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¦Ä13C(75 MHz, MeOD): 12.63, 17.33, 19.21, 22.31, 22.48, 25.22, 29.34, 31.61, 31.68, 32.09, 33.49, 34.89, 35.26, 35.99, 36.99, 39.30, 41.41, 41.49, 43.96, 46.55, 57.43, 57.51, 68.32, 76.51, 76.79, 106.88, 157.73.
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²éѯ½á¹û£º¹²²éµ½13052¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼)
1 .     24-methylenecholesta-3¦Â,5¦Á,6¦Â-triol
    ÏàËÆ¶È:96.4%
Natural Product Research          1997          10          231-237
Two 11¦Á-Acetoxysterols from the Palauan Soft Coral lobophytum cf. Pauciflorum
Qing Lu; D. John Faulkner
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
2 .     ergost-24(28)-en-3¦Â,5¦Á,6¦Â-triol
C28H48O3     ÏàËÆ¶È:96.4%
Acta Scientiarum Naturalium Universitatis Sunyatseni          2003          42(3)          105-107
Studies on the Secondary Metabolites of the Soft Coral, Sinularia sp. Collected from the South China Sea
LAN Wen-jian, SU Jing-yu, ZENGLong-mei
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
3 .     24-methylenecholestane-3¦Â,5¦Á,6¦Â-triol
    ÏàËÆ¶È:96.4%
Indian Journal of Chemistry Section B          2000          39B          42-56
Two new terpenoid derivatives from a new soft coral species of the Nephthea genus of the India ocean
A S R Anjaneyulu, M V R Krishna Murthy
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
4 .     24-methylenecholesta-3,5,6-triol
C28H48O3     ÏàËÆ¶È:92.8%
Journal of Instrumental Analysis          2004          23          5-8
Studies on the Secondary Metabolites of the Soft Coral Sarcophyton sp
MA Xiang-quan, ZHANG Guang-wen, SU Jing-yu, ZENG Long-mei, LI Hong
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
5 .     24-methylene-cholest-4-en-3¦Â,5¦Á,6¦Â-triol
C28H48O3     ÏàËÆ¶È:92.8%
Acta Scientiarum Naturalium Universitatis Sunyatseni          2004          43(1)          122-124
Studies on the Secondary Metabolites of the Soft Coral Lobophyton sp.
LIU Hong, SU Jing-yu, ZENG Lang-mei
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
6 .     ergost-24(28)-en-3¦Â,5¦Á,6¦Â-triol
C28H48O3     ÏàËÆ¶È:92.8%
Journal of Pharmaceutical Practice          2010          28          274-278
Bioactive constituents from Sinularia sp
MENG Li-Yuan, LI Xiu-bao, ZHANG Wen, LI Ling, SUN Peng, TANG Hua, LIU Bao-shu, YI Yang-hua
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
7 .     (3¦Â,5¦Á,6¦Â)-24-methylcholest-24(28)-ene-3,5,6,19-tetrol
    ÏàËÆ¶È:89.2%
Helvetica Chimica Acta          2006          Vol. 89          1330
Two New Polyhydroxylated Steroids from the Hainan Soft Coral Sinularia sp.
Rui Jia, Yue-Wei Guo, Ernesto Mollo, Margherita Gavagnin, and Guido Cimino
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
8 .     24R-methylcholesta-3¦Â,5¦Á,6¦Â-triol
    ÏàËÆ¶È:89.2%
Natural Product Research          1997          10          231-237
Two 11¦Á-Acetoxysterols from the Palauan Soft Coral lobophytum cf. Pauciflorum
Qing Lu; D. John Faulkner
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
9 .     (24S)-ergostane-1¦Â,3¦Â,5¦Á,6¦Â-tetraol 1,3,6-triacetate
    ÏàËÆ¶È:89.2%
Indian Journal of Chemistry Section B          1995          34B          221-226
Alcyonacean metabolitesart 3-Three new lobanes from a soft coral,Lobophytum hirsutum,.of the Andaman and Nicobar coasts
B Lakshmana Raju & Gottumukkala V subbaraju
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
10 .     ergost-3¦Â,5¦Á,6¦Â-triol
    ÏàËÆ¶È:89.2%
Acta Scientiarum Naturalium Universitatis Sunyatseni          2007          46(4)          116-118
The Secondary Metabolite of the Soft Coral Cespitularia cocerulea May(¢ò)
HE Xi-xin, YAN Su-jun, SU Jing-yu, ZENG Long-mei
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
11 .     3¦Â,5¦Á,6¦Â,19-ËÄôÇ»ù,24-ÑǼ׻ùµ¨çÞÍé´¼
C28H46O2     ÏàËÆ¶È:89.2%
Chinese Journal of Marine Drugs          1993                   1-7
Studies on the chemical constituents of the Chinese soft coral Nephthea capnelliformis
Li Ruisheng, Tan Guili
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
12 .     compound 15
    ÏàËÆ¶È:88.8%
Steroids          2007          72          643-652
Atypical regioselective biohydrolysis on steroidal oxiranes by Aspergillus niger whole cells: Some stereochemical features
Fabricio R. Bisogno, Alejandro A. Orden, Celeste Aguirre Pranzoni, Diego A. Cifuente, Oscar S. Giordano, Marcela Kurina Sanz
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
13 .     cholest-3¦Â,5¦Á,6¦Â-triol
    ÏàËÆ¶È:88.8%
Journal of Shenyang Pharmaceutical University          2010          27          191-194
Steroids from marine spongeSpheciospongia sp. from the South China Sea
LIU Dong, LIN Wen-han, DENG Zhi-wei, WU Li-jun
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
14 .     cholestane-3U,5T,6U-triol
C27H48O3     ÏàËÆ¶È:88.8%
Chinese Journal of Spectroscopy Laboratory
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