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1 .     (22E,24R)-3¦Â,5¦Á,9¦Á-trihydroxyergosta-7,22-dien-6-one
     ÏàËÆ¶È:75%
Chinese Journal of Marine Drugs          2009          28(5)          11-16
Cytotoxic metabolites from symbiotic fungus Penicilliom sp.HK13-8 with Rhizophora stylosa
HAN Xiu-li, LIN Zhen-jian, TAO Hong-wen, LIU Pei-pei, WANG Yi, ZHU Wei-ming
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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2 .     3¦Â,5¦Á,9¦Á-trihydroxyl-(22E,24R)-ergosta-7,22-diene-6-one
     ÏàËÆ¶È:75%
Natural Product Research and Development          2012          24          1047-1050
Secondary Metabolites from Marine Fungus Fusarium sp.
LIU Tao; LI Zhan-lin; WANG Yu; TIAN Li; PEI Yue-hu; HUA Hui-ming
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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3 .     3¦Â,5¦Á,9¦Á-trihydroxy-(22E,24R)-ergosta-7,22-dien-6-one
C28H44O4     ÏàËÆ¶È:71.4%
Chemistry of Natural Compounds          2009          45          759-761
STEROIDS AND OTHER CONSTITUENTS FROMTHE MUSHROOM Armillaria lueo-virens
Hui-Yan Xiong, Dong-Qing Fei, Jin-Song Zhou,Chun-Jiang Yang,and Guo-Liang Ma
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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4 .     (22E,24R)-ergosta-7,22-dien-3¦Â,5¦Á,9¦Á-trihydroxy-6-one
C28H44O4     ÏàËÆ¶È:71.4%
Natural Product Research and Development          2007          19          436-438
Chemical Constituents of Basidiomycetes Russula subnigricans
GONG Qing-fang; ZHANG Yu-mei; TAN Ning-hua; CHEN Zuo-hong
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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5 .     3¦Â,5¦Á,9¦Á-ÈýôÇ»ù-(22E,24R)-Âó½ÇçÞ-7,22-¶þÏ©-6-ͪ
    ÏàËÆ¶È:71.4%
Journal of Chinese Medicinal Materials          2007          30          655-657
Studies on Chemical Constituents of Marine Bryozoan Bugula neritina L.
TANG Hua, CHENG Ping, LIN Hou-wen, GAO Wen, LU Yi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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6 .     3¦Â,5¦Á,9¦Á-trihydroxy-(22E,24R)-ergosta-7,22-dien-6-one
     ÏàËÆ¶È:71.4%
Journal of Chinese Medicinal Materials          2011          34          180-183
Sterols of Marine Bryozoan Bugula neritina from the South China Sea
LEI Hui, ZHOU Xue-feng, YANG Ya-ling, SUN Jian-fan, HU Jing, LIU Yong-hong
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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7 .     dehydro ergosterol peroxide
     ÏàËÆ¶È:70.8%
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

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8 .     3¦Â,5¦Á,9¦Á-trihydroxyergosta-7,22-dien-6-one
     ÏàËÆ¶È:67.8%
Natural Product Research and Development          2012          24          1747-1749
Chemical Constituents of Favolus arcularius
YIN Wei, LIU Jin-song, WU Pei-yun, LIANG Yi-min, WANG Gang*
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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9 .     24E-ergosta-7,22-dien-6-one-3¦Â,5¦Á-diol
C28H44O3     ÏàËÆ¶È:66.6%
Natural Product Research and Development          1992          4(2)          44-47
CHEMICAL RESEARCH ON THE METABOLITES OF LACTARIUS HYSGINUS (¢ñ)
Dong Ding* Wang Huaibin Li Guangyi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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10 .     9,11-Dehydroergosterol peroxide
     ÏàËÆ¶È:65.3%
Korean Journal of Pharmacognosy          2007          38(2)          164-169
Antioxidative Activities of Phenolic Compounds Isolated from Inonotus obliquus
Kim, Hyoung-Ja; Jin, Chang-Bae; Lee, Yong-Sup
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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11 .     (22E,24R)-ergosta-6,9,22-trien-3¦Â,5¦Á,8¦Á-triol
     ÏàËÆ¶È:64.2%
Natural Products and Bioprospecting          2012          2          240-244
Six novel steroids from culture of basidiomycete Polyporus ellisii
Shuang Wang, Ling Zhang, Liang-Yan Liu, Ze-Jun Dong, Zheng-Hui Li, Ji-Kai Liu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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12 .     3 ¦Â,5¦Á-dihydroxy-(22E,24R)-ergosta-7,22-dien-6-one
C28H44O3     ÏàËÆ¶È:64.2%
Natural Product Research          2013          27          1611-1619
Bioactive ergostanoids and a new polyhydroxyoctane from Lentinus polychrous mycelia and their inhibitory effects on E2-enhanced cell proliferation of T47D cells
Niramai Fangkrathok, Bungorn Sripanidkulchai, Kaoru Umehara & Hiroshi Noguchi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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13 .     13-epi-homoverrucosan-5¦Â,6¦Â-diol
C20H34O2     ÏàËÆ¶È:60.8%
Phytochemistry          1995          40          199-203
13-Epi-homoverrucosane derivatives and other diterpenes from Plagiochila (hepaticae)
Susanne Valcic, Volker Huch, Michael Veith, Hans Becker
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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14 .     ent-3¦Â-hydroxy-beyer-15-ene-2-one
C20H30O2     ÏàËÆ¶È:60.8%
Phytochemistry          1992          31          699-702
Diterpenoids from Spirostachys africana
Zvitendo James Duri, Neil Arthur Hughes, Namboole Moses Munkombwe
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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15 .     ent-3¦Â,18-isopropylidenedioxy-beyer-15-ene-2-one
C23H34O3     ÏàËÆ¶È:60.8%
Phytochemistry          1992          31          699-702
Diterpenoids from Spirostachys africana
Zvitendo James Duri, Neil Arthur Hughes, Namboole Moses Munkombwe
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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16 .     senepodine A
     ÏàËÆ¶È:60.8%
Heterocycles          2009          77          679-729
The Lycopodium Alkaloids
Yusuke Hirasawa, Jun'ichi Kobayashi, and Hiroshi Morita
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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17 .     3¦Â-Hydroxy-14-oxo-14,15-seco-5¦Â-card-20( 22)-enolide-15-nitrile
C23H31NO4     ÏàËÆ¶È:60.8%
Steroids          1996          61          572-582
Digitalis-like compounds: Synthesis and biological evaluation of seco-D and D-homo derivatives
Mauro Gobbini, Alessandra Benicchio, Giuseppe Marazzi, Gloria Padoani, Marco Torri, Piero Melloni
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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18 .     (1R,3aR,5R,7aR,1'R,2'E,4'R)-5,6,7,7a-Tetrahydro-5-bromoacetoxy-7a-methyl-1-(1',4',5'-trimethyl-2'-hexenyl)-3aH-indan-4-one
C21H33O3Br     ÏàËÆ¶È:60.8%
Tetrahedron          2012          68          1729-1735
Synthesis of two osteoclast-forming suppressors, demethylincisterol A3 and chaxine A
Arata Yajima, Yuuma Kagohara, Keisuke Shikai, Ryo Katsuta, Tomoo Nukada
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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19 .     (3aR,3bR,5aR,6R,8aR,1'R,2'E,4'R)-3a,3b,4,5,5a,7,8,8a-Octahydro-3a-hydroxy-5a-methyl-6-(1',4',5'-trimethyl-2'-hexenyl)-2H-indeno[5,4-b]dihydrofuran-2-one
C21H34O3     ÏàËÆ¶È:60.8%
Tetrahedron          2012          68          1729-1735
Synthesis of two osteoclast-forming suppressors, demethylincisterol A3 and chaxine A
Arata Yajima, Yuuma Kagohara, Keisuke Shikai, Ryo Katsuta, Tomoo Nukada
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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20 .     (3bR,5aR,6R,8aR,1'R,20E,4'R)-3a,3b,4,5,5a,7,8,8a-Octahydro-5a-methyl-6-(1',4',5'-trimethyl-2'-hexenyl)-2H-indeno[5,4-b]furan-2-one
C21H32O2     ÏàËÆ¶È:60.8%
Tetrahedron          2012          68          1729-1735
Synthesis of two osteoclast-forming suppressors, demethylincisterol A3 and chaxine A
Arata Yajima, Yuuma Kagohara, Keisuke Shikai, Ryo Katsuta, Tomoo Nukada
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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21 .     volemolide
C22H34O3     ÏàËÆ¶È:60.8%
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

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22 .     volemolide
C22H36O3     ÏàËÆ¶È:60.8%
Natural Product Research and Development          2010          22          786-788
Chemical Constituents of Culture Broth of Hebeloma westraliense
SHAO Hong-jun;FANG Li-zhen; LIU Ji-kai
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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23 .     Voulkens in E
C20H32O2     ÏàËÆ¶È:60.8%
Bioorganic & Medicinal Chemistry Letters          2013          23          3088-3095
Voulkensin C¨CE, new 11-oxocassane-type diterpenoids and a steroid glycoside from Caesalpinia volkensii stem bark and their antiplasmodial activities
Charles O. Ochieng, Lawrence A.O. Manguro, Philip O. Owuor, Hosea Akala
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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24 .     (22E)-5a,8a-epidioxyergosta-6,9(11),22-trien-3b-ol
     ÏàËÆ¶È:60.7%
Chemistry & Biodiversity          2008          Vol. 5          743
Chemical Constituents of Stereum subtomentosum and Two Other Birch-Associated Basidiomycetes: An Interspecies Comparative Study
Simona Hybelbauerov¨¢, Jan Sejbal, Martin Drač¨ªnský , Alice Hahnov¨¢, and Bohum¨ªr Koutek
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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25 .     9(11)-dehydroaxinysterol
C28H40O3     ÏàËÆ¶È:60.7%
Chemical & Pharmaceutical Bulletin          2002          50(9)          1286-1289
New Biologically Active Marine Sesquiterpenoid and Steroid from the Okinawan Sponge of the Genus Axinyssa
Makoto IWASHIMA,Ikuo TERADA,Kazuo IGUCHI,and Takao YAMORI
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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