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寂静绽放: 金币+15, ★有帮助 2014-05-11 10:47:45
感谢参与，应助指数 +1
寂静绽放: 金币+15, ★有帮助 2014-05-11 10:47:45
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查询结果：共查到96个化合物(查询结果仅供参考) -------------------------------------------------------------------------------- 1 . 1-O-β-D-glucopyranosyl-(2S,3S,4R,8E/Z)-2-(2'-hydroxylignoceroyl amino)-8-octadecene-1,3,4-triol 相似度:71.4% Natural Product Sciences 2008 14 161-166 Phytochemical Studies on Paeoniae Radix (4);Cerebrosides and Other Constituents Kim, Yoon-Jung; Yean, Min-Hye; Lee, Eun-Ju; Kim, Ju-Sun; Lee, Je-Hyun; Kang, Sam-Sik Structure 13C NMR 碳谱模拟图 -------------------------------------------------------------------------------- 2 . 1-O-β-D-glucopyranosyl-(2S,3S,4R,8E/Z)-2-(2'-hydroxytricosanoyl amino)-8-octadecene-1,3,4-triol 相似度:71.4% Natural Product Sciences 2008 14 161-166 Phytochemical Studies on Paeoniae Radix (4);Cerebrosides and Other Constituents Kim, Yoon-Jung; Yean, Min-Hye; Lee, Eun-Ju; Kim, Ju-Sun; Lee, Je-Hyun; Kang, Sam-Sik Structure 13C NMR 碳谱模拟图 -------------------------------------------------------------------------------- 3 . 1-O-β-D-glucopyranosyl-(2S,3S,4R,8E)-2-[(2'R)-2'-hydroxypalmitoylamino]-8-octadecene-1,3,4-triol 相似度:70.9% Journal of Shenyang Pharmaceutical University 2013 30 674-682 Constituents from starfish Asterina pectinifer LI Zhan-qiang, CHEN Gang, WANG Hai-feng, LU Xuan, FENG Bao-min, PEI Yu Structure 13C NMR 碳谱模拟图 -------------------------------------------------------------------------------- 4 . 1-O-β-D-glucopyranosyl-(2S,3S,4R,8E/Z)-2-(2'-hydroxydocosanoyl amino)-8-octadecene-1,3,4-triol 相似度:69.6% Natural Product Sciences 2008 14 161-166 Phytochemical Studies on Paeoniae Radix (4);Cerebrosides and Other Constituents Kim, Yoon-Jung; Yean, Min-Hye; Lee, Eun-Ju; Kim, Ju-Sun; Lee, Je-Hyun; Kang, Sam-Sik Structure 13C NMR 碳谱模拟图 -------------------------------------------------------------------------------- 5 . 1-O-β-D-glucopyranosyl-(2S,3S,4R,8E/Z)-2-(2'-hydroxypalmitoyl amino)-8-octadecene-1,3,4-triol 相似度:69.4% Natural Product Sciences 2008 14 161-166 Phytochemical Studies on Paeoniae Radix (4);Cerebrosides and Other Constituents Kim, Yoon-Jung; Yean, Min-Hye; Lee, Eun-Ju; Kim, Ju-Sun; Lee, Je-Hyun; Kang, Sam-Sik Structure 13C NMR 碳谱模拟图 -------------------------------------------------------------------------------- 6 . 1,3,5-trihydroxy-2-hexadecanoylamino-9-(E)-heptacosene β-D-glucopyranoside derivative C48H93NO9 相似度:68.7% Phytochemistry 2002 61 1005-1008 Sphingolipids from Conyza canadensis Naveen Mukhtar, Kiran Iqbal, Itrat Anis, Abdul Malik Structure 13C NMR 碳谱模拟图 -------------------------------------------------------------------------------- 7 . aralia cerebroside C40H77NO10 相似度:67.7% 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 碳谱模拟图 -------------------------------------------------------------------------------- 8 . aralia cerebroside (1-O-β-D-glucopyranosyl-(2S,3S,4R,8E)-2-[(2'R)-2'-hydorxypalmitoylamino]-8-octadecene-1,3,4-triol) 相似度:67.7% 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 碳谱模拟图 -------------------------------------------------------------------------------- 9 . astrocerebroside A 相似度:67.7% 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 碳谱模拟图 -------------------------------------------------------------------------------- 10 . hylodendroside-I C48H91NO9 相似度:66.6% Phytochemistry 2008 69 2400-2405 A triterpenoidal saponin and sphingolipids from Pteleopsis hylodendron Atta-ur-Rahman,Seema Zareen,M. Iqbal Choudhary,M. Nadeem Akhtar,F.N. Ngounou Structure 13C NMR 碳谱模拟图 -------------------------------------------------------------------------------- 11 . rouremin C45H87NO9 相似度:66.6% Phytochemistry 2006 67 1378-1384 Rourinoside and rouremin, antimalarial constituents from Rourea minor Zhen-Dan He, Cui-Ying Ma, Ghee Teng Tan, Kongmany Sydara, Pamela Tamez,Bounhoong Southavong, Somsanith Bouamanivong, D. Doel Soejarto,John M. Pezzuto, Harry H.S. Fong, Hong-Jie Zhang Structure 13C NMR 碳谱模拟图 -------------------------------------------------------------------------------- 12 . 1-O-(9Z,12Z,15Z-octadecatrienoyl)-2-O-hexadecanoyl-3-O-α-(6-sulfoquinovopyranosyl)glycerol 相似度:65.7% Phytochemistry Letters 2008 1 207-210 Glyceroglycolipids, a novel class of platelet-activating factor antagonists from Kalimeris indica Gao-jun Fan, Sanghee Kim, Byung Hoon Han, Yong Nam Han Structure 13C NMR 碳谱模拟图 -------------------------------------------------------------------------------- 13 . Cerebroside 相似度:65.7% Natural Product Sciences 2010 16 32-38 Phytochemical Studies on Lonicerae Flos (1) - Isolation of Iridoid Glycosides and other Constituents Lee, Eun-Ju; Lee, Joo-Young; Kim, Ju-Sun; Kang, Sam-Sik Structure 13C NMR 碳谱模拟图 -------------------------------------------------------------------------------- 14 . aralia cerebroside 相似度:64.5% Archives of Pharmacal Research 2006 29 548-555 Cytotoxic and COX-2 inhibitory constituents from the aerial parts ofAralia cordata Ik Soo Lee, Wen Yi Jin, Xinfeng Zhang, Tran Manh Hung and Kyung Sik Song, et al. Structure 13C NMR 碳谱模拟图 -------------------------------------------------------------------------------- 15 . (2S,3S,4R)-1-O-(5a-Carba-α-D-galactopyranosyl)-2-hexacosanoylaminooctadecane-1,3,4-triol C51H101NO8 相似度:64.5% 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 碳谱模拟图 -------------------------------------------------------------------------------- 16 . (2'S,3'S,4'R)-1D-(1,2,3/4,5)-5-O-(2'-hexacosanoylamino-3',4'-dihydroxyoctadecyl)cyclohexanepentol C50H99NO8 相似度:64.5% 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 碳谱模拟图 -------------------------------------------------------------------------------- 17 . (2S,3S,4R)-2-hexacosanoylamino-1-O-(6-O-methyl-5a-carba-α-D-galactopyranosyl)octadecane-1,3,4-triol C52H101NO8 相似度:64.5% 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 碳谱模拟图 -------------------------------------------------------------------------------- 18 . aralia cerebroside 相似度:64.5% 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 碳谱模拟图 -------------------------------------------------------------------------------- 19 . vibratilicin C43H80N2O7 相似度:61.7% Helvetica Chimica Acta 2004 Vol. 87 1912 Vibratilicin: a Novel Compound from the Basidiomycete Cortinarius vibratilis Fei Wang, Jian-Wen Tan, and Ji-Kai Liu Structure 13C NMR 碳谱模拟图 -------------------------------------------------------------------------------- 20 . soya-cerebroside I C40H75NO9 相似度:61.2% Natural Product Sciences 2001 7 27-32 Isolation of Soya-cerebroside I from the Roots of Trichosanthes kirilowii Kim, Ju-Sun; Byun, Ji-Hye; Kang, Sam-Sik Structure 13C NMR 碳谱模拟图 -------------------------------------------------------------------------------- 21 . toxadocial C C50H94S4O18 相似度:61.2% Tetrahedron 1993 49 11183-11188 Toxadocials B, C and toxadocic acid A: thrombin-inhibitory aliphatic tetrasulfates from the marine sponge, toxadocia cylindrica Youichi Nakao, Shigeki Matsunaga, Nobuhiro Fusetani Structure 13C NMR 碳谱模拟图 -------------------------------------------------------------------------------- 22 . (2S,3S,4R)-3,4-dihydroxy-2-[(2'R,3'R)-2',3'-(dihydroxy)hex-acosanoyloxy]octadecyl α-D-galactopyranoside C50H98O12 相似度:61.2% Tetrahedron 2013 69 9710-9725 Synthesis and biological activity of hydroxylated analogs of RCAI-80 Original Research Article Masao Shiozaki, Takuya Tashiro, Hiroyuki Koshino, Tomokuni Shigeura, Hiroshi Watarai, Masaru Taniguchi, Kenji Mori Structure 13C NMR 碳谱模拟图 -------------------------------------------------------------------------------- 23 . (2S,3S,4R)-1-O-(6-Deoxy-6-methyl-α-D-galactopyranosyl)-2-(hexacosanamido)octadecane-1,3,4-triol C51H101NO9 相似度:61.2% Bioorganic & Medicinal Chemistry 2013 23 3066-3079 RCAI-61 and related 6′-modified analogs of KRN7000: Their synthesis and bioactivity for mouse lymphocytes to produce interferon-γ in vivo Takuya, Tashiro, Ryusuke, Nakagawa, Tomokuni, Shigeura, Hiroshi, Watarai, Masaru, Taniguchi, Kenji, Mori Structure 13C NMR 碳谱模拟图 -------------------------------------------------------------------------------- 24 . (2S,3S,4R)-1-O-(β-L-rabinopyranosyl)-2-(hexacosanamido)octadecane-1,3,4-triol C49H97NO8 相似度:61.2% Bioorganic & Medicinal Chemistry 2013 23 3066-3079 RCAI-61 and related 6′-modified analogs of KRN7000: Their synthesis and bioactivity for mouse lymphocytes to produce interferon-γ in vivo Takuya, Tashiro, Ryusuke, Nakagawa, Tomokuni, Shigeura, Hiroshi, Watarai, Masaru, Taniguchi, Kenji, Mori Structure 13C NMR 碳谱模拟图 -------------------------------------------------------------------------------- 25 . 6'-O-linoleylsucrose C30H52O12 相似度:61.2% Journal of Agricultural and Food Chemistry 2013 61 7081-7088 NF-κB Inhibitory Activity of Sucrose Fatty Acid Esters and Related Constituents from Astragalus membranaceus Wei Li, Ya Nan Sun, Xi Tao Yan, Seo Young Yang, Seok Bean Song, Young Mi Lee, and Young Ho Kim Structure 13C NMR 碳谱模拟图 -------------------------------------------------------------------------------- 26 . 6-O-linoleylsucrose 相似度:61.2% Journal of Agricultural and Food Chemistry 2013 61 7081-7088 NF-κB Inhibitory Activity of Sucrose Fatty Acid Esters and Related Constituents from Astragalus membranaceus Wei Li, Ya Nan Sun, Xi Tao Yan, Seo Young Yang, Seok Bean Song, Young Mi Lee, and Young Ho Kim Structure 13C NMR 碳谱模拟图 -------------------------------------------------------------------------------- 27 . (2S,3S,4R)-1-O-(α-D-Galactopyranosyl)-2-[3-(5-phenylpentyl)ureido]octadecane-1,3,4-triol C36H64N2O9 相似度:60.6% Bioorganic & Medicinal Chemistry 2012 20 4540-4548 RCAI-84, 91, and 105-108, ureido and thioureido analogs of KRN7000: Their synthesis and bioactivity for mouse lymphocytes to produce Th1-biased cytokines Takuya Tashiro, Tomokuni Shigeura, Hiroshi Watarai, Masaru Taniguchi, Kenji Mori Structure 13C NMR 碳谱模拟图 -------------------------------------------------------------------------------- 28 . cus-2 相似度:59.3% Chemical & Pharmaceutical Bulletin 1996 44 481-485 Resin Glycosides. XXIII. Two Novel Acylated Trisaccharides Related to Resin Glycoside from the Seeds of Cuscuta chinensis Kazumoto MIYAHARA,Xiao-ming DU,Minae WATAMABE,Chizuko SUGIMURA,Shoji YAHARA and Toshihiro NOHARA Structure 13C NMR 碳谱模拟图 -------------------------------------------------------------------------------- 29 . AGL-584 C56H108NO14 相似度:59.3% Bioorganic & Medicinal Chemistry 1997 5 2245-2249 Immunostimulatory activities of monoglycosylated α-d-pyranosylceramides Akira Uchimura, Toshiyuki Shimizu, Masahiro Morita, Hitomi Ueno, Kazuhiro Motoki, Hideaki Fukushima, Takenori Natori, Yasuhiko Koezuka Structure 13C NMR 碳谱模拟图 -------------------------------------------------------------------------------- 30 . (2S,3S,4R)-1-O-(α-D-galactopyranosyl)-2-(3-octylureido)octadecane-1,3,4-triol C33H66N2O9 相似度:59.3% Bioorganic & Medicinal Chemistry 2012 20 4540-4548 RCAI-84, 91, and 105-108, ureido and thioureido analogs of KRN7000: Their synthesis and bioactivity for mouse lymphocytes to produce Th1-biased cytokines Takuya Tashiro, Tomokuni Shigeura, Hiroshi Watarai, Masaru Taniguchi, Kenji Mori Structure 13C NMR 碳谱模拟图 -------------------------------------------------------------------------------- 31 . (2S,3R,4R,5S,6S)-2-[(2'R,3'R)-2',3'-(dihydroxy)hex-acosanoyloxy]-3,4,5,6-(tetrahydroxy)octadecyl α-D-galactopyranoside C50H98O14 相似度:59.3% Tetrahedron 2013 69 9710-9725 Synthesis and biological activity of hydroxylated analogs of RCAI-80 Original Research Article Masao Shiozaki, Takuya Tashiro, Hiroyuki Koshino, Tomokuni Shigeura, Hiroshi Watarai, Masaru Taniguchi, Kenji Mori Structure 13C NMR 碳谱模拟图 -------------------------------------------------------------------------------- 32 . (2S,3S,4R)-1-O-(6-O-Methyl-α-D-galactopyranosyl)-2-(hexacosanamido)octadecane-1,3,4-triol C51H101NO9 相似度:59.3% Bioorganic & Medicinal Chemistry 2013 23 3066-3079 RCAI-61 and related 6′-modified analogs of KRN7000: Their synthesis and bioactivity for mouse lymphocytes to produce interferon-γ in vivo Takuya, Tashiro, Ryusuke, Nakagawa, Tomokuni, Shigeura, Hiroshi, Watarai, Masaru, Taniguchi, Kenji, Mori Structure 13C NMR 碳谱模拟图 -------------------------------------------------------------------------------- 33 . (2S,3S,4R)-1-O-(α-D-Fucopyranosyl)-2-(hexacosanamido)octadecane-1,3,4-triol C50H99NO8 相似度:59.3% Bioorganic & Medicinal Chemistry 2013 23 3066-3079 RCAI-61 and related 6′-modified analogs of KRN7000: Their synthesis and bioactivity for mouse lymphocytes to produce interferon-γ in vivo Takuya, Tashiro, Ryusuke, Nakagawa, Tomokuni, Shigeura, Hiroshi, Watarai, Masaru, Taniguchi, Kenji, Mori Structure 13C NMR 碳谱模拟图 -------------------------------------------------------------------------------- 34 . termitomycesphin C C41H77NO10 相似度:58.8% Tetrahedron 2000 56 5835-5841 Termitomycesphins A-D, Novel Neuritogenic Cerebrosides from the Edible Chinese Mushroom Termitomyces albuminosus Jianhua Qi, Makoto Ojika, Youji Sakagami Structure 13C NMR 碳谱模拟图 -------------------------------------------------------------------------------- 35 . termitomycesphin D C43H81NO10 相似度:58.8% Tetrahedron 2000 56 5835-5841 Termitomycesphins A-D, Novel Neuritogenic Cerebrosides from the Edible Chinese Mushroom Termitomyces albuminosus Jianhua Qi, Makoto Ojika, Youji Sakagami Structure 13C NMR 碳谱模拟图 -------------------------------------------------------------------------------- 36 . (2S,3S,4R)-1-O-[6-O-(2-hydroxyethyl)-α-D-galactopyranosyl]-2-(hexacosanamido)octadecane-1,3,4-triol C52H103NO10 相似度:58.8% Bioorganic & Medicinal Chemistry 2013 23 3066-3079 RCAI-61 and related 6′-modified analogs of KRN7000: Their synthesis and bioactivity for mouse lymphocytes to produce interferon-γ in vivo Takuya, Tashiro, Ryusuke, Nakagawa, Tomokuni, Shigeura, Hiroshi, Watarai, Masaru, Taniguchi, Kenji, Mori Structure 13C NMR 碳谱模拟图 -------------------------------------------------------------------------------- 37 . 1,2-diacyl-3-O-(6'-sulpho-α-D-quinovopyranosyl)-glycerol 相似度:58.3% Phytochemistry 1990 29 307-309 Glycolipids from Gracilaria verrucosa Byeng Wha Son Structure 13C NMR 碳谱模拟图 -------------------------------------------------------------------------------- 38 . termitomycesphin A C41H77NO10 相似度:58.3% Tetrahedron 2000 56 5835-5841 Termitomycesphins A-D, Novel Neuritogenic Cerebrosides from the Edible Chinese Mushroom Termitomyces albuminosus Jianhua Qi, Makoto Ojika, Youji Sakagami Structure 13C NMR 碳谱模拟图 -------------------------------------------------------------------------------- 39 . termitomycesphin B C43H81NO10 相似度:58.3% Tetrahedron 2000 56 5835-5841 Termitomycesphins A-D, Novel Neuritogenic Cerebrosides from the Edible Chinese Mushroom Termitomyces albuminosus Jianhua Qi, Makoto Ojika, Youji Sakagami Structure 13C NMR 碳谱模拟图 -------------------------------------------------------------------------------- 40 . (2S,3S,4R)-1-O-(5a-Carba-α-D-fucopyranosyl)-2-hexacosanoylaminooctadecane-1,3,4-triol C51H101NO7 相似度:58.3% 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 碳谱模拟图 -------------------------------------------------------------------------------- 41 . soyacerebroside II 相似度:58.0% Chinese Pharmaceutical Journal 2008 43 971-973 Studies on Chemical Constituents of Acetyl Acetate Extracted Fraction from Veratrum dahuricum NIE Li-yue TANG Jian~LI Hui-liang JIN Hui-zi ZHANG Wei-dong Structure 13C NMR 碳谱模拟图 -------------------------------------------------------------------------------- 42 . AGL-585 C50H98NO9 相似度:58.0% Bioorganic & Medicinal Chemistry 1997 5 2245-2249 Immunostimulatory activities of monoglycosylated α-d-pyranosylceramides Akira Uchimura, Toshiyuki Shimizu, Masahiro Morita, Hitomi Ueno, Kazuhiro Motoki, Hideaki Fukushima, Takenori Natori, Yasuhiko Koezuka Structure 13C NMR 碳谱模拟图 -------------------------------------------------------------------------------- 43 . (2S,3S,4R)-5-Cyclopentyl-1-O-(α-D-galactosyl)-2-tetracosanoylamino-1,3,4-pentanetriol C40H77NO9 相似度:58.0% Bioorganic & Medicinal Chemistry 2012 20 2850-2859 Synthesis and biological evaluation of truncated α-galactosylceramide derivatives focusing on cytokine induction profile 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 碳谱模拟图 -------------------------------------------------------------------------------- 44 . lucyobroside C39H73O9N 相似度:58.0% Natural Product Research and Development 1996 8(3) 20-25 A NEW CEREBROSIDE FROM LUFFA CYLINDRICA (L)ROEM Fang Zhapu; Zeng Xianyi; Xiong Shuling Structure 13C NMR 碳谱模拟图 -------------------------------------------------------------------------------- 45 . agelasphin-11 C49H97NO10 相似度:58.0% 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 碳谱模拟图 -------------------------------------------------------------------------------- 46 . agelasphin-13 C50H99NO10 相似度:58.0% 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 碳谱模拟图 -------------------------------------------------------------------------------- 47 . (2'S,3'S,4'R)-2-O-(2'-hexacosanoylamino-3',4'-dihydroxyoctadecyl)-neo-inositol C50H99NO9 相似度:58.0% 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 碳谱模拟图 -------------------------------------------------------------------------------- 48 . (2S,3S,4R)-1-O-(α-D-galactopyranosyl)-2-(3-tetracosy-lureido)octadecane-1,3,4-triol C49H98N2O9 相似度:58.0% Bioorganic & Medicinal Chemistry 2012 20 4540-4548 RCAI-84, 91, and 105-108, ureido and thioureido analogs of KRN7000: Their synthesis and bioactivity for mouse lymphocytes to produce Th1-biased cytokines Takuya Tashiro, Tomokuni Shigeura, Hiroshi Watarai, Masaru Taniguchi, Kenji Mori Structure 13C NMR 碳谱模拟图 -------------------------------------------------------------------------------- 49 . (2S,3S,4R)-1-O-(α-D-galactopyranosyl)-2-(3-hexadecy-lureido)octadecane-1,3,4-triol C41H82N2O9 相似度:58.0% Bioorganic & Medicinal Chemistry 2012 20 4540-4548 RCAI-84, 91, and 105-108, ureido and thioureido analogs of KRN7000: Their synthesis and bioactivity for mouse lymphocytes to produce Th1-biased cytokines Takuya Tashiro, Tomokuni Shigeura, Hiroshi Watarai, Masaru Taniguchi, Kenji Mori Structure 13C NMR 碳谱模拟图 -------------------------------------------------------------------------------- 50 . (2S,3S,4R)-1-O-(α-D-galactopyranosyl)-2-(N-hexacosanoylamino)-1,3,4-octadecanetriol C50H99NO9 相似度:58.0% 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 碳谱模拟图 -------------------------------------------------------------------------------- 51 . (2S,3S,4S,5S,6R,2'R,3'R)-2-[2',3'-(dihydroxy)hexacosanoylamino]-3,4,5,6-(tetrahydroxy)octadecyl α-D-galactopyranoside C50H99NO13 相似度:58.0% Bioorganic & Medicinal Chemistry 2014 22 827-833 Synthesis of RCAI-172 (C6 epimer of RCAI-147) and its biological activity Masao Shiozaki, Takuya Tashiro, Hiroyuki Koshino, Tomokuni Shigeura, Hiroshi Watarai, Masaru Taniguchi, Kenji Mori Structure 13C NMR 碳谱模拟图 -------------------------------------------------------------------------------- 52 . AGL-588 C56H108NO14 相似度:57.5% Bioorganic & Medicinal Chemistry 1997 5 2245-2249 Immunostimulatory activities of monoglycosylated α-d-pyranosylceramides Akira Uchimura, Toshiyuki Shimizu, Masahiro Morita, Hitomi Ueno, Kazuhiro Motoki, Hideaki Fukushima, Takenori Natori, Yasuhiko Koezuka Structure 13C NMR 碳谱模拟图 -------------------------------------------------------------------------------- 53 . (2'S,3'S,4'R)-1D-(1,2,3/4,5)-5-O-(2'-hexacosanoylamino-3',4'-dihydroxyoctadecyl)-1-O-methylcyclohexanepentol C51H101NO8 相似度:57.5% 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 碳谱模拟图 -------------------------------------------------------------------------------- 54 . (2S,3R,4E)-2-[(3''-stearoyloxy)triacontanamido]octadec-4-ene-1,3-diol C66H129NO5 相似度:57.5% Bioscience, Biotechnology, and Biochemistry 2012 76 1715-1720 Synthesis of Sphingolipids with an ω-Esterified Long Acyl Chain, Ceramide Components of the Human Epidermis Takuya TASHIRO, Kenji MORI Structure 13C NMR 碳谱模拟图 -------------------------------------------------------------------------------- 55 . (2'S,3'S,4'R)-2-O-(2'-hexacosanoylamino-3',4'-dihydroxyoctadecyl)-myo-inositol C50H99NO9 相似度:57.1% 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 碳谱模拟图 -------------------------------------------------------------------------------- 56 . (2S,3S,4R)-1-O-(6-O-Ethyl-α-D-galactopyranosyl)-2-(hexacosanamido)octadecane-1,3,4-triol C52H103NO9 相似度:57.1% Bioorganic & Medicinal Chemistry 2013 23 3066-3079 RCAI-61 and related 6′-modified analogs of KRN7000: Their synthesis and bioactivity for mouse lymphocytes to produce interferon-γ in vivo Takuya, Tashiro, Ryusuke, Nakagawa, Tomokuni, Shigeura, Hiroshi, Watarai, Masaru, Taniguchi, Kenji, Mori Structure 13C NMR 碳谱模拟图 -------------------------------------------------------------------------------- 57 . 1,3,5-trihydroxy-2-hexadecanoylamino-(6E,9E)-heptacosdiene-1-O-glucopyranoside C48H91NO9 相似度:56.2% Chemical & Pharmaceutical Bulletin 2002 50(12) 1558-1560 Novel Sphingolipids from Conyza canadensis Naveen MUKHTAR, Kiran IQBAL, and Abdul MALIK Structure 13C NMR 碳谱模拟图 -------------------------------------------------------------------------------- 58 . AGL-586 C56H108NO14 相似度:56.2% Bioorganic & Medicinal Chemistry 1997 5 2245-2249 Immunostimulatory activities of monoglycosylated α-d-pyranosylceramides Akira Uchimura, Toshiyuki Shimizu, Masahiro Morita, Hitomi Ueno, Kazuhiro Motoki, Hideaki Fukushima, Takenori Natori, Yasuhiko Koezuka Structure 13C NMR 碳谱模拟图 -------------------------------------------------------------------------------- 59 . agelasphin-10 C49H90NO9 相似度:56.2% 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 碳谱模拟图 -------------------------------------------------------------------------------- 60 . agelasphin-12 C50H93NO9 相似度:56.2% 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 碳谱模拟图 -------------------------------------------------------------------------------- 61 . (2S,3S,4R)-1-O-(6-Deoxy-6-fluoro-α-D-galactopyranosyl)-2-(hexacosanamido)octadecane-1,3,4-triol C50H98NO8F 相似度:56.2% Bioorganic & Medicinal Chemistry 2013 23 3066-3079 RCAI-61 and related 6′-modified analogs of KRN7000: Their synthesis and bioactivity for mouse lymphocytes to produce interferon-γ in vivo Takuya, Tashiro, Ryusuke, Nakagawa, Tomokuni, Shigeura, Hiroshi, Watarai, Masaru, Taniguchi, Kenji, Mori Structure 13C NMR 碳谱模拟图 -------------------------------------------------------------------------------- 62 . (2S,3S,4R)-1-O-[6-O-(methoxylmethyl)-α-D-galactopyranosyl]-2-(hexacosanamido)octadecane-1,3,4-triol C52H103NO10 相似度:56.2% Bioorganic & Medicinal Chemistry 2013 23 3066-3079 RCAI-61 and related 6′-modified analogs of KRN7000: Their synthesis and bioactivity for mouse lymphocytes to produce interferon-γ in vivo Takuya, Tashiro, Ryusuke, Nakagawa, Tomokuni, Shigeura, Hiroshi, Watarai, Masaru, Taniguchi, Kenji, Mori Structure 13C NMR 碳谱模拟图 -------------------------------------------------------------------------------- 63 . 1,3,5-trihydroxy-2-hexadecanoylamino-(6E,9E)-heptacosdiene C42H81NO4 相似度:54.8% Chemical & Pharmaceutical Bulletin 2002 50(12) 1558-1560 Novel Sphingolipids from Conyza canadensis Naveen MUKHTAR, Kiran IQBAL, and Abdul MALIK Structure 13C NMR 碳谱模拟图 -------------------------------------------------------------------------------- 64 . 1,3,5-trihydroxy-2-hexadecanoylamino-9-(E)-heptacosene C42H83NO4 相似度:54.8% Phytochemistry 2002 61 1005-1008 Sphingolipids from Conyza canadensis Naveen Mukhtar, Kiran Iqbal, Itrat Anis, Abdul Malik Structure 13C NMR 碳谱模拟图 -------------------------------------------------------------------------------- 65 . typhonoside C46H89O10N 相似度:54.8% Journal of Asian Natural Products Research 2001 3 277-283 CHEMICAL CONSTITUENTS OF TYPHONIUM GIGANTEUM ENGL XUE-SONG CHEN, DI-HUA CHEN, JIAN-YONG SI and GUANG-ZHONG Tu Structure 13C NMR 碳谱模拟图 -------------------------------------------------------------------------------- 66 . (2S,3S,4R)-1-O-(α-D-Galactosyl)-2-icosanoylamino-1,3,4-nonanetriol C35H69NO9 相似度:54.8% Bioorganic & Medicinal Chemistry 2012 20 2850-2859 Synthesis and biological evaluation of truncated α-galactosylceramide derivatives focusing on cytokine induction profile 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 碳谱模拟图 -------------------------------------------------------------------------------- 67 . (2S,3S,4R)-1-O-(α-D-Galactosyl)-2-docosanoylamino-1,3,4-nonanetriol C37H73NO9 相似度:54.8% Bioorganic & Medicinal Chemistry 2012 20 2850-2859 Synthesis and biological evaluation of truncated α-galactosylceramide derivatives focusing on cytokine induction profile 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 碳谱模拟图 -------------------------------------------------------------------------------- 68 . (2S,3S,4R)-1-O-(α-D-Galactosyl)-2-pentacosanoylamino-1,3,4-nonanetriol C40H79NO9 相似度:54.8% Bioorganic & Medicinal Chemistry 2012 20 2850-2859 Synthesis and biological evaluation of truncated α-galactosylceramide derivatives focusing on cytokine induction profile 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 碳谱模拟图 -------------------------------------------------------------------------------- 69 . (2S,3S,4R)-1-O-(α-D-Galactosyl)-2-hexacosanoylamino-1,3,4-nonanetriol C41H81NO9 相似度:54.8% Bioorganic & Medicinal Chemistry 2012 20 2850-2859 Synthesis and biological evaluation of truncated α-galactosylceramide derivatives focusing on cytokine induction profile 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 碳谱模拟图 -------------------------------------------------------------------------------- 70 . (2S,3S,4R)-1-O-(α-D-Galactosyl)-2-octacosanoylamino-1,3,4-nonanetriol C43H85NO9 相似度:54.8% Bioorganic & Medicinal Chemistry 2012 20 2850-2859 Synthesis and biological evaluation of truncated α-galactosylceramide derivatives focusing on cytokine induction profile 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 碳谱模拟图 -------------------------------------------------------------------------------- 71 . (2S,3S,4R)-1-O-(α-D-Galactosyl)-6-oxa-2-tetracosanoy lamino-1,3,4-octadecanetriol C47H93NO10 相似度:54.8% Bioorganic & Medicinal Chemistry 2012 20 2850-2859 Synthesis and biological evaluation of truncated α-galactosylceramide derivatives focusing on cytokine induction profile 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 碳谱模拟图 -------------------------------------------------------------------------------- 72 . agelasphin-9b C48H95NO10 相似度:54.8% 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 碳谱模拟图 -------------------------------------------------------------------------------- 73 . (2S,3S,4R)-1-O-(α-D-Galactopyranosyl)-2-(3-hexadecylthioureido)octadecane-1,3,4-triol C41H82N2O8S 相似度:54.8% Bioorganic & Medicinal Chemistry 2012 20 4540-4548 RCAI-84, 91, and 105-108, ureido and thioureido analogs of KRN7000: Their synthesis and bioactivity for mouse lymphocytes to produce Th1-biased cytokines Takuya Tashiro, Tomokuni Shigeura, Hiroshi Watarai, Masaru Taniguchi, Kenji Mori Structure 13C NMR 碳谱模拟图 -------------------------------------------------------------------------------- 74 . (2S,3R)-2-(N-docosanoylainino)-1-O-(α-D-galactopyranosyl)-1,3-octadecanediol C46H91NO8 相似度:54.8% 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 碳谱模拟图 -------------------------------------------------------------------------------- 75 . (2S,3R)-2-(N-tetradecanoylamino)-1-O-(α-D-galactopyranosyl)-1,3-octadecanediol C38H75NO8 相似度:54.8% 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 碳谱模拟图 -------------------------------------------------------------------------------- 76 . ascotrichic acid B C30H52O5 相似度:54.8% Acta Pharmaceutica Sinica 2013 48 89-93 A new 3, 4-seco-lanostane triterpenoid from a marine-derived fungus Ascotricha sp. ZJ-M-5 XIE Lei-rui, LI Dan-yi, WANG Pei-le, HUA Hui-ming, WU Xin, LI Zhan-lin, Structure 13C NMR 碳谱模拟图 -------------------------------------------------------------------------------- 77 . iotroridoside-B C48H93NO10 相似度:54.5% 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 碳谱模拟图 -------------------------------------------------------------------------------- 78 . (2S,3S,4R)-1-O-(6-O-methyl-α-D-galactopyranosyl)-2-(3-tetracosylureido)octadecane-1,3,4-triol C50H100N2O9 相似度:54.5% Bioorganic & Medicinal Chemistry 2012 20 4540-4548 RCAI-84, 91, and 105-108, ureido and thioureido analogs of KRN7000: Their synthesis and bioactivity for mouse lymphocytes to produce Th1-biased cytokines Takuya Tashiro, Tomokuni Shigeura, Hiroshi Watarai, Masaru Taniguchi, Kenji Mori Structure 13C NMR 碳谱模拟图 -------------------------------------------------------------------------------- 79 . ophidiacerebroside E C49H91NO9 相似度:54.5% European Journal of Organic Chemistry 2007 2007 5277-5283 Oreacerebrosides: Bioactive Cerebrosides with a Triunsaturated Sphingoid Base from the Sea Star Oreaster reticulatus Valeria Costantino, Caterina de Rosa, Ernesto Fattorusso, Concetta Imperatore, Alfonso Mangoni, Carlo Irace, Carmen Maffettone, Domenica Capasso, Livia Malorni, Rosanna Palumbo and Carlo Pedone Structure 13C NMR 碳谱模拟图 -------------------------------------------------------------------------------- 80 . oreacerebroside I C49H91NO9 相似度:54.5% European Journal of Organic Chemistry 2007 2007 5277-5283 Oreacerebrosides: Bioactive Cerebrosides with a Triunsaturated Sphingoid Base from the Sea Star Oreaster reticulatus Valeria Costantino, Caterina de Rosa, Ernesto Fattorusso, Concetta Imperatore, Alfonso Mangoni, Carlo Irace, Carmen Maffettone, Domenica Capasso, Livia Malorni, Rosanna Palumbo and Carlo Pedone Structure 13C NMR 碳谱模拟图 -------------------------------------------------------------------------------- 81 . oreacerebroside D C46H85NO9 相似度:54.5% European Journal of Organic Chemistry 2007 2007 5277-5283 Oreacerebrosides: Bioactive Cerebrosides with a Triunsaturated Sphingoid Base from the Sea Star Oreaster reticulatus Valeria Costantino, Caterina de Rosa, Ernesto Fattorusso, Concetta Imperatore, Alfonso Mangoni, Carlo Irace, Carmen Maffettone, Domenica Capasso, Livia Malorni, Rosanna Palumbo and Carlo Pedone Structure 13C NMR 碳谱模拟图 -------------------------------------------------------------------------------- 82 . (2S,3S,4R)-1-O-[6-O-(2-methoxyethoxymethyl)-α-Dgalactopyranosyl]-2-(hexacosanamido)octadecane-1,3,4-triol C54H107NO11 相似度:54.2% Bioorganic & Medicinal Chemistry 2013 23 3066-3079 RCAI-61 and related 6′-modified analogs of KRN7000: Their synthesis and bioactivity for mouse lymphocytes to produce interferon-γ in vivo Takuya, Tashiro, Ryusuke, Nakagawa, Tomokuni, Shigeura, Hiroshi, Watarai, Masaru, Taniguchi, Kenji, Mori Structure 13C NMR 碳谱模拟图 -------------------------------------------------------------------------------- 83 . oreacerebroside A C46H85NO9 相似度:53.1% European Journal of Organic Chemistry 2007 2007 5277-5283 Oreacerebrosides: Bioactive Cerebrosides with a Triunsaturated Sphingoid Base from the Sea Star Oreaster reticulatus Valeria Costantino, Caterina de Rosa, Ernesto Fattorusso, Concetta Imperatore, Alfonso Mangoni, Carlo Irace, Carmen Maffettone, Domenica Capasso, Livia Malorni, Rosanna Palumbo and Carlo Pedone Structure 13C NMR 碳谱模拟图 -------------------------------------------------------------------------------- 84 . agelasphin-7b C47H93NO10 相似度:52.9% 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 碳谱模拟图 -------------------------------------------------------------------------------- 85 . (2S,3S,4R)-2-(Hexacosanamido)-1-O-(6-O-propyl-α-Dgalactopyranosyl)octadecane-1,3,4-triol C53H105NO9 相似度:52.9% Bioorganic & Medicinal Chemistry 2013 23 3066-3079 RCAI-61 and related 6′-modified analogs of KRN7000: Their synthesis and bioactivity for mouse lymphocytes to produce interferon-γ in vivo Takuya, Tashiro, Ryusuke, Nakagawa, Tomokuni, Shigeura, Hiroshi, Watarai, Masaru, Taniguchi, Kenji, Mori Structure 13C NMR 碳谱模拟图 -------------------------------------------------------------------------------- 86 . neoengleromycin C45H84N2O7 相似度:52.7% Helvetica Chimica Acta 2002 Vol. 85 1439 Neoengleromycin, a Novel Compound from Engleromyces goetzii Liu Jikai, Tan Jianwen, Dong Zejun, Ding Zhihui, Wang Xianghua, and Liu Peigui Structure 13C NMR 碳谱模拟图 -------------------------------------------------------------------------------- 87 . Pancovioside C48H93NO10 相似度:51.6% Helvetica Chimica Acta 2010 93 2210-2217 New Sphingolipids and Other Constituents of Pancovia laurentii Ferdinand Tantangmo, Bruno Ndjakou Lenta, Silvère Ngouela, Louis Marie Kamdem, Bernard Weniger, Etienne Tsamo, Annelise Lobstein and Catherine Vonthron-Sénécheau Structure 13C NMR 碳谱模拟图 -------------------------------------------------------------------------------- 88 . betulafoliene-oxide-II 相似度:51.6% Phytochemistry 1978 17 1353-1358 Dammarane saponins of leaves of Panax pseudo-ginseng subsp. himalaicus Osamu Tanaka, Shoji Yahara Structure 13C NMR 碳谱模拟图 -------------------------------------------------------------------------------- 89 . (2S,3S,4R)-1-O-(α-D-Galactosyl)-2-tetracosanoylamino-1,3,4-octanetriol C38H75NO9 相似度:51.6% Bioorganic & Medicinal Chemistry 2012 20 2850-2859 Synthesis and biological evaluation of truncated α-galactosylceramide derivatives focusing on cytokine induction profile 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 碳谱模拟图 -------------------------------------------------------------------------------- 90 . (2S,3S,4R)-1-O-(α-D-Galactosyl)-2-tricosanoylamino-1,3,4-decanetriol C39H77NO9 相似度:51.6% Bioorganic & Medicinal Chemistry 2012 20 2850-2859 Synthesis and biological evaluation of truncated α-galactosylceramide derivatives focusing on cytokine induction profile 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 碳谱模拟图 -------------------------------------------------------------------------------- 91 . (2S,3S,4R)-1-O-(α-D-Galactosyl)-5-(p-tolyl)-2-tetracosano ylamino-1,3,4-pentanetriol C42H75NO9 相似度:51.6% Bioorganic & Medicinal Chemistry 2012 20 2850-2859 Synthesis and biological evaluation of truncated α-galactosylceramide derivatives focusing on cytokine induction profile 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 碳谱模拟图 -------------------------------------------------------------------------------- 92 . (2S,3S,4R)-1-O-(α-D-Galactosyl)-5-phenoxy-2-tetracosanoylamino-1,3,4-pentanetriol C41H73NO10 相似度:51.6% Bioorganic & Medicinal Chemistry 2012 20 2850-2859 Synthesis and biological evaluation of truncated α-galactosylceramide derivatives focusing on cytokine induction profile 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 碳谱模拟图 -------------------------------------------------------------------------------- 93 . Momordicine I 相似度:51.6% Zeitschrift für Naturforschung C 2006 61 81-86 Cucurbitane Glucosides from Momordica charantia Leaves as Oviposition Deterrents to the Leafminer, Liriomyza trifolii D. B. Mekuria, T. Kashiwagi, S.-i. Tebayashi, and C.-S. Kim Structure 13C NMR 碳谱模拟图 -------------------------------------------------------------------------------- 94 . 6'-O-linolenoylsucrose 相似度:51.6% Journal of Agricultural and Food Chemistry 2013 61 7081-7088 NF-κB Inhibitory Activity of Sucrose Fatty Acid Esters and Related Constituents from Astragalus membranaceus Wei Li, Ya Nan Sun, Xi Tao Yan, Seo Young Yang, Seok Bean Song, Young Mi Lee, and Young Ho Kim Structure 13C NMR 碳谱模拟图 -------------------------------------------------------------------------------- 95 . 1-O-(9Z,12Z,15Z-octadecatrienoyl)-2-O-hexadecanoyl-3-O-[α-D-galactopyranosyl(1 →6)-O-β-D-galactopyranosyl]glycerol 相似度:50% Phytochemistry Letters 2008 1 207-210 Glyceroglycolipids, a novel class of platelet-activating factor antagonists from Kalimeris indica Gao-jun Fan, Sanghee Kim, Byung Hoon Han, Yong Nam Han Structure 13C NMR 碳谱模拟图 -------------------------------------------------------------------------------- 96 . amphidinol 2 相似度:50% Bioorganic & Medicinal Chemistry Letters 2004 14 3117-3120 Lingshuiol, a novel polyhydroxyl compound with strongly cytotoxic activity from the marine dinoflagellate Amphidinium sp Xiao-Chun Huang, Di Zhao, Yue-Wei Guo, Hou-Ming Wu, Li-Ping Lin, Zhong-Hua Wang, Jian Ding, Yong-Shui Lin Structure 13C NMR 碳谱模拟图 |
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