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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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×Ä£Äâͼ
2Â¥2013-12-08 16:02:56
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