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6788591

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13C NMR (126 MHz, Pyr) ¦Ä 173.70, 130.59, 130.46, 76.55, 76.09, 73.44, 72.62, 61.67, 52.82, 33.65, 33.09, 32.76, 32.31, 31.89, 30.02, 29.93, 29.82, 29.75, 29.68, 29.64, 29.59, 29.37, 29.29, 26.46, 26.34, 22.70, 14.04.ÈܼÁ·åÒѳýÈ¥~~лл~~~
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6788591: ½ð±Ò+5, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸, лл£¬ÐÁ¿àÀ²~~ 2013-03-19 15:35:12
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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×Ä£Äâͼ
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