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1 . ceramide ÏàËÆ¶È:78.5% 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 2 . phytoceramide C36H71NO4 ÏàËÆ¶È:78.5% Molecules 2011 16 9090-9100 Phytoceramide Shows Neuroprotection and Ameliorates Scopolamine-Induced Memory Impairment Jae-Chul Jung, Yeonju Lee, Sohyeon Moon, Jong Hoon Ryu and Seikwan Oh Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . 1-O-¦Â-D-glucopyranosyl-(2S,3S,4R,8E)-2-[(2'R)-2'-hydroxypalmitoyl amino]-8-octadecene-1,3,4-triol ÏàËÆ¶È:75% Natural Product Research and Development 2005 17 298-300 Studies on Chemical Constituents of Polygala aureocauda HUANG Zhao-hui; XU Kang-ping; ZHOU Ying-jun; HU Gao-yun; TAN Gui-shan Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . paxillamide C42H85NO6 ÏàËÆ¶È:74.0% 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 5 . N-palmitoyl-octadecasphinga-4(E),8(E)-dienine C34H65NO3 ÏàËÆ¶È:74.0% Journal of Natural Products 1995 Vol 58 948-953 Isolation of New Ceramides from the Gorgonian Acabaria undulata Jongheon Shin, Youngwan Seo Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . drechslerol-B C40H76O3 ÏàËÆ¶È:74.0% Phytochemistry 1989 28 2089-2091 Drechslerol-B,A host-selective phytotoxin produced by Drechslera maydis R.S. Shukla,K. Agrawal,R.S. Thakur,A. Husain Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . (2'S,3'S,4'R)-1D-(1,2,3/4,5)-5-O-(2'-hexacosanoylamino-3',4'-dihydroxyoctadecyl)cyclohexanepentol C50H99NO8 ÏàËÆ¶È:74.0% Bioorganic & Medicinal Chemistry 2009 17 6360-6373 RCAI-37, 56, 59, 60, 92, 101, and 102, cyclitol and carbasugar analogs of KRN7000: Their synthesis and bioactivity for mouse lymphocytes to produce Th1-biased cytokines Takuya Tashiro, Ryusuke Nakagawa, Takatsugu Hirokawa, Sayo Inoue, Hiroshi Watarai, Masaru Taniguchi, Kenji Mori Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . (2'S,3'S,4'R)-2-O-(2'-hexacosanoylamino-3',4'-dihydroxyoctadecyl)-neo-inositol C50H99NO9 ÏàËÆ¶È:71.4% Bioorganic & Medicinal Chemistry 2009 17 6360-6373 RCAI-37, 56, 59, 60, 92, 101, and 102, cyclitol and carbasugar analogs of KRN7000: Their synthesis and bioactivity for mouse lymphocytes to produce Th1-biased cytokines Takuya Tashiro, Ryusuke Nakagawa, Takatsugu Hirokawa, Sayo Inoue, Hiroshi Watarai, Masaru Taniguchi, Kenji Mori Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . 1,3,5-trihydroxy-2-hexadecanoylamino-(6E,9E)-heptacosdiene C42H81NO4 ÏàËÆ¶È:70.3% 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 10 . 1,3,5-trihydroxy-2-hexadecanoylamino-9-(E)-heptacosene C42H83NO4 ÏàËÆ¶È:70.3% Phytochemistry 2002 61 1005-1008 Sphingolipids from Conyza canadensis Naveen Mukhtar, Kiran Iqbal, Itrat Anis, Abdul Malik Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . aralia cerebroside C40H77NO10 ÏàËÆ¶È:70.3% Journal of Natural Products 1999 62 1059-1060 Isolation of a New Cerebroside from the Root Bark of Aralia elata Sam Sik Kang, Ju Sun Kim, Yong Nan Xu, and Young Hee Kim Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . Di-O-alkadienyl ethers C86H162O4 ÏàËÆ¶È:70.3% Phytochemistry 1995 40 543-554 n-alkenylpyrogallol dimethyl ethers, aliphatic diol monoesters and some minor ether lipids from Botryococcus braunii a race P. Metzger, Y. Pouet Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . 1-O-¦Â-D-glucopyranosyl-(2S,3S,4R,8E)-2-[(2'R)-2'-hydroxy-tetracosanoyl]-8-octadecene-1,3,4-triol C48H93NO10 ÏàËÆ¶È:70.3% Chinese Journal of Natural Medicines 2009 7 115-118 Chemical Constituents from the Fruits of Ziziphus jujuba GUO Sheng; TANG Yu-Ping; DUAN Jin-Ao; SU Shu-Lan; QIAN Da-Wei Jiangsu Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . 1,3-dieaproyl-2-oleoyl-glycerol ÏàËÆ¶È:70.3% Bioorganic & Medicinal Chemistry 1996 4 345-348 Two step synthesis of 1,3-aeetylated, -butyroylated and -eaproylated triglycerides from a microorganism oil rich in Docosahexaenoic Acid (DHA) Yves Bayon , and Ran¨¦ Dolmazon Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . AGL-585 C50H98NO9 ÏàËÆ¶È:70.3% 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 16 . (11E,19Z)-3-Acetoxy-11,19-octacosadien-1-ol C30H56O3 ÏàËÆ¶È:70.3% Tetrahedron 2012 68 3750-3760 Pheromone synthesis. Part 250: Determination of the stereostructure of CH503, a sex pheromone of male Drosophila melanogaster, as (3R,11Z,19Z)-3-acetoxy-11,19-octacosadien-1-ol by synthesis and chromatographic analysis of its eight isomers Original Resear Yasumasa Shikichi, Kazuaki Akasaka, Shigeyuki Tamogami, Shruti Shankar, Joanne Y. Yew, Kenji Mori Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . (2S,3S,4R)-1-O-(5a-Carba-¦Á-D-galactopyranosyl)-2-hexacosanoylaminooctadecane-1,3,4-triol C51H101NO8 ÏàËÆ¶È:70.3% Bioorganic & Medicinal Chemistry 2009 17 6360-6373 RCAI-37, 56, 59, 60, 92, 101, and 102, cyclitol and carbasugar analogs of KRN7000: Their synthesis and bioactivity for mouse lymphocytes to produce Th1-biased cytokines Takuya Tashiro, Ryusuke Nakagawa, Takatsugu Hirokawa, Sayo Inoue, Hiroshi Watarai, Masaru Taniguchi, Kenji Mori Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . aralia cerebroside ÏàËÆ¶È:70.3% Archives of Pharmacal Research 2012 35 1771-1777 Inhibitory Activity of Aralia continentalis Roots on Protein Tyrosine Phosphatase 1B and Rat Lens Aldose Reductase Hee Jin Jung, Hyun Ah Jung, Sam Sik Kang, Je-Hyun Lee, Yoon Sook Cho, Kyong Ho Moon, and Jae Sue Choi, Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . (2S,3S,4R)-1-O-(¦Á-D-galactopyranosyl)-2-(N-hexacosanoylamino)-1,3,4-octadecanetriol C50H99NO9 ÏàËÆ¶È:70.3% Journal of Medicinal Chemistry 1995 38 2176-2187 Structure-Activity Relationship of .alpha.-Galactosylceramides against B16-Bearing Mice Masahiro Morita, Kazuhiro Motoki, Kohji Akimoto, Takenori Natori, Teruyuki Sakai, Eiji Sawa, Kazuo Yamaji, Yasuhiko Koezuka, Eiichi Kobayashi, Hideaki Fukushima Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . 1-O-¦Â-D-glucopyranosyl(2S,3S,4R,8E)-2-[(2'R)-2'-hydroxytetra cosanamino]-8-octadecene-1,3,4-triol ÏàËÆ¶È:70% Natural Product Research and Development 2005 17 298-300 Studies on Chemical Constituents of Polygala aureocauda HUANG Zhao-hui; XU Kang-ping; ZHOU Ying-jun; HU Gao-yun; TAN Gui-shan Structure 13C NMR ̼Æ×Ä£Äâͼ 21 . reticulatain-1 C37H66O4 ÏàËÆ¶È:68.9% Tetrahedron Letters 2004 45 973-977 Synthesis of two possible diastereomers of reticulatain-1 Hidefumi Makabe, Aya Miyawaki, Ryoko Takahashi, Yasunao Hattori, Hiroyuki Konno, Masato Abe, Hideto Miyoshi Structure 13C NMR ̼Æ×Ä£Äâͼ 22 . cerebroside ÏàËÆ¶È:68.7% 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 23 . aralia cerebroside (1-O-¦Â-D-glucopyranosyl-(2S,3S,4R,8E)-2-[(2'R)-2'-hydorxypalmitoylamino]-8-octadecene-1,3,4-triol) ÏàËÆ¶È:67.8% Korean Journal of Pharmacognosy 2006 37(2) 81-84 Isolation of a Cerebroside from Panax notoginseng Cho, Min-Jung; Lee, So-Young; Kim, Ju-Sun; Lee, Je-Hyun; Choi, Hwan-Soo; Lee, Ho-Young; Ha, Hye-Kyung; Kim, Chung-Sook; Kang, Sam-Sik Structure 13C NMR ̼Æ×Ä£Äâͼ 24 . 6,6'-Di-O-oleoyl-2,3,4,2',3',4'-hexakis-O-(trimethylsilyl)-¦Á,¦Á-trehalose C66H134O13Si6 ÏàËÆ¶È:67.8% The Journal of Organic Chemistry 2011 76 6866-6870 Synthesis of Maradolipid Vikram A. Sarpe and Suvarn S. Kulkarni Structure 13C NMR ̼Æ×Ä£Äâͼ |

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