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11.91,14.05,14.12,17.24,18.86,19.73,20.98,21.15,22.62,22.99,26.03,26.26,29.63,31.07,31.86,33.88,36.01,36.28,38.23,38.63,41.72,45.35,45.76,49.87,54.64,60.37,70.44,126.01,165.22,171.18,177.75,202.41

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12.06,12.18,19.01,19.26,19.34,19.49,20.10,21.00,23.02,24.26,25.85,27.61,28.12,29.12,29.66,31.78,31.83,33.75,35.88,36.61,45.56,50.02,55.83,56.89,61.49,70.49,73.86,77.11,77.15,77.38,101.20,121.59,129.08,131.97,140.86
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1 .     7-Keto-¦Â-sitosterol
    ÏàËÆ¶È:78.1%
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   Ì¼Æ×Ä£Äâͼ

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2 .     3¦Â-hydroxystigmast-5-en-7-one
    ÏàËÆ¶È:78.1%
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   Ì¼Æ×Ä£Äâͼ

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3 .     7-Oxo-¦Â-sitosterol
C29H48O2     ÏàËÆ¶È:75%
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   Ì¼Æ×Ä£Äâͼ

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4 .     compound 9
    ÏàËÆ¶È:75%
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   Ì¼Æ×Ä£Äâͼ

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5 .     7-ketositosterol
C29H48O2     ÏàËÆ¶È:75%
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

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6 .     7¦Â-hydroxystigmast-4-en-3-one
C29H48O2     ÏàËÆ¶È:75%
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   Ì¼Æ×Ä£Äâͼ

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7 .     3¦Â-hydroxystigmast-5-en-7-one
    ÏàËÆ¶È:75%
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   Ì¼Æ×Ä£Äâͼ

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8 .     3¦Â-hydroxy-stigmast-5-en-7-one
    ÏàËÆ¶È:75%
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   Ì¼Æ×Ä£Äâͼ

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9 .     3¦Â-hydroxystigmast-5-en-7-one
C29H48O2     ÏàËÆ¶È:75%
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   Ì¼Æ×Ä£Äâͼ

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10 .     7-Oxo-¦Â-sitosterol
    ÏàËÆ¶È:75%
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   Ì¼Æ×Ä£Äâͼ
2Â¥2012-11-04 13:09:23
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1 .     ¦Â-sitosterol-3-O-¦Â-D-glucopyranoside
    ÏàËÆ¶È:88.5%
Korean Journal of Pharmacognosy          1996          27(1)          75-79
Phytochemical Constituents from Aconitum pseudolaeve Var. erectum
Kim, Dae-Keun; Kwak, Jong-Hwan; Song, Ki-Won; Kwon, Hack-Cheol; Zee, Ok-Pyo; Lee, Kang-Ro
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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2 .     Stigmast-5-en-3-O-¦Â-D-glucoside
C35H60O6     ÏàËÆ¶È:88.5%
Magnetic Resonance in Chemistry          2001          39          399-405
Complete 1H and 13C NMR assignments of stigma-5-en-3-O-¦Â-glucoside and its acetyl derivative
Shaheen Faizi, Muhammad Ali, Rubeena Saleem, Irfanullah and Sarah Bibi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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3 .     daucosterol
C35H60O4     ÏàËÆ¶È:88.5%
Chinese Journal of Natural Medicines          2006          4          257-259
Chemical Constituents of Sibiraea angustata
TAO Ting-Ting; SEI Yasuo; WANG Tian-Zhi; BAI Chuan; CHANG Yan-Bo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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4 .     Sitosterol-3-O-¦Â-D-glucopyranoside
    ÏàËÆ¶È:88.5%
Archives of Pharmacal Research          2002          25          628-635
Phytochemical constituens of Cirsium setidens Nakai and their cytotoxicity against human cancer cell lines
Won Bin Lee, Hak Cheol Kwon, Ock Ryun Cho, Kang Choon Lee and Sang Un Choi, et al.
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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5 .     ¦Â-Sitosterol-3-O-¦Â-D-glycoside
    ÏàËÆ¶È:88.5%
Archives of Pharmacal Research          2004          27          1016-1019
A new sesquiterpene lactone from Artemisia rubripes nakai
Kyu Ha Lee, Yong Deuk Min, Sang Zin Choi, Hak Cheol Kwon and Ock Ryun Cho, et al.
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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6 .     ¦Â-Sitosterol-3-O-glucoside
    ÏàËÆ¶È:88.5%
Archives of Pharmacal Research          2005          28          39-43
Antitumor and antiinflammatory constituents from celtis sinensis
Dae Keun Kim, Jong Pil Lim, Jin Wook Kim, Hee Wook Park and Jae Soon Eun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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7 .     ¦Â-daucosterol
    ÏàËÆ¶È:88.5%
Chinese Pharmaceutical Journal          2011          46          341-343
Chemical Constituents of Lysimachia clethroides Duby
YUE Shu-mei, CHEN Bai-quan, YUAN Peng-fei, CUI Wei-heng, KANG Wen-yi*
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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8 .     daucosterol
    ÏàËÆ¶È:88.5%
Chinese Journal of Medicinal Chemistry          2006          16          303-305
The constituents of Veratrum japonicum Loes. f.
ZHOU Jian-xia, KANG Lu, SHEN Zheng-wu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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9 .     daucosterol
C35H60O6     ÏàËÆ¶È:88.5%
Journal of Shenyang Pharmaceutical University          2008          25          630-632
Chemical constituents from the fruits of Xanthium sibiricum
DAI Ying-hui, CUI Zheng, WANG Dong, LI Jian-lin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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10 .     daucosterol
    ÏàËÆ¶È:88.5%
Natural Product Research and Development          2009          21          784-786
Study on the Chemical Constituents of Fruits of Cannabis Sativa L.
SHEN Qian;CAI Guang-ming; HE Gui-xia; DU Fang-lu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3Â¥2012-11-04 13:19:59
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