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1 .     ergosterol
     ÏàËÆ¶È:92.8%
Phytochemistry          1997          45          1669-1671
Ergosta-4, 6, 8, 22-tetraen-3-one from the edible fungus, Pleurotus ostreatus (oyster fungus)
Vladimir Chobot, Lubom¨ªr Opletal, Ludk J¨¢hod¨¢, Asmita V. Patel, Christopher G. Dacke, Gerald Blunden
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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2 .     ergosterol
C28H44O     ÏàËÆ¶È:92.8%
Natural Product Sciences          2009          15          173-179
Steroids and Triterpenoid from the Fruit Bodies of Ganoderma lucidum and Their Cytotoxic Activity
Lee, Joon-Seok; Lee, Mi-Kyoung; Hung, Tran-Manh; Lee, Ik-Soo; Min, Byung-Sun; Bae, Ki-Hwan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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3 .     ergosterol
     ÏàËÆ¶È:92.8%
Phytochemistry          1996          41          1301-1308
Sterol analysis of DMI-resistant and -sensitive strains of Venturia inaequalis
Noboru Shirane, Hideyuki Takenaka, Kazuo Ueda, Yutaka Hashimoto, Kenji Katoh, Hideo Ishii
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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4 .     (3¦Â,22E)-Ergosta-5,7,22-trien-3-ol
     ÏàËÆ¶È:92.8%
Chemistry of Natural Compounds          2011          Vol. 47, No. 4          541-544
BIOACTIVE METABOLITES FROM Penicillium sp. P-1,A FUNGAL ENDOPHYTE IN Huperzia serrata
You-Min Ying, Zha-Jun Zhan, Zhi-Shan Ding,and Wei-Guang Shan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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5 .     ergosterol
     ÏàËÆ¶È:92.8%
Phytochemistry          1990          29          2513-2520
Effect on ergosterol biosynthesis of a fungicide,SSF-109,in Botrytis cinerea
Noboru Shirane,Akira Murabayashi,Michio Masuko,Atsuko Uomori,Yohko Yoshimura,Shujiro Seo,Kiyohisa Uchida,Ken'ichi Takeda
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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6 .     (22E,24R)-ergosta-5,7,22-trien-3¦Â-ol
C28H44O     ÏàËÆ¶È:92.8%
Chinese Traditional and Herbal Drugs          2008          39          1776-1778
Chemical constituents of Russula virescens
TANG Jian-guo; SHAO Hong-jun; LIU Ji-kai
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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7 .     ¦Â-ergosterol
     ÏàËÆ¶È:92.8%
Chinese Traditional and Herbal Drugs          2000          31          328-330
ºÖÔ²¿×Å£¸Î¾ú»¯Ñ§³É·ÖµÄÑо¿
Íò»Ô
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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8 .     Ergosterol
     ÏàËÆ¶È:92.8%
Archives of Pharmacal Research          2009          32          1573-1579
Steroids and triterpenes from the fruit bodies of Ganoderma lucidum and their anti-complement activity
Hyo Won Seo, Tran Manh Hung, MinKyun Na, Hyun Ju Jung and Jin Cheol Kim, et al.
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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9 .     ergosta-5, 7, 22-trien-3¦Â-ol
C28H44O     ÏàËÆ¶È:92.8%
Acta Bot. Boreal. -Occident. Sin.          2010          30          601-603
Chemical Constituents in the Fruiting Bodies of Sarcodon scabrosus
MA Bing-ji, SHEN Jin-wen, YU Hai-you, ZHOU Hang, ZHAO Xu, RUAN Yuan, WU Ting-ting
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------


10 .     ergosta-5,7,22-trien-3¦Â-ol
     ÏàËÆ¶È:92.8%
Chinese Pharmaceutical Journal          2009          44          418-421
Studies on Chemical Constituents in Forsythia suspensa (Thunb.) Vahl
FENG Wei-sheng, LI Ke-ke, ZHENG Xiao-ke
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------


11 .     22 E-ergosta-5,7,22-trien-3¦Â-ol
     ÏàËÆ¶È:92.8%
Chinese Journal of Medicinal Chemistry          2006          16          98-101
The constituents of marine fungus 97F49
ZHANG Qing-hua, WANG Nai-li, GAO Hao, LIU Hong-wei, SONG Shan-shan, MICHIO Namikoshi, YAO Xin-sheng
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------


12 .     (3¦Â,22E)-Âó½ÇçÞ-5,7,22-ÈýÏ©-3-´¼
C28H44O     ÏàËÆ¶È:92.8%
Chinese Journal of Medicinal Chemistry          2009          19          200-205
Chemical constituents from the endophytic fungus Acremonium sp. J1 of Antiaris toxicaria
QUE Dong-mei, DAI Hao-fu, ZENG Yan-bo, WU Jiao, MEI Wen-li
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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13 .     ergosterol
     ÏàËÆ¶È:92.8%
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   Ì¼Æ×Ä£Äâͼ

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14 .     Âó½ÇçÞ´¼
    ÏàËÆ¶È:92.8%
Journal of Shenyang Pharmaceutical University          2007          24          245-248
Fermentation products of endophyte HCCB00167
XIE Cui-hua, RUAN Li-jun, XIA Huan-zhang, CHEN Dai-jie, GE Mei
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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15 .     24(R)-methylcholesta-5,7,22-tiene-3-ol
     ÏàËÆ¶È:92.8%
Bulletin of the Korean Chemical Society          2008          29          615-619
Human Acyl-CoA: Cholesterol Acyltransferase (hACAT) Inhibitory Activities of Triterpenoids from Roots of Glycine max (L.) Merr.
Jin Hwan Lee, Young Bae Ryu, Byong Won Lee, Jin Hyo Kim, Woo Song Lee, Yong-Dae Park, Tae-Sook Jeong, Ki Hun Park*
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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16 .     ergosterol
     ÏàËÆ¶È:92.8%
Bioscience, Biotechnology, and Biochemistry          1994          58          1542-1544
Volemolide, a Novel Norsterol from the Fungus Lactarius volemus
Kenji Kobata, Tomonari Wada, Yasuo Hayashi, Hisao Shisata
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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17 .     ergosterol
C28H44O     ÏàËÆ¶È:92.8%
Natural Product Research and Development          2010          22          998-1000
Chemical Constituents and Identification of the Caules of Clematis armandii Franch. and Clematis montana Buch.-Ham.
LIU Jing-jing;CHEN Xing; WEI Zhi-qi; LI Bin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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18 .     ergosta-5,7,22-trien-3-ol
     ÏàËÆ¶È:92.8%
Natural Product Research and Development          2007          19          420-422
Isolation and Structures of Two Steroids from Mangrove Endophyte Penicillium sp.
LI Xiang;SUN Guang-zhi; ZHENG Yi-nan; LIN Wen-han; Isabel Sattler
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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19 .     ergosta-5,7,22-trien-3¦Â-o-l
C28H44O     ÏàËÆ¶È:92.8%
Natural Product Research and Development          2004          16          204-206
THE CHEMICAL CONSTITUENTS OF BASIDIOMYCETE CALODON SUAVEOLENS
WANG Fei; LIU Ji-kai *
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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20 .     ¦Â-ergosterol
     ÏàËÆ¶È:92.8%
Natural Product Research and Development          1999          11(6)          18-21
THREE STEROLS FROM GYROPORUS CASTANEUS
Wan Hui; Sun Rongqi; Wu Dajun; Guo Beishu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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