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12.12,12.34,12.39,15.53,17.46,18.40,18.99,19.07,19.14,19.18,19.94,20.35,21.20,21.36,21.56,23.19,25.51,26.23,26.46,26.55,28.69,29.19,29.27,30.46,31.33,32.02,32.55,33.86,34.09,35.97,36.23,36.49,38.43,38.73,38.85,38.96,40.39,41.96,43.13,43.24,45.54,45.56,45.96,50.09,50.18,51.36,54.84,70.66,77.37,126.26,129.64,138.23,165.25,202.39,202.48
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ºúÐÓÈÊ103: ½ð±Ò+10, ¡ï¡ï¡ïºÜÓаïÖú 2015-05-15 12:07:12
1 .     daucosterol+stigmasterol-3-O-glucopyranoside
    ÏàËÆ¶È:67.2%
Chinese Traditional and Herbal Drugs          2004          35          608-611
Studies on chemical constituents of Indigofera carlesii
SU Yan-fang; ZHANG Xin-xin; YANG Jing; GUO Zeng-jun; L¨¹ Ju-xian; GUO De-an
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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2 .     ¦Â-sitosterol and stigmasterol
    ÏàËÆ¶È:65.5%
China Journal of Chinese Materia Medica          2001          26          692-694
Chemical Constituents of loxocalyx urticifolius Hemsl
ZHANG Xiaorong, WANG Ming'an, ZHANG Yong, WANG Mingkui, IDNG Lisheng
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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3 .     pseudolaridimer A
C50H78O5     ÏàËÆ¶È:63.6%
Organic Letters          2012          14          5432-5435
Pseudolaridimers A and B, Hetero-Cycloartane¨CLabdane Diels¨CAlder Adducts from the Cone of Pseudolarix amabilis
Bo Li, De-Yun Kong, Yun-Heng Shen, Hu Yuan, Rong-Cai Yue, Yi-Ren He, Lu Lu, Lei Shan, Hui-Liang Li, Ji Ye, Xian-Wen Yang, Juan Su, Run-Hui Liu, and Wei-Dong Zhang
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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4 .     hamigerol A
C56H84Na4O20S4     ÏàËÆ¶È:62.5%
Journal of Natural Products          2007          70          1195-1199
Hamigerols A and B, Unprecedented Polysulfate Sterol Dimers from the Mediterranean Sponge Hamigera hamigera
Jie-Fei Cheng, Jong-Soo Lee, Furong Sun, Elizabeth A. Jares-Erijman, Sue Cross, and Kenneth L. Rinehart
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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5 .     7-ketositosteryl-9,10-dihydroxystearate
C50H86O5     ÏàËÆ¶È:61.8%
Steroids          2008          73          1098-1109
Synthesis of highly pure oxyphytosterols and (oxy)phytosterol esters: Part II. (Oxy)-sitosterol esters derived from oleic acid and from 9,10-dihydroxystearic acid [1]
Diane Julien-David, Philippe Geoffroy, Eric Marchioni, Françis Raul, Dalal Aoud¨¦-Werner, Michel Miesch
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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6 .     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:61.8%
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    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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7 .     bisconicasterone
    ÏàËÆ¶È:61.8%
Chemistry Letters          1994          23          419-420
Structure and Absolute Stereochemistry of Bisconicasterone from the Marine Sponge Theonella swinhoei
Yoshinobu Inouye, Yumi Sugo, Takenori Kusumi and Nobuhiro Fusetani
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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8 .     Citruslanosteroside
C56H100O7     ÏàËÆ¶È:60.7%
Natural Product Research          2010          24          610-620
Phytochemical investigation of the fruit peels of Citrus reticulata Blanco
M. Aasim Khan; M. Ali; Prawez Alam
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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9 .     ergosterol
    ÏàËÆ¶È:60.7%
Chemical Communications          1986                   1139-1140
Biosynthesis of Sitosterol in Tissue Cultures of Rabdosia japonica Hara and Ergosterol in Yeast from [2-13C, 2-2H3]Acetate
Shujiro Seo, * Ushio Sankawa, Haruo Seto, Atsuko Uomori, Yohko Yoshimura, Yutaka Ebizuka, Hiroshi Noguchi, and Ken'ichi Takeda
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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10 .     sitosterol
    ÏàËÆ¶È:60.3%
Chemical Communications          1986                   1139-1140
Biosynthesis of Sitosterol in Tissue Cultures of Rabdosia japonica Hara and Ergosterol in Yeast from [2-13C, 2-2H3]Acetate
Shujiro Seo, * Ushio Sankawa, Haruo Seto, Atsuko Uomori, Yohko Yoshimura, Yutaka Ebizuka, Hiroshi Noguchi, and Ken'ichi Takeda
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
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