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1 .     stigmast-5-ene-3¦Â,7¦Á-diol
    ÏàËÆ¶È:80.6%
Planta Medica          1988          54          33-36
In vitro Fibrinolytic Phytosterols Isolated from the Roots of Spatholobus suberetus
Yoshiyasu Fukuyama, Yoshinori Nakano, Geng Pei-Wu, Wang Rui, Junko Sumitomo, Bao Jinxian,and Kazuyuki Nakagawa
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     topsentinol E
C30H52O2     ÏàËÆ¶È:80.6%
Chemical & Pharmaceutical Bulletin          1997          45          1435-1438
Topsentinols A-J, New Sterols with Highly Branched Side Chains from Marine Sponge Topsentia sp.
Masami ISHIBASHI,Emiko YAMAGISHI and Jun'ichi KOBAYASHI
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     Stigmast-5-ene-3¦Â,7¦Á-diol
    ÏàËÆ¶È:80.6%
Journal of Asian Natural Products Research          2005          7          165-169
Sterols from the pericarp of Sphaerophysa salsula DC
GUO-YU LI, JIN-HUI WANG and XIAN LI
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     7¦Á-hydroxysitosterol
    ÏàËÆ¶È:80.6%
Chinese Journal of Natural Medicines          2007          5          105-107
Chemical Constituents of African Plant Harpagophytum procumbens
QI Jin; CHEN Ji-Jun; TU Ying; CHEN Lu; YU Bo-Yang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     7 ¦Á-Hydroxysitosterol (Stigmast-5-ene-3¦Â,7¦Â-diol)
    ÏàËÆ¶È:80.6%
Pharmazie          2004          59          885-888
Terpenoids and steroids from Lappula anocarpa
Yuan-Peng Jin, and Yan-Ping Shi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     7¦Á-dydroxysitosterol
    ÏàËÆ¶È:80.6%
Chinese Pharmaceutical Journal          2008          43          897-899
Study on Steroids from the Stem of Croton caudatus Geisel.var.tomentosus Hook
WANG Yuan, ZOU Zhong-mei
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     stigmast-5-ene-3¦Â,7¦Á-diol
    ÏàËÆ¶È:80.6%
Natural Product Research and Development          2007          19          55-58
Chemical Constituents of Daphne tangutica
YUAN Xiao-hong;XU Chun-xia; ZHOU Min; ZHANG Xiu-yun; LI Bo-gang *
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     5-stigmasten-3¦Â,7¦Á-diol
    ÏàËÆ¶È:80.6%
Journal of the Chinese Chemical Society          2004          51          437-441
New Prenylated Flavones from the Roots of Ficus beecheyana
Ching-kuo Lee*, Chung-kuang Lu, Yuen-Hsiung Kuo,Jian-Zhi Chen and Guang-Zhong Sun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     Stigmast-5-en-3¦Â,7¦Á-diol
C29H50O2     ÏàËÆ¶È:80.6%
Journal of Tropical and Subtropical Botany          2013          21          52-56
Chemical Constituents from Twigs of Aglaia testicularis C. Y. Wu
XIA Ying, JIA Ji-rong, WANG Zhe, YANG Shu-min
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     topsentinol B
C30H50O2     ÏàËÆ¶È:77.4%
Chemical & Pharmaceutical Bulletin          1997          45          1435-1438
Topsentinols A-J, New Sterols with Highly Branched Side Chains from Marine Sponge Topsentia sp.
Masami ISHIBASHI,Emiko YAMAGISHI and Jun'ichi KOBAYASHI
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     7¦Á-Hydroxysitosterol
C29H50O2     ÏàËÆ¶È:77.4%
Journal of Chinese Pharmaceutical Sciences          2007          16          288-293
Chemical constituents of the flower buds of Tussilago farfara
Yu-Feng Liu; Xiu-Wei Yang and Bin Wu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     7¦Á-hydroxysitosterol
C29H50O2     ÏàËÆ¶È:77.4%
Steroids          2005          70          886-895
Gram-scale chromatographic purification of ¦Â-sitosterol: Synthesis and characterization of ¦Â-sitosterol oxides
Xin Zhang, Philippe Geoffroy, Michel Miesch, Diane Julien-David, Francis Raul, Dalal Aoud¨¦-Werner, Eric Marchioni
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
13 .     (24S)-stigmast-5-ene-3¦Â,7¦Á-diol
    ÏàËÆ¶È:77.4%
Journal of Asian Natural Products Research          2005          7          165-169
Sterols from the pericarp of Sphaerophysa salsula DC
GUO-YU LI, JIN-HUI WANG and XIAN LI
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
14 .     7¦Á-hydroxysitosterol
    ÏàËÆ¶È:77.4%
China Journal of Chinese Materia Medica          2008          33          1566-1568
Studies on chemical constituents from stem bark of Trwia nudiflora
WU Shaohua, SHENG Yuemao, CHEN Youwei, YANG Liyuan, LI Shaolan, LI Zhiying
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
15 .     stigmast-5-en-3¦Â,7¦Á-diol
    ÏàËÆ¶È:77.4%
Chinese Traditional and Herbal Drugs          2010          41          195-197
ºÚÀÏ»¢¸ù»¯Ñ§³É·ÖµÄÑо¿
Íõéª;ÀîÕ¼ÁÖ;»ª»áÃ÷
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
16 .     stigmasta-5-en-3¦Â,7¦Á-diol
C29H50O2     ÏàËÆ¶È:77.4%
Chinese Traditional and Herbal Drugs          2006          37          831-833
ÓñÃ×ÐëµÄ»¯Ñ§³É·ÖÑо¿
ÐìÑà;Áº¾´îÚ
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
17 .     stigmast-5-en-3¦Â,7¦Á-diol
C29H50O2     ÏàËÆ¶È:77.4%
Chinese Traditional and Herbal Drugs          2005          36          510-511+544
Å£¶ú¶ä»¯Ñ§³É·ÖµÄÑо¿
²ÌÏ麣,µËµÂɽ,ÂíÔÆ±£,ÂÞÏþ¶«
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
18 .     stigmast-5-ene-3¦Â,7¦Á-diol
    ÏàËÆ¶È:77.4%
Archives of Pharmacal Research          2005          28          1147-1151
Antimicrobial constituents from fruits of Ailanthus altissima SWINGLE
Chun-Chao Zhao, Jian-Hua Shao, Xian Li, Jing Xu and Peng Zhang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
19 .     7¦Á-hydroxysitosterol
    ÏàËÆ¶È:77.4%
Archives of Pharmacal Research          2010          33          1347-1353
Structural implication in cytotoxic effects of sterols from Sellaginella tamariscina
Eun Mi Roh, Qinglong Jin, Hong-Guang Jin, Ji Eun Shin and Eun Jin Choi, et al.
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
20 .     7¦Á-ôÇ»ù-¦Â-¹ÈçÞ´¼
    ÏàËÆ¶È:77.4%
Chinese Pharmaceutical Journal          2004          39          173-175
Studies on the chemical constituents of Caragana rosea
CUI Yi-ling, MU Qing, HU Chang-qi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
21 .     7¦Á-hydroxysitosterol
    ÏàËÆ¶È:77.4%
Chinese Pharmaceutical Journal          2010          45          1615-1617
Chemical Constituents of Tetrastigma planicaule(Hook.) Gagnep.
SHAO Jia-chun, HE Cui-hong, LEI Ting, HONGi-hua, CEN Ying-zhou
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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