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mlkyingгæ (³õÈëÎÄ̳)
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mlkying: ½ð±Ò+8, ¡ï¡ï¡ïºÜÓаïÖú 2015-03-10 15:30:53
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mlkying: ½ð±Ò+8, ¡ï¡ï¡ïºÜÓаïÖú 2015-03-10 15:30:53
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1 . AS-1-3 C40H75NO9 ÏàËÆ¶È:89.4% Chemical & Pharmaceutical Bulletin 1998 46 1153-1156 Isolation and Structure Determination of cerebrosides from Garlic, the Bulbs of Allium sativum L. Masanori INAGAKI,Yasuo HARADA,Koji YAMADA,Ryuichi ISOBE,Ryuichi HIGUCHI,Hiromichi MATSUURA and Yoichi ITAKURA Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 2 . ´ó¶¹ÄÔÜÕI ÏàËÆ¶È:89.4% 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 . SJC-4 ÏàËÆ¶È:85.7% Chemical & Pharmaceutical Bulletin 2005 53(4) 382-386 Constituents of Holothuroidea, 14.1) Isolation and Structure of New Glucocerebroside Molecular Species from the Sea Cucumber Stichopus japonicus Fumiaki KISA, Koji YAMADA, Masafumi KANEKO, Masanori INAGAKI, and Ryuichi HIGUCHI Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 4 . mixture of (2S,3R,4E,8E,10E)-1-(¦Â-D-glucopyranosyloxy)-3-hydroxy-2-[(R)-2-hydroxyheptadecanoyl)amino]-9-methyl-4,8,10-octadecatriene and (2S,3R,4E,8E,10E)-1-(¦Â-D-glucopyranosyloxy)-3-hydroxy-2-[(R)-2-hydroxyoctadecanoyl)amino]-9-methyl-4,8,10-octadecatrie ÏàËÆ¶È:85% Lipids 1998 33 825-827 Isolation and structure of glucosylceramides from the starfish Cosmasterias lurida Marta S. Maier, Anabel Kuriss and Alicia M. Seldes Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 5 . S-1 ÏàËÆ¶È:85% European Journal of Organic Chemistry 1996 1996 593-599 Biologically Active Glycosides from Asteroidea, XXXIV. Isolation and Structure of Cerebrosides from the Starfish Stellaster equestris Ryuichi Higuchi, Yoichiro Harano, Mika Mitsuyuki, Ryuichi Isobe, Koji Yamada, Tomofumi Miyamoto and Tetsuya Komori Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 6 . S-1-3 ÏàËÆ¶È:85% European Journal of Organic Chemistry 1996 1996 593-599 Biologically Active Glycosides from Asteroidea, XXXIV. Isolation and Structure of Cerebrosides from the Starfish Stellaster equestris Ryuichi Higuchi, Yoichiro Harano, Mika Mitsuyuki, Ryuichi Isobe, Koji Yamada, Tomofumi Miyamoto and Tetsuya Komori Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 7 . S-1-5 ÏàËÆ¶È:85% European Journal of Organic Chemistry 1996 1996 593-599 Biologically Active Glycosides from Asteroidea, XXXIV. Isolation and Structure of Cerebrosides from the Starfish Stellaster equestris Ryuichi Higuchi, Yoichiro Harano, Mika Mitsuyuki, Ryuichi Isobe, Koji Yamada, Tomofumi Miyamoto and Tetsuya Komori Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 8 . AS-1-1 C38H71NO9 ÏàËÆ¶È:84.2% Chemical & Pharmaceutical Bulletin 1998 46 1153-1156 Isolation and Structure Determination of cerebrosides from Garlic, the Bulbs of Allium sativum L. Masanori INAGAKI,Yasuo HARADA,Koji YAMADA,Ryuichi ISOBE,Ryuichi HIGUCHI,Hiromichi MATSUURA and Yoichi ITAKURA Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 9 . AS-1-2 C38H71NO9 ÏàËÆ¶È:84.2% Chemical & Pharmaceutical Bulletin 1998 46 1153-1156 Isolation and Structure Determination of cerebrosides from Garlic, the Bulbs of Allium sativum L. Masanori INAGAKI,Yasuo HARADA,Koji YAMADA,Ryuichi ISOBE,Ryuichi HIGUCHI,Hiromichi MATSUURA and Yoichi ITAKURA Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 10 . AS-1-4 C40H75NO9 ÏàËÆ¶È:84.2% Chemical & Pharmaceutical Bulletin 1998 46 1153-1156 Isolation and Structure Determination of cerebrosides from Garlic, the Bulbs of Allium sativum L. Masanori INAGAKI,Yasuo HARADA,Koji YAMADA,Ryuichi ISOBE,Ryuichi HIGUCHI,Hiromichi MATSUURA and Yoichi ITAKURA Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 11 . acanthaccrebroside D C46H87O9N ÏàËÆ¶È:84.2% European Journal of Organic Chemistry 1988 1988 19-24 Biologically active glycosides from asteroidea, XIII. Glycosphingolipids from the starfish Acanthaster planci, 2. Isolation and structure of six new cerebrosides Yasuhiro Kawano, Ryuichi Higuchi, Ryuichi Isobe and Tetsuya Komori Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 12 . acanthaccrebroside E C47H89O9N ÏàËÆ¶È:84.2% European Journal of Organic Chemistry 1988 1988 19-24 Biologically active glycosides from asteroidea, XIII. Glycosphingolipids from the starfish Acanthaster planci, 2. Isolation and structure of six new cerebrosides Yasuhiro Kawano, Ryuichi Higuchi, Ryuichi Isobe and Tetsuya Komori Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 13 . acanthaccrebroside F C48H91O9N ÏàËÆ¶È:84.2% European Journal of Organic Chemistry 1988 1988 19-24 Biologically active glycosides from asteroidea, XIII. Glycosphingolipids from the starfish Acanthaster planci, 2. Isolation and structure of six new cerebrosides Yasuhiro Kawano, Ryuichi Higuchi, Ryuichi Isobe and Tetsuya Komori Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 14 . 1-O-(¦Â-D-glucopyranosyl)-(2S,3R,4E)-2-[(2R,13Z)-2-hydroxy-13-docosenoylamino]-1,3-dihydroxy-4-hexadecene ÏàËÆ¶È:84.2% Chemical & Pharmaceutical Bulletin 2004 52 1307-1311 Constituents of Crinoidea, 4. Isolation and Structure of Ceramides and Glucocerebrosides from the Feather Star Comanthus japonica Masanori Inagaki, Akemi Oyama, Kazuyoshi Arao, Ryuichi Higuchi Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 15 . HLC-2 ÏàËÆ¶È:84.2% Chemical & Pharmaceutical Bulletin 2005 53 788-791 Constituents of Holothuroidea, 15. Isolation of Ante-iso Type Regio-isomer on Long Chain Base Moiety of Glucocerebroside from the Sea Cucumber Holothuria leucospilota Koji Yamada, Noriko Wada, Hiroyuki Onaka, Rei Matsubara, Ryuichi Isobe, Masanori Inagaki, Ryuichi Higuchi Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 16 . soyacerebroside I ÏàËÆ¶È:80.9% 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 17 . soyacerebroside II ÏàËÆ¶È:80.9% 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 18 . 1-O-¦Â-D-glucopyranosyl-(2S,3R,4E,8Z)-2[(2(R)-hydroxyhexadecanoyl)amido]-4,8-octadecadiene-1,3-diol ÏàËÆ¶È:80% Natural Product Research and Development 2005 17 409-411 Chemical Constituents in the Roots of Linum usitatissimum L. LIANG Zhi;WANG Ying-hong; LI Zhi-hong; QIN Hai-lin Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 19 . S-1-4 ÏàËÆ¶È:80% European Journal of Organic Chemistry 1996 1996 593-599 Biologically Active Glycosides from Asteroidea, XXXIV. Isolation and Structure of Cerebrosides from the Starfish Stellaster equestris Ryuichi Higuchi, Yoichiro Harano, Mika Mitsuyuki, Ryuichi Isobe, Koji Yamada, Tomofumi Miyamoto and Tetsuya Komori Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 20 . SJC-1 ÏàËÆ¶È:78.9% Chemical & Pharmaceutical Bulletin 2005 53(4) 382-386 Constituents of Holothuroidea, 14.1) Isolation and Structure of New Glucocerebroside Molecular Species from the Sea Cucumber Stichopus japonicus Fumiaki KISA, Koji YAMADA, Masafumi KANEKO, Masanori INAGAKI, and Ryuichi HIGUCHI Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |
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