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²éѯģʽ£ºÄ£ºý²éѯ ̼Æ×Êý¾ÝÊäÈ룺 °´´ÓСµ½´ó˳ÐòÊäÈ룬Êý×Ö¼äÓÃÓ¢Îİë½Ç¶ººÅ(,)·Ö¸ôÀýÈ磺 21.4,30.4,37.4,73.2,73.7,125.6,126.6,139.6,140.2,168.2 ÈܼÁÑ¡Ï Æ¥ÅäÈݲ (Êý×Ö¸ñʽ£¬¿É×ÔÐÐÉ趨) ÏàËÆ¶È£º %(ÏàËÆ¶È>=50%) ²éѯ½á¹û£º¹²²éµ½2960¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×Ä£Äâͼ 5 . »ìºÏÎï 22E)-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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×Ä£Äâͼ |

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