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1 .     ergosta-7,22-diene-2¦Â,3¦Á,9¦Á-triol 2¦Â,3¦Á-diacetate
    ÏàËÆ¶È:75%
Journal of Natural Products          1991          Vol 54          998
Novel Cytotoxic Principles of Formosan Ganoderma lucidum
Chun-Nan Lin, Whey-Pim Tome, Shen-Jeu Won
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     ergosta-7,22-dien-2¦Â,3¦Á,9¦Á-triol 2¦Â,3¦Á-diacetate
    ÏàËÆ¶È:75%
Phytochemistry          1993          32          1549-1551
Steroids of formosan Ganoderma amboinense
Lin Chun-Nan, Kuo Shih-Hsieh, Won Shen-Jeu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     3¦Â,16¦Â,30-trihydroxycycloart-20,24-diene
C30H52O3     ÏàËÆ¶È:75%
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
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     (22E,24R)-6-Acetoxy-ergosta-7,22-dien-3¦Â,5¦Á,6¦Â-triol
    ÏàËÆ¶È:75%
Natural Product Communications          2009          4          1449-1454
Ring B Aromatic Steroids from an Endophytic Fungus, Colletotrichum sp.
Wen Zhang , Siegfried Draeger, Barbara Schulz and Karsten Krohn
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     (22E,24R)-6-Acetoxy-ergosta-7,22-dien-3¦Â,5¦Á,6¦Â-triol
    ÏàËÆ¶È:75%
Natural Product Communications          2009          4          1449-1454
Ring B Aromatic Steroids from an Endophytic Fungus, Colletotrichum sp.
Wen Zhang , Siegfried Draeger, Barbara Schulz and Karsten Krohn
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     ergosteryl myristate
C42H70O2     ÏàËÆ¶È:73.5%
Natural Product Sciences          1999          5          93-96
Ergosteryl Myristate, a New Ergosterol Derivative from Unidentified Marine Algicolous Fungus
Lee, Dong-Ick; Choi, Jin-Souk; Yang, Mi-Rim; Lee, Won-Kap; Kim, Dong-Soo; Choi, Hong-Dae; Son, Byeng-Wha
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     3¦Â,5¦Á,6¦Á-Trihydroxyergosta-7,22-diene 6-O-benzoate
C35H50O4     ÏàËÆ¶È:72.7%
Journal of Natural Medicines          2011          65          307-312
Constituents of cultivated Agaricus blazei
Yumi Ueguchi ,Katsuyoshi Matsunami ,Hideaki Otsuka ,Kazunari Kondo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     Globosterol
C29H47O3     ÏàËÆ¶È:71.8%
Steroids          2009          74          786-790
Polyhydroxylated steroids from an endophytic fungus, Chaetomium globosum ZY-22 isolated from Ginkgo biloba
Jian-Chun Qin, Jin-Ming Gao, Ya-Mei Zhang, Sheng-Xiang Yang, Ming-Sheng Bai, Ya-Tuan Ma, Hartmut Laatsch
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     ergosta-7,22-dien-3¦Â-ylpentadecanoate
    ÏàËÆ¶È:71.8%
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   Ì¼Æ×Ä£Äâͼ
10 .     24-Ethylcholesta-7,22-diene-3¦Â,5¦Á,6¦Â-triol
    ÏàËÆ¶È:71.8%
Bulletin of the Korean Chemical Society          2011          32          697-700
Isolation of Protein Tyrosine Phosphatase 1B Inhibitory Constituents from the Sclerotia of Polyporus umbellatus Fries
Hee Sang Lee, In Hyun Hwang, Jeong Ah Kim, Ji Young Choi, Tae Su Jang, Hiruyuki Osada, Jong Seog Ahn*, MinKyun Na*, Seung Ho Lee*
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     methylsirosterol
C48H63O7     ÏàËÆ¶È:71.8%
Canadian Journal of Chemistry          1992          70          1905-1913
Sirosterol and dehydroazasirosterol, unusual steroidal adducts from a Sirococcus species
William A. Ayer, Yu-Ting Ma
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     (22E,24R)-3,6-Diacetoxy-ergosta-7,22-dien-3¦Â,5¦Á,6¦Â-triol
    ÏàËÆ¶È:71.8%
Natural Product Communications          2009          4          1449-1454
Ring B Aromatic Steroids from an Endophytic Fungus, Colletotrichum sp.
Wen Zhang , Siegfried Draeger, Barbara Schulz and Karsten Krohn
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
13 .     ergosta-7,22-diene-3¦Â-yl pentadecanoate
    ÏàËÆ¶È:71.8%
Journal of Chinese Medicinal Materials          2008          31          41-44
Chemical Constituents of the Spores of Ganoderma lucidum
ZHANG Xiao-qi, PANG Guo-liang, CHENG Yan, WANG Ying, YE Wen-cai
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
14 .     (22E)-6 -Methoxy-3 ¦Á,5-cyclo-24 -methyl-5 ¦Á-cholest-22-ene
C29H48O     ÏàËÆ¶È:68.7%
Steroids          2002          67          597-603
[3,3]-Claisen rearrangements in 24¦Á-methyl steroid synthesis: Application to campesterol, crinosterol, and ¦¤25-crinosterol side chain construction
Vladimir A. Khripach, Vladimir N. Zhabinskii, Olga V. Konstantinova, Natalya B. Khripach, Andrey P. Antonchick, Bernd Schneider
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
15 .     (24R,241R)-24(241)-epoxyisoavenasteryl acetate
    ÏàËÆ¶È:68.7%
Phytochemistry          1999          52          1601-1605
(24R)- and (24S)-24-hydoxy-24-vinyllathosterols and other sterols from the aerial part of Bryonia dioica
Toshihiro Akihisa, Yumiko Kimura, Kazuo Koike, Wilhelmus C.M.C. Kokke, Tadashi Ohkawa, Tamotsu Nikaido
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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