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wgqyaokaoyan: ½ð±Ò+5, ¡ïÓаïÖú 2015-03-23 22:04:26
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1 . ferulaeone A C25H34O5 ÏàËÆ¶È:57.6% Phytochemistry 2013 86 151-158 Sesquiterpenoid derivatives from Ferula ferulaeoides (Steud.) Korov. He Meng, Guoyu Li, Jian Huang, Ke Zhang, Xiuyan Wei, Yueping Ma, Cui Zhang, Jinhui Wang Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . Tetrapterol C C26H30O6 ÏàËÆ¶È:53.8% Phytochemistry 1995 39 667-672 Flavonoid compounds in roots of Sophora tetraptera Munekazu Iinuma, Masayoshi Ohyama, Yoko Kawasaka, Toshiyuki Tanaka Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . acetoxy lycopersene C42H68O2 ÏàËÆ¶È:53.8% Phytochemistry 1988 27 887-890 Polyprenols and hydroxylated lycopersenes from Myriophyllum verticillatum Rosa Lanzetta,Pietro Monaco,Lucio Previtera,Antonella Simaldone Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . Neovibsanine A C26H38O5 ÏàËÆ¶È:53.8% Tetrahedron Letters 1996 37 6767-6770 Neovibsanines A and B, unprecedented diterpenes from Viburnum awabuki Yoshiyasu Fukuyama, Hiroyuki Minami, Kumiko Takeuchi, Mitsuaki Kodama, Kazuyoshi Kawazu Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . Sarcophytolin B C26H36O8 ÏàËÆ¶È:53.8% Tetrahedron 2010 66 7129-7135 Steroid and cembranoids from the Dongsha atoll soft coral Lobophytum sarcophytoides Yi Lu, You-Cheng Lin, Zhi-Hong Wen, Jui-Hsin Su, Ping-Jyun Sung, Chi-Hsin Hsu, Yao-Haur Kuo, Michael Y. Chiang, Chang-Feng Dai, Jyh-Horng Sheu Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . shaliuin I C26H38O5 ÏàËÆ¶È:53.8% Journal of the Chinese Chemical Society 2008 55 401-405 Acyclic Diterpene-¦Ã-lactones and Flavonoid from Salix cheilophila Omitted Tong Shen*, Yong-Qiang Tian,Wu-Xia Liu and Shang-Zhen Zheng Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . compound 8 C25H32O8 ÏàËÆ¶È:53.8% Natural Product Communications 2010 5 675-680 Acid Rearrangment of Epoxy-germacranolides andAbsolute Configuration of 1¦Â,10¦Á-Epoxy-salonitenolide Sergio Rosselli, Antonella Maria Maggio, Rosa Angela Raccuglia, Susan L. Morris-Natschke,Kenneth F. Bastow, Kuo-Hsiung Lee and Maurizio Bruno Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . (1S,4R,5S,6R,7R,8S,9R,10S)-1,8-Diacetoxy-9-benzoyloxy-6-nicotinoyloxy-dihydro-¦Â-agarofuran C32H37NO9 ÏàËÆ¶È:53.3% Bioorganic & Medicinal Chemistry 2011 19 2182-2189 Dihydro-¦Â-agarofuran sesquiterpenes isolated from Celastrus vulcanicola as potential anti-Mycobacterium tuberculosis multidrug-resistant agents David Torres-Romero,Ignacio A. Jim¨¦nez ,Rosario Rojas,Robert H. Gilman ,Mat¨ªas L¨®pez ,Isabel L. Bazzocchi Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . eunicenone A acetate C31H46O5 ÏàËÆ¶È:51.8% Tetrahedron 1993 49 9277-9284 Eunicenones A and B: Diterpenoid cyclohexenones of a rare skeletal class from a new species of the caribbean gorgonian eunicea Jongheon Shin, William Fenical Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . pacamycin ÏàËÆ¶È:51.8% The Journal of Antibiotics 1986 39 1779-1783 8"-HYDROXYPACTAMYCIN AND 7-DEOXYPACTAMYCIN, NEW MEMBERS OF THE PACTAMYCIN GROUP KAZUYUKI DOBASHI, KUNIO ISSHIKI, TSUTOMU SAWA, TAMAMI OBATA, MASA HAMADA, HIROSHI NAGANAWA, TOMOHISA TAKITA, TOMIO TAKEUCHI, HAMAO UMEZAWA, HONGSHENG BEI, BAOQUAN ZHU, CUN TONG, WENSI XU Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . pactamycin C28H38N4O8 ÏàËÆ¶È:51.8% Angewandte Chemie International Edition 2011 50 3497-3500 Total Synthesis of Pactamycin Stephen Hanessian, Ramkrishna Reddy Vakiti, St phane Dorich, Shyamapada Banerjee, Fabien Lecomte, Juan R. DelValle, Jianbin Zhang, and Beno t DeschTnes-Simard Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . Tryptoquialanine A C27H25O7N4 ÏàËÆ¶È:51.8% Journal of Agricultural and Food Chemistry 2002 50 6361-6365 Penicillium digitatum Metabolites on Synthetic Media and Citrus Fruits Marta R. Ariza, Thomas O. Larsen, Bent O. Petersen, Jens Ø. Duus, and Alejandro F. Barrero Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . dehydroaustin ÏàËÆ¶È:51.8% Journal of the Brazilian Chemical Society 2003 14 722-727 Structures of Meroterpenes Produced by Penicillium sp, an Endophytic Fungus Found Associated with Melia azedarach Regina M. Geris dos Santos and Edson Rodrigues-Filho Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . 4-acetoxy-2-geranyl-5- hydroxy-3-n-pentylphenol C23H34O4 ÏàËÆ¶È:50% Journal of Natural Products 2009 72 906-911 Biologically Active Cannabinoids from High-Potency Cannabis sativa Mohamed M. Radwan, Mahmoud A. ElSohly, Desmond Slade, Safwat A. Ahmed, Ikhlas A. Khan, and Samir A. Ross Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . pancherin B C25H40O6 ÏàËÆ¶È:50% Phytochemistry 2007 68 604-608 Cytotoxic farnesyl glycosides from Pittosporum pancheri V¨¦ronique ¨¦parvier, Odile Thoison, Hadjira Bousserouel, Françoise Gu¨¦ritte,Thierry S¨¦venet, Marc Litaudon Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . fukanedone B C24H32O5 ÏàËÆ¶È:50% Journal of Natural Products 2005 68 365-368 Sesquiterpene Phenylpropanoids from Ferula fukanensis and Their Nitric Oxide Production Inhibitory Effects Tsunetake Motai, and Susumu Kitanaka Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . 4-acetoxy-9-deoxoidiadione C27H40O4 ÏàËÆ¶È:50% Journal of Natural Products 2004 67 1748-1751 New Sesterterpenes from the Sponge Smenospongia sp. Jung-Rae Rho, Hyi-Seung Lee, Hee Jae Shin, Jong-Woong Ahn, Ji-Yun Kim, Chung J. Sim, and Jongheon Shin Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . malonganenone G C27H43N4O3 ÏàËÆ¶È:50% Journal of Natural Products 2007 70 1104-1109 Nuttingins A-F and Malonganenones D-H, Tetraprenylated Alkaloids from the Tanzanian Gorgonian Euplexaura nuttingi Hagit Sorek,Amira Rudi,Yehuda Benayahu,Nathalie Ben-Califa, Drorit Neumann, and Yoel Kashman Structure 13C NMR ̼Æ×Ä£Äâͼ |

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