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20071070088Ìú³æ (СÓÐÃûÆø)
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CÆ×ÈçÏ£º 13C NMR (126 MHz, Pyr): 17.64,18.08,19.38,20.89,25.25,29.49,34.17,34.27,34.36, 38.67,40.22,40.36,50.03,52.00,52.12,52.50,54.28,76.90,80.60,111.26,122.38,129.26,131.71,142.64,143.74,171.42,175.46,220.49 |
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20071070088(jiangchunyong´ú·¢): ½ð±Ò+12, лл 2013-08-27 10:32:57
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20071070088(jiangchunyong´ú·¢): ½ð±Ò+12, лл 2013-08-27 10:32:57
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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£º¹²²éµ½227¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . proceranolide C27H34O7 ÏàËÆ¶È:71.4% Chemical & Pharmaceutical Bulletin 1990 38 639-651 Constituents of the Seeds of Swietenia mahagoni JACQ. I. : Isolation, Structures, and 1H- and 13C-Nuclear Magnetic Resonance Signal Assignments of New Tetranortriterpenoids Related to Swietenine and Swietenolide Shigetoshi KADOTA,Lamek MARPAUNG,Tohru KIKUCHI and Hisao EKIMOTO Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . proceranolide ÏàËÆ¶È:67.8% Natural Product Research 2008 22 763-800 13C NMR spectroscopy of D and B, D-ring seco-limonoids of Meliaceae family T. Narender; T. Khaliq; Shweta Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . swietenolide ÏàËÆ¶È:64.2% Chemical & Pharmaceutical Bulletin 1990 38 639-651 Constituents of the Seeds of Swietenia mahagoni JACQ. I. : Isolation, Structures, and 1H- and 13C-Nuclear Magnetic Resonance Signal Assignments of New Tetranortriterpenoids Related to Swietenine and Swietenolide Shigetoshi KADOTA,Lamek MARPAUNG,Tohru KIKUCHI and Hisao EKIMOTO Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . swietenolide ÏàËÆ¶È:64.2% Chemical & Pharmaceutical Bulletin 1990 38 894-901 Constitutents of the Seeds of Swietenia mahagoni JACQ.II. : Structures of Swietemahonin A, B, C, D, E, F, and G and Swietemahonolide Shigetoshi KADOTA,Lamek MARPAUNG,Tohru KIKUCHI and Hisao EKIMOTO Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . swietenolide ÏàËÆ¶È:60.7% Natural Product Research 2008 22 763-800 13C NMR spectroscopy of D and B, D-ring seco-limonoids of Meliaceae family T. Narender; T. Khaliq; Shweta Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . Swietenolide C27H34O8 ÏàËÆ¶È:60.7% Journal of Natural Medicines 2009 63 41-45 Antibacterial activity of two limonoids from Swietenia mahagoni against multiple-drug-resistant (MDR) bacterial strains A. K. M. Shahidur Rahman, A. K. Azad Chowdhury, Husne-Ara Ali, Sheikh Z. Raihan and Mohammad S. Ali, et al. Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . (1S,4aS,8aR)-N-(3-Methoxy-1-phenylpropyl)-5-[2-(furan-3-yl)ethyl]-1,4a,6-trimethyl-1,2,3,4,4a,7,8,8aoctahydronaphthalen- 1-carboxamide C30H39NO4 ÏàËÆ¶È:59.3% Chemistry of Natural Compounds 2010 46 233-241 Synthetic transformations of higher terpenoids. XXI.* Preparation of phlomisoic acid and its N-containing derivatives M. E. Mironov, Yu. V. Kharitonov, E. E. Shul¡¯ts, M. M. Shakirov and I. Yu. Bagryanskaya, et al. Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . siraitic acid F C29H40O5 ÏàËÆ¶È:58.6% Journal of Asian Natural Products Research 2005 7 37-41 Siraitic acid F, a new nor-cucurbitacin with novel skeleton,from the roots of Siraitia grosvenorii JIAN-YONG SI, DI-HUA CHEN and GUAN-ZHONG TU Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . Fissinolide C29H36O8 ÏàËÆ¶È:58.6% Phytochemistry 1998 49 1769-1772 limonoids from Khaya senegalensis Sami A. Khalid, Gerda M. Friedrichsen, Arsalan Kharazmi, Thor G. Theander, Carl E. Olsen, S. Br[oslash]gger Christensen Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . 2,6-dihydroxy fissinolide ÏàËÆ¶È:57.1% Natural Product Research 2008 22 763-800 13C NMR spectroscopy of D and B, D-ring seco-limonoids of Meliaceae family T. Narender; T. Khaliq; Shweta Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . 2¦Á,3¦Â-dihydroxy-3-deoxymcxicanolide C27H34O8 ÏàËÆ¶È:57.1% Phytochemistry 1998 47 1423-1425 Tetranortriterpenoids from Khaya senegalensis T. R. Govindachari, G. N. Krishna Kumari Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . Compound 9 C27H34O6S ÏàËÆ¶È:57.1% Bioorganic & Medicinal Chemistry Letters 2010 20 4233-4236 In vitro and in vivo antimalarial evaluation of semi-synthetic derivatives of gomphostenin Manisha Sathe, M.P. Kaushik Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . demethylisoswietenolide C26H32O8 ÏàËÆ¶È:57.1% Pest Management Science 2010 66 1298-1303 Identification of new limonoids from Swietenia and their biological activity against insects Robert Fowles, Baldwin Mootoo, Russel Ramsewak, Ayub Khan, Adesh Ramsubhag, William Reynolds and Muraleedharan Nair Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . Ganolucidate F C30H47O6 ÏàËÆ¶È:56.6% Planta Medica 2012 78 368-376 Isolation and Bioactivity Evaluation of Terpenoids from the Medicinal Fungus Ganoderma sinense Jie-Qing Liu, Cui-FangWang, Yan Li , Huai-Rong Luo, Ming-Hua Qiu Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . 21-oxo-1¦Â,3¦Â-dihydroxy-urs-12-en-28-oic acid ÏàËÆ¶È:56.6% Fitoterapia 2013 86 123-128 Biotransformation of ursolic acid by Syncephalastrum racemosum CGMCC 3.2500 and anti-HCV activity Shao-bin Fu, Jun-shan Yang, Jin-long Cui, Di-An Sun Structure 13C NMR ̼Æ×Ä£Äâͼ |

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