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13C NMR (101 MHz, CDCl3) ¦Ä 11.9, 17.3, 18.9, 19.0, 19.8, 21.2, 23.0, 26.1, 26.3, 28.5, 29.1, 31.2, 33.9, 36.0, 36.3, 38.2, 38.7, 41.8, 43.1, 45.4, 45.8, 49.9, 49.9, 54.7, 70.5, 126.1, 165.0, 202.3.
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meitianyxs: ½ð±Ò+15 2014-04-02 09:06:38
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1 .     7-ketositosterol
C29H48O2     ÏàËÆ¶È:100%
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    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
2 .     7-ketositosterol
    ÏàËÆ¶È:100%
Journal of Chinese Pharmaceutical Sciences          2012          21          88-92
Chemical constituents from Aquilaria sinensis(Lour.) Gilg
Dong Chen; Yue-Lin Song; Chun-Xiao Nie; Xu Ma; Peng-Fei Tu
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
3 .     stigmast-5-ene-3¦Â-ol-7-one
C29H48O2     ÏàËÆ¶È:100%
Chinese Traditional and Herbal Drugs          2013          44          2208-2212
Chemical constituents from stems of Ficus auriculata
SHAO Tai-ming, SONG Xiao-ping, CHEN Guang-ying, HAN Chang-ri, ZHENG Cai-juan, YAO Guo-gui
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
4 .     3¦Â-hydroxystigmast-5-en-7-one
    ÏàËÆ¶È:96.5%
China Journal of Chinese Materia Medica          2009          34          1809-1811
Steroids from Monascus purpureus metabolite
SHANG Xiaoya, WANG Ruolan, YI N Suqin, LI Jinjie, JIN Zonglian
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
5 .     3¦Â-hydroxy-stigmast-5-en-7-one
    ÏàËÆ¶È:96.5%
China Journal of Chinese Materia Medica          2006          31          131-133
Chemical constituents from roots of Ficus hirta
LI Chun, BU Pengbin, YUE Dangkun, SUN Youfu
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
6 .     3¦Â-hydroxystigmast-5-en-7-one
C29H48O2     ÏàËÆ¶È:96.5%
China Journal of Chinese Materia Medica          2001          26          762-764
Studies on the Chemical Constitutents of Asarum longerhizomatosum C. F. Liang et C. S. Yang
ZHANG Shuxing, CAI Shaoqing, ZHAO Yuying
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
7 .     7-Keto-¦Â-sitosterol
    ÏàËÆ¶È:96.5%
Natural Product Sciences          2007          13          332-336
Norsesquiterpene and Steroid Constituents of Humulus japonicus
Yu, Byung-Chul; Yang, Min-Cheol; Lee, Kyu-Ha; Kim, Ki-Hyun; Lee, Kang-Ro
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
8 .     7-Oxo-¦Â-sitosterol
    ÏàËÆ¶È:96.5%
Korean Journal of Pharmacognosy          2008          39(3)          186-193
Phytochemical Studies on Astragalus Root (3);Triterpenoids and Sterols
Jung, Hye-Sil; Lee, Eun-Ju; Lee, Je-Hyun; Kim, Ju-Sun; Kang, Sam-Sik
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
9 .     stigmasta-5-en-3¦Â-ol-7-one
    ÏàËÆ¶È:96.5%
China Journal of Chinese Materia Medica          2011          Vol 36,Issue 7          891-895
Chemical constituents from petroleum ether portion of Abelmoschus esculentus
JIA Lu, GUO M ingm ing, LI Dong, JING Lin lin
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
10 .     stigmast-5-en-7-oxo-3¦Â-ol
    ÏàËÆ¶È:96.5%
Chinese Traditional and Herbal Drugs          2010          41          195-197
ºÚÀÏ»¢¸ù»¯Ñ§³É·ÖµÄÑо¿
Íõéª;ÀîÕ¼ÁÖ;»ª»áÃ÷
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
11 .     3¦Â-hydroxy-stigmast-5-en-7-one
    ÏàËÆ¶È:96.5%
Chinese Traditional and Herbal Drugs          2007          38          14-17
Chemical constituents of whole herb of Dicliptera chinensis
GAO Yu-tao; YANG Xiu-wei; AI Tie-min
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
12 .     stigmast-5-ene-3¦Â-ol-7-one
    ÏàËÆ¶È:96.5%
Pharmazie          2002          57          209-211
Two new steroids from Adenophora stenanthina subsp. xifengensis
Zhen-Fu Hou - Yong-Qiang Tu - Yu Li
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
13 .     3¦Â-hydroxystigmast-5-en-7-one
    ÏàËÆ¶È:96.5%
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    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
14 .     7-oxo-3¦Â-stigmasterol
    ÏàËÆ¶È:96.5%
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    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
15 .     ¶¹çÞÍé-5-Ï©-3¦Â-´¼-7-ͪ
    ÏàËÆ¶È:96.5%
Chinese Journal of Medicinal Chemistry          2004          14          294-297
Isolation, identification of the chemical constituents from Bauhinia variegata L.
ZHAO Yan-yan, CUI Cheng-bin, CAI Bing, SUN Qi-shi
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
16 .     3-hydroxy-stigmast-5-en-7-one
    ÏàËÆ¶È:96.5%
Chinese Journal of Medicinal Chemistry          2007          17          170-172
Chemical constituents of Tribulus terrestris L.
L¨¹ A-li, ZHANG Nan, MA Hong-yu, WANG Ding, DANG Quan, PEI Yue-hu
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
17 .     stigmastanone
    ÏàËÆ¶È:96.5%
Chemistry of Natural Compounds          2012          48          594-596
A novel C29 sterol from Clerodendrum cyrtophyllum
Peng Wang, Fujiang Guo, Junjie Tan, Cheng Huang and Guangyin Wang, et al.
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
18 .     3¦Â-hydroxy-Stigmasta-5-en-7-one
C29H48O2     ÏàËÆ¶È:96.5%
Acta Scientiarum Naturalium Universitatis Sunyatseni          2001          40(2)          54-57
Steroids from the Marine Sponge Stelletta tenuis Lindgren
YAN Su-jun, SU Jing-yu, ZHANG Guang-wen, WANG Yan-hong, LI Hong
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
19 .     7-oxositosterol
    ÏàËÆ¶È:96.5%
Chinese Traditional and Herbal Drugs          2012          43          2346-2350
Chemical constituents from fruits of Vitex negundo
ZHAO Xiang-xiang; ZHENG Cheng-jian; QIN Lu-ping
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
20 .     (24R)-24-¶¹çÞ-3¦Â-ôÇ»ù-5-Ï©-7-ͪ
    ÏàËÆ¶È:96.5%
China Journal of Chinese Materia Medica          2012          37          2092-2099
Non-anthraquinones constituents from the roots of Knoxia valerianoides
ZHAO Feng; WANG Sujuan; WU Xiuli; YU Yang; YUE Zhenggang; LIU Bo; LIN Sheng; ZHU Chenggen; YANG Yongchun; SHI Jiangong
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
21 .     7-oxo-¦Â-sitosterol
C29H48O2     ÏàËÆ¶È:96.5%
Journal of Chinese Medicinal Materials          2006          29          1186-1187
µÆÐIJݻ¯Ñ§³É·ÖÑо¿
Àîºìϼ, ³ÂÓñ, ÷֮ÄÏ, Ñî¹âÖÒ
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
22 .     3¦Â-hydroxystigmast-5-en-7-one
C29H48O2     ÏàËÆ¶È:96.5%
Yakugaku Zasshi          1991          111          299-305
Studies on the Anticomplementary Activity of Jozann. Antlcomplementary Activity of Steroid Derivatives
Tsuyoshi EBIHARA, Tomoko KAWAI, Masanori KUROYANAGI, Seigo FUKUSHIMA, Akira UENO
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
23 .     compound 1a
    ÏàËÆ¶È:96.5%
Yakugaku Zasshi          1991          111          299-305
Studies on the Anticomplementary Activity of Jozann. Antlcomplementary Activity of Steroid Derivatives
Tsuyoshi EBIHARA, Tomoko KAWAI, Masanori KUROYANAGI, Seigo FUKUSHIMA, Akira UENO
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
24 .     mangdesisterol
    ÏàËÆ¶È:96.5%
Lishizhen Medicine and Materia Medica Research          2013          24          591-593
Antimicrobial constituents from the twigs of Trigonostemon xyphophylloides
YU Li, MEI Wen-li, ZUO Wen-jian, WANG Hui, GUO Zhi-kai, AN Xue-qin, DAI Hao-fu*
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
25 .     7-Oxo-¦Â-sitosterol
C29H48O2     ÏàËÆ¶È:96.4%
Journal of Natural Products          2000          63          72-78
Isolation and Structures of Schleicherastatins 1-7 and Schleicheols 1 and 2 from the Teak Forest Medicinal Tree Schleichera oleosa1
George R. Pettit,Atsushi Numata, Gordon M. Cragg, Delbert L. Herald, Tamie Takada,Chika Iwamoto,Roland Riesen, Jean M. Schmidt, Dennis L. Doubek, and Animesh Goswami
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
26 .     7-oxo-¦Â-sitosterol
    ÏàËÆ¶È:96.4%
Natural Product Research and Development          2009          21          593-599
Chemical Constituents of Osmanthus yunnanensis
MA Xiao-li;LIN Wen-bing; ZHANG Guo-lin
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
27 .     7-Oxo-¦Â-sitosterol
    ÏàËÆ¶È:96.4%
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    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
28 .     compound 9
    ÏàËÆ¶È:93.1%
Chemistry of Natural Compounds          1999          35          646-649
13C NMR SPECTRA OF II-SITOSTEROL DERIVATIVES WITH OXIDIZED RINGS A AND B
N. V. Kovganko, Zh. N. Kashkan,E. V. Borisov, and E. V. Batura
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
29 .     7-Oxositosterol (3¦Â-hydroxystigmast-5-en-7-one)
    ÏàËÆ¶È:93.1%
Pharmazie          2004          59          885-888
Terpenoids and steroids from Lappula anocarpa
Yuan-Peng Jin, and Yan-Ping Shi
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
30 .     stigmast-5-en-3¦Â-ol-7-one
    ÏàËÆ¶È:93.1%
Pharmazie          2005          60          464-467
Steroids from Saussurea ussuriensis
Jia-Tao Feng and Yan-Ping Shi
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
31 .     ¶¹çÞ-5-Ï©-3¦Â-´¼-7-ͪ
    ÏàËÆ¶È:93.1%
Journal of Shenyang Pharmaceutical University          2005          22          422-424
Studies on the chemical constituents of Malt
LING Jun-hong, WANG Jin-hui, WANG Nan, LI Wen, SHA Yi, LI Xian
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
32 .     3¦Â-hydroxystigmast-5-en-7-one
    ÏàËÆ¶È:93.1%
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    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
33 .     7-oxo-¦Â-sitosterol
C29H48O2     ÏàËÆ¶È:89.6%
Journal of Tropical and Subtropical Botany          2007          15          35-39
Chemical Constituents from Barks of Endospermum chinense Benth.
LI, Xiao-hua, LIN, Li-dong, WU, Ping, LIU, Mei-fang, WEI, Xiao-yi
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
34 .     7¦Â-hydroxystigmast-4-en-3-one
C29H48O2     ÏàËÆ¶È:86.2%
Natural Product Research          2006          20          327-334
Potential cancer chemopreventive agents from Arbutus unedo
Esperanza J. Carcache-Blanco; Muriel Cuendet; Eun Jung Park; Bao-Ning Su; J. Fausto Rivero-Cruz; Norman R. Farnsworth; John M. Pezzuto; A. Douglas Kinghorn
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
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