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yjl2007: ½ð±Ò+10 2014-08-08 15:24:11
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yjl2007: ½ð±Ò+10 2014-08-08 15:24:11
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²éѯ½á¹û£º¹²²éµ½61¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . ardisiphenol B C23H36O4 ÏàËÆ¶È:65.2% Chemical & Pharmaceutical Bulletin 2002 50(11) 1484-1487 Ardisiphenols and Other Antioxidant Principles from the Fruits of Ardisia colorata Megumi SUMINO,Toshikazu SEKINE, Nijsiri RUANGRUNGSI,Kazuei IGARASHI,and Fumio IKEGAMI Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . O-oleyl-L-glutamine C23H42N2O4 ÏàËÆ¶È:65.2% Tetrahedron 1999 55 11275-11280 New fatty acid amides from regurgitant of Lepidopteran (Noctuidae, Geometridae) caterpillars Georg Pohnert, Verena Jung, Erkki Haukioja, Kyösti Lempa, Wilhelm Boland Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . tornabeatin B C24H42O3 ÏàËÆ¶È:62.5% Phytochemistry 2004 65 2605-2612 The tornabeatins, four tetrahydro-2-furanone derivatives from the lichenized ascomycete Tornabea scutellifera (With.) J.R. Laundon Tom¨¢š Řezanka, Marina Temina, Lum¨ªr Hanuš, Valery M. Dembitsky Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . tornabeatin A C22H38O3 ÏàËÆ¶È:60.8% Phytochemistry 2004 65 2605-2612 The tornabeatins, four tetrahydro-2-furanone derivatives from the lichenized ascomycete Tornabea scutellifera (With.) J.R. Laundon Tom¨¢š Řezanka, Marina Temina, Lum¨ªr Hanuš, Valery M. Dembitsky Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . N-linolyl-L-glutamine C23H40N2O4 ÏàËÆ¶È:60.8% Tetrahedron 1999 55 11275-11280 New fatty acid amides from regurgitant of Lepidopteran (Noctuidae, Geometridae) caterpillars Georg Pohnert, Verena Jung, Erkki Haukioja, Kyösti Lempa, Wilhelm Boland Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . N-linolyl-L-glutamate C22H39NO5 ÏàËÆ¶È:60.8% Tetrahedron 1999 55 11275-11280 New fatty acid amides from regurgitant of Lepidopteran (Noctuidae, Geometridae) caterpillars Georg Pohnert, Verena Jung, Erkki Haukioja, Kyösti Lempa, Wilhelm Boland Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . 1,4-dideoxy-5-O-[(9Z)-octadec-9-en-1-yl]-1,4-imino-D-ribitol C23H45NO3 ÏàËÆ¶È:60.8% Bioorganic & Medicinal Chemistry 2011 19 7720-7727 Anti-cancer activity of 5-O-alkyl 1,4-imino-1,4-dideoxyribitols Claudia Bello, Giovanna Dal Bello, Michele Cea, Aimable Nahimana, Dominique Aubry, Anna Garuti, Giulia Motta, Eva Moran, Floriana Fruscione, Paolo Pronzato, Francesco Grossi, Franco Patrone, Alberto Ballestrero, Marc Dupuis, Bernard Sordat, Kaspar Zimmermann, Jacqueline Loretan, Markus Wartmann, Michel A. Duchosal, Alessio Nencioni, et al. Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . gerronemin B C24H32O4 ÏàËÆ¶È:56.5% Phytochemistry 2002 59 643-648 Gerronemins A¨CF, cytotoxic biscatechols from a Gerronema species Sven Silberborth, Anja Stumpf, Gerhard Erkel, Timm Anke, Olov Sterner Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . gerronemin D C26H36O4 ÏàËÆ¶È:56.5% Phytochemistry 2002 59 643-648 Gerronemins A¨CF, cytotoxic biscatechols from a Gerronema species Sven Silberborth, Anja Stumpf, Gerhard Erkel, Timm Anke, Olov Sterner Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . gerronemin F C28H38O4 ÏàËÆ¶È:56.5% Phytochemistry 2002 59 643-648 Gerronemins A¨CF, cytotoxic biscatechols from a Gerronema species Sven Silberborth, Anja Stumpf, Gerhard Erkel, Timm Anke, Olov Sterner Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . 1-methyl-2-[(Z)-7-tridecenyl]-4(1H)-quinolone ÏàËÆ¶È:56.5% Phytochemistry 1996 43 719-722 Quinolone alkaloids from Evodia rutaecarpa Yuan-Qing Tang, Xiao-Zhang Feng, Liang Huang Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . 1-methyl-2-[(Z)-7-tridecenyl]-4(1H)-evocarpine ÏàËÆ¶È:56.5% Phytochemistry 1996 43 719-722 Quinolone alkaloids from Evodia rutaecarpa Yuan-Qing Tang, Xiao-Zhang Feng, Liang Huang Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . Compound 1b C24H46N3O2 ÏàËÆ¶È:56.5% Bioorganic & Medicinal Chemistry Letters 2007 17 4584-4587 Design, synthesis, and preliminary biological evaluation of a novel triazole analogue of ceramide Sanghee Kim, Minjae Cho, Taeho Lee, Sukjin Lee, Hye-Young Min, Sang Kook Lee Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . (2S,3R,2'S,4E)-2'-hydroxy-C4-ceramide C22H49NO4 ÏàËÆ¶È:56.5% Bioorganic & Medicinal Chemistry 2010 18 7565-7579 Synthesis, NMR characterization and divergent biological actions of 2'-hydroxy-ceramide/dihydroceramide stereoisomers in MCF7 cells Zdzislaw M. Szulc, Aiping Bai, Jacek Bielawski, Nalini Mayroo, Doreen E. Miller, Hanna Gracz, Yusuf A. Hannun, Alicja Bielawska Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . N-palmitoleyl-L-glutamine C21H38N2O4 ÏàËÆ¶È:56.5% Tetrahedron 1999 55 11275-11280 New fatty acid amides from regurgitant of Lepidopteran (Noctuidae, Geometridae) caterpillars Georg Pohnert, Verena Jung, Erkki Haukioja, Kyösti Lempa, Wilhelm Boland Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . 7,8-dihydroxy-3-decyl-4-methylcoumarin C20H28O4 ÏàËÆ¶È:56.5% Bioorganic & Medicinal Chemistry 2009 17 1550-1556 Specificities of Calreticulin Transacetylase to acetoxy derivatives of 3-alkyl-4-methylcoumarins: Effect on the activation of nitric oxide synthase Abha Kathuria, Anjali Gupta, Nivedita Priya, Prabhjot Singh, Hanumantharao G. Raj, Ashok K. Prasad, Virinder S. Parmar, Sunil K. Sharma Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . (S)-N-(12-aminododecyl)-4-hydroxy-¦Á-[(1-oxobutyl)amino]benzenepropanamide trifluoroacetate ÏàËÆ¶È:56.5% Journal of Medicinal Chemistry 2000 43 4526-4533 Solid-Phase Synthesis and Biological Evaluation of a Combinatorial Library of Philanthotoxin Analogues Kristian Strømgaard, Tim J. Brier, Kim Andersen, Ian R. Mellor, Alex Saghyan, Denis Tikhonov, Peter N. R. Usherwood, Povl Krogsgaard-Larsen, and Jerzy W. Jaroszewski Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . (E)-9-octadecenoic acid C18H34O2 ÏàËÆ¶È:56.5% Journal of Agricultural and Food Chemistry 2002 50 6993-6996 Repellent Activity of Constituents Identified in Foeniculum vulgare Fruit against Aedes aegypti (Diptera: Culicidae) Do-Hyoung Kim, Soon-Il Kim, Kyu-Sik Chang, and Young-Joon Ahn Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . linoleic acid C18H32O2 ÏàËÆ¶È:56.5% Chinese Journal of Medicinal Chemistry 2012 22 47-50 Chemical constituents of Lysimachia stenosepala CAO Xian-ping; LIANG Xin; ZHONG Hui-min Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . N-(3,5-Dimethoxy-4-hydroxy-E-cinnamoyl)-L-tyrosine Dodecyl Ester C32H45NO7 ÏàËÆ¶È:55.5% Journal of Agricultural and Food Chemistry 2003 51 4596-4602 Synthesis of Lipophilic Clovamide Derivatives and Their Antioxidative Potential against Lipid Peroxidation Jakob P. Ley and Heinz-J¨¹rgen Bertram Structure 13C NMR ̼Æ×Ä£Äâͼ 21 . (E)-2,11,12,13,15,16-Hexachloro-14-hydroxytetracos-1-en-1-yl sulfate C24H41Cl6O5S ÏàËÆ¶È:54.1% Journal of Natural Products 2010 73 279-283 Structure Revision and Absolute Configuration of Malhamensilipin A from the Freshwater Chrysophyte Poterioochromonas malhamensis Alban R. Pereira, Tara Byrum, Grant M. Shibuya, Christopher D. Vanderwal and William H. Gerwick Structure 13C NMR ̼Æ×Ä£Äâͼ 22 . tert-butyl {(4R,5S)-4-[8'-(2''-hexyl-1'',3''-dioxolan-2''-yl)octyl]-5-(hydroxymethyl)-2,2-dimethyl-1,3-dioxan-5-yl}carbamate C29H55NO7 ÏàËÆ¶È:54.1% Chemical Papers 2013 67 1317-1329 Stereoselective total synthesis of protected sulfamisterin and its analogues Jana Špakov¨¢ Raschmanov¨¢, Miroslava Martinkov¨¢*, Jozef Gonda, Alena Uhr¨ªkov¨¢ Structure 13C NMR ̼Æ×Ä£Äâͼ 23 . 1-oleoyl-3-O-¦Â-D-galactopyranosyl-sn-glycerol ÏàËÆ¶È:53.8% 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 24 . 1-O-11'-(Z)-icosen-1'-ynyl-2-hydroxy-sn-glycero-3-phosphoethanolamine C25H48NO6P ÏàËÆ¶È:53.5% Bioorganic & Medicinal Chemistry 2014 22 2966-2973 Synthesis and evaluation of immunostimulant plasmalogen lysophosphatidylethanolamine and analogues for natural killer T cells Guanghui Ni, Zhiyuan Li, Kangjiang Liang, Ting Wu, Gennaro De Libero, Chengfeng Xia Structure 13C NMR ̼Æ×Ä£Äâͼ 25 . Alkylresorcinol B ÏàËÆ¶È:52.1% Chemical & Pharmaceutical Bulletin 2002 50(11) 1484-1487 Ardisiphenols and Other Antioxidant Principles from the Fruits of Ardisia colorata Megumi SUMINO,Toshikazu SEKINE, Nijsiri RUANGRUNGSI,Kazuei IGARASHI,and Fumio IKEGAMI Structure 13C NMR ̼Æ×Ä£Äâͼ |

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