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| 13C NMR (201 MHz, MeOD) ¦Ä 14.5,23.8,26.2,27.9,28.3,33.1,33.7,35.9,54.7,62.7,69.8,71.6,72.9,73.1,75.0,77.9,78.0,104.7,129.9,131.4,131.4,134.4,177.3 |
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1012caijuan: ½ð±Ò+10, ¡ï¡ï¡ïºÜÓаïÖú 2015-01-14 20:10:25
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1012caijuan: ½ð±Ò+10, ¡ï¡ï¡ïºÜÓаïÖú 2015-01-14 20:10:25
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1 . (4E)-1-O-(¦Â-glucopyranosyl)-N-(2'-hydroxytetracosanoyl)-4,8-sphingadienine C48H91NO9 ÏàËÆ¶È:88.4% Records of Natural Products 2014 4 348-353 New Compounds from the Tree Fern Metaxya rostrata C. Presl Kerstin Kainz, Martin Zehl, Johanna Bleier, Barbara Merkinger, Teresa Pemmer, Natalie Schmidt, Johannes Winkler, Hanspeter Kählig and Liselotte Krenn Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . ´ó¶¹ÄÔÜÕI ÏàËÆ¶È:82.6% Chinese Pharmaceutical Journal 2010 45 16-18 A New Flavone from Reineckea carnea ZHOU Xin, LIU Hai, GONG Xiao-jian, ZHAO Chao, CHENG Hua-guo Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . soyacerebroside II ÏàËÆ¶È:82.6% China Journal of Chinese Materia Medica 2014 39 258-261 Chemical constituents from leaves of Ilex latifolia WANG Cun-qin, WANG Lei, LI Bao-jing, FAN Chun-lin, HUANG Xiao-jun, YE Wen-cai Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . soyacerebroside I ÏàËÆ¶È:78.2% China Journal of Chinese Materia Medica 2010 35 2704-2707 Nonvolatile chemical constituents from Pogostemon cablin WANG Dahai; YIN Zhiqi; ZHANG Qingwen; YE Wencai; ZHANG Xiaoqi; ZHANG Jian Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . (2S,3R,4E,8E,2'R-)-1-O-(¦Â-D-Glucopyranosyl)-N-(2'-hydroxyhexadecanoyl)-4,8-sphinyadienine ÏàËÆ¶È:76.9% European Journal of Organic Chemistry 1988 1988 807-814 Synthesis of sphingosine relatives, VII. Synthesis of anti-ulcerogenic cerebrosides isolated from Tetragonia tetragonoides Kenji Mori and Takeshi Kinsho Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . (2S,3R,4E,8 Z,2'R)-1-O-(¦Â-D-Glucopyranosyl)-N-(2'-hydrox yhexadecanoyl)-4,8-sphingadienin ÏàËÆ¶È:76.9% European Journal of Organic Chemistry 1988 1988 807-814 Synthesis of sphingosine relatives, VII. Synthesis of anti-ulcerogenic cerebrosides isolated from Tetragonia tetragonoides Kenji Mori and Takeshi Kinsho Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . 1-O-¦Â-D-glucopyranosyl-(2S,3S,4R,10Z)-2-[(2'R)-2'-hydroxylignocenoyl-amino]-10-octadecene-1,3,4-triol C48H93O10N ÏàËÆ¶È:75% Natural Product Research 2009 23 1330-1336 A new cerebroside from Gynura divaricata Lei Chen; Jin-Jiang Wang; Guo-Gang Zhang; Hong-Tao Song; Lu-Ping Qin Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . aralia cerebroside (1-O-¦Â-D-glucopyranosyl-(2S,3S,4R,8Z)-2-[(2'R)-2'-hydorxypalmitoylamino]-8-octadecene-1,3,4-triol) ÏàËÆ¶È:75% Korean Journal of Pharmacognosy 2006 37(2) 81-84 Isolation of a Cerebroside from Panax notoginseng Cho, Min-Jung; Lee, So-Young; Kim, Ju-Sun; Lee, Je-Hyun; Choi, Hwan-Soo; Lee, Ho-Young; Ha, Hye-Kyung; Kim, Chung-Sook; Kang, Sam-Sik Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 9 . glucocerebroside ÏàËÆ¶È:73.9% Acta Botanica Yunnanica 2001 23(3) 385-393 The Constituents of Russula ochroleuca Basidiomycetes GAO Jin-Ming,SHENGJie,YANG Xue,LIU Ji-Kai Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 10 . Eriophytonoide ÏàËÆ¶È:73.9% Steroids 2004 69 809-815 Phytoecdysteroids and glycoceramides from Eriophyton wallchii Jinhai Yi, Yinggang Luo, Bogang Li, Guolin Zhang Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |
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