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monkey514: ½ð±Ò+15, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸, ·Ç³£¸Ðл£¡ 2013-07-10 20:38:41
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²éѯ½á¹û£º¹²²éµ½165¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . 1,3,5-trihydroxy-2-hexadecanoylamino-(6E,9E)-heptacosdiene-1-O-glucopyranoside C48H91NO9 ÏàËÆ¶È:62.5% 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 2 . cerebroside C48H91NO9 ÏàËÆ¶È:62.5% Phytochemistry 1998 49 2403-2408 Glycosides from Stenochlaena palustris Hongmei Liu, Jimmy Orjala, Topul Rali, Otto Sticher Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . phalluside 4 C42H77NO9 ÏàËÆ¶È:61.2% Tetrahedron 1998 54 14597-14602 Phallusides, new glucosphingolipids from the ascidian Phallusia fumigata Rosario Dur¨¢n, Eva Zub¨ªa, Mar¨ªa J. Ortega, Santiago Naranjo, Javier Salv¨¢ Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . (+)-araguspongine L C28H50O5N2 ÏàËÆ¶È:60% Journal of Natural Products 2002 65 1782-1785 Araguspongines K and L, New Bioactive Bis-1-oxaquinolizidine N-Oxide Alkaloids from Red Sea Specimens of Xestospongia exigua Khaled Y. Orabi,Khalid A. El Sayed, Mark T. Hamann, D. Chuck Dunbar, Mansour S. Al-Said,Tatsuo Higa,and Michelle Kelly Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . gallicaside J C30H50O11 ÏàËÆ¶È:60% Phytochemistry 2010 71 1410-1417 Cyclic fatty acyl glycosides in the glandular trichome exudate of Silene gallica Teigo Asai, Yoshinori Fujimoto Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . 1-oleoyl-3-O-¦Â-D-galactopyranosyl-sn-glycerol ÏàËÆ¶È:60% 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 7 . lucyobroside C39H73O9N ÏàËÆ¶È:60% 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 ̼Æ×Ä£Äâͼ 8 . agelasphin-12 C50H93NO9 ÏàËÆ¶È:59.3% 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 9 . PX26 ÏàËÆ¶È:58.0% Journal of the Chemical Society, Perkin Transactions 1 1996 2651-2656 Preparative transformation of natural phospholipids catalysed by phospholipase D from Streptomyces Paola D'Arrigo, Lorenzo de Ferra, Valentino Piergianni, Antonio Selva, Stefano Servi and Alberto Strini Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . phalluside 1 C41H75NO9 ÏàËÆ¶È:58.0% Tetrahedron 1998 54 14597-14602 Phallusides, new glucosphingolipids from the ascidian Phallusia fumigata Rosario Dur¨¢n, Eva Zub¨ªa, Mar¨ªa J. Ortega, Santiago Naranjo, Javier Salv¨¢ Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . phalluside 3 C42H77NO9 ÏàËÆ¶È:58.0% Tetrahedron 1998 54 14597-14602 Phallusides, new glucosphingolipids from the ascidian Phallusia fumigata Rosario Dur¨¢n, Eva Zub¨ªa, Mar¨ªa J. Ortega, Santiago Naranjo, Javier Salv¨¢ Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . 16-O-acetyldarutoside ÏàËÆ¶È:56.6% Journal of Natural Products 2009 72 2005-2008 ent-Pimarane Diterpenoids from Siegesbeckia orientalis and Structure Revision of a Related Compound Fei Wang, Xue-Lian Cheng, Ya-Ju Li, Song Shi, and Ji-Kai Liu Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . aralia cerebroside C40H77NO10 ÏàËÆ¶È:56.6% 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 14 . frameroside C27H38O15 ÏàËÆ¶È:56.6% Phytochemistry 2000 55 275-284 Secoiridoid glucosides from Fraxinus americana Yukiko Takenaka, Takao Tanahashi, Masashi Shintaku, Takeshi Sakai, Naotaka Nagakura, Parida Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . typhonoside C46H89O10N ÏàËÆ¶È:56.6% 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 ̼Æ×Ä£Äâͼ 16 . soya-cerebroside I C40H75NO9 ÏàËÆ¶È:56.6% 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 ̼Æ×Ä£Äâͼ 17 . Pancovioside C48H93NO10 ÏàËÆ¶È:56.6% Helvetica Chimica Acta 2010 93 2210-2217 New Sphingolipids and Other Constituents of Pancovia laurentii Ferdinand Tantangmo, Bruno Ndjakou Lenta, Silv¨¨re Ngouela, Louis Marie Kamdem, Bernard Weniger, Etienne Tsamo, Annelise Lobstein and Catherine Vonthron-S¨¦n¨¦cheau Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . aralia cerebroside ÏàËÆ¶È:56.6% 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 ̼Æ×Ä£Äâͼ 19 . astrocerebroside A ÏàËÆ¶È:56.6% 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 . bengazole E C28H46N2O8 ÏàËÆ¶È:56.6% The Journal of Organic Chemistry 1996 61 4073-4079 Bengazoles C−G from the Sponge Jaspis sp. Synthesis of the Side Chain and Determination of Absolute Configuration Philip A. Searle, Rowena K. Richter, and Tadeusz F. Molinski Structure 13C NMR ̼Æ×Ä£Äâͼ 21 . glucolipsin A C50H92O14 ÏàËÆ¶È:56.6% The Journal of Antibiotics 1999 52 245-255 Glucolipsin A and B, Two New Glucokinase Activators Produced by Streptomyces purpurogeniscleroticus and Nocardia vaccinii JINGFANG QIAN-CUTRONE, T. UEKI, STELLA HUANG, KASIM A. MOOKHTIAR, REGINA EZEKIEL, STEVEN S. KALINOWSKI, KAREN S. BROWN, JERZY GOLIK, SUSAN LOWE, DOLORES M. PIRNIK, ROBERT HUGILL, JUDY A. VEITCH, STEVEN E. KLOHR, JEFFREY L. WHITNEY, SUSAN P. MANLY Structure 13C NMR ̼Æ×Ä£Äâͼ 22 . compound 3 ÏàËÆ¶È:56.6% The Journal of Antibiotics 1999 52 245-255 Glucolipsin A and B, Two New Glucokinase Activators Produced by Streptomyces purpurogeniscleroticus and Nocardia vaccinii JINGFANG QIAN-CUTRONE, T. UEKI, STELLA HUANG, KASIM A. MOOKHTIAR, REGINA EZEKIEL, STEVEN S. KALINOWSKI, KAREN S. BROWN, JERZY GOLIK, SUSAN LOWE, DOLORES M. PIRNIK, ROBERT HUGILL, JUDY A. VEITCH, STEVEN E. KLOHR, JEFFREY L. WHITNEY, SUSAN P. MANLY Structure 13C NMR ̼Æ×Ä£Äâͼ 23 . compound 14 C238H462Br14N14O28 ÏàËÆ¶È:56.6% Molecules 2011 16 1508-1518 Polycationic Glycosides Robert Engel, Ishrat Ghani, Diego Montenegro, Marie Thomas, Barbara Klaritch-Vrana, Alejandra Castaño, Laura Friedman, Jay Leb, Leah Rothman, Heidi Lee, et al. Structure 13C NMR ̼Æ×Ä£Äâͼ 24 . 1,3,5-trihydroxy-2-hexadecanoylamino-9-(E)-heptacosene ¦Â-D-glucopyranoside derivative C48H93NO9 ÏàËÆ¶È:56.2% Phytochemistry 2002 61 1005-1008 Sphingolipids from Conyza canadensis Naveen Mukhtar, Kiran Iqbal, Itrat Anis, Abdul Malik Structure 13C NMR ̼Æ×Ä£Äâͼ 25 . agelasphin-10 C49H90NO9 ÏàËÆ¶È: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 ̼Æ×Ä£Äâͼ 26 . (25S)-3¦Â-hydroxy-5¦Á-spirostan-6¦Á-yl-O-¦Â-D-xylopyranoside C32H52O8 ÏàËÆ¶È:56.2% Phytochemistry 2013 86 137-143 Steroidal saponins from the fruits of Solanum torvum Alida P¨¦rez Colmenares, Luis B. Rojas, Anne-Claire Mitaine-Offer, Laurent Pouys¨¦gu, St¨¦phane Quideau, Tomofumi Miyamoto, Chiaki Tanaka, Thomas Paululat, Alfredo Usubillaga, Marie-Aleth Lacaille-Dubois Structure 13C NMR ̼Æ×Ä£Äâͼ 27 . termitomycesphin C C41H77NO10 ÏàËÆ¶È:55.8% 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 ̼Æ×Ä£Äâͼ 28 . termitomycesphin D C43H81NO10 ÏàËÆ¶È:55.8% 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 ̼Æ×Ä£Äâͼ 29 . soyacerebroside II ÏàËÆ¶È:54.8% 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 ̼Æ×Ä£Äâͼ 30 . glycoside 3 C33H54O9 ÏàËÆ¶È:54.5% Chemical & Pharmaceutical Bulletin 2007 55(1) 145-149 Steroidal Glycosides from Agave utahensis Akihito YOKOSUKA and Yoshihiro MIMAKI Structure 13C NMR ̼Æ×Ä£Äâͼ 31 . iotroridoside-B C48H93NO10 ÏàËÆ¶È: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 ̼Æ×Ä£Äâͼ 32 . (4E)-1-S-(2-Acetamido-3,4,6-tri-O-acetyl-2-deoxy-¦Á-D-galactopyranosyl)-2,4,5-trideoxy-3-O-(methoxymethyl)- 2-(octadecanoylamino)-1-thio-6-O-undecyl-d-erythro-hex-4-enitol C51H92N2O12S ÏàËÆ¶È:54.5% Helvetica Chimica Acta 2009 92 918-927 Synthesis and Evaluation of N-Acetyl-2-amino-2-deoxy-¦Á-D-galactosyl 1-Thio-7-oxaceramide, a New Analogue of ¦Á-D-Galactosyl Ceramide Roshini Rajan, Thresen Mathew, Radovan Buffa, Fr¨¦d¨¦ric Bornancin, Marco Cavallari, Peter Nussbaumer, Gennaro De Libero, Andrea Vasella Structure 13C NMR ̼Æ×Ä£Äâͼ 33 . (25R)-5¦Á-spirostan-3¦Â,6¦Á-diol(chlorogenin) 6-O-¦Â-D-glucopyranoside C33H54O9 ÏàËÆ¶È:54.5% Phytochemistry 1991 30 3721-3727 Steroidal saponins from the bulbs ofCamassia cusickii Yoshihiro Mimaki, Yutaka Sashida, Kazuhiro Kawashima Structure 13C NMR ̼Æ×Ä£Äâͼ 34 . 1-O-(9 Z-octadecenoyl)-2-O-(8Z,11Z-octadecadienoyl)-sn-glycero-3-phosphorylcholine ÏàËÆ¶È:54.5% Archives of Pharmacal Research 2003 26 471-477 Phospholipids from Bombycis corpus and their neurotrophic effects Hak Cheol Kwon, I Yeon Jung, Se Yeon Cho, Ock Ryun Cho and Min Cheol Yang, et al. Structure 13C NMR ̼Æ×Ä£Äâͼ 35 . ircicerebroside C45H85NO9 ÏàËÆ¶È:53.3% Helvetica Chimica Acta 2005 Vol. 88 885 Two New Ceramides from the Marine Sponge Ircinia fasciculata Guang-Wen Zhang, Xiang-Quan Ma, Cui-Xian Zhang, Jing-Yu Su, Wen-Cai Ye, Xiao-Qi Zhang, Xin-Sheng Yao, Long-Mei Zeng Structure 13C NMR ̼Æ×Ä£Äâͼ 36 . siphonellinol D C30H52O4 ÏàËÆ¶È:53.3% Journal of Natural Products 2009 72 1291-1298 Sipholane Triterpenoids: Chemistry, Reversal of ABCB1/P-Glycoprotein-Mediated Multidrug Resistance, and Pharmacophore Modeling Sandeep Jain, Ioana Abraham, Paulo Carvalho,Ye-Hong Kuang,Lamiaa A. Shaala, Diaa T. A. Youssef, Mitchell A. Avery, Zhe-Sheng Chen,and Khalid A. El Sayed Structure 13C NMR ̼Æ×Ä£Äâͼ 37 . siphonellinol E C30H52O6 ÏàËÆ¶È:53.3% Journal of Natural Products 2009 72 1291-1298 Sipholane Triterpenoids: Chemistry, Reversal of ABCB1/P-Glycoprotein-Mediated Multidrug Resistance, and Pharmacophore Modeling Sandeep Jain, Ioana Abraham, Paulo Carvalho,Ye-Hong Kuang,Lamiaa A. Shaala, Diaa T. A. Youssef, Mitchell A. Avery, Zhe-Sheng Chen,and Khalid A. El Sayed Structure 13C NMR ̼Æ×Ä£Äâͼ 38 . dihomodehydrobatzelladine C C29H50N6O2 ÏàËÆ¶È:53.3% Journal of Natural Products 2009 72 1589-1594 Bioactive Guanidine Alkaloids from Two Caribbean Marine Sponges Remi Laville, Olivier P. Thomas,Fabrice Berrue, Diana Marquez, Jean Vacelet, and Philippe Amad Structure 13C NMR ̼Æ×Ä£Äâͼ 39 . siphonellinol C C30H52O5 ÏàËÆ¶È:53.3% Journal of Natural Products 2007 70 928-931 Reversal of P-Glycoprotein-Mediated Multidrug Resistance by Sipholane Triterpenoids Sandeep Jain, Surat Laphookhieo, Zhi Shi, Li-wu Fu, Shin-ichi Akiyama,Zhe-Sheng Chen, Diaa T. A. Youssef,Rob W. M. van Soest,3 and Khalid A. El Sayed Structure 13C NMR ̼Æ×Ä£Äâͼ 40 . (+)-araguspongine A ÏàËÆ¶È:53.3% Journal of Natural Products 2002 65 1782-1785 Araguspongines K and L, New Bioactive Bis-1-oxaquinolizidine N-Oxide Alkaloids from Red Sea Specimens of Xestospongia exigua Khaled Y. Orabi,Khalid A. El Sayed, Mark T. Hamann, D. Chuck Dunbar, Mansour S. Al-Said,Tatsuo Higa,and Michelle Kelly Structure 13C NMR ̼Æ×Ä£Äâͼ 41 . grayanoside D ÏàËÆ¶È:53.3% Journal of Natural Products 1998 61 1473-1475 Grayanane Diterpenoids from Pieris formosa Li-Quan Wang, Shao-Nong Chen, Guo-Wei Qin, and Kin-Fai Cheng Structure 13C NMR ̼Æ×Ä£Äâͼ 42 . 1-O-(9Z,12Z,15Z-octadecatrienoyl)-2-Ohexadecanoylglycerol ÏàËÆ¶È:53.3% 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 ̼Æ×Ä£Äâͼ 43 . 3¦Â,3¦Â'-dimethylxestospongin C C30H54N2O2 ÏàËÆ¶È:53.3% Natural Product Research 1997 11 53-59 3¦Â,3'¦Â-Dimethylxestospongin C, a New Bis-1-Oxaquinolizidine Alkaloid from the Palauan Sponge Xestospongia sp M. Venkata Rami Reddy; D. John Faulkner Structure 13C NMR ̼Æ×Ä£Äâͼ 44 . darutoside C24H39O6 ÏàËÆ¶È:53.3% Natural Product Research 2005 19 503-507 NMR studies of darutoside, a rare ENT-pimarane glucoside Phan Tong Son; Phan Minh Giang; Walter C. Taylor Structure 13C NMR ̼Æ×Ä£Äâͼ 45 . 1-O-¦Â-D-glucopyranosyl-(2S,3R,4E,9E)-2-(2'R-hydroxyhexadecenoy)-4,9-octadecadiene-1,3-diol C40H75O9N ÏàËÆ¶È:53.3% Natural Product Research 2006 20 1187-1191 A new cerebroside from fruits of Ailanthus altissima Swingle Chun-Chao Zhao; Jian-Hua Shao; Nan Wang; Xian Li; Jin-Hui Wang Structure 13C NMR ̼Æ×Ä£Äâͼ 46 . Crambine Cl C25H48N6O3 ÏàËÆ¶È:53.3% Journal of Natural Products 1992 Vol 55 528 Crambines C1 and C2: Two Further Ichthyotoxic Guanidine Alkaloids from the Sponge Crambe crambe R. G. S. Gerlinck, J. C. Braekman, D. Daloze, I. Bruno, R. Riccio, D. Rogeau, P. Amade Structure 13C NMR ̼Æ×Ä£Äâͼ 47 . Cerebroside Blb ÏàËÆ¶È:53.3% Phytochemistry 1995 38 1537-1545 Alkaloids and other compounds from Psychotria correae Hans Achenbach, Monika Lottes, Reiner Waibel, George A. Karikas, Mireya D. Correa, Mahabir P. Gupta Structure 13C NMR ̼Æ×Ä£Äâͼ 48 . aralia cerebroside (1-O-¦Â-D-glucopyranosyl-(2S,3S,4R,8E)-2-[(2'R)-2'-hydorxypalmitoylamino]-8-octadecene-1,3,4-triol) ÏàËÆ¶È:53.3% 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 49 . 3-tetradecanoate-ingenol-5,20-diacetate ÏàËÆ¶È:53.3% Phytochemistry 1988 27 207-212 Diterpenes from the latex of Euphorbia broteri Julio Gonz¨¤lez Urones,Pilar Basabe Barcala,Ma Jos¨¨ Sexmero Cuadrado,Isidro S¨¤nchez Marcos Structure 13C NMR ̼Æ×Ä£Äâͼ 50 . Panajaponin C27H49NO9 ÏàËÆ¶È:53.3% Natural Product Research 2010 24 86-91 Panajaponin, a new glycosphingolipid from Panax japonicus Zhiyong Guo; Kun Zou; Feijun Dan; Junzhi Wang; Shu Zhu; Katsuko Komatsu Structure 13C NMR ̼Æ×Ä£Äâͼ 51 . 1,2-Di-O-9Z-octadecenoyl-sn-glycero-3-phosphorylcholine ÏàËÆ¶È:53.3% Archives of Pharmacal Research 2003 26 471-477 Phospholipids from Bombycis corpus and their neurotrophic effects Hak Cheol Kwon, I Yeon Jung, Se Yeon Cho, Ock Ryun Cho and Min Cheol Yang, et al. Structure 13C NMR ̼Æ×Ä£Äâͼ 52 . 1-linoleoyl-3-O-¦Â-D-galactopyranosyl-sn-glycerol ÏàËÆ¶È:53.3% 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 53 . PX23 ÏàËÆ¶È:53.3% Journal of the Chemical Society, Perkin Transactions 1 1996 2651-2656 Preparative transformation of natural phospholipids catalysed by phospholipase D from Streptomyces Paola D'Arrigo, Lorenzo de Ferra, Valentino Piergianni, Antonio Selva, Stefano Servi and Alberto Strini Structure 13C NMR ̼Æ×Ä£Äâͼ 54 . inseparable III+IV |

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