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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.   Ð»Ð»£¡
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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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×Ä£Äâͼ
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