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12.96,18.27,19.24,20.28,21.85,22.86,23.92,28.91,33.08,33.79,34.28,38.52,40.36,41.28,42.42,43.52,44.21,55.70,56.60,68.02,74.71,76.57,120.92,124.25,132.56,136.26,136.63,150.68
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1 .     cerevisterol
C28H46O3     ÏàËÆ¶È:89.2%
Acta Botanica Yunnanica          2006          28(3)          315-318
A New Steroidal Glycoside from the Fruiting Bodies of Tylopilus virens (Boletaceae)
WANG Fei,ZHANGLing, DONG Ze-Jun,LIU Ji-Kai
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     ergosta-7,22-diene-3,5,6-triol
C28H46O3     ÏàËÆ¶È:89.2%
Chemistry of Natural Compounds          2009          45          124-125
COMPONENTS OF THE SCLEROTIAOF Polyporus umbellatus
Weiwei Zhou, Shunxing Guo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     ergosta-7,22E-diene-3¦Â,5¦Á,6¦Â-triol
    ÏàËÆ¶È:89.2%
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 .     stigma-7,22-dien-3¦Â,5¦Á,6¦Â-triol
C28H46O3     ÏàËÆ¶È:89.2%
Natural Product Research          2008          22          154-166
Antifouling and antibacterial compounds from the gorgonians Subergorgia suberosa and Scripearia gracillis
S. H. Qi; S. Zhang; L. H. Yang; P. Y. Qian
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     6,9-epidioxyergosta-7,22-dien-3¦Â-ol
    ÏàËÆ¶È:89.2%
China Journal of Chinese Materia Medica          2007          32          235-237
Studies on chemical constituents from the fruiting bodies of Ganoderma sinense Zhao,Xu et Zhang
LIU Chao , WANG Hongqing, LI Baoming, CHEN Ruoyun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     (22E,24R)-24-methyl-5¦Á-cholesta-7,22-diene-3¦Â,5,6¦Â-triol
    ÏàËÆ¶È:89.2%
Journal of Natural Products          1987          Vol 50          915
Four New Trihydroxylated Sterols from the Sponge Spongionella gracilis Four New Trihydroxylated Sterols from the Sponge Spongionella gracilis
Vincenzo Piccialli, Donato Sica
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     cerevisterol(3¦Â,5¦Á,6¦Â-trihydroxyergosta-7,22-diene)
C28H46O3     ÏàËÆ¶È:89.2%
Phytochemistry          1991          30          4117-4120
Glycosides of ergosterol derivatives from Hericum erinacens
Yoshihisa Takaishi, Minoru Uda, Takashi Ohashi, Kimiko Nakano, Koutarou Murakami, Toshiaki Tomimatsu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     (22E,24R)-ergosta-7,22-dien-3¦Â,5¦Á,6¦Â-triol
    ÏàËÆ¶È:89.2%
Chinese Traditional and Herbal Drugs          2010          41          1065-1068
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Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     stigma-7,22-dien-3¦Â,5¦Á,6¦Â-triol
    ÏàËÆ¶È:89.2%
Chinese Traditional and Herbal Drugs          2008          39          1606-1609
Chemical constituents of Amtipathes dichotoma
SU Guo-chen; ZHANG Si; QI Shu-hua
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     (22E,24S)-24-methyl-5¦Á-cholesta-7,22-diene-3¦Â,5,6¦Â-triol
C28H46O3     ÏàËÆ¶È:89.2%
Chinese Traditional and Herbal Drugs          1994          25          342-343+390
Studies on the Chemical Constituents of Kuhonggu (Russula rosacea)(¢ò)
Wang Huaibin; Xu Weishen; et al(Institute of Materia Medica; Chinese Academy of Medica Sciences; Beijing);
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     cerevisterol
    ÏàËÆ¶È:89.2%
Archives of Pharmacal Research          2005          28          889-891
Antibacterial constituents from fruit bodies of Ascomyce Bulgaria inquinans
Peng Zhang, Xian Li, Ning Li, Jing Xu and Zhan-Lin Li, et al.
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     ergosta-7,22-diene-3,5,6-triol
C28H46O3     ÏàËÆ¶È:89.2%
Chinese Pharmaceutical Journal          2003          38          499-5001
Studies on chemical constituents of Cordyceps sinensis(Berk) Sacc
LI Jie-xiu, LI Jin, XU Li-zhen, YANG Shi-lin, ZOU Zhong-mei
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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2Â¥: Originally posted by wangwang1989 at 2013-06-17 19:24:38
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21.4,30.4,37.4,73.2,73.7,125.6,126.6,139.6,140.2,168.2

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12.96,18.27,19.24,20.28,20.58,21.85,22.86,23.92,28.91,33.08,33.79,34.28,38.52,40.36,41.28,42.42,43.52,44.21,55.70,56.60,68.02,74.71,76.57,120.92,124.25,132.56,136.26,136.63,150.68
3Â¥2013-06-17 20:18:32
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wangwang1989

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1 .     cerevisterol
C28H46O3     ÏàËÆ¶È:89.6%
Acta Botanica Yunnanica          2006          28(3)          315-318
A New Steroidal Glycoside from the Fruiting Bodies of Tylopilus virens (Boletaceae)
WANG Fei,ZHANGLing, DONG Ze-Jun,LIU Ji-Kai
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     ergosta-7,22-diene-3,5,6-triol
C28H46O3     ÏàËÆ¶È:89.6%
Chemistry of Natural Compounds          2009          45          124-125
COMPONENTS OF THE SCLEROTIAOF Polyporus umbellatus
Weiwei Zhou, Shunxing Guo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     ergosta-7,22E-diene-3¦Â,5¦Á,6¦Â-triol
    ÏàËÆ¶È:89.6%
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 .     stigma-7,22-dien-3¦Â,5¦Á,6¦Â-triol
C28H46O3     ÏàËÆ¶È:89.6%
Natural Product Research          2008          22          154-166
Antifouling and antibacterial compounds from the gorgonians Subergorgia suberosa and Scripearia gracillis
S. H. Qi; S. Zhang; L. H. Yang; P. Y. Qian
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     6,9-epidioxyergosta-7,22-dien-3¦Â-ol
    ÏàËÆ¶È:89.6%
China Journal of Chinese Materia Medica          2007          32          235-237
Studies on chemical constituents from the fruiting bodies of Ganoderma sinense Zhao,Xu et Zhang
LIU Chao , WANG Hongqing, LI Baoming, CHEN Ruoyun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     (22E,24R)-24-methyl-5¦Á-cholesta-7,22-diene-3¦Â,5,6¦Â-triol
    ÏàËÆ¶È:89.6%
Journal of Natural Products          1987          Vol 50          915
Four New Trihydroxylated Sterols from the Sponge Spongionella gracilis Four New Trihydroxylated Sterols from the Sponge Spongionella gracilis
Vincenzo Piccialli, Donato Sica
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     cerevisterol(3¦Â,5¦Á,6¦Â-trihydroxyergosta-7,22-diene)
C28H46O3     ÏàËÆ¶È:89.6%
Phytochemistry          1991          30          4117-4120
Glycosides of ergosterol derivatives from Hericum erinacens
Yoshihisa Takaishi, Minoru Uda, Takashi Ohashi, Kimiko Nakano, Koutarou Murakami, Toshiaki Tomimatsu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     (22E,24R)-ergosta-7,22-dien-3¦Â,5¦Á,6¦Â-triol
    ÏàËÆ¶È:89.6%
Chinese Traditional and Herbal Drugs          2010          41          1065-1068
СҶÈ̶¬ÌٵĻ¯Ñ§³É·ÖÑо¿
Áõΰ;°×ËØÆ½;Áº»á¾ê;Ô¬ÓÀÁÁ
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     stigma-7,22-dien-3¦Â,5¦Á,6¦Â-triol
    ÏàËÆ¶È:89.6%
Chinese Traditional and Herbal Drugs          2008          39          1606-1609
Chemical constituents of Amtipathes dichotoma
SU Guo-chen; ZHANG Si; QI Shu-hua
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     (22E,24S)-24-methyl-5¦Á-cholesta-7,22-diene-3¦Â,5,6¦Â-triol
C28H46O3     ÏàËÆ¶È:89.6%
Chinese Traditional and Herbal Drugs          1994          25          342-343+390
Studies on the Chemical Constituents of Kuhonggu (Russula rosacea)(¢ò)
Wang Huaibin; Xu Weishen; et al(Institute of Materia Medica; Chinese Academy of Medica Sciences; Beijing);
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     cerevisterol
    ÏàËÆ¶È:89.6%
Archives of Pharmacal Research          2005          28          889-891
Antibacterial constituents from fruit bodies of Ascomyce Bulgaria inquinans
Peng Zhang, Xian Li, Ning Li, Jing Xu and Zhan-Lin Li, et al.
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     ergosta-7,22-diene-3,5,6-triol
C28H46O3     ÏàËÆ¶È:89.6%
Chinese Pharmaceutical Journal          2003          38          499-5001
Studies on chemical constituents of Cordyceps sinensis(Berk) Sacc
LI Jie-xiu, LI Jin, XU Li-zhen, YANG Shi-lin, ZOU Zhong-mei
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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4Â¥2013-06-17 20:38:22
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4Â¥: Originally posted by wangwang1989 at 2013-06-17 20:38:22
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