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1 .     (2S,3S,4R,10E)-2-[(2R)-2-hydroxytetracosanoylamino]10-octadecene-1,3,4-triol
    ÏàËÆ¶È:75%
Natural Product Research and Development          2006          18          411-414
Phytochemical Study on Zehneria maysorensis
LI Hong-juan;LUO Ying-gang; HE Zhi-heng; ZHANG Guo-lin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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2 .     ¦Â-D-Galactopyranosyl-(1¡ú1)-3-O-palmitate-¦Á-D-mannopyranoside
C12H22O11     ÏàËÆ¶È:72%
Bioorganic & Medicinal Chemistry          2011          19          4803-4811
Synthesis, gp120 binding and anti-HIV activity of fatty acid esters of 1, 1-linked disaccharides
Stewart Bachan, Jacques Fantini, Anjali Joshi, Himanshu Garg, David R. Mootoo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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3 .     (3S,4S,5R)-1-(¦Á-D-Galactopyranosyl)-3-tetracosanoylamino-4,5-decanediol
C40H79NO8     ÏàËÆ¶È:72%
Bioorganic & Medicinal Chemistry          2012          20          2850-2859
Synthesis and biological evaluation of truncated ¦Á-galactosylceramide derivatives focusing on cytokine induction profile Original Research Article
Tetsuya Toba, Kenji Murata, Junko Futamura, Kyoko Nakanishi, Bitoku Takahashi, Naohiro Takemoto, Minako Tomino, Takashi Nakatsuka, Seiichi Imajo, Megumi Goto, Takashi Yamamura, Sachiko Miyake, Hirokazu Annoura
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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4 .     ceramide
    ÏàËÆ¶È:71.4%
Indian Journal of Chemistry          2007          46B          1868-1872
Antifungal and phytochemical studies of Eupatorium birmanicum DC.
Devi,L Reena; Singh,Th Shyamkeshor; Laitonjam,Warjeet S
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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5 .     paxillamide
C42H85NO6     ÏàËÆ¶È:70.8%
Helvetica Chimica Acta          2004          Vol. 87          1483
Paxillamide: a Novel Phytosphingosine Derivative from the Fruiting Bodies of Paxillus panuoides
Jin-Ming Gao, An-Ling Zhang, Cun-Li Zhang, and Ji-kai Liu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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6 .     (2S,3S,4R)-2-[(2'R-2'-hydroxydocosanoylamino]-1,3,4-octadecanetriol
C40H81NO5     ÏàËÆ¶È:70.8%
Chemical & Pharmaceutical Bulletin          2000          48(9)          1356-1358
Structures of New Ceramides from the Fruit Bodies of Grifola frondasa
Yasunori YAOITA,Takaaki ISHIZUKA, Rie KAKUDA,Koichi MACHIDA and Masao KIKUCHI
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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7 .     (2S,3S,4R)-2-[(2'R-2'-hydroxytricosanoylamino]-1,3,4-octadecanetriol
C41H83NO5     ÏàËÆ¶È:70.8%
Chemical & Pharmaceutical Bulletin          2000          48(9)          1356-1358
Structures of New Ceramides from the Fruit Bodies of Grifola frondasa
Yasunori YAOITA,Takaaki ISHIZUKA, Rie KAKUDA,Koichi MACHIDA and Masao KIKUCHI
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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8 .     (2S,3S,4R)-2-[(2'R-2'-hydroxypentacosanoylamino]-1,3,4-octadecanetriol
C43H87NO5     ÏàËÆ¶È:70.8%
Chemical & Pharmaceutical Bulletin          2000          48(9)          1356-1358
Structures of New Ceramides from the Fruit Bodies of Grifola frondasa
Yasunori YAOITA,Takaaki ISHIZUKA, Rie KAKUDA,Koichi MACHIDA and Masao KIKUCHI
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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9 .     (2S,3S,4R)-2-[(2'R-2'-hydroxyhexacosanoylamino]-1,3,4-octadecanetriol
C44H89NO5     ÏàËÆ¶È:70.8%
Chemical & Pharmaceutical Bulletin          2000          48(9)          1356-1358
Structures of New Ceramides from the Fruit Bodies of Grifola frondasa
Yasunori YAOITA,Takaaki ISHIZUKA, Rie KAKUDA,Koichi MACHIDA and Masao KIKUCHI
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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10 .     (2S,3S,4R,8E)-2-[(2'R)-2'-Hydroxylignoceroylamino]-8(E)-octadecene-1,3,4-triol
C42H83O5N     ÏàËÆ¶È:70.8%
Archives of Pharmacal Research          2005          28          1239-1243
Norditerpenoid alkaloids and other components from the processed tubers of aconitum carmichaeli
Sang Hee Shim, So Young Lee, Ju Sun Kim, Kun Ho Son and Sam Sik Kang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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11 .     (2S,3S,4R)-1-O-(¦Á-D-Galactosyl)-2-tricosanoylamino-1,3,4-nonanetriol
C38H75NO9     ÏàËÆ¶È:70.8%
Bioorganic & Medicinal Chemistry          2012          20          2850-2859
Synthesis and biological evaluation of truncated ¦Á-galactosylceramide derivatives focusing on cytokine induction profile Original Research Article
Tetsuya Toba, Kenji Murata, Junko Futamura, Kyoko Nakanishi, Bitoku Takahashi, Naohiro Takemoto, Minako Tomino, Takashi Nakatsuka, Seiichi Imajo, Megumi Goto, Takashi Yamamura, Sachiko Miyake, Hirokazu Annoura
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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12 .     ¦Â-GalCer
    ÏàËÆ¶È:70.3%
Bioorganic & Medicinal Chemistry Letters          2006          16          2195-2199
Synthesis and biological evaluation of ¦Á-galactosylceramide (KRN7000) and isoglobotrihexosylceramide (iGb3)
Chengfeng Xia, Qingjia Yao, Jens Sch¨¹mann, Emmanuel Rossy, Wenlan Chen, Lizhi Zhu, Wenpeng Zhang, Gennaro De Libero, Peng George Wang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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13 .     AGL-585
C50H98NO9     ÏàËÆ¶È:69.2%
Bioorganic & Medicinal Chemistry          1997          5          2245-2249
Immunostimulatory activities of monoglycosylated ¦Á-d-pyranosylceramides
Akira Uchimura, Toshiyuki Shimizu, Masahiro Morita, Hitomi Ueno, Kazuhiro Motoki, Hideaki Fukushima, Takenori Natori, Yasuhiko Koezuka
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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14 .     1-linoleoyl-3-O-¦Â-D-galactopyranosyl-sn-glycerol
    ÏàËÆ¶È:68%
Chinese Pharmaceutical Journal          2006          41          1374-1375
Studies on Non-Alkaloid Constituent of Amaryllidaceae Species Hippeastrun vittatum(L'Herit.) Herb.
WANG Guang-shu, WANG Ling-yan, YANG Xiao-hong, XU Jingda
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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15 .     agelasphin-7a
C46H91NO10     ÏàËÆ¶È:68%
Tetrahedron          1994          50          2771-2784
Agelasphins, novel antitumor and immunostimulatory cerebrosides from the marine sponge Agelas mauritianus
Takenori Natori, Masahiro Morita, Kohji Akimoto, Yasuhiko Koezuka
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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16 .     agelasphin-9a
C47H93NO10     ÏàËÆ¶È:68%
Tetrahedron          1994          50          2771-2784
Agelasphins, novel antitumor and immunostimulatory cerebrosides from the marine sponge Agelas mauritianus
Takenori Natori, Masahiro Morita, Kohji Akimoto, Yasuhiko Koezuka
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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17 .     sphingolipid
C43H87NO5     ÏàËÆ¶È:66.6%
Chemical & Pharmaceutical Bulletin          2003          51(10)          1193-1195
New Sphingolipids from Marine Sponge Iotrochota baculifera
Pendyala MURALIDHAR,Nallamothu KRISHNA,Muthyala Muralikrishna KUMAR,Chaganty Bheemasankara RAO, and Desaraju Venkata RAO
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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18 .     compound 1
C41H83O4N     ÏàËÆ¶È:66.6%
Journal of Natural Products          2008          71(1)          513-515
Antiepileptic Ceramides from the Red Sea Sponge Negombata corticata
Safwat A. Ahmed, Sherief I. Khalifa, and Mark T. Hamann
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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19 .     acanthacerebroside A
    ÏàËÆ¶È:66.6%
Bulletin of the Chemical Society of Japan          1998          71          259-272
Total Synthesis of Acanthacerebroside A and Astrocerebroside A via a Chiral Epoxide Intermediate Derived from L-Quebrachitol
Noritaka Chida, Noboru Sakata, Katsuyuki Murai, Takahiko Tobe, Toshihiko Nagase, Seiichiro Ogawa
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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20 .     (2S,3S,4R)-1-O-(¦Á-D-Galactosyl)-2-hexacosanoylamino-1,3,4-nonanetriol
C41H81NO9     ÏàËÆ¶È:66.6%
Bioorganic & Medicinal Chemistry          2012          20          2850-2859
Synthesis and biological evaluation of truncated ¦Á-galactosylceramide derivatives focusing on cytokine induction profile Original Research Article
Tetsuya Toba, Kenji Murata, Junko Futamura, Kyoko Nakanishi, Bitoku Takahashi, Naohiro Takemoto, Minako Tomino, Takashi Nakatsuka, Seiichi Imajo, Megumi Goto, Takashi Yamamura, Sachiko Miyake, Hirokazu Annoura
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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21 .     (2S,3S,4R,2'S,3'S)-2-(2',3'-O-isopropylideneicosanoylamino)-1,3,4-docosanetriol
C49H89NO6     ÏàËÆ¶È:66.6%
Journal of Medicinal Chemistry          2006          49          5830-5839
Isolation, Structure Elucidation, Total Synthesis, and Evaluation of New Natural and Synthetic Ceramides on Human SK-MEL-1 Melanoma Cells
Francisco Le¨®n, Ignacio Brouard, Augusto Rivera, Fernando Torres, Sara Rubio, Jos¨¦ Quintana, Francisco Est¨¦vez, and Jaime Bermejo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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22 .     (2S)-2,3-O-Dioctadeca-9Z,12Z-dienoylglyceryl-O-¦Â-D-galactopyranoside
C45H78O10     ÏàËÆ¶È:66.6%
Archives of Pharmacal Research          2012          35          2135-2142
Inhibitory effect on TNF-¦Á-induced IL-8 secretion in HT-29 cell line by glyceroglycolipids from the leaves of Ficus microcarpa
Phan Van Kiem, Chau Van Minh, Nguyen Xuan Nhiem, Nguyen Xuan Cuong, Bui Huu Tai, Tran Hong Quang, Hoang Le Tuan Anh, Pham Hai Yen, Ninh Khac Ban, Seung Hyun Kim, et al.
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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23 .     1,3,5-trihydroxy-2-hexadecanoylamino-(6E,9E)-heptacosdiene
C42H81NO4     ÏàËÆ¶È:65.3%
Chemical & Pharmaceutical Bulletin          2002          50(12)          1558-1560
Novel Sphingolipids from Conyza canadensis
Naveen MUKHTAR, Kiran IQBAL, and Abdul MALIK
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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24 .     (2S,3R,4E,8E,2'R-)-1-O-(¦Â-D-Glucopyranosyl)-N-(2'-hydroxyhexadecanoyl)-4,8-sphinyadienine
    ÏàËÆ¶È:65.3%
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

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25 .     (2S,3S,4R)-1-O-(¦Á-D-Galactosyl)-2-icosanoylamino-1,3,4-nonanetriol
C35H69NO9     ÏàËÆ¶È:64.2%
Bioorganic & Medicinal Chemistry          2012          20          2850-2859
Synthesis and biological evaluation of truncated ¦Á-galactosylceramide derivatives focusing on cytokine induction profile Original Research Article
Tetsuya Toba, Kenji Murata, Junko Futamura, Kyoko Nakanishi, Bitoku Takahashi, Naohiro Takemoto, Minako Tomino, Takashi Nakatsuka, Seiichi Imajo, Megumi Goto, Takashi Yamamura, Sachiko Miyake, Hirokazu Annoura
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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26 .     (2S,3S,4R)-1-O-(¦Á-D-Galactosyl)-2-docosanoylamino-1,3,4-nonanetriol
C37H73NO9     ÏàËÆ¶È:64.2%
Bioorganic & Medicinal Chemistry          2012          20          2850-2859
Synthesis and biological evaluation of truncated ¦Á-galactosylceramide derivatives focusing on cytokine induction profile Original Research Article
Tetsuya Toba, Kenji Murata, Junko Futamura, Kyoko Nakanishi, Bitoku Takahashi, Naohiro Takemoto, Minako Tomino, Takashi Nakatsuka, Seiichi Imajo, Megumi Goto, Takashi Yamamura, Sachiko Miyake, Hirokazu Annoura
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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27 .     (2S,3S,4R)-1-O-(¦Á-D-Galactosyl)-2-pentacosanoylamino-1,3,4-nonanetriol
C40H79NO9     ÏàËÆ¶È:64.2%
Bioorganic & Medicinal Chemistry          2012          20          2850-2859
Synthesis and biological evaluation of truncated ¦Á-galactosylceramide derivatives focusing on cytokine induction profile Original Research Article
Tetsuya Toba, Kenji Murata, Junko Futamura, Kyoko Nakanishi, Bitoku Takahashi, Naohiro Takemoto, Minako Tomino, Takashi Nakatsuka, Seiichi Imajo, Megumi Goto, Takashi Yamamura, Sachiko Miyake, Hirokazu Annoura
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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28 .     (2S,3S,4R)-1-O-(¦Á-D-Galactosyl)-2-octacosanoylamino-1,3,4-nonanetriol
C43H85NO9     ÏàËÆ¶È:64.2%
Bioorganic & Medicinal Chemistry          2012          20          2850-2859
Synthesis and biological evaluation of truncated ¦Á-galactosylceramide derivatives focusing on cytokine induction profile Original Research Article
Tetsuya Toba, Kenji Murata, Junko Futamura, Kyoko Nakanishi, Bitoku Takahashi, Naohiro Takemoto, Minako Tomino, Takashi Nakatsuka, Seiichi Imajo, Megumi Goto, Takashi Yamamura, Sachiko Miyake, Hirokazu Annoura
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

29 .     agelasphin-9b
C48H95NO10     ÏàËÆ¶È:64.2%
Tetrahedron          1994          50          2771-2784
Agelasphins, novel antitumor and immunostimulatory cerebrosides from the marine sponge Agelas mauritianus
Takenori Natori, Masahiro Morita, Kohji Akimoto, Yasuhiko Koezuka
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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30 .     M-2
    ÏàËÆ¶È:64%
Chemical & Pharmaceutical Bulletin          1982          30          3544-3547
Marine Natural Products. X. Pharmacologically Active Glycolipids from the Okinawan Marine Sponge Phyllospongia foliascens (PALLAS)
HIROYUKI KIKUCHI,YASUMASA TSUKITANI,TOSHITAKA MANDA,TAKASHI FUJII,HAJIME NAKANISHI,MOTOMASA KOBAYASHI and ISAO KITAGAWA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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