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1 .     stigmasta-7,22-diene-3¦Â,5¦Á,6¦Á-triol
    ÏàËÆ¶È:88.8%
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
2 .     (3¦Â,5¦Á,6¦Á,7¦Â,22E)-ergosta-7,22-diene-3,5,6-triol
C28H46O3     ÏàËÆ¶È:85.7%
Chinese Journal of Marine Drugs          2008          27(4)          9-13
Studies on the chemical constituents from the endophytic fungus Penicillium sp.091402 of managrove plant Brugurera sexangula
HAN Zhuang, MEI Wen-li, CUI Hai-bin, LIN Hai-peng, HONG Kui, DAI Hao-fu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     cerevisterol
C28H44O3     ÏàËÆ¶È:85.7%
Chinese Traditional and Herbal Drugs          2009          40          1211-1214
Ó¡¶È¿é¾úµÄ»¯Ñ§³É·ÖÑо¿
ÎâÉÙ»ª;³ÂÓÐΪ;ÑîÀöÔ´;ÀîÉÜÀ¼;ÀîÖÎäÞ
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     (3¦Â,5¦Á,6¦Á,22E)-Âó½ÇçÞ-7,22-¶þÏ©-3,5,6-Èý´¼
C28H46O3     ÏàËÆ¶È:85.7%
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
5 .     ergosta-7,11-dien-3¦Â,5¦Á,6¦Â-triol
C28H46O3     ÏàËÆ¶È:85.7%
Natural Product Research and Development          2010          22          235-237
Studies on the Chemical Constituents of Rhodobryum giganteum (schwaegr.) Par.
JIAO Wei; LU Gai-li; SHAO Hua-wu; LU Run-hua;
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     7,22-¶þÏ©-3,5,6-ÈýôÇ»ù-Âó½ÇçÞ´¼
    ÏàËÆ¶È:85.7%
Acta Scientiarum Naturalium Universitatis Sunyatseni          2001          40(4)          70-72
Metabolites of Marine Fungus Hypoxylon oceanicum from the South China Sea
LI Hou-jin, UN Yong-cheng, WANG Li, ZHOU Shi-ning, L. L. P. RJJMOED
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     cerevisterol
C28H46O3     ÏàËÆ¶È:85.1%
Chemistry of Natural Compounds          2011          47          858-861
Secondary metabolites of endophytic fungus Xylaria sp. YC-10 of Azadirachta indica
Shao-Hua Wu, You-Wei Chen and Cui-Ping Miao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     Globosterol
C29H47O3     ÏàËÆ¶È:82.7%
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 .     24-methyl-cholesta-7,22E-diene-3¦Â,5¦Á,6¦Â-triol
    ÏàËÆ¶È:82.1%
Chinese Journal of Marine Drugs          2011          30(1)          31-36
Studies on Chemical Constituents of Subergorgia ret iculata
LI Jun, LI Yong-ai, XU Jing, TANG Xu-li, LI Ping-lin, LI Guo-qiang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     (22E,24R)-Ergosta-7,22-diene-3¦Â,5¦Á,6¦Â-triol
    ÏàËÆ¶È:82.1%
Chinese Traditional and Herbal Drugs          2005          36          1126-1130
Chemical constituents of basidiomycete Hydnum repandum
WANG Xing-na; DU Jian-chang; TAN Ren-xiang; LIU Ji-kai
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     24-Ethylcholesta-7,22-diene-3¦Â,5¦Á,6¦Â-triol
    ÏàËÆ¶È:78.5%
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
12 .     (22E,24R)-ergosta-5,7,22-trien-3¦Â-ol
C28H44O     ÏàËÆ¶È:75%
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
13 .     dehydro ergosterol peroxide
    ÏàËÆ¶È:75%
Archives of Pharmacal Research          1994          17          1-4
Some sesquiterpenoids and 5¦Á,8¦Á-epidioxysterols from Solanum lyratum
Su Mi Yu, Hyoung Ja Kim, Eun-Rhan Woo and Hokoon Park
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
14 .     ergosta-5, 7, 22-trien-3¦Â-ol
C28H44O     ÏàËÆ¶È:75%
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
15 .     ergoaterol
    ÏàËÆ¶È:75%
Natural Product Research and Development          2010          22          1018-1020
Chemical Constituents from Fruiting Bodies of Ganoderma lucidum.(¢ò)
CHEN Man; ZHANG Mi; SUN Shi; XIA Bing; ZHANG Han-qing
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
16 .     ergosterol
    ÏàËÆ¶È:72%
China Journal of Chinese Materia Medica          2002          27          674-676
Studies on the Chemical Constituents of Shiraia bambusicola
SHEN Yuxiu, RONG Xianguo, GAO Zonghua
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
17 .     5¦Á,6¦Á-epoxy-24(R)-methylcholesta-7,22-dien-3¦Â-ol
C28H44O2     ÏàËÆ¶È:71.4%
Phytochemistry          1999          51          891-898
Antitumor sterols from the mycelia of Cordyceps sinensis
Jin Woo Bok, Leonard Lermer, Jeff Chilton, Hans G. Klingeman, G.H. Neil Towers
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
18 .     ergosterol
    ÏàËÆ¶È:71.4%
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
19 .     ergosterol-7,22-dien-3¦Â-ol
    ÏàËÆ¶È:71.4%
Acta Pharmaceutica Sinica          2000          Vol 35          367-369
THE STEROL CONSTITUENTS OF MYCENA DENDROBII
CHEN Xiao Mei; YANG Jun Shan; GUO Shun Xing
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
20 .     ergosterol
C28H44O     ÏàËÆ¶È:71.4%
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
21 .     ergosterol
    ÏàËÆ¶È:71.4%
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
22 .     (3¦Â,22E)-Ergosta-5,7,22-trien-3-ol
    ÏàËÆ¶È:71.4%
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
23 .     ergosterol
    ÏàËÆ¶È:71.4%
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
24 .     ergosterol
    ÏàËÆ¶È:71.4%
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
25 .     ¦Â-ergosterol
    ÏàËÆ¶È:71.4%
Chinese Traditional and Herbal Drugs          2000          31          328-330
ºÖÔ²¿×Å£¸Î¾ú»¯Ñ§³É·ÖµÄÑо¿
Íò»Ô
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
26 .     Ergosterol
    ÏàËÆ¶È:71.4%
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
27 .     ergosta-5,7,22-trien-3¦Â-ol
    ÏàËÆ¶È:71.4%
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
28 .     22 E-ergosta-5,7,22-trien-3¦Â-ol
    ÏàËÆ¶È:71.4%
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
29 .     (3¦Â,22E)-Âó½ÇçÞ-5,7,22-ÈýÏ©-3-´¼
C28H44O     ÏàËÆ¶È:71.4%
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
30 .     ergosterol
    ÏàËÆ¶È:71.4%
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
31 .     Âó½ÇçÞ´¼
    ÏàËÆ¶È:71.4%
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
32 .     24(R)-methylcholesta-5,7,22-tiene-3-ol
    ÏàËÆ¶È:71.4%
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
33 .     ergosterol
    ÏàËÆ¶È:71.4%
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
34 .     ergosterol
C28H44O     ÏàËÆ¶È:71.4%
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
35 .     ergosteryl palmitate
    ÏàËÆ¶È:71.4%
Natural Product Research and Development          2010          22          1018-1020
Chemical Constituents from Fruiting Bodies of Ganoderma lucidum.(¢ò)
CHEN Man; ZHANG Mi; SUN Shi; XIA Bing; ZHANG Han-qing
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
36 .     ergosta-5,7,22-trien-3-ol
    ÏàËÆ¶È:71.4%
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
37 .     (22E,24R)-ergosta-5,7,22-triene-3¦Â-ol
C28H44O     ÏàËÆ¶È:71.4%
Natural Product Research and Development          2007          19          620-622
Chemical Constituents of Piper pedicellatum C. DC
LI Jun-zhu; LIU Hai-yang; DONG Qiu; CHEN Chang-xiang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
38 .     ergosta-5,7,22-trien-3¦Â-o-l
C28H44O     ÏàËÆ¶È:71.4%
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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