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²éѯ½á¹û£º¹²²éµ½329¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . (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 ̼Æ×Ä£Äâͼ 2 . (2S,3R,4E,8 Z,2'R)-1-O-(¦Â-D-Glucopyranosyl)-N-(2'-hydrox yhexadecanoyl)-4,8-sphingadienin ÏàËÆ¶È:73.0% 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 ̼Æ×Ä£Äâͼ 3 . soyacerebroside I ÏàËÆ¶È:72.7% 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 ̼Æ×Ä£Äâͼ 4 . (2S,3S,4R,8Z)-N-Octadecanoyl-1-O-¦Â-D-glucopyranosyl-4-hydroxy-8-sphingenine ÏàËÆ¶È:72.7% Archives of Pharmacal Research 2003 26 132-137 Cerebrosides and terpene glycosides from the root of aster scaber Kwon Hak Cheol, Cho Ock Ryun, Lee Kang Choon and Lee Kang Ro Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . ´ó¶¹ÄÔÜÕI ÏàËÆ¶È:72.7% 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 ̼Æ×Ä£Äâͼ 6 . 1-O-¦Â-D-glucopyranosyl-(2S,3R,4E,8Z)-2[(2(R)-hydroxyhexadecanoyl)amido]-4,8-octadecadiene-1,3-diol ÏàËÆ¶È:72.7% 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 ̼Æ×Ä£Äâͼ 7 . synthetic glucocerebroside ÏàËÆ¶È:69.5% 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 ̼Æ×Ä£Äâͼ 8 . asteriacerebroside G C42H79NO9 ÏàËÆ¶È:68.1% Journal of Natural Products 2006 69 1080-1082 A Ceramide and Cerebroside from the Starfish Asterias amurensis L¨¹tken and Their Plant-Growth Promotion Activities Takahiro Ishii, Tatsufumi Okino, and Yosuke Mino Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . AS-1-1 C38H71NO9 ÏàËÆ¶È:68.1% 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 ̼Æ×Ä£Äâͼ 10 . AS-1-2 C38H71NO9 ÏàËÆ¶È:68.1% 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 ̼Æ×Ä£Äâͼ 11 . AS-1-4 C40H75NO9 ÏàËÆ¶È:68.1% 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 ̼Æ×Ä£Äâͼ 12 . soya-cerebroside I ÏàËÆ¶È:68.1% China Journal of Chinese Materia Medica 2007 32 921-923 Chemical constituents from root of Psammosilene tunicoides LIU Xiaoxiao, WANG Lei, WANG Qiang, QIU Bin Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . (2S,3S,4R,2'R,8Z)-N-2'-Hydroxy-hexadecanoyl-1-O-¦Â-D-glucopyranosyl-4-hydroxy-8-sphingenine ÏàËÆ¶È:68.1% Archives of Pharmacal Research 2003 26 132-137 Cerebrosides and terpene glycosides from the root of aster scaber Kwon Hak Cheol, Cho Ock Ryun, Lee Kang Choon and Lee Kang Ro Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . (2S,3R,4E,8E,2'R)-2-N-(2-hydroxypalmitoyl)-1-O-¦Â-D-glucopyranosyl-9-methyl-4,8-sphingadienine C41H77NO9 ÏàËÆ¶È:68.1% Natural Product Research and Development 2004 16 204-206 THE CHEMICAL CONSTITUENTS OF BASIDIOMYCETE CALODON SUAVEOLENS WANG Fei; LIU Ji-kai * Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . 1-O-(¦Â-D-3-benzoyl-glucopyranosyl)octacosanol C41H72O7 ÏàËÆ¶È:68.1% Indian Journal of Chemistry Section B 1996 35B 988-989 Arundinoide B,a new acylated glucoside from Chlorophytum arundinaceum Mamta Tandon & Y N Shukla Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . CE-1-2 ÏàËÆ¶È:68.1% European Journal of Organic Chemistry 1998 1998 371-378 Isolation and Structure of Biologically Active Glycosphingolipids from the Sea Cucumber Cucumaria echinata Koji Yamada, Eiji Hara, Tomofumi Miyamoto, Ryuichi Higuchi, Ryuichi Isobe and Seiichiroh Honda Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . (2S,3S,4R,2'R,8Z,15'Z)-N-2'-Hydroxy-15'-tetracosenoyl-1-O-¦Â-D-glucopyranosyl-4-hydroxy-8-sphingenine ÏàËÆ¶È:68% Archives of Pharmacal Research 2003 26 132-137 Cerebrosides and terpene glycosides from the root of aster scaber Kwon Hak Cheol, Cho Ock Ryun, Lee Kang Choon and Lee Kang Ro Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . bonaroside C54H91NO17 ÏàËÆ¶È:65.3% Phytochemistry 2001 58 645-651 Glycosides and xanthine oxidase inhibitors from Conyza bonariensis L.D. Kong, Z. Abliz, C.X. Zhou, L.J. Li, C.H.K. Cheng, R.X. Tan Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . compound YA-3-2 ÏàËÆ¶È:65.3% Archives of Pharmacal Research 2003 26 138-142 Cerebrosides from longan arillus Ryu Jiyoung, Kim Ju Sun and Kang Sam Sik Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . rivulacerebroside C46H87NO9 ÏàËÆ¶È:65.3% Chemistry of Natural Compounds 2013 49 694-695 A new cerebroside from Anemone rivularis Jian-Hua Shao, Chun-Chao Zhao, Rui Zhao Structure 13C NMR ̼Æ×Ä£Äâͼ 21 . Ophidiacerebroside D C48H87NO7 ÏàËÆ¶È:65.3% The Journal of Organic Chemistry 1994 59 144-147 Ophidiacerebrosides: cytotoxic glycosphingolipids containing a novel sphingosine from a sea star Wenzao Jin, Kenneth L. Rinehart, Elizabeth A. Jares-Erijman Structure 13C NMR ̼Æ×Ä£Äâͼ 22 . (2S,3R,4E,8E,2R)-1-O-(¦Â-D-glucopyrancosyl)-N-(2'-hydroxyiosanoyl)-4,8-sphingadienine C44H83O9N ÏàËÆ¶È:65.2% Journal of the Chinese Chemical Society 2003 50 1103-1107 Two Cerebrosides and One Acylglycosyl Sterol from Monochoria vaginalis Lie-Ching Row, Chiu-Ming Chen and Jiau-Ching Ho* Structure 13C NMR ̼Æ×Ä£Äâͼ 23 . AS-1-3 C40H75NO9 ÏàËÆ¶È:63.6% 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 ̼Æ×Ä£Äâͼ |
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