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Ë®ÐǤÎÎÀ: ½ð±Ò+20, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸, ·Ç³£¸Ðл£¡ 2013-05-13 21:26:01
1 .     5¦Á,14¦Á-cevanin-6-O-20¦Â-hydroxy-3¦Â-yl-3¦Á,7¦Á-dihydroxy-5¦Â-cholan-24-oate
C51H81NO6     ÏàËÆ¶È:70.5%
Steroids          2009          74          424-434
Structural analysis and antitussive evaluation of five novel esters of verticinone and bile acids
Jiu-liang Zhang, Hui Wang, Hui-fang Pi, Han-li Ruan, Peng Zhang, Ji-zhou Wu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

2 .     5¦Á,14¦Á-cevanin-6-O-20¦Â-hydroxy-3¦Â-yl-3¦Á,7¦Â-dihydroxy-5¦Â-cholan-24-oate
C51H81NO6     ÏàËÆ¶È:70.5%
Steroids          2009          74          424-434
Structural analysis and antitussive evaluation of five novel esters of verticinone and bile acids
Jiu-liang Zhang, Hui Wang, Hui-fang Pi, Han-li Ruan, Peng Zhang, Ji-zhou Wu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

3 .     5¦Á,14¦Á-cevanin-6-O-20¦Â-hydroxy-3¦Â-yl-3¦Á,6¦Á-dihydroxy-5¦Â-cholan-24-oate
C51H81NO6     ÏàËÆ¶È:70.5%
Steroids          2009          74          424-434
Structural analysis and antitussive evaluation of five novel esters of verticinone and bile acids
Jiu-liang Zhang, Hui Wang, Hui-fang Pi, Han-li Ruan, Peng Zhang, Ji-zhou Wu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

4 .     (3S,20S)-20-[(1R,S)-(1,2-dimethyl-propylamino)-methyl]-pregn-7-en-3-ol
C24H39NO     ÏàËÆ¶È:67.3%
Bioorganic & Medicinal Chemistry          2009          17          8123-8137
Side chain azasteroids and thiasteroids as sterol methyltransferase inhibitors in ergosterol biosynthesis
Delphine Renard, Johann Perruchon, Martin Giera, Jörg M¨¹ller, Franz Bracher
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

5 .     N-hydroxysolasodine
C27H43NO3     ÏàËÆ¶È:65.2%
Phytochemistry          1992          31          1837-1839
N-Hydroxysolasodine from Solanum robustum
Helmut Ripperger, Andrea Porzel
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

6 .     7-hydroxysitosteryl-3-O-¦Â-D-glucopyranoside tetraacetate
    ÏàËÆ¶È:65.2%
Phytochemistry          1991          30          3383-3387
Steroids and triterpenoids from Rosa laevigata
Jim-Min Fang, Kuang-Chaun Wang, Yu-Shia Cheng
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

7 .     glucoraphenin
    ÏàËÆ¶È:65.2%
Natural Product Research and Development          2010          22          58-59
Studies on the Chemical Constituents of Cirsium henryi
ZHANG Yue; RUAN Han-li; ZHANG Yong-hui; PI Hui-fang; WU Ji-zhou
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

8 .     (cis)-2-(4-{2-[(ethoxycarbonyl)amino]ethoxy}benzyl)cyclohexyl (3¦Â,22E)-stigmasta-5,22-dien-3-yl butanedioate
    ÏàËÆ¶È:64.5%
Bioorganic & Medicinal Chemistry          2010          18          8194-8203
Steroid conjugates: Synthesis and preliminary biological testing of pro-juvenoids
Hana Svobodov¨¢, Hana Ryšav¨¢, Milan Pavl¨ªk, David Šaman, Pavel Drašar, Zden¨§k Wimmer
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

9 .     N-(Cholest-5-en-3¦Â-yl)-3¦Â-hydroxyandrost-5-ene-17¦Â-carboxamide
C47H75NO2     ÏàËÆ¶È:63.8%
Steroids          2009          74          88-94
Steroids linked with amide bond¡ªExtended cholesterol
Ivan Černy, Miloš Bud¨§š¨ªnsky, Vladim¨ªr Pouzar, Pavel Drašar
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

10 .     3¦Â-hydroxy-35-(cyclohexyl-5'-propan-7'-one)-33-ethyl-34-methyl-bactereohopane
C47H82O2     ÏàËÆ¶È:63.8%
Chinese Chemical Letters          2011          22          81-84
A novel bacteriohopanoid from Celtis australis L. bark
Ruchi Badoni, Deepak Kumar Semwal, Prabhakar P. Badoni, Sudhir Kumar Kothiyal, Usha Rawat
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

11 .     ¦Â-sitosteryl linoleate
    ÏàËÆ¶È:63.8%
Natural Product Research and Development          2012          24          1738-1742
Chemical Constituents of Ceratocarpus arenarius L£®
LIU Shan-shan, SUN Wen, YANG Hong-bing*, SUN Wan-fu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

12 .     3-Oxo-5¦Â-cholan-24-oic acid (cholan-24-oic acidmethyl ester)-3-yl ester
C49H79O5     ÏàËÆ¶È:63.2%
Steroids          2003          68          1157-1161
Synthesis of ester-linked lithocholic acid dimers
Lutfun Nahar, Alan B. Turner
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

13 .     3¦Á-Hydroxy-5¦Â-cholan-24-oic acid (cholan-24-oicacid methyl ester)-3-yl ester
C49H81O5     ÏàËÆ¶È:63.2%
Steroids          2003          68          1157-1161
Synthesis of ester-linked lithocholic acid dimers
Lutfun Nahar, Alan B. Turner
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

14 .     procrim a
C46H80O3     ÏàËÆ¶È:63.0%
Chemical & Pharmaceutical Bulletin          2002          50(3)          439-440
Two Novel Long-Chain Alkanoic Acid Esters of Lupeol from Alecrim-Propolis
Satomi FURUKAWA,Naomichi TAKAGI,Tsuyoshi IKEDA,Masateru ONO,Alaa Mohamed NAFADY,Toshihiro NOHARA,Hiroyuki SUGIMOTO,Shima DOI,and Hideo YAMADA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

15 .     lanoscopariol
C46H80O3     ÏàËÆ¶È:63.0%
Journal of Natural Products          1996          59          181-184
New 9¦Â-Lanostane-Type Triterpenic and 13, 14-seco-Steroidal Esters from the Roots of Artemisia scoparia
Surendra Kumar Sharma and Mohammad Ali
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

16 .     ¦Â-sitosterol ¦Â-D-glucopyranoside tetraacetate
    ÏàËÆ¶È:63.0%
Planta Medica          1993          59          369-372
A New Oleanolic Acid Derivative from Securinega tinctoria
LuisM. Carvalho and J. Seita
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

17 .     colebrin C
C52H90O7     ÏàËÆ¶È:63.0%
Fitoterapia          2000          71          641-648
New steroids from Clerodendrum colebrookianum
Hui Yang, Jia Wang, Ai-Jun Hou, Yun-Pin Guo,Zhong-Wen Lin, Han-Dong Sun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

18 .     sitosteryl-¦Â-D-glucopyranoside tetraacetate
    ÏàËÆ¶È:63.0%
Phytochemistry          1991          30          3383-3387
Steroids and triterpenoids from Rosa laevigata
Jim-Min Fang, Kuang-Chaun Wang, Yu-Shia Cheng
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

19 .     3,5-¶þôÇ»ù¶þÊ®ÍéËáÓðÉȶ¹´¼õ¥
C50H88O4     ÏàËÆ¶È:63.0%
Chemical Journal of Chinese Universities          2003          24          436-441
Chemical Constituents from the Roots of Biondia Hemsleyana
TAN Xing-Gen, ZHANG Xiao-Rong, PENG Shu-Lin, LIAO Xun, DING Li-Sheng
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

20 .     mixture of compound 1a and compound 1b
    ÏàËÆ¶È:63.0%
Phytochemistry          1989          28          1721-1724
Acylglucosyl sterols from Momordica charantia
Amelia P. Guevara,Clara Y. Lim-Sylianco,Fabian M. Dayrit,Paul Finch
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
΢΢һЦ
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