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1 .     ergosta-5,7,---triene-3¦Â-ol
    ÏàËÆ¶È:96.1%
Chinese Journal of Marine Drugs          2006          25(1)          6-10
Studies on the chemical constituents of the fermentation liquid from marine actinomyces Micromonos por a sp. and bacteria Ocea nos pi rillum sp.
SHI Ying, TIAN Li, WANG Jing, PEI Yue-hu
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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2 .     ergosta-5,7,22-t riene-3¦Â-ol
    ÏàËÆ¶È:96.1%
Chinese Journal of Marine Drugs          2004          23(1)          14-16
Study on the chemical constituents of the fermentation liquid from marine fungus Aspergillus versicolor
ZHANG Hai-long, MA Li, TIAN Li
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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3 .     ergosterol derived
    ÏàËÆ¶È:96.1%
Tetrahedron Letters          2000          41          2791-2795
Stereochemistry of hydrogen introduction at C-25 in ergosterol synthesized by the mevalonate-independent pathway
Wen-xu Zhou, W. David Nes
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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4 .     Ergosterol
    ÏàËÆ¶È:96.1%
Archives of Pharmacal Research          2002          25          851-855
Cytotoxic ergosterols from paecilomyces sp. J300
Hak Cheol Kwon, Sang Deuk Zee, Sae Yun Cho, Sang Un Choi and Kang Ro Lee
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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5 .     ergosterol
    ÏàËÆ¶È:96.1%
Natural Product Research          2012          26          2008-2012
A new phenol compound from endophytic Phomopsis sp. DC01
Jun-Tian Li, Qian-Qian Chen, Ying Zeng, Qi Wang & Pei-Ji Zhao
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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6 .     ergosterol
    ÏàËÆ¶È:96.1%
Canadian Journal of Chemistry          1992          70          2276-2284
Phytotoxic metabolites of Phomopsisconvolvulus, a host-specific pathogen of field bindweed
Youla S. Tsantrizos, Kelvin K. Ogilvie, Alan K. Watson
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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7 .     ergosta-5,7,22-triene-3¦Â-ol
C28H44O     ÏàËÆ¶È:96.1%
Chinese Pharmaceutical Journal          2014          49          26-29
Chemical Constituents of a Marine Fungus Nigrospora sphaerica
ZHANG Qi-hui, TIAN Li, YAN Zheng-qing, LIU Si, ZHANG Zhong-shan, PEI Yue-hu
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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8 .     ergostatrien-3¦Â-ol
    ÏàËÆ¶È:96.1%
Journal of Agricultural and Food Chemistry          2010          58          7445-7452
Analgesic Effects and the Mechanisms of Anti-inflammation of Ergostatrien-3¦Â-ol from Antrodia camphorata Submerged Whole Broth in Mice
Guan-Jhong Huang, Shyh-Shyun Huang, Shiang-Shiou Lin, Yi-Yuan Shao, Chin-Chu Chen, Wen-Chi Hou and Yueh-Hsiung Kuo
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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9 .     ergosterol
    ÏàËÆ¶È:96.1%
Journal of Agricultural and Food Chemistry          2002          50          7581-7585
Cyclooxygenase Inhibitory and Antioxidant Compounds from the Mycelia of the Edible Mushroom Grifola frondosa
Yanjun Zhang, Gary L. Mills, and Muraleedharan G. Nair
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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10 .     (22E,24R)-Ergosta-5,7,22E-trien-3¦Â-ol
    ÏàËÆ¶È:96.1%
Chemistry of Natural Compounds          2012          48          771-773
A new sulfo-xanthone from the marine-derived fungus Penicillium sacculum
Tao Liu, Limin Zhang, Zhanlin Li, Yu Wang, Li Tian, Yuehu Pei, Huiming Hua
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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11 .     Ergosterol
    ÏàËÆ¶È:96.1%
Mycosystema          2011          30          636-643
The bioactive metabolites of Aspergillus versicolor F62 isolated from Haliclona simulans
DONG Shi-Hao GONG Ting ZHU Ping
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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12 .     ergosterol
    ÏàËÆ¶È:96.1%
Chinese Joumal of Experimental Traditional Medical Fomulae          2011          17          97-101
Investigations on Chemical Constituents of Methanolic Extract from Penicillium jiangxiense
CHEN Chao, PAN Wei-dong, XIAO Jian-hui, LIANG Guang-yi
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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13 .     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    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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14 .     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    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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15 .     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    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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16 .     (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    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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17 .     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    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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18 .     (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    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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

19 .     ergosterol
    ÏàËÆ¶È:92.8%
Chinese Traditional and Herbal Drugs          2005          36          1601-1603
Chemical constituents from fruiting bodies of Ganoderma lucidum
ZHANG Xiao-qi; YIN Zhi-qi; YE Wen-cai; ZHAO Shou-xun
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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

20 .     ¦Â-ergosterol
    ÏàËÆ¶È:92.8%
Chinese Traditional and Herbal Drugs          2000          31          328-330
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Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
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