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ÂíÐùpacino: ½ð±Ò+10 2014-10-26 18:26:46
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²éѯ½á¹û£º¹²²éµ½3284¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . (3R)-hydroxy-14-methyldocos-(4E)-en-1-yne C23H42O ÏàËÆ¶È:71.4% Journal of Natural Products 1992 Vol 55 1275 Further Bioactive Acetylenic Compounds from the Caribbean Sponge Cribrochalina vasculum Anna Aiello, Ernesto Fattorusso, Marialuisa Menna, Maurizio Pansini Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 2 . (3R)-hydroxy-16-methyleicos-1-yne C21H40O ÏàËÆ¶È:71.4% Journal of Natural Products 1992 Vol 55 1275 Further Bioactive Acetylenic Compounds from the Caribbean Sponge Cribrochalina vasculum Anna Aiello, Ernesto Fattorusso, Marialuisa Menna, Maurizio Pansini Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 3 . compound R-1(a) ÏàËÆ¶È:71.4% Bioscience, Biotechnology, and Biochemistry 2001 65 2065-2069 Synthesis of Methyl (5Z,9Z,17R)-17-Methylnonadeca-5,9-dienoate, the (R)-Enantiomer of the Structure Proposed for a Metabolite of the Philippine Sponge Plakinastrella sp. Miho TAKAGI, Hirosato TAKIKAWA, Kenji MORI Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 4 . (-)-(3S)-1-[(3S,6R,7S)-3-(tert-butyldimethylsilyloxy)-1-azaspiro[5.5]undec-7-yl]-nonan-3-ol C25H51NO2Si ÏàËÆ¶È:71.4% Chemistry-A European Journal 2005 11 639-649 An Asymmetric Formal Synthesis of Fasicularin Michaël D. B. Fenster and Gregory R. Dake Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 5 . (R)-10,14-Dimethyl-1-pentadecanol C17H34 ÏàËÆ¶È:71.4% Journal of Chemical Ecology 1995 21 627-634 Absolute configuration of sex pheromone for tea tussock moth,Euproctis pseudoconspersa (strand)via synthesis of (R)- and (S)-10, 14-dimethyl-1-pentadecyl isobutyrates Akio Ichikawa, Tetsuya Yasuda, Sadao Wakamura Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 6 . 3-Hydroxy-16-methyleicos-4(E)-en-1-yne C21H38O ÏàËÆ¶È:71.4% The Journal of Organic Chemistry 1990 55 6223-6225 New acetylenic alcohols from the sponge Cribrochalina vasculum Sarath P. Gunasekera, Glynn T. Faircloth Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 7 . strongylodiol G C24H42O2 ÏàËÆ¶È:70.8% Journal of Natural Products 2005 68 1001-1005 Acetylenic Strongylodiols from a Petrosia (Strongylophora) Okinawan Marine Sponge Kinzo Watanabe, Yuichiro Tsuda, Maki Hamada, Miki Omori, Go Mori,Kazuo Iguchi, Hideo Naoki, Tsuyoshi Fujita, and Rob W. M. Van Soest Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 8 . Microginin 91-A oxazolizinone C29H48N4O7 ÏàËÆ¶È:69.5% Tetrahedron 2000 56 8643-8656 Microginins, Zinc Metalloproteases Inhibitors from the Cyanobacterium Microcystis aeruginosa Keishi Ishida, Taku Kato, Masahiro Murakami, Masayuki Watanabe, Mariyo F. Watanabe Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 9 . Cycloartenol ÏàËÆ¶È:68.1% Phytochemistry 1984 23 2077-2079 Uvariastrol, a novel cycloartane triterpene from the stem bark of Uvariastrum zenkeri Peter G. Waterman, Ilias Mohammad Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 10 . Officinoic acid B C22H38O4 ÏàËÆ¶È:68.1% Journal of Natural Products 2011 74 1241-1247 Bioactive Terpenes from Spongia officinalis Emiliano Manzo, M. Letizia Ciavatta, Guido Villani, Mario Varcamonti, S. M. Abu Sayem, Rob van Soest, and Margherita Gavagnin Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 11 . Methyl (2R,3R,23R)-3-acetoxy-2-docosyl-23-methyl-24-oxotetracosanoate ÏàËÆ¶È:68.1% Tetrahedron 2014 70 7322-7335 Synthetic epoxy-mycolic acids Dakhil Z. Al Kremawi, Juma'a R. Al Dulayymi, Mark S. Baird Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 12 . melophlin S C21H37NO ÏàËÆ¶È:66.6% Chemical & Pharmaceutical Bulletin 2006 54(6) 852-854 Melophlins P, Q, R, and S: Four New Tetramic Acid Derivatives, from Two Palauan Marine Sponges of the Genus Melophlus Jinzhong XU,Masateru HASEGAWA,Ken-ichi HARADA,Hisayoshi KOBAYASHI, Hiroshi NAGAI,and Michio NAMIKOSHI Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 13 . compound 1 C41H83O4N ÏàËÆ¶È:66.6% Journal of Natural Products 2008 71(1) 513-515 Antiepileptic Ceramides from the Red Sea Sponge Negombata corticata Safwat A. Ahmed, Sherief I. Khalifa, and Mark T. Hamann Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 14 . (5Z,9Z)-17-methylnonadeca-5,9-dienoate C21H38O2 ÏàËÆ¶È:66.6% Journal of Natural Products 1998 61 1539-1542 New Cyclic Peroxides from the Philippine Sponge Plakinastrella sp. Asfia Qureshi, Javier Salv¨¢ , Mary Kay Harper, and D. John Faulkner Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 15 . methyl 11-methylpentadecanoate C17H34O2 ÏàËÆ¶È:66.6% Journal of Natural Products 1998 61 1049-1052 Identification and Total Synthesis of Novel Fatty Acids from the Caribbean Sponge Calyx podatypa N¨¦stor M. Carballeira, Mayra Pag¨¢n, and Abimael D. Rodr¨ªguez Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 16 . (5S)-hydroxy-16-methyleicos-(3Z)-en-1-yne C21H38O ÏàËÆ¶È:66.6% Journal of Natural Products 1995 Vol 58 1801-1807 Antitumor Activity and Stereochemistry of Acetylenic Alcohols from the Sponge Cribrochalina vasculum Yali F. Hallock, John H. Cardellina, Michael S. Balaschak, Mark R. Alexander, Tanya R. Prather, Robert H. Shoemaker, Micheal R. Boyd Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 17 . Methyl 10-ketolactobacillate (Methyl (Z)-10-(2-hexylcyclopropane-1-yl)-10-oxodecanoate) C20H36O3 ÏàËÆ¶È:66.6% Organic Letters 2006 Vol. 8, No. 1 79-81 Configurational Analysis of Cyclopropyl Fatty Acids Isolated from Escherichia coli Laura J. Stuart, James P. Buck, Amy E. Tremblay, and Peter H. Buist Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 18 . Methyl 13-ketolactobacillate (Methyl (Z)-10-(2-(1-oxo)-hexylcyclopropane-1-yl)-decanoate) C20H36O3 ÏàËÆ¶È:66.6% Organic Letters 2006 Vol. 8, No. 1 79-81 Configurational Analysis of Cyclopropyl Fatty Acids Isolated from Escherichia coli Laura J. Stuart, James P. Buck, Amy E. Tremblay, and Peter H. Buist Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 19 . N,N,N-Trimethyl-3-(6-(2-dodecanoyloxazol-5-yl)hexylsulfonyl)-propan-1-ammonium iodide C27H51N2O4S ÏàËÆ¶È:66.6% Bioorganic & Medicinal Chemistry 2012 20 1100-1112 Design, synthesis and evaluation of polar head group containing 2-keto-oxazole inhibitors of FAAH Marion Rusch,Stefan Zahov,Ingrid R. Vetter, Matthias Lehr, Christian Hedberg Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 20 . 1-(tetrahydropyran-2-yloxy)-heptadecan-8-ol ÏàËÆ¶È:66.6% Indian Journal of Chemistry Section B 2010 49B 1648-1652 Total synthesis of three natural products: Decyl 8-hydroxyheptadecanoate,undecyl hexadecanoate and 2,3-dihydroxypropyl hexadecanoate Ashima Singh,M L Sharma & Jasvinder Singh* Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ Ï´ÎÇë °´´ÓСµ½´ó˳ÐòÊäÈ룬Êý×Ö¼äÓÃÓ¢Îİë½Ç¶ººÅ(,)·Ö¸ôÀýÈ磺 È磺21.4,30.4,37.4,73.2,73.7,125.6,126.6,139.6,140.2,168.2 |
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