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2Â¥2013-01-13 20:13:36
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3Â¥2013-01-13 21:13:16
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²éѯ½á¹û£º¹²²éµ½760¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ |

4Â¥2013-01-14 13:42:16














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