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wangwang1989
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²éѯģʽ£ºÄ£ºý²éѯ ̼Æ×Êý¾ÝÊäÈ룺 °´´ÓСµ½´ó˳ÐòÊäÈ룬Êý×Ö¼äÓÃÓ¢Îİë½Ç¶ººÅ(,)·Ö¸ôÀýÈ磺 21.4,30.4,37.4,73.2,73.7,125.6,126.6,139.6,140.2,168.2 ÈܼÁÑ¡Ï Æ¥ÅäÈݲ (Êý×Ö¸ñʽ£¬¿É×ÔÐÐÉ趨) ÏàËÆ¶È£º %(ÏàËÆ¶È>=50%) ²éѯ½á¹û£º¹²²éµ½1014¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . leucoceramides A¨CG C34H67NO5,C35H69NO5,C36H71NO5,C37H73NO5,C38H75NO5,C39H77NO5,C40H79NO5 ÏàËÆ¶È:72.2% Phytochemistry 2006 67 1143-1150 Immunosuppressive diacetylenes, ceramides and cerebrosides from Hydrocotyle leucocephala Freddy Ramos, Yoshihisa Takaishi, Kazuyoshi Kawazoe, Coralia Osorio,Carmenza Duque, Ricardo Acuña, Yoshinori Fujimoto, Mitsunobu Sato,Masato Okamoto, Tetsuya Oshikawa, Sharif Uddin Ahmed Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . ¦¤(4,5)(E),¦¤(8,9)(E)-Çʰ·´¼-ÕýÊ®Áù̼õ£°· C34H65NO3 ÏàËÆ¶È:72.2% Chinese Journal of Marine Drugs 2000 19(3) 5-7 STUDIES ON THE CHEM ICAL CONSTITUENTS OF THE SOFT CORAL LOBOPH Y TUM SP1FROM SOU TH CH INA SEA Liang Liyan, Deng Songzhi, Wu Houming Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . Cameroonemide A C43H85NO5 ÏàËÆ¶È:72.2% Journal of Asian Natural products Research 2010 12 629-633 Cameroonemide A: a new ceramide from Helichrysum cameroonense Kakam Zanetsie Antoine; Hidayat Hussain; Etienne Dongo; Simeon F. Kouam; Barbara Schulz; Karsten Krohn Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . lobophytamide L8 C34H65NO3 ÏàËÆ¶È:72.2% Acta Scientiarum Naturalium Universitatis Sunyatseni 1989 28(4) 22-27 Studies on the Chemical Constituents of the Chinese Soft Coral¡ªLobophytum chevalieri Tixier Duriult (XXI) Li Ruisheng, Di Li, Long Kanghou Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . hexadecanoic acid (2-hydroxy-1-hydroxymethyl-heptadeca-3,7dienyl)-amide ÏàËÆ¶È:68.4% Natural Product Research and Development 2003 15 109-112 STUDIES ON CHEMICAL CONSTITUENTS FROM ACROPORA PULCHRA XU Shi hai; YANG Kai; GUO Shu hao; LIU Ying ping Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . N-1-ôÇ»ù¼×»ù-2-ôÇ»ù-(E,E)-3,7-Ê®Æß̼¶þÏ©»ùÊ®ÁùËáõ£õ£°· ÏàËÆ¶È:68.4% Journal of Chinese Medicinal Materials 2001 24 640-641 Isolation and Identification of Chemical Constituents from Acropora pulchra Liu Yingping, Xu Shihai, Guo Shuhao, Li Xiaolin Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . compound 3 C42H80NO4 ÏàËÆ¶È:68.1% Natural Product Research 2009 23 44-50 Isolation and structure determination of the biologically active sphingolipids from marine sponge Haliclona species Seif-Eldin N. Ayyad; Saleh Omar S. Bahaffi; Nadia E. Hashish Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . rigidiusculamide D C18H25NO5 ÏàËÆ¶È:66.6% Journal of Natural Products 2009 72 2184-2187 Pyrrolidinones from the Ascomycete Fungus Albonectria rigidiuscula Jian Li, Shuchun Liu, Shubin Niu,Wenying Zhuang, and Yongsheng Che Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . (4E,8E)-2(hexadecanoylamino)-4,8-O-ctadecadiene-1,3-diol ÏàËÆ¶È:66.6% Chinese Journal of Marine Drugs 2005 24(6) 37-40 Ceramides and cerebrosides from Bugul a neritina ZHOU Guang-xiong, HUANG Mei-yan, SHI Jiang-gong Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . Tithoniamide B C42H83NO5 ÏàËÆ¶È:66.6% Zeitschrift f¨¹r Naturforschung B 2006 61b 78-82 Tithoniaquinone A and Tithoniamide B: A New Anthraquinone and a New Ceramide from Leaves of Tithonia diversifolia Meffo Yemele Bouberte, Karsten Krohn, Hidayat Hussain, Etienne Dongo, Barbara Schulz, and Qunxiu Hu Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . (4E,8E)-2(hexadecanoylamino)-4,8-octadecad-iene-1,3-diol ÏàËÆ¶È:66.6% Chinese Pharmaceutical Journal 2009 44 740-742 Study on Chemical Constituents of Soft Coral Dendronephthya gigantea from the South China Sea WANG Ying-li, LIAO Xiao-jian, XU Shi-hai Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . 6,7,10-trihydroxy-8-octadecenoic acid ÏàËÆ¶È:66.6% Chinese Pharmaceutical Journal 2009 44 1137-1140 Studies on Chemical Constituents of Acanthopanax brachypus(¢ò) HU Hao-bin, FAN Jun Structure 13C NMR ̼Æ×Ä£Äâͼ |

2Â¥2013-06-20 08:20:47
jasminelw
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zhiwu1983: ½ð±Ò+15, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2013-06-20 14:21:14
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zhiwu1983: ½ð±Ò+15, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2013-06-20 14:21:14
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²éѯ½á¹û£º¹²²éµ½10202¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) -------------------------------------------------------------------------------- 1 . leucoceramides A¨CG C34H67NO5,C35H69NO5,C36H71NO5,C37H73NO5,C38H75NO5,C39H77NO5,C40H79NO5 ÏàËÆ¶È:88.8% Phytochemistry 2006 67 1143-1150 Immunosuppressive diacetylenes, ceramides and cerebrosides from Hydrocotyle leucocephala Freddy Ramos, Yoshihisa Takaishi, Kazuyoshi Kawazoe, Coralia Osorio,Carmenza Duque, Ricardo Acuña, Yoshinori Fujimoto, Mitsunobu Sato,Masato Okamoto, Tetsuya Oshikawa, Sharif Uddin Ahmed Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . compound (9S,10S)-2 C18H32O4 ÏàËÆ¶È:88.8% Tetrahedron 2012 68 5583-5589 Enantio-selective reduction of the flowering related compound KODA and its analogues in Pharbitis nil cv. Violet Ariaki Murata, Kenji Kai, Ken Tsutsui, Jun Takeuchi, Yasushi Todoroki, Kazuo Furihata, Mineyuki Yokoyama, Susanne Baldermann, Naoharu Watanabe Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . compound (9R,10R)-2 C18H32O4 ÏàËÆ¶È:88.8% Tetrahedron 2012 68 5583-5589 Enantio-selective reduction of the flowering related compound KODA and its analogues in Pharbitis nil cv. Violet Ariaki Murata, Kenji Kai, Ken Tsutsui, Jun Takeuchi, Yasushi Todoroki, Kazuo Furihata, Mineyuki Yokoyama, Susanne Baldermann, Naoharu Watanabe Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . triumfettamide C43H85NO5 ÏàËÆ¶È:84.2% Helvetica Chimica Acta 2008 Vol. 91 1326 Triumfettamide and Triumfettoside Ic, Two Ceramides and Other Secondary Metabolites from the Stems of Wild Triumfetta cordifolia A. Rich. (Tiliaceae) Louis Pergaud Sandjo, Paul Hannewald, Mehdi Yemloul, Gilbert Kirsch, and Bonaventure Tchaleu Ngadjui Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . (2S,3S,4R,8E)-2-[(2'R)-2'-Hydroxylignoceroylamino]-8(E)-octadecene-1,3,4-triol C42H83O5N ÏàËÆ¶È:84.2% Archives of Pharmacal Research 2005 28 1239-1243 Norditerpenoid alkaloids and other components from the processed tubers of aconitum carmichaeli Sang Hee Shim, So Young Lee, Ju Sun Kim, Kun Ho Son and Sam Sik Kang Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . hexadecanoic acid (2-hydroxy-1-hydroxymethyl-heptadeca-3,7dienyl)-amide ÏàËÆ¶È:84.2% Natural Product Research and Development 2003 15 109-112 STUDIES ON CHEMICAL CONSTITUENTS FROM ACROPORA PULCHRA XU Shi hai; YANG Kai; GUO Shu hao; LIU Ying ping Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . N-1-ôÇ»ù¼×»ù-2-ôÇ»ù-(E,E)-3,7-Ê®Æß̼¶þÏ©»ùÊ®ÁùËáõ£õ£°· ÏàËÆ¶È:84.2% Journal of Chinese Medicinal Materials 2001 24 640-641 Isolation and Identification of Chemical Constituents from Acropora pulchra Liu Yingping, Xu Shihai, Guo Shuhao, Li Xiaolin Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . longifoamide A C43H85NO4 ÏàËÆ¶È:83.3% 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 -------------------------------------------------------------------------------- 9 . longifoamide B C43H85NO5 ÏàËÆ¶È:83.3% 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 -------------------------------------------------------------------------------- 10 . (4E,8E)-2(hexadecanoylamino)-4,8-O-ctadecadiene-1,3-diol ÏàËÆ¶È:83.3% Chinese Journal of Marine Drugs 2005 24(6) 37-40 Ceramides and cerebrosides from Bugul a neritina ZHOU Guang-xiong, HUANG Mei-yan, SHI Jiang-gong Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 11 . ¦¤(4,5)(E),¦¤(8,9)(E)-Çʰ·´¼-ÕýÊ®Áù̼õ£°· C34H65NO3 ÏàËÆ¶È:83.3% Chinese Journal of Marine Drugs 2000 19(3) 5-7 STUDIES ON THE CHEM ICAL CONSTITUENTS OF THE SOFT CORAL LOBOPH Y TUM SP1FROM SOU TH CH INA SEA Liang Liyan, Deng Songzhi, Wu Houming Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 12 . (4E,8E)-2(hexadecanoylamino)-4,8-octadecad-iene-1,3-diol ÏàËÆ¶È:83.3% Chinese Pharmaceutical Journal 2009 44 740-742 Study on Chemical Constituents of Soft Coral Dendronephthya gigantea from the South China Sea WANG Ying-li, LIAO Xiao-jian, XU Shi-hai Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 13 . isisamide C33H63NO3 ÏàËÆ¶È:83.3% Natural Product Research and Development 1994 6(1) 32-35 A NEW CERAMIDE FROM GORHONIAN ISIS SP. OF THE SOUTH CHINA SEA Deng Songzhi; Li Fengying; Tan Xiefeng Chen Jiefei Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 14 . lobophytamide L8 C34H65NO3 ÏàËÆ¶È:83.3% Acta Scientiarum Naturalium Universitatis Sunyatseni 1989 28(4) 22-27 Studies on the Chemical Constituents of the Chinese Soft Coral¡ªLobophytum chevalieri Tixier Duriult (XXI) Li Ruisheng, Di Li, Long Kanghou Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 15 . compound 3 C42H80NO4 ÏàËÆ¶È:81.8% Natural Product Research 2009 23 44-50 Isolation and structure determination of the biologically active sphingolipids from marine sponge Haliclona species Seif-Eldin N. Ayyad; Saleh Omar S. Bahaffi; Nadia E. Hashish Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 16 . PGF2¦Á ÏàËÆ¶È:80% Bioorganic & Medicinal Chemistry Letters 1999 9 1853-1858 Lipase-catalysed acylation of prostanoids Omar Parve, Ivar Järving, Ivar Martin, Andrus Metsala, Imre Vallikivi, Madis Aidnik, Tõnis Pehk, Nigulas Samel Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 17 . gracilamide A C43H83NO5 ÏàËÆ¶È:78.9% Journal of Natural Products 2006 69 1488-1491 Gracilarioside and Gracilamides from the Red Alga Gracilaria asiatica Yi Sun, Youjun Xu, Kai Liu, Huiming Hua, He Zhu, and Yuehu Pei Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 18 . ÐÁ»ù-4,5-¶þôÇ»ù-3-(ÈÉ-4-ϩ̪Ñõ»ù)ßÁ¿©Íé-2-ôÈËáõ¥ ÏàËÆ¶È:78.9% Chinese Traditional and Herbal Drugs 2007 38 1157-1159 СҶÈýµã½ð»¯Ñ§³É·ÖÑо¿ ëÉÜ´º;ÀîÖñÓ¢;Àî´Ï Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 19 . N-(2'-hydroxyeicosanoyl0-1,3,4-trihydroxy-2-aminoheptadec-5-ene C37H73NO5 ÏàËÆ¶È:78.9% Indian Journal of Chemistry 1999 38B 357-360 A new sphingosine derivative and a new polyhydroxy steroidal glycoside from sinularia gravis Tixier-Durivault of the Aandaman and Nicobar Islands V Anjaneyulu, P V subba Rao&Padhika Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 20 . (9S*,10R*,11R*,12Z,15Z)-9,10,11-trihydroxyoctadeca-12,15-dienoic acid C18H32O5 ÏàËÆ¶È:77.7% 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 -------------------------------------------------------------------------------- 21 . gracilamide B C43H85NO5 ÏàËÆ¶È:77.7% Journal of Natural Products 2006 69 1488-1491 Gracilarioside and Gracilamides from the Red Alga Gracilaria asiatica Yi Sun, Youjun Xu, Kai Liu, Huiming Hua, He Zhu, and Yuehu Pei Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 22 . tithoniamide C43H85NO5 ÏàËÆ¶È:77.7% Natural Product Research 2006 20 842-849 Tithoniamarin and tithoniamide: a structurally unique isocoumarin dimer and a new ceramide from Tithonia diversifolia Meffo Yemele Bouberte; Karsten Krohn; Hidayat Hussain; Etienne Dongo; Barbara Schulz; Qunxiu Hu Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 23 . corchorifatty acid F C18H32O5 ÏàËÆ¶È:77.7% Chemical & Pharmaceutical Bulletin 1998 46 1008-1014 Medicinal Foodstuffs. XIV. On the Bioactive Constituents of Moroheiya. (2) : New Fatty Acids, Corchorifatty Acids A, B, C, D, E, and F, from the Leaves of Corchorus olitorius L. (Tiliaceae) : Structures and Inhibitory Effect on NO Production in Mouse Peri Masayuki YOSHIKAWA,Toshiyuki MURAKAMI,Hiromi SHIMADA,Satoshi YOSHIZUMI,Masami SAKA,Johji YAMAHARA and Hisashi MATSUDA Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 24 . synurus cerebrosides ÏàËÆ¶È:77.7% Natural Product Sciences 2006 12 193-196 Cerebrosides and Triterpenoids from the Roots of Synurus deltoides Lee, Hyun-Young; Min, Byung-Sun; Son, Kun-Ho; Chang, Hyeun-Wook; Kim, Hyun-Pyo; Kang, Sam-Sik; Bae, Ki-Hwan Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 25 . Laportomide A C42H83NO5 ÏàËÆ¶È:77.7% Zeitschrift f¨¹r Naturforschung B 2007 62b 1208-1212 Laportoside A and Laportomide A: A New Cerebroside and a New Ceramide from Leaves of Laportea ovalifolia Dagobert Tazoo, Karsten Krohn, Hidayat Hussain, Simeon F. Kouam, and Etienne Dongo Structure 13C NMR ̼Æ×Ä£Äâͼ |
3Â¥2013-06-20 08:21:41














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