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11.93,16.23,17.55,18.20,18.65,18.98,19.90,20.16,21.05,22.94,28.24,31.94,33.03,33.66,35.84,36.95,38.31,38.76,39.02,40.37,40.73,42.76,46.19,54.50,55.67,70.40,116.22,119.53,131.91,135.50,139.69,141.31,
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wanfeier1212: ½ð±Ò+10, Ì«¸ÐлÁË 2015-03-29 09:21:23
1 .     ergosterol
    ÏàËÆ¶È:84.3%
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
2 .     ergosterol
    ÏàËÆ¶È:84.3%
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
3 .     (3¦Â,22E)-Ergosta-5,7,22-trien-3-ol
    ÏàËÆ¶È:84.3%
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
4 .     ergosterol
    ÏàËÆ¶È:84.3%
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
5 .     ergosta-5,7,22-trien-3¦Â-ol
    ÏàËÆ¶È:84.3%
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    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
6 .     22 E-ergosta-5,7,22-trien-3¦Â-ol
    ÏàËÆ¶È:84.3%
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    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
7 .     (3¦Â,22E)-Âó½ÇçÞ-5,7,22-ÈýÏ©-3-´¼
C28H44O     ÏàËÆ¶È:84.3%
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    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
8 .     Âó½ÇçÞ´¼
    ÏàËÆ¶È:84.3%
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    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
9 .     ergosterol
    ÏàËÆ¶È:84.3%
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    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
10 .     ergosterol
C28H44O     ÏàËÆ¶È:84.3%
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    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
11 .     (22E,24R)-ergosta-5,7,22-trien-3¦Â-ol
    ÏàËÆ¶È:84.3%
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    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
12 .     ergosta-5,7,22-trien-3-ol
    ÏàËÆ¶È:84.3%
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    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
13 .     (22E,24R)-ergosta-5,7,22-trine-3¦Â-ol
    ÏàËÆ¶È:84.3%
Natural Product Research and Development          2007          19          605-609
Study on the Chemical Constitutes of Hydnellum concrescens
YANG Xiao-long;WANG Fei; SHAO Hong-jun; DONG Ze-jun; DING Zhi-hui; YANG Wan-qiu; LIU Ji-kai
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
14 .     ergosta-5,7,22-trien-3¦Â-o-l
C28H44O     ÏàËÆ¶È:84.3%
Natural Product Research and Development          2004          16          204-206
THE CHEMICAL CONSTITUENTS OF BASIDIOMYCETE CALODON SUAVEOLENS
WANG Fei; LIU Ji-kai *
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
15 .     ergosterol
    ÏàËÆ¶È:84.3%
Journal of the Chinese Chemical Society          1991          38          71-76
Studies on the Constituents of Ganoderma lucidum
½ªºêÕÜ(Hung-Cheh Chiang);ÖìÊÀ²ý(Shih-Chang Chu)
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
16 .     16¦Â-hydroxylanosta-2,8,23-triene
C30H48O     ÏàËÆ¶È:84.3%
Zeitschrift f¨¹r Naturforschung C          2002          57          489-495
Microbial Transformation of a Mixture of Argentatin A and Incanilin
Key words: Argentatin A, Incanilin, Biotransformation
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