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wdzhengqun: ½ð±Ò+12, ¡ïÓаïÖú 2014-12-02 12:17:30
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wdzhengqun: ½ð±Ò+12, ¡ïÓаïÖú 2014-12-02 12:17:30
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²éѯ½á¹û£º¹²²éµ½227¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . (8R*,9R*,10S*,6Z)-trihydroxyoctadec-6-enoic acid C18H34O5 ÏàËÆ¶È:72.2% Journal of Natural Products 2009 72 813-817 Oxylipins from Dracontium loretense Angelyne Benavides, Assunta Napolitano, Carla Bassarello, Virginia Carbone, Patrizia Gazzerro, AnnaMaria Malfitano, Paola Saggese, Maurizio Bifulco, Sonia Piacente, and Cosimo Pizza Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . porrigenic Acid C18H30O4 ÏàËÆ¶È:72.2% Chemical & Pharmaceutical Bulletin 2007 55(12) 1748-1749 Cytotoxic Fatty Acid from Pleurocybella porrigens Tatsuya HASEGAWA, Mayumi ISHIBASHI, Takanobu TAKATA, Fumihide TAKANO, and Tomihisa OHTA Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . (14RS)-(10E,12E)-14-hydroxy- 9-oxo-10,12-octadecadienoic acid C18H30O4 ÏàËÆ¶È:72.2% Chemical & Pharmaceutical Bulletin 2006 54(8) 1213-1215 Conjugated Ketonic Fatty Acids from Pleurocybella porrigens Yoshiaki AMAKURA,Kazunari KONDO,Hiroshi AKIYAMA,Hideyuki ITO,Tsutomu HATANO,Takashi YOSHIDA,and Tamio MAITANI Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . (12RS)-(8E,10E)-12-hydroxy-7-oxo-8,10-octadecadienoic acid C18H30O4 ÏàËÆ¶È:72.2% Chemical & Pharmaceutical Bulletin 2006 54(8) 1213-1215 Conjugated Ketonic Fatty Acids from Pleurocybella porrigens Yoshiaki AMAKURA,Kazunari KONDO,Hiroshi AKIYAMA,Hideyuki ITO,Tsutomu HATANO,Takashi YOSHIDA,and Tamio MAITANI Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . (8E,12Z)-10,11-Dihydroxyoctadeca-8,12-dienoic acid C18H32O4 ÏàËÆ¶È:72.2% Magnetic Resonance in Chemistry 2011 49 366-369 Steroids and an oxylipin from an algicolous isolate of Aspergillus flavus Ming-Feng Qiao,Nai-Yun Ji, Feng-PingMiaoa and Xiu-Li Yin Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . 1¦Â,2¦Â,3¦Á-cyclopent-4-ene-1,2,3-triol-2--tridecanoicAcidEster C18H32O4 ÏàËÆ¶È:72.2% Chemistry of Natural Compounds 2013 49 219-221 A new compound from the roots of Ligularia vellerea Cai-Fang Wang, Ling Zhu, Yuan Zhao, Jing Zhou, Yu Zhao, Zhen-Zhong Zhang Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . linoleic acid C18H32O2 ÏàËÆ¶È:72.2% 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 8 . (9E)-8,11,12-ÈýôÇ»ù-Ê®°Ë̼ϩËá C18H34O5 ÏàËÆ¶È:72.2% Journal of Tropical and Subtropical Botany 2013 21 57-62 Chemical Constituents from Roots of Achyranthes bidentata TANG Xin, PEI Gang, ZHOU Zhong-yu, TAN Jian-wen Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . (9R,10R,7E)-6,9,10-trihydroxyoctadec-7-enoic acid C18H34O5 ÏàËÆ¶È:72.2% Journal of Jinan University (Natural Science) 2013 34 324-327 Chemical constituents in petroleum ether fraction of Nerviliae fordii CHEN Jinman, WEI Liubin, ZHANG Ying, YE Wencai, ZHOU Guangxiong Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . (9S,10R,11E,13R)-9,10,13-trihydroxyoctadec-11-enoic Acid C18H34O5 ÏàËÆ¶È:66.6% Chemistry & Biodiversity 2008 Vol. 5 1780 Chemical Characterization of New Oxylipins from Cestrum parqui, and Their Effects on Seed Germination and Early Seedling Growth Antonio Fiorentino, Brigida D!Abrosca, Marina DellaGreca, Angelina Izzo, Angela Natale, Maria Teresa Pascarella, Severina Pacifico, Armando Zarrelli, and Pietro Monaco Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . (9S,10R,11E,13S)-9,10,13-trihydroxyoctadec-11-enoic Acid C18H34O5 ÏàËÆ¶È:66.6% Chemistry & Biodiversity 2008 Vol. 5 1780 Chemical Characterization of New Oxylipins from Cestrum parqui, and Their Effects on Seed Germination and Early Seedling Growth Antonio Fiorentino, Brigida D!Abrosca, Marina DellaGreca, Angelina Izzo, Angela Natale, Maria Teresa Pascarella, Severina Pacifico, Armando Zarrelli, and Pietro Monaco Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . 9,12,13-trihydroxyoctadeca-10(E)-dienoic acid C18H34O5 ÏàËÆ¶È:66.6% Journal of Natural Products 2006 69 1366-1369 Phytochemical Constituents from Salsola tetrandra M. Habib Oueslati, Hichem Ben Jannet, Zine Mighri, J. Chriaa, and Pedro M. Abreu Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . ÌìʦËá ÏàËÆ¶È:66.6% Chinese Traditional and Herbal Drugs 2009 40 1715-1719 ËÕÃŰ׾ƲݵĻ¯Ñ§³É·ÖÑо¿ ½âЦè¤;ËÕÑÞ·¼;²ñÐÀ;ÖÜάÒå;µËС¾ê;¹ùÀöƼ;¸ßÐã÷;ÕŲ®Àñ Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . 9(S),12(S),13(S)-Trihydroxy-10(E)-octadecenoic acid ÏàËÆ¶È:66.6% Archives of Pharmacal Research 2007 30 665-669 Two new ¦Á-pyrones and other components from the cladodes of Opuntia dillenii Ying Kun Qiu, Yan Yan Zhao, De Qiang Dou, Bi Xia Xu and Ke Liu Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . compound 4 C18H34O5 ÏàËÆ¶È:66.6% Tetrahedron Letters 2002 43 1265-1268 Total synthesis of pinellic acid, a potent oral adjuvant for nasal influenza vaccine. Determination of the relative and absolute configuration Toshiaki Sunazuka, Tatsuya Shirahata, Kiminari Yoshida, Daisuke Yamamoto, Yoshihiro Harigaya, Takayuki Nagai, Hiroaki Kiyohara, Haruki Yamada, Isao Kuwajima, Satoshi ¨mura Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . compound 5 C18H34O5 ÏàËÆ¶È:66.6% Tetrahedron Letters 2002 43 1265-1268 Total synthesis of pinellic acid, a potent oral adjuvant for nasal influenza vaccine. Determination of the relative and absolute configuration Toshiaki Sunazuka, Tatsuya Shirahata, Kiminari Yoshida, Daisuke Yamamoto, Yoshihiro Harigaya, Takayuki Nagai, Hiroaki Kiyohara, Haruki Yamada, Isao Kuwajima, Satoshi ¨mura Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . ¦Á-dimorphecolic acid C18H32O3 ÏàËÆ¶È:66.6% Journal of Ethnopharmacology 2008 116 554-560 Antibacterial compounds from Planchonia careya leaf extracts Jacqui M. McRae, Qi Yang, Russell J. Crawford, Enzo A. Palombo Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . pinellic acid ÏàËÆ¶È:66.6% Korean Journal of Pharmacognosy 2011 42 127-137 Phytochemical Studies on Rehmanniae Radix Lee, So-Young; Yean, Min-Hye; Kim, Ju-Sun; Lee, Je-Hyun; Kang, Sam-Sik Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . 9(S),12(R),13(S)-trihydroxystearic acid C18H32O4 ÏàËÆ¶È:66.6% Tetrahedron 1980 36 993-996 Malyngic acid, a new fatty acid from Lyngbya majuscula Original Research Article John H. Cardellina II, Richard E. Moore Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . tianshic acid C18H34O5 ÏàËÆ¶È:66.6% Natural Product Research and Development 2013 25 1665-1668 Chemical Constituents from Corydalis bungeana Turcz. XIAO Yang, YANG Chun-juan, ZHONG Ming-liang, JIANG Xue-chun, LIU Gao-feng* Structure 13C NMR ̼Æ×Ä£Äâͼ 21 . Tianshic Acid ÏàËÆ¶È:66.6% Journal of Agricultural and Food Chemistry 2002 50 6318-6321 Antifungal Constituents from the Seeds of Allium fistulosum L. Shengmin Sang, Aina Lao, Yanseng Wang, Chee-Kok Chin, Robert T. Rosen, and Chi-Tang Ho Structure 13C NMR ̼Æ×Ä£Äâͼ 22 . (9S,12S,13S)-(E)-9,12,13-trihydroxy-10-octadecaenoic acid ÏàËÆ¶È:66.6% Chinese Traditional and Herbal Drugs 2012 43 649-652 Chemical constituents from barks of Ailanthus altissima WANG Yan; ZHANG Hai-ning; WANG Wen-jing; ZHANG Sheng-yuan; ZHANG Xiao-qi; YE Wen-cai Structure 13C NMR ̼Æ×Ä£Äâͼ 23 . Pinellic acid C18H34O5 ÏàËÆ¶È:66.6% Journal of Tropical and Subtropical Botany 2012 20 413-417 Antibacterial Activity Components from Elephantopus tomentosus WANG Bei, MEI Wen-li, ZUO Wen-jian, ZENG Yan-bo, LIU Guo-dao, DAI Hao-fu Structure 13C NMR ̼Æ×Ä£Äâͼ 24 . ÑÇÓÍËá C18H32O2 ÏàËÆ¶È:66.6% Journal of Tropical and Subtropical Botany 2013 21 57-62 Chemical Constituents from Roots of Achyranthes bidentata TANG Xin, PEI Gang, ZHOU Zhong-yu, TAN Jian-wen Structure 13C NMR ̼Æ×Ä£Äâͼ 25 . 7,10-dihydroxy-8(E)-octadecenoic acid ÏàËÆ¶È:66.6% Journal of the American Oil Chemists' Society 1992 69 367-371 7,10-Dihydroxy-8(E)-Octadecenoic acid: Stereochemistry and a novel derivative, 7,10-Dihydroxyoctadecanoic acid G. Knothe, M. O. Bagby, R. E. Peterson, C. T. Hou Structure 13C NMR ̼Æ×Ä£Äâͼ 26 . sugiol ÏàËÆ¶È:65% Natural Product Research and Development 2012 24 47-51 Chemical Constituents of Scrophularia ningpoensis Hemsl. LI Yuan; SONG Bao-an; YANG Song; HU De-yu; JIN Lin-hong Structure 13C NMR ̼Æ×Ä£Äâͼ 27 . dehydrohaliclocyclin F C19H29N ÏàËÆ¶È:63.1% Journal of Natural Products 2013 76 1997-2001 Cyclic 3-Alkyl Pyridinium Alkaloid Monomers from a New Zealand Haliclona sp. Marine Sponge Vidhiya Damodaran, Jason L. Ryan, and Robert A. Keyzers Structure 13C NMR ̼Æ×Ä£Äâͼ 28 . Oleioyl-¦Â-D-arabinoside C23H42O6 ÏàËÆ¶È:61.9% Journal of Agricultural and Food Chemistry 2013 61 8039-8048 New Chemical Constituents from Oryza sativa Straw and Their Algicidal Activities against Blue-Green Algae Ateeque Ahmad, Seung-Hyun Kim, Mohd Ali, Inmyoung Park, Jin-Seog Kim, Eun-Hye Kim, Ju-Jin Lim, Seul-Ki Kim, and Ill-Min Chung Structure 13C NMR ̼Æ×Ä£Äâͼ 29 . (9S*,10R*,11R*,12Z,15Z)-9,10,11-trihydroxyoctadeca-12,15-dienoic acid C18H32O5 ÏàËÆ¶È:61.1% Journal of Natural Products 2009 72 813-817 Oxylipins from Dracontium loretense Angelyne Benavides, Assunta Napolitano, Carla Bassarello, Virginia Carbone, Patrizia Gazzerro, AnnaMaria Malfitano, Paola Saggese, Maurizio Bifulco, Sonia Piacente, and Cosimo Pizza Structure 13C NMR ̼Æ×Ä£Äâͼ 30 . (9R*,10S*,7E)-6,9,10-trihydroxyoctadec-7-enoic acid C18H34O5 ÏàËÆ¶È:61.1% Journal of Natural Products 2009 72 813-817 Oxylipins from Dracontium loretense Angelyne Benavides, Assunta Napolitano, Carla Bassarello, Virginia Carbone, Patrizia Gazzerro, AnnaMaria Malfitano, Paola Saggese, Maurizio Bifulco, Sonia Piacente, and Cosimo Pizza Structure 13C NMR ̼Æ×Ä£Äâͼ 31 . (9R*,10R*,7E)-6,9,10-trihydroxyoctadec-7-enoic acid C18H34O5 ÏàËÆ¶È:61.1% Journal of Natural Products 2009 72 813-817 Oxylipins from Dracontium loretense Angelyne Benavides, Assunta Napolitano, Carla Bassarello, Virginia Carbone, Patrizia Gazzerro, AnnaMaria Malfitano, Paola Saggese, Maurizio Bifulco, Sonia Piacente, and Cosimo Pizza Structure 13C NMR ̼Æ×Ä£Äâͼ 32 . clathriadic acid C18H28N3O2 ÏàËÆ¶È:61.1% 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 33 . longifoamide A C43H85NO4 ÏàËÆ¶È:61.1% Natural Product Research 2006 20 953-960 Longifoamide-A and B: Two new ceramides from Mentha longifolia (Lamiaceae) Muhammad Shaiq Ali; Waqar Ahmed; Muhammad Saleem; Taous Khan Structure 13C NMR ̼Æ×Ä£Äâͼ 34 . Pinellic acid ÏàËÆ¶È:61.1% Korean Journal of Pharmacognosy 2009 40(4) 326-333 Phytochemical Studies on Lonicera Caulis (2) - Aliphatic and Phenolic Compounds Kim, Ju-Sun; Yean, Min-Hye; Seo, Hyun-Kyu; Lee, Je-Hyun; Kang, Sam-Sik Structure 13C NMR ̼Æ×Ä£Äâͼ 35 . (2R,3S,4R)-2-Methanesulfonyloxy-pentadecane-1,3,4-triol C16H34SO6 ÏàËÆ¶È:61.1% Bioorganic & Medicinal Chemistry 2011 19 221-228 Synthesis of truncated analogues of the iNKT cell agonist,¦Á-galactosyl ceramide (KRN7000), and their biological evaluation Natacha Veerapen, Faye Reddington, Mariolina Salio, Vincenzo Cerundolo, Gurdyal S. Besra Structure 13C NMR ̼Æ×Ä£Äâͼ 36 . Compound 6 ÏàËÆ¶È:61.1% Bioorganic & Medicinal Chemistry Letters 2001 11 1063-1064 Novel, lipophilic derivatives of 2,5-dideoxy-2,5-imino-D-mannitol (DMDP) are powerful ¦Â-glucosidase inhibitors Tanja M. Wrodnigg, Stephen G. Withers, Arnold E. St¨¹tz Structure 13C NMR ̼Æ×Ä£Äâͼ 37 . (S)-2-amino-oleyl alcohol ÏàËÆ¶È:61.1% Bioorganic & Medicinal Chemistry Letters 2003 13 375-377 Synthesis and In vivo anti-inflammatory activity of long-chain 2-amino-alcohols Victoria Magrioti, Dimitra Hadjipavlou-Litina, Violetta Constantinou-Kokotou Structure 13C NMR ̼Æ×Ä£Äâͼ 38 . Moluccanic acid C17H22O3 ÏàËÆ¶È:61.1% Tetrahedron Letters 2008 49 5150-5151 Three novel 3, 4-seco-podocarpane trinorditerpenoids from Aleurites moluccana Haiyang Liu, Yingtong Di, Junyun Yang, Fei Teng, Yi Lu, Wei Ni, Changxiang Chen, Xiaojiang Hao Structure 13C NMR ̼Æ×Ä£Äâͼ |

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