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| 13C NMR (101 MHz, MeOD) ¦Ä14.1,22.4,24.6,26.3,27.4,28.6,28.8,28.9,29.2,29.3,31.5,33.5,51.4,52.6,56.4,69.9,73.4,76.6,77.3,101.3,114.7,119.0,121.0,123.1,146.2,150.1,169.0,173.7. |
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ÖÁ×ðľ³æ (ÖªÃû×÷¼Ò)
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Ñ©µØÀïµÄÐÇÐÇ: ½ð±Ò+8, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2015-06-05 12:50:20
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Ñ©µØÀïµÄÐÇÐÇ: ½ð±Ò+8, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2015-06-05 12:50:20
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1 . hydroxybenzoic acid 2,3-bis-hexadecanoyloxypropyl esters(d) ÏàËÆ¶È:60.7% Canadian Journal of Chemistry 2006 84 1411-1415 Synthesis and characterization of a series of novel phenol- and polyphenol-based glycerolipids1 Rolf Schmidt, Joseph G. Carrigan, and Christine E. DeWolf Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 2 . (2S,3S,4R)-1-O-(¦Á-D-galactopyranosyl)-2-(N-tetracosanoylamino)-1,3,4-octadecanetriol C48H95NO9 ÏàËÆ¶È:60.7% Journal of Medicinal Chemistry 1995 38 2176-2187 Structure-Activity Relationship of .alpha.-Galactosylceramides against B16-Bearing Mice Masahiro Morita, Kazuhiro Motoki, Kohji Akimoto, Takenori Natori, Teruyuki Sakai, Eiji Sawa, Kazuo Yamaji, Yasuhiko Koezuka, Eiichi Kobayashi, Hideaki Fukushima Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 3 . (2S,3S,4R)-1-O-(¦Á-D-galactopyranosyl)-2-(N-hexacosanoylamino)-1,3,4-octadecanetriol C50H99NO9 ÏàËÆ¶È:60.7% Journal of Medicinal Chemistry 1995 38 2176-2187 Structure-Activity Relationship of .alpha.-Galactosylceramides against B16-Bearing Mice Masahiro Morita, Kazuhiro Motoki, Kohji Akimoto, Takenori Natori, Teruyuki Sakai, Eiji Sawa, Kazuo Yamaji, Yasuhiko Koezuka, Eiichi Kobayashi, Hideaki Fukushima Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 4 . 2-(4'-Hydroxy-3'-methoxyphenyl)ethyl oleate C27H44O4 ÏàËÆ¶È:60.7% Journal of Agricultural and Food Chemistry 2008 56 8897-8904 Convenient Synthesis of Hydroxytyrosol and Its Lipophilic Derivatives from Tyrosol or Homovanillyl Alcohol Roberta Bernini, Enrico Mincione, Maurizio Barontini and Fernanda Crisante Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 5 . Glomeraside F C28H52O7 ÏàËÆ¶È:60.7% Phytochemistry 2012 82 149-157 Cyclic glycolipids from glandular trichome exudates of Cerastium glomeratum Teigo Asai, Yuki Nakamura, Yui Hirayama, Kiyoshi Ohyama, Yoshinori Fujimoto Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 6 . Glomeraside G C28H52O7 ÏàËÆ¶È:60.7% Phytochemistry 2012 82 149-157 Cyclic glycolipids from glandular trichome exudates of Cerastium glomeratum Teigo Asai, Yuki Nakamura, Yui Hirayama, Kiyoshi Ohyama, Yoshinori Fujimoto Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 7 . 28-hydroxysipholenol A C30H52O5 ÏàËÆ¶È:60% Journal of Natural Products 2007 70 928-931 Reversal of P-Glycoprotein-Mediated Multidrug Resistance by Sipholane Triterpenoids Sandeep Jain, Surat Laphookhieo, Zhi Shi, Li-wu Fu, Shin-ichi Akiyama,Zhe-Sheng Chen, Diaa T. A. Youssef,Rob W. M. van Soest,3 and Khalid A. El Sayed Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |

2Â¥2015-06-04 18:18:13

3Â¥2015-06-05 09:42:17













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