Fang, YANG Xiu-wei Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 20 . (2S)-1-O-eicosapentaenoyl-2-O-palmitoyl-3-O-(6-sulfo-¦Á-D-quinovopyranosyl)-glycerol C45H52O12S ÏàËÆ¶È:62.5% Phytochemistry 2014 101 101-108 Polar lipids from the marine macroalga Palmaria palmata inhibit lipopolysaccharide-induced nitric oxide production in RAW264.7 macrophage cells Arjun H. Banskota, Roumiana Stefanova, Sandra Sperker, Santosh P. Lall, James S. Craigie, Jeff T. Hafting, Alan T. Critchley Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 21 . glyceryl-1-octadec-9',12',15'-trienoyl-2-octadec-9'',12''-dienoyl-3-hexadecanoate C55H96O6 ÏàËÆ¶È:62.5% Asian Journal of Chemistry 2012 24 885-889 Chemical Constituents from the Fruits of Lycium chinense and Antioxidant Activity ILL-MIN CHUNG, NAGELLA PRAVEEN, SUN-JIN KIM and ATEEQUE AHMAD Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |

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