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»¯ºÏÎï1------13C NMR (101 MHz, CDCl3) ¦Ä  £º12.27,16.51,17.83,19.87,20.17,21.32,21.34,23.22,28.51,32.22,33.32,37.26,38.60,39.32,40.64,41.02,43.05,43.07,46.49,54.79,55.97,70.69,116.52,119.82,132.21,135.80,140.01,141.58.

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1 .     ZL-5
C28H40O     ÏàËÆ¶È:96.4%
Chemical & Pharmaceutical Bulletin          2004          52(8)          1005-1008
Six Immunosuppressive Features from an Ascomycete, Zopfiella longicaudata, Found in a Screening Study Monitored by Immunomodulatory Activity
Haruhiro FUJIMOTO,Etsuko NAKAMURA, Emi OKUYAMA, and Masami ISHIBASHI
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     (22E,24R)-Ergosta-4,6,8(14),22-tetraen-3-one
    ÏàËÆ¶È:96.4%
Steroids          2001          66          771-775
A novel sterol from Chinese truffles Tuber indicum
Gao Jinming, Hu Lin, Liu Jikai
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     ergosta-4,6,8(14),22-tetraen-3-one
C28H40O     ÏàËÆ¶È:96.4%
Natural Product Research          2008          22          901-906
Ergosta-4,6,8(14),22-tetraen-3-one from Vietnamese Xylaria sp. possessing inhibitory activity of nitric oxide production
Dang Ngoc Quang; Dang Dinh Bach
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     ergosta-4,6,8(14),22-tetraen-3-one
    ÏàËÆ¶È:96.4%
China Journal of Chinese Materia Medica          2005          30          193-195
Studies on chemical constituents in the mycelia from fermented culture of Flammulian velutipes
KANG Jie, CHEN Ruoyun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     24R-ergosta-4,6,8(14),22-tetraen-3-one
    ÏàËÆ¶È:96.4%
China Journal of Chinese Materia Medica          2011          Vol 36,Issue 7          874-880
Studies on constituents of cultures of fungus Phellinu signiarius
WU Xiu li,LIN Sheng, ZHU Chenggen, ZHAO Feng, YU Yang, YUE Zhenggang, LIU Bo,YANG Yong chun, DAI Jungui, SHI Jiangong
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     (24R)-ergosta-4,6,8(14),22-tetraene-3-one
    ÏàËÆ¶È:96.4%
Chinese Journal of Natural Medicines          2008          6          348-353
Chemical Constituents of Marine Sponge Biemna fortis Topsent
HUANG Xiao-Chun; LIU Hai-Li; GUO Yue-Wei
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     ergosta-4,6,8(14),22-tetraene-3-one
    ÏàËÆ¶È:96.4%
Archives of Pharmacal Research          2010          33          1347-1353
Structural implication in cytotoxic effects of sterols from Sellaginella tamariscina
Eun Mi Roh, Qinglong Jin, Hong-Guang Jin, Ji Eun Shin and Eun Jin Choi, et al.
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     22-tetaren-3-one
    ÏàËÆ¶È:96.4%
Chinese Pharmaceutical Journal          2005          40          414-416
Chemical constituents of Pterocarya tonkinesis and their antitumor activity in vitro
LIU Hong-bing, CUI Cheng-bin, GU Qian-qun, CAI Bing, ZHAO Qing-chun, GUAN Hua-shi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     3-subfraction
    ÏàËÆ¶È:96.4%
Bulletin of the Korean Chemical Society          2005          26          1464-1466
Cytotoxic Activity of Ergosta-4,6,8(14),22-tetraen-3-one from the Sclerotia of Polyporus umbellatus
Wi Young Lee, Youngki Park, Jin-Kwon Ahn, So-Young Park, Hak-Ju Lee*
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     ergosta-4,6,8(14),22-tetraen-3-one
    ÏàËÆ¶È:96.4%
Natural Product Research and Development          2010          22          972-975
Chemical Constitutes of Termitomyces schimperi Collected from Africa
YANG Xiao-long;ZHU Ying-cheng; FANG Sheng-tao; JIANG Meng-yuan; LIU Ji-kai
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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²éѯ½á¹û£º¹²²éµ½6596¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼)
1 .     Ergosterol
C28H440     ÏàËÆ¶È:100%
Chemistry of Natural Compounds          2000          36          170-172
LOW-MOLECULAR-WEIGHT MUSHROOM METABOLITES.IV. SLIGHTLY POLAR COMPONENTS OF Stachybotrys alternans
L. S. Kamalov, M. A. Agzamova,S. F. Aripova, and M. I. Isaev
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     ergosterol
    ÏàËÆ¶È:100%
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
3 .     ergosterol
C28H44O     ÏàËÆ¶È:100%
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
4 .     ergosterol
    ÏàËÆ¶È:100%
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
5 .     ergosterol(3¦Â-hydroxyergosta-5,7,22-triene)
C28H44O     ÏàËÆ¶È:100%
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
6 .     (3¦Â,22E)-Ergosta-5,7,22-trien-3-ol
    ÏàËÆ¶È:100%
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
7 .     ergosterol
    ÏàËÆ¶È:100%
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