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1 .     3¦Â-hydroxy-(22E,24R)-ergosta-5,8,22-trien-7-one
C28H42O2     ÏàËÆ¶È:96.4%
Chemical & Pharmaceutical Bulletin          1997          45          1756-1760
Sterol Constituents from the Fruit Bodies of Grifola frondosa (FR.) S. F. Gray
Takaaki ISHIZUKA,Yasunori YAOITA and Masao KIKUCHI
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     3¦Â-hydroxy-(22E,24R)-ergosta-5,8,22-trien-7-one
C28H42O2     ÏàËÆ¶È:96.4%
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
3 .     compound 7
    ÏàËÆ¶È:96.4%
Steroids          2008          73          19-26
Six new ergosterols from the marine-derived fungus Rhizopus sp.
Fazuo Wang, Yuchun Fang, Min Zhang, Aiqun Lin, Tianjiao Zhu, Qianqun Gu, Weiming Zhu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     (22E,24R)-3¦Â-ôÇ»ùÂó½ÇçÞ-5,8,22-ÈýÏ©-7-ͪ
C24H42O2     ÏàËÆ¶È:96.4%
Journal of Chinese Medicinal Materials          2008          31          1343-1347
Studies on the Anti-tumor Activity Principles of a Marine-derived Fungus BZYT-21
GAO Zong-hua, MA Li-ying, SHEN Yun-xiu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     »ìºÏÎï22E)-3¦Â-ôÇ»ùµ¨çÞ-5,8,22-ÈýÏ©-7-ͪ;(22E,24¦Î)-3¦Â-ôÇ»ù-24-¼×»ùµ¨çÞ-5,8,22-ÈýÏ©-7-ͪ;(22E,24¦Î)-3¦Â-ôÇ»ù-24-ÒÒ»ùµ¨çÞ-5,8,22-ÈýÏ©-7-ͪ
    ÏàËÆ¶È:96.2%
Chinese Journal of Marine Drugs          1999          2          1-3
STUDIES ON THE CHEMICAL CONSTITUENTS OF THE SPONGE BIEMNA FORTIS FROM SOUTH CHINA SEA
Deng Songzhi, Tian Chunlei, Xiao DingJun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     3¦Â-hydroxy-(22E,24R)-ergosta-5,8,22-trien-7-one
    ÏàËÆ¶È:92.8%
Journal of the Chinese Chemical Society          2011          58          893-898
Sterols from the Stems of Momordica charantia
Yun-Wen Liao,Chiy-Rong Chen,Jue-Liang Hsu, Hsueh-Ling Cheng, Wen-Ling Shih,Yueh-Hsiung Kuo, Tzou-Chi Huanga,* and Chi-I Chang*
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     3¦Â-hydroxy-24R*-ethylcholesta-5,8-dien-7-one
C29H46O2     ÏàËÆ¶È:75.8%
Journal of Natural Products          2002          65          1161-1164
Novel Cytotoxic Oxygenated C29 Sterols from the Colombian Marine Sponge Polymastia tenax
Gilmar Santaf¨¦, Vanessa Paz, Jaime Rodr¨ªguez, and Carlos Jim¨¦nez
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     topsentisterol D3
C28H42O2     ÏàËÆ¶È:71.4%
Journal of Natural Products          2006          69          1760-1768
26,27-Cyclosterols and Other Polyoxygenated Sterols from a Marine Sponge Topsentia sp.
Xuan Luo, Famei Li, Pramod B. Shinde, Jongki Hong, Chong-O. Lee, Kwang Sik Im, and Jee H. Jung
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     (24R) ergosta-8,22-diene-3¦Â,6¦Â,7¦Á-triol
C28H46O3     ÏàËÆ¶È:71.4%
Natural Product Research          2001          15          111-118
Two New Polyhydroxylated Sterols from Ruppia maritima
Marina Dellagreca; Antonio Fiorentino; Pietro Monaco; Armando Zarrelli
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     compound 4
C28H42O3     ÏàËÆ¶È:71.4%
Tetrahedron          2011          67          6576-6581
Osteoclast-forming suppressing compounds, gargalols A, B, and C, from the edible mushroom Grifola gargal
Jing Wu, Jae-Hoon Choi, Miyuki Yoshida, Hirofumi Hirai, Etsuko Harada, Kikuko Masuda, Tomoyuki Koyama, Kazunaga Yazawa, Keiichi Noguchi, Kazuo Nagasawa, Hirokazu Kawagishi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     5¦Á,6¦Á-epoxy-3¦Â-hydroxy-(22E,24R)-ergosta-8,22-dien-7-one
C28H40O2     ÏàËÆ¶È:71.4%
Journal of the Chinese Chemical Society          2011          58          893-898
Sterols from the Stems of Momordica charantia
Yun-Wen Liao,Chiy-Rong Chen,Jue-Liang Hsu, Hsueh-Ling Cheng, Wen-Ling Shih,Yueh-Hsiung Kuo, Tzou-Chi Huanga,* and Chi-I Chang*
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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