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holmessakura: ½ð±Ò+10, ¡ïÓаïÖú 2013-08-12 19:44:36
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holmessakura: ½ð±Ò+10, ¡ïÓаïÖú 2013-08-12 19:44:36
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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£º¹²²éµ½28¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . zythiostromic acid A C20H26O3 ÏàËÆ¶È:55% Phytochemistry 1996 42 1647-1652 Zythiostromic acids, diterpenoids from an antifungal Zythiostroma species associated with aspen William A. Ayer, Abdul Q. Khan Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . 9-(4-Aminophenyl)-3,7-dihydroxy-2,4,6-trimethyl-9-oxo-nonoic acid C18H27NO5 ÏàËÆ¶È:55% Molecules 2010 15 2782-2790 p-Aminoacetophenonic Acids Produced by a Mangrove Endophyte Streptomyces sp. (strain HK10552) Fangfang Wang, Minjuan Xu, Qingshan Li, Isable Sattler and Wenhan Lin Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . myricananins A ÏàËÆ¶È:55% Natural Product Communications 2010 5 1687 - 1708 Naturally Occurring Diarylheptanoids Haining Lv and Gaimei She Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . 5,6-Dihydro-7-(tricyclo[3.3.1.13,7]dec-1-yl)benzo[c]acridine C27H27N ÏàËÆ¶È:55% Helvetica Chimica Acta 2012 95 1003-1017 Novel Route to 4-(Adamantan-1-yl)quinoline Derivatives Based on the Friedlnder Condensation Zuzana Kozubkov¨¢, Michal Rouchal, Marek Nečas and Robert V¨ªcha Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . Coleon S C22H30O6 ÏàËÆ¶È:54.5% Chinese Chemical Letters 2001 12 339-342 The Diterpenoid Quinones from Coleus forskohlii Chun Suo YAO, Yun Long XU Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . coleon S C22H30O6 ÏàËÆ¶È:54.5% Natural Product Research and Development 2002 14(2) 1-6 THE CHEMICAL CONSTITUENTS OF COLEUS FORSKOHLII YAO Chun-suo SHEN Yun-heng XU Yun-long Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . 4¦Á-hydroxy-18-normanoyl oxide C25H42O6 ÏàËÆ¶È:50% Journal of Natural Products 2005 68 554-558 Manoyl Oxide Diterpenoids from Grindelia scorzonerifolia Mara Ins Ybarra, Susana Popich, Susana A. Borkosky, Yoshinori Asakawa, and Alicia Bardn Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . agallochaexcoerin B C20H32O3 ÏàËÆ¶È:50% Helvetica Chimica Acta 2009 92 1419-1427 Three New ent-Labdane Diterpenoids from the Wood of Excoecaria agallocha Linn. Ponnapalli Mangala Gowri, Sri Vedavyasa Srirangaraja Radhakrishnan Bhattar, Poreddy Guruva Reddy, Yerraballi Rakesh, Shaik Jeelani Basha, Akella Venkata Subrahmanya Sarma, Janaswamy Madhusudana Rao Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . 3¦Â-hydroxy-2-oxo-manoyloxid C20H32O3 ÏàËÆ¶È:50% Phytochemistry 1998 47 1583-1600 Diterpenes from Euphorbia segetalis J. Jakupovic, F. Jeske, T. Morgenstern, F. Tsichritzis, J. A. Marco, W. Berendsohn Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . 2¦Á,5-epoxy-5,10-dihydroxy-6¦Á-angeloyloxy-9¦Â-isobutyloxy-germacran-8¦Á,12-olide C24H34O9 ÏàËÆ¶È:50% Phytochemistry 1997 46 1245-1247 Sesquiterpene lactones from Carpesium divaricatum Dae Keun Kim, Kang Ro Lee, Ok Pyo Zee Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . (trans-Diastereomers)[4-(3,4-dichlorophenyl)-1,2,3,4-tetrahydro-naphthalen-2-ylmethyl]-dimethylamine ÏàËÆ¶È:50% Bioorganic & Medicinal Chemistry 2011 19 663-676 Synthesis and pharmacological evaluation of 4-(3,4-dichlorophenyl)-N-methyl-1,2,3,4-tetrahydronaphthalenyl amines as triple reuptake inhibitors Liming Shao, Fengjiang Wang, Scott C. Malcolm, Jianguo Ma, Michael C. Hewitt, Una C. Campbell,Larry R. Bush, Nancy A. Spicer, Sharon R. Engel, Lakshmi D. Saraswat, Larry W. Hardy, Patrick Koch,Rudy Schreiber , Kerry L. Spear, Mark A. Varney Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . (3aS,4R,7aR)-4-ethyl-1-(3-(naphthalen-2-yl)propyl)-tetrahydro-1H-pyrano[4,3-d]oxazole-2,6-dione C20H22N2O4 ÏàËÆ¶È:50% Canadian Journal of Chemistry 2005 83 801-811 Design and synthesis of oxazolidinone ketolide antibiotic segment mimetics1 Stephen Hanessian and Kiran Kumar Kothakonda Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . diosbulbin J C19H22O8 ÏàËÆ¶È:50% Chemical & Pharmaceutical Bulletin 2009 57 625-627 Two New Furanoid Norditerpenes from Dioscorea bulbifera Gang Wang, Jin-Song Liu, Bin-Bin Lin, Guo-Kai Wang and Ji-Kai Liu Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . syringopicroside ÏàËÆ¶È:50% Chinese Traditional and Herbal Drugs 2010 41 1598-1601 Chemical constituents in seed crust of Syringa oblata WANG Jin-lan; ZHANG Gang-feng; DONG Li-wei; ZHAO Ming; ZHANG Shu-jun Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . 2¦Á,5-Epoxy-5,10-dihydroxy-6¦Á-angeloyloxy-9¦Â-isobutyloxy-germacran-8¦Á,12-olide C24H34O9 ÏàËÆ¶È:50% Archives of Pharmacal Research 2007 30 556-560 cytotoxic germacranolide sesquiterpene lactones fromCarpesium triste var.manshuricum Mi- Ran Kim, Bang Yeon Hwang, Eun-Sook Jeong, Yong-Moon Lee and Hwan-Soo Yoo, et al. Structure 13C NMR ̼Æ×Ä£Äâͼ |

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