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jinglingle: ½ð±Ò+10, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2013-03-29 16:41:27
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²éѯ½á¹û£º¹²²éµ½17¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . petroraspailyne A1 C15H24O3 ÏàËÆ¶È:61.1% Journal of Natural Products 1999 62 122-126 New Acetylenic Enol Ethers of Glycerol from the Sponge Petrosia sp. Youngwan Seo, Ki Woong Cho, Hyi-Seung Lee, Jung-Rae Rho, and Jongheon Shin Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . Cytosporone R C19H28O7 ÏàËÆ¶È:52.6% Marine drugs 2012 10 762-774 Epigenetic Tailoring for the Production of Anti-Infective Cytosporones from the Marine Fungus Leucostoma persoonii Jeremy Beau, Nida Mahid, Whittney N. Burda, Lacey Harrington, Lindsey N. Shaw,Tina Mutka, Dennis E. Kyle, Betty Barisic, Alberto van Olphen and Bill J. Baker Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . Compound 6d C22H41N3O5 ÏàËÆ¶È:52.6% Bioorganic & Medicinal Chemistry Letters 2008 18 6265-6267 Synthesis of Arabino glycosyl triazoles as potential inhibitors of mycobacterial cell wall biosynthesis Brendan L. Wilkinson, Hilary Long, Edith Sim, Antony J. Fairbanks Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . petroside C16H26O8 ÏàËÆ¶È:50% Chemical & Pharmaceutical Bulletin 2000 48(7) 1039-1044 Medicinal Foodstuffs. XVIII. Phytoestrogens from the Aerial Part of Petroselinum crispum MILL. (PARSLEY) and Structures of 6"-Acetylapiin and a New Monoterpene Glycoside, Petroside Masayuki YOSHIKAWA,Toshiaki UEMURA,Hiroshi SHIMODA,Akinobu KISHI,Yuzo KAWAHARA and Hisashi MATSUDA Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . petroraspailyne A2 C16H26O3 ÏàËÆ¶È:50% Journal of Natural Products 1999 62 122-126 New Acetylenic Enol Ethers of Glycerol from the Sponge Petrosia sp. Youngwan Seo, Ki Woong Cho, Hyi-Seung Lee, Jung-Rae Rho, and Jongheon Shin Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . petroraspailyne B1 C15H26O3 ÏàËÆ¶È:50% Journal of Natural Products 1999 62 122-126 New Acetylenic Enol Ethers of Glycerol from the Sponge Petrosia sp. Youngwan Seo, Ki Woong Cho, Hyi-Seung Lee, Jung-Rae Rho, and Jongheon Shin Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . 1,2-di-O-miristoyl-3-O-(6-sulpho-¦Á-D-quinovopyranosyl)-glycerol C37H69O12SNa ÏàËÆ¶È:50% Phytochemistry 1997 45 647-650 Glycolipids from Byrsonima crassifolia Luca Rastrelli, Nunziatina De Tommasi, Ingeborg Berger, Armando Caceres, Amarillis Saravia, Francesco De Simone Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . ¦Â-D-Galactopyranosyl-(1¡ú1)-6-O-palmitate-¦Á-D-mannopyranoside C28H52O12 ÏàËÆ¶È:50% Bioorganic & Medicinal Chemistry 2011 19 4803-4811 Synthesis, gp120 binding and anti-HIV activity of fatty acid esters of 1, 1-linked disaccharides Stewart Bachan, Jacques Fantini, Anjali Joshi, Himanshu Garg, David R. Mootoo Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . N-ocyl-4-epi-¦Â-valienamine (NOEV) ÏàËÆ¶È:50% Bioorganic & Medicinal Chemistry Letters 2011 21 7189-7192 Transformation of quercitols into 4-methylenecyclohex-5-ene-1,2,3-triol derivatives, precursors for thechemical chaperones N-octyl-4-epi-¦Â-valienamine (NOEV) and N-octyl-¦Â-valienamine (NOV) Shinichi Kuno, Atsushi Takahashi, Seiichiro Ogawa Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . (+)-Raspailyne-A C21H36O4 ÏàËÆ¶È:50% Chemical Communications 1986 77-78 (+)-Raspailyne-A, a Novel, Acid-sensitive Acetylenic Enol Ether Glyceride from the Marine Sponge Raspailia pumila Graziano Guella, lnes Mancini, and Francesco Pietra Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . 3'-(4-pentyl-1,2,3-triazol-1-yl)-3'-deoxythymidine C17H25N5O4 ÏàËÆ¶È:50% Bioorganic & Medicinal Chemistry 2010 18 3261-3269 3'-(1, 2, 3-Triazol-1-yl)-3'-deoxythymidine analogs as substrates for human and Ureaplasma parvum thymidine kinase for structure¨Cactivity investigations Jay Lin, Vincent Roy, Liya Wang, Li You, Luigi A. Agrofoglio, Dominique Deville-Bonne, Tamara R. McBrayer, Steven J. Coats, Raymond F. Schinazi, Staffan Eriksson Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . octyl ¦Á-D-arabinofuranosyl-(1¡ú5)-3-deoxy-¦Á-D-arbinofuranoside C18H34O8 ÏàËÆ¶È:50% Bioorganic & Medicinal Chemistry 2009 17 872-881 Synthesis of deoxygenated ¦Á(1 ¡ú 5)-linked arabinofuranose disaccharides as substrates and inhibitors of arabinosyltransferases of Mycobacterium tuberculosis Ashish K. Pathak, Vibha Pathak, William J. Suling, James R. Riordan, Sudagar S. Gurcha, Gurdyal S. Besra, Robert C. Reynolds Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . octyl 2-deoxy-¦Á-D-arabino-hexopyranoside C14H28O5 ÏàËÆ¶È:50% Bioorganic & Medicinal Chemistry 2008 16 4083-4092 Alkyl deoxy-arabino-hexopyranosides: Synthesis, surface properties, and biological activities Filipa V.M. Silva, Margarida Goulart, Jorge Justino, Ana Neves, Fernando Santos, João Caio, Susana Lucas, Ana Newton, Diana Sacoto, Ester Barbosa, Maria-Soledade Santos, Am¨¦lia P. Rauter Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . octyl 2-deoxy¦Â-D-arabino-hexopyranoside C14H28O5 ÏàËÆ¶È:50% Bioorganic & Medicinal Chemistry 2008 16 4083-4092 Alkyl deoxy-arabino-hexopyranosides: Synthesis, surface properties, and biological activities Filipa V.M. Silva, Margarida Goulart, Jorge Justino, Ana Neves, Fernando Santos, João Caio, Susana Lucas, Ana Newton, Diana Sacoto, Ester Barbosa, Maria-Soledade Santos, Am¨¦lia P. Rauter Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . dodecyl 2-deoxy-¦Á-D-arabino-hexopyranoside C14H36O5 ÏàËÆ¶È:50% Bioorganic & Medicinal Chemistry 2008 16 4083-4092 Alkyl deoxy-arabino-hexopyranosides: Synthesis, surface properties, and biological activities Filipa V.M. Silva, Margarida Goulart, Jorge Justino, Ana Neves, Fernando Santos, João Caio, Susana Lucas, Ana Newton, Diana Sacoto, Ester Barbosa, Maria-Soledade Santos, Am¨¦lia P. Rauter Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . dodecyl 2-deoxy-¦Â-D-arabino-hexopyranoside C14H36O5 ÏàËÆ¶È:50% Bioorganic & Medicinal Chemistry 2008 16 4083-4092 Alkyl deoxy-arabino-hexopyranosides: Synthesis, surface properties, and biological activities Filipa V.M. Silva, Margarida Goulart, Jorge Justino, Ana Neves, Fernando Santos, João Caio, Susana Lucas, Ana Newton, Diana Sacoto, Ester Barbosa, Maria-Soledade Santos, Am¨¦lia P. Rauter Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . Loniceracetalide A C21H32O11 ÏàËÆ¶È:50% Chemical & Pharmaceutical Bulletin 2007 55 689-728 Naturally Occurring Secoiridoids and Bioactivity of Naturally Occurring Iridoids and Secoiridoids. A Review, Part 2 Biswanath DINDA, Sudhan DEBNATH and Yoshihiro HARIGAYA Structure 13C NMR ̼Æ×Ä£Äâͼ |

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