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| 13C NMR (75 MHz, MeOD) ¦Ä 12.66,29.08,30.39,30.47,59.74,62.72,65.22,69.44,71.58,75.05,76.32,78.01,81.11,81.97,103.68,106.59,108.82,111.01,128.92,129.63,131.54,139.57,140.37,142.49,143.96,144.11,145.00,146.42,169.14. лл£¡ |
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ÄÄ¡¢Alone: ½ð±Ò+20, ¡ïÓаïÖú 2014-09-14 21:17:27
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ÄÄ¡¢Alone: ½ð±Ò+20, ¡ïÓаïÖú 2014-09-14 21:17:27
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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£º¹²²éµ½15¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . (2R,5R,6R,8R,9S,10S,12S)-15,16-epoxy-2-hydroxy-6-O-(¦Â-D-glucopyranosyl)-cleroda-3,13(16),14-trien-17,12-olid-18-oic acid methyl ester C27H37O12 ÏàËÆ¶È:55.1% Journal of Natural Products 2010 73 541-547 cis-Clerodane-Type Furanoditerpenoids from Tinospora crispa M. Iqbal Choudhary, Muhammad Ismail, Khozirah Shaari, Ahmed Abbaskhan, Samina A. Sattar, Nordin H. Lajis and Atta-ur-Rahman Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . fucatoside A C28H34O15 ÏàËÆ¶È:51.7% Journal of Natural Products 2009 72 1424-1428 Phenylethanoid Glycosides from Lantana fucata with in Vitro Anti-inflammatory Activity Lisieux de Santana Juliao,Anna Lisa Piccinelli, Stefania Marzocco, Suzana Guimaraes Leitao,Cinzia Lotti,Giuseppina Autore,and Luca Rastrelli Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . 3¡ä-O-trans-cinnamoylmangiferin C28H24O12 ÏàËÆ¶È:51.7% Journal of Natural Products 2008 71(11) 1887-1890 Antioxidant C-Glucosylxanthones from the Leaves of Arrabidaea patellifera Fr¨¦d¨¦ric Martin, Anne-Emmanuelle Hay, Delphine Cressend, Marianne Reist,Livia Vivas, Mahabir P. Gupta, Pierre-Alain Carrupt, and Kurt Hostettmann Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . calceolarioside E C28H34O15 ÏàËÆ¶È:51.7% Planta Medica 1988 54 347-348 Polar Constituents of Calceolana ascendens M. Nicoletti, C. Galeffi, G. Multari, J. A. Garbarino, andY. Gambaro Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . calceolarioside E ÏàËÆ¶È:51.7% Phytochemistry 1993 34 239-243 Iridoids and verbascosides in Retzia Søren Damtoft, Henrik Franzyk, Søren Rosendal Jensen, Bent Juhl Nielsen Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . penproside A C24H34O11 ÏàËÆ¶È:51.7% Phytochemistry 1993 33 1211-1213 Two phenylpropanoid glucosides from Penstemon procerus Silke Ofterdinger-Daegel, Peter Junior Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . (Z)-2-(2-((2-(Nitrooxy)ethyl)disulfanyl)ethoxy)-2-oxoethyl-2-(5-fluoro-2-methyl-1-(4-(methylsulfinyl)benzylidene)-1H-inden-3-yl)acetate C26H26FNO8S3 ÏàËÆ¶È:51.7% Chemical & Pharmaceutical Bulletin 2012 60 465-481 NO-NSAIDs. Part 3: Nitric Oxide-Releasing Prodrugs of Non-steroidal Anti-inflammatory Drugs Namdev Borhade,Asif Rahimkhan Pathan,Somnath Halder,Manoj Karwa,Mini Dhiman,Venu Pamidiboina,Machhindra Gund,Jagannath Janardhan Deshattiwar,Sunil Vasantrao Mali,Nitin Janardanrao Deshmukh,Subrayan Palanisamy Senthilkumar,Parikshit Gaikwad,Santhosh Goud T Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . (-)-5,6,13,14-tetrahydro-9-¦Â-D-glucosyl-10-methoxy-2,3-(methylenedioxy)-8H-dibenzo[a,g]quinolizine ÏàËÆ¶È:51.7% Bioorganic & Medicinal Chemistry 2013 21 62-69 Chemical and microbial semi-synthesis of tetrahydroprotoberberines as inhibitors on tissue factor procoagulant activity Hai-Xia Ge, Jian Zhang, Ling Chen, Jun-Ping Kou, Bo-Yang Yu Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . (+)-5,6,13,14-tetrahydro-9-¦Â-D-glucosyl-10-methoxy-2,3-(methylenedi oxy)-8H-dibenzo[a,g]quinolizine ÏàËÆ¶È:51.7% Bioorganic & Medicinal Chemistry 2013 21 62-69 Chemical and microbial semi-synthesis of tetrahydroprotoberberines as inhibitors on tissue factor procoagulant activity Hai-Xia Ge, Jian Zhang, Ling Chen, Jun-Ping Kou, Bo-Yang Yu Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . (2S,3R,4S,5R,E)-3,4,5-tris(benzyloxy)-2-methoxy-8-methyl-N-((S)-2-oxoazepan-3-yl)non-6-enamide C38H48N2O6 ÏàËÆ¶È:51.7% Tetrahedron 2013 69 664-672 Concise synthesis and antitumor activity of Bengamide E and its analogs Wenxuan Zhang, Qingzhao Liang, Hui Li, Xiangbao Meng, Zhongjun Li Structure 13C NMR ̼Æ×Ä£Äâͼ |

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