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0.08, 12.36, 12.54, 13.27, 14.29, 19.84, 21.13, 21.72, 23.11, 23.72, 26.60, 29.81, 30.13, 32.39, 34.75, 37.57, 37.68, 45.26, 55.92, 55.61, 63.82, 65.95, 69.37, 70.22, 72.82, 73.74, 76.68
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mlkying: ½ð±Ò+10, ¡ïÓаïÖú 2015-03-06 09:37:07
1 .     (20R,22R)-5¦Á-Cholestane-3¦Â,20,22-triol
C27H48O3     ÏàËÆ¶È:65.3%
Steroids          2008          73          1452-1464
Synthesis of ponasterone A derivatives with various steroid skeleton moieties and evaluation of their binding to the ecdysone receptor of Kc cells
Hirokazu Arai, Bunta Watanabe, Yoshiaki Nakagawa, Hisashi Miyagawa
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     muriflasteroid A
C28H46O4     ÏàËÆ¶È:64.2%
Steroids          2013          78          108-114
3¦Â,5¦Á,6¦Â-Oxygenated sterols from the South China Sea gorgonian Muriceopsis flavida and their tumor cell growth inhibitory activity and apoptosis-inducing function
Tao-Fang Liu, Xin Lu, Hua Tang, Min-Min Zhang, Pan Wang, Peng Sun, Zhi-Yong Liu, Zeng-Lei Wang, Ling Li, Yao-Cheng Rui, Tie-Jun Li, Wen Zhang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     24-ethyl-4¦Á-methyl-cholestane-3,20-diol
C30H45O2     ÏàËÆ¶È:63.3%
Fitoterapia          2005          76          433-438
A new dihydroxysterol from the marine phytoplankton Diacronema sp.
Am¨¦lia P. Rauter, Manuela M. Filipe, Carla Prata,João P. Noronha, Maria A.M. Sampayo,Jorge Justino,Jaime Bermejo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     (20S)-5¦Á-pregnane-3¦Â,20-diol 20-O-¦Â-D-glucopyranoside
C27H46O7     ÏàËÆ¶È:62.9%
Chinese Chemical Letters          2002          13          1189-1192
A New Pregnane Glycoside from Fermented Leaves of Agave americana
Jian Ming JIN, Xi Kui LIU, Chong Ren YANG
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     compound 6
C31H52O6     ÏàËÆ¶È:62.9%
Tetrahedron          1998          54          179-186
New cytotoxic sterols from the soft coral Gersemia fruticosa
Reet Koljak, Annika Lopp, Tõnis Pehk, K¨¹lliki Varvas, Aleksander-Mati M¨¹¨¹risepp, Ivar Järving, Nigulas Samel
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     stigmast-7-en-3¦Â-ol
    ÏàËÆ¶È:62.0%
Acta Pharmaceutica Sinica          2000          Vol 35          29-31
STRUCTURE IDENTIFICATION OF VULGARSAPONIN A
Tian Jing; Xiao Zhiyan; Chen Yayan; Zhao Yuying and Wang Zhuju
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     stigmast-7-en-3¦Â-ol
    ÏàËÆ¶È:62.0%
Phytochemistry          1990          29          2351-2355
Sterol glucosides from Prunella vulgaris
Hisashi Kojima,Noriko Sato,Akiko Hatano,Haruo Ogura
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     stigmast-7-en-3¦Â-ol
    ÏàËÆ¶È:62.0%
Chinese Traditional and Herbal Drugs          2009          40          1039-1042
ɽ·¯µÄ»¯Ñ§³É·ÖÑо¿
»ô³¤ºç;Áººè;ÕÅÇìÓ¢;Íõß“;ÕÔÓñÓ¢
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     stigmastane-3¦Â,6¦Á-diol
    ÏàËÆ¶È:62.0%
Journal of Shenyang Pharmaceutical University          2009          26          357-360
Isolation and identification of chemical constituents from testa of Castanea mollissima Blume
LU Chuan, WU Zhao-hua, GAO Hui-yuan, SUN Bo-hang, HUANG Jian, WU Li-jun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     22-dihydrochondrillasterol
    ÏàËÆ¶È:62.0%
Journal of the Chemical Society, Perkin Transactions 1          1989                   1969-1974
Biosynthesis of 24¦Â-ethylsterols in cultured cells of Trichosanthes kirilowii(cucurbitaceae) fed with [1,2-13C2]- and [2-13C2H3]-acetate: reinvestigation of the stereochemistry at C-25
Shujiro Seo, Atsuku Uomori, Yohko Yoshimura, Ken'ichi Takeda, Haruo Seto, Yutaka Ebizuka, Hiroshi Noguchi and Ushio Sankawa
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     (22R,23R)-Stigmasta-3¦Â,22,23-triol(6-deoxo-28-homoteasterone
C29H52O3     ÏàËÆ¶È:62.0%
Tetrahedron          2012          68          3685-3691
Synthesis of aromatic stigmastanes: application to the synthesis of aromatic analogs of brassinosteroids
Sof¨ªa L. Acebedo, Fernando Alonso, Javier A. Ram¨ªrez, Lydia R. Galagovsky
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     5¦Á-stigmastane-3¦Â,6¦Á-diol
C29H52O2     ÏàËÆ¶È:62.0%
Natural Product Research and Development          2005          17          301-302
Chemical Constituents of Tripterygium wilfordii
CHEN Yu; YANG Guang-zhong *; LI Yuan-chao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
13 .     5¦Á-sitgmasta-7-en-3¦Â-ol
    ÏàËÆ¶È:62.0%
Journal of the Chinese Chemical Society          2000          47          1131-1136
The Low Polar Constituents from Bidens Pilosa L. var. minor (Blume) Sherff
Ming-Huey Chang, Guei-Jane Wang,Yueh-Hsiung Kuo and Ching-Kuo Lee*
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
14 .     stigmast-7-en-3¦Â-ol
    ÏàËÆ¶È:62.0%
Modern Chinese Medicine          2012          14          7-11
Separation and Identification of Chemical Constituents from Agriophyllum squarrosum( L. ) Moq.
GONG Bang, ZHAN Kai-xuan, ZHOU Yu-hua, ZHANG Lan, HUI Ye-qian, LI Yu-shan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
15 .     (22R,23R)-3,3-difluoro-22,23-dihydroxy-5¦Á-stigmastan-6-one
C29H48F2O3     ÏàËÆ¶È:62.0%
Steroids          2011          76          1016-1020
Synthesis and biological activity of ring-A difluorinated brassinosteroids
Sof¨ªa L. Acebedo, Fernando Alonso, Lydia R. Galagovsky, Javier A. Ram¨ªrez
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
16 .     compound 7(24S)
    ÏàËÆ¶È:62.0%
Shoyakugaku Zasshi          1992          46          302-309
Chemical Components of a Commercial Crude Drug "Byakken" (Ampelopsis Radix)
KATO TAKESHI, SUYAMA TETSUO, YAMANE FUJITOSHI, MORITA YUTAKA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
17 .     ¡÷7-¶¹çÞÏ©´¼
    ÏàËÆ¶È:62.0%
Journal of Chinese Medicinal Materials          2011          34          553-555
Study on the Chemical Constituents of Codonopsis lanceolata
WANG Wen-yong, ZHAO Shi-cheng, LIU Dong-xin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
18 .     stigmastane-3¦Â,6¦Á-diol
C29H52O2     ÏàËÆ¶È:62.0%
Chinese Tladitional Patent Medicine          2008          30          419-423
»¨Éú¾¥Ò¶»¯Ñ§³É·ÖÑо¿
Áõ¾¢ËÉ, Íõ ¸ÕH, ¶­ ³¬, Âé±ø¼Ì, Áõ¼ª¿ª
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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