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1 .     deoxycholic acid
    ÏàËÆ¶È:100%
Journal of Natural Products          2002          65          1793-1797
Isolation of Labradorins 1 and 2 from Pseudomonas syringae pv. Coronafaciens
George R. Pettit, John C. Knight, Delbert L. Herald, Richard Davenport, Robin K. Pettit, Bruce E. Tucker, and Jean M. Schmidt
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

2 .     compound C
    ÏàËÆ¶È:100%
Applied Microbiology and Biotechnology          2005          67          679-683
Bile acids are new products of a marine bacterium, Myroides sp.strain SM1
Suppasil Maneerat, Teruhiko Nitoda, Hiroshi Kanzaki, Fusako Kawai
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

3 .     deoxycholic acid
    ÏàËÆ¶È:100%
Applied Microbiology and Biotechnology          2005          67          679-683
Bile acids are new products of a marine bacterium, Myroides sp.strain SM1
Suppasil Maneerat, Teruhiko Nitoda, Hiroshi Kanzaki, Fusako Kawai
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

4 .     compound 14
    ÏàËÆ¶È:92%
Organic Magnetic Resonance          1983          21          305-309
Carbon-13 NMR spectra of hydroxylated bile acid stereoisomers
Takashi Iida, Toshitake Tamura, Taro Matsumoto and Frederic C. Chang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

5 .     Methyl 3¦Á,12¦Á-dihydroxy-5¦Â-cholan-24-oate
C25H42O4     ÏàËÆ¶È:92%
Organic Magnetic Resonance          1977          9          439-464
13C N.m.r. Spectra of steroids¡ªA Survey and Commentary
J.W.Blunt and J.B.Stothers
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

6 .     Deoxycholic acid
    ÏàËÆ¶È:91.6%
Journal of Natural Medicines          2008          62          83-86
Bioproduction of bile acids and the glycine conjugates by Penicillium fungus
Kazuyoshi Ohashi, Yoshitaka Miyagawa, Yuhki Nakamura and Hirotaka Shibuya
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

7 .     3¦Á,12¦Á-Dihydroxy-5¦Â-cholan-24-oic acid desoxycholic acid
C24H40O4     ÏàËÆ¶È:91.6%
Organic Magnetic Resonance          1977          9          439-464
13C N.m.r. Spectra of steroids¡ªA Survey and Commentary
J.W.Blunt and J.B.Stothers
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

8 .     compound B1
    ÏàËÆ¶È:88.4%
Applied Microbiology and Biotechnology          2005          67          679-683
Bile acids are new products of a marine bacterium, Myroides sp.strain SM1
Suppasil Maneerat, Teruhiko Nitoda, Hiroshi Kanzaki, Fusako Kawai
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

9 .     GDCA
    ÏàËÆ¶È:88.4%
Applied Microbiology and Biotechnology          2005          67          679-683
Bile acids are new products of a marine bacterium, Myroides sp.strain SM1
Suppasil Maneerat, Teruhiko Nitoda, Hiroshi Kanzaki, Fusako Kawai
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

10 .     compound IV
    ÏàËÆ¶È:88%
Acta Pharmaceutica Sinica          1992          27          674-678
STUDIES ON CHEMICAL CONSTITUENTS OF THE GALL OF PYTHON MOLURUS BIVITTATUS SCHLEGEL
YJ You; JG Lin; LF Ji
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

11 .     compound 24
    ÏàËÆ¶È:88%
Organic Magnetic Resonance          1983          21          305-309
Carbon-13 NMR spectra of hydroxylated bile acid stereoisomers
Takashi Iida, Toshitake Tamura, Taro Matsumoto and Frederic C. Chang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

12 .     3¦Á,12¦Á-dihydroxy-5¦Â-cholane-24-phosphonic acid
    ÏàËÆ¶È:87.5%
Steroids          2005          70          681-689
Synthesis and in vitro cholesterol dissolution by 23- and 24-phosphonobile acids
Ponnusamy Babu, Uday Maitra
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2Â¥2013-08-30 08:18:46
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