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273047565ZS

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13C-NMR (125 MHz, DMSO-D6) ¦Ä: 61.6, 70.6, 73.4, 85.9, 87.8, 119.3, 139.8, 149.0, 152.2,152.4,156.1,185.8.
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273047565ZS(׿Խ_ÏÈ·æ´ú·¢): ½ð±Ò+10 2015-05-07 09:07:16
1 .     ¦Â-adenosine
    ÏàËÆ¶È:83.3%
Phytochemistry          2004          65          181-187
¦Â-Adenosine, a bioactive compound in grass chaff stimulating mushroom production
Denisa L. Domondon, Weidong He, Norbert De Kimpe, Monica Höfte,Joseph Poppea
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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2 .     compound 10
    ÏàËÆ¶È:83.3%
Chemical & Pharmaceutical Bulletin          1996          44          337-342
Five New Monoterpene Glycosides and Other Compounds form Foeniculi Fructus (Fruit of Foeniculum vulgare MILLER)
Masateru ONO,Yasuyuki ITO,Thoru ISHIKAWA,Junichi KITAJIMA,Yasuko TANAKA,Yujiro NIIHO and Toshihiro NOHARA
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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3 .     A
    ÏàËÆ¶È:83.3%
Chemical & Pharmaceutical Bulletin          1981          29          2199-2204
Studies on Nucleosides and Nucleotides. LXXXVIII. : Purine Cyclonucleosides. XLIII. : 13C NMR Spectra of 2'-Substituted 2'-Deoxyadenosines. Substituent Effects on the Chemical Shifts in the Furanose Ring System
SEIICHI UESUGI,HIROKO MIKI and MORIO IKEHARA
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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4 .     adenosine
C10H13N5O4     ÏàËÆ¶È:83.3%
Chemistry of Natural Compounds          2007          43          181-183
CHEMICAL COMPOSITION OF Capparis spinosa FRUIT
X. P. Fu, H. A. Aisa, M. Abdurahim, A. Yili,S. F. Aripova, and B. Tashkhodzhaev
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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5 .     compound 2b
    ÏàËÆ¶È:83.3%
Chinese Chemical Letters          2006          17          1149-1151
Microwave-assisted Green and Efficient Synthesis of N6-(2-Hydroxyethyl)adenosine and its Analogues
Gui Rong QU, Ming Wei GENG, Su Hui HAN, Zhi Guang ZHANG, Feng XUE
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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6 .     6-(2',3'-dihydroxy-4'-hydroxymethyltetrahydrofuran-1'-yl)cyclo-pentadiene[c]pyrrole-1,3-diol
C12H13NO6     ÏàËÆ¶È:83.3%
Chinese Chemical Letters          2008          19          832-834
A new alkaloid from Castanea mollissima Blume
Dong Song Zhang, Hui Yuan Gao, Xiao Mei Song, Zhi Shu Tang, Li Jun Wu
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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7 .     adeno-sine
    ÏàËÆ¶È:83.3%
Journal of Chinese Pharmaceutical Sciences          1998          7          98-99
The Chemical Constituents from the Roots of Bupleurum chinense DC.
Hong Liang , Yan-Jing Bai , Yu-Ying Zhao and Ru-Yi Zhang
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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8 .     adenosine
    ÏàËÆ¶È:83.3%
Journal of Chinese Pharmaceutical Sciences          2005          14          86-88
Chemical Constituents from Potentilla multifida L.
XUE Pei-feng; LIANG Hong; WANG Bin; and ZHAO Yu-ying
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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9 .     Adenosine
C10H13N5O4     ÏàËÆ¶È:83.3%
Journal of Asian Natural Products Research          2005          7          761-765
A new cerebroside, Asperiamide A, from the marine fungus Asperillus sp
MING-AN OUYANG, RONG LIU and YUEH-HSIUNG KUO
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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10 .     adenosine
    ÏàËÆ¶È:83.3%
China Journal of Chinese Materia Medica          2007          32          688-691
Studies on chemical constituents in root of Isatis indigotica
ZUO Li, LI Jianbei, XU Jing, YANG Jingzhi, ZHANG Dongming, TONG Yongling
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
2Â¥2015-04-09 16:01:22
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