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ÂÌË®ÏÐÖñ: ½ð±Ò+10, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2014-12-15 21:44:30
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1 . (22E,24R)-3¦Â-ôÇ»ùÂó½ÇçÞ-5,8,22-ÈýÏ©-7-ͪ C28H42O2 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 Structure & 13C NMR ̼Æ×Ä£Äâͼ 2 . 3¦Â,5¦Á,9¦Á-ÈýôÇ»ù-(22E,24R)-Âó½ÇçÞ-7,22-¶þÏ©-6-ͪ ÏàËÆ¶È:96.4% Journal of Tropical and Subtropical Botany 2011 19 75-78 Steroidal Metabolites of Fimetariella rabenhorstii,Endophytic Fungus from Aquilaria sinensis TAO, Meihua, YAN, Jian, WEI, Xiaoyi, LI, Dongli, ZHANG, Weimin, TAN, Jianwen Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 3 . 22E,24R-3¦Â,5¦Á,9¦Á-trihydroxy-ergosta-7,22-diene-6-one C28H44O4 ÏàËÆ¶È:96.4% Chinese Joumal of Experimental Traditional Medical Fomulae 2012 18 120-123 Study on Secondary Metabolites of Endophytic Fungal Strain Botryosphaeria sp.MHF of Maytenus hookeri YUAN Lin, SHEN Fang, MA Yin-hai, CHEN Xiao-ni, HUANG Xing-nan, GU Xue-zhu, KANG Wen-yi Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 4 . (22E,24R)-3¦Â,5¦Á,9¦Á-trihydroxy-ergosta-7,22-dien-6-one ÏàËÆ¶È:92.8% Chinese Journal of Oceanology and Limnology 2011 29 63-67 Chemical constituents of marine algal-derived endophytic fungus Exophiala oligosperma EN-21* LI Fang, LI Ke, LI Xiaoming, WANG Bingui Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 5 . (22E,22R)-ergost-7,22-diene-3¦Â,5¦Á,6¦Â,9¦Á-tetraol ÏàËÆ¶È:78.5% Chinese Journal of Marine Drugs 2013 32 8-12 Secondary metabolites from the fungus Engyodontium album associated with the South China Sea starfish Anthenea pentagonula E Heng-chao, ZHOU Wei, LIU Bao-shu, TANG Hua, SUN Peng, LI Ling, ZHANG Wen* Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 6 . (22E,24R)-3¦Â,5¦Á,9¦Á-trihydroxyergosta-7,22-diene-6-one C28H44O4 ÏàËÆ¶È:78.5% Chinese Tladitional Patent Medicine 2012 34 1304-1308 Chemical constituents of Hexagonia speciosa DU Zi-wei, LIU Jin-song, WU Pei-yan, HE Qi-wei, XIANG Chen, WANG Gang Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 7 . 3¦Â,5¦Á,9¦Á-trihydroxyergosta-7,22-dien-6-one ÏàËÆ¶È:78.5% China Journal of Chinese Materia Medica 2013 38 4329-4334 Chemical constituents of Osmanthus fragrans fruits YIN Wei, LIU Jin-qi, ZHANG Guo-sheng Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 8 . 3,5,9-trihydroxyergosta-7-22-dien-6-one C28H44O4 ÏàËÆ¶È:78.5% Natural Product Research and Development 2014 26 1034-1037 Study on Chemical Constituents of Polygonatum odoratum YIN Wei*, TAO A-li, LIU Jin-qi, ZHANG Guo-sheng Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 9 . compound 12 ÏàËÆ¶È:75% Steroids 1995 60 666-673 New cytotoxic steroids from the marine sponge Dysidea fragilis coming from the lagoon of Venice Anna Aiello, Ernesto Fattorusso, Marialuisa Menna, Rosa Carnuccio, Teresa Iuvone Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 10 . 3¦Â,5¦Á,9¦Á-trihydroxyergosta-7,22-dien-6-one ÏàËÆ¶È:75% 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 Structure & 13C NMR ̼Æ×Ä£Äâͼ 11 . ergosterol peroxide ÏàËÆ¶È:75% Lishizhen Medicine and Materia Medica Research 2013 24 591-593 Antimicrobial constituents from the twigs of Trigonostemon xyphophylloides YU Li, MEI Wen-li, ZUO Wen-jian, WANG Hui, GUO Zhi-kai, AN Xue-qin, DAI Hao-fu* Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 12 . 3¦Â,5¦Á,9¦Á-trihydroxycholesta-7,22-dien-6-one C27H42O4 ÏàËÆ¶È:74.0% Tropic Oceanology 2013 32 55-59 Steroids from South China Sea sponge Halichondria sp. SUN Jian-fan, LI Yun-qiu, YANG Bin, HU Jing, DONG Guang, LIU Yong-hong Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 13 . topsentisterol C1 C29H46O4 ÏàËÆ¶È:72.4% 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 Structure & 13C NMR ̼Æ×Ä£Äâͼ 14 . (24S)-stigmast-3¦Â,5¦Á,6¦Â-triol ÏàËÆ¶È:72.4% Chinese Traditional and Herbal Drugs 2010 41 1065-1068 СҶÈ̶¬ÌٵĻ¯Ñ§³É·ÖÑо¿ Áõΰ;°×ËØÆ½;Áº»á¾ê;Ô¬ÓÀÁÁ Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 15 . 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 Structure & 13C NMR ̼Æ×Ä£Äâͼ 16 . compound 5a ÏàËÆ¶È:71.4% Chemistry of Natural Compounds 1999 35 646-649 13C NMR SPECTRA OF II-SITOSTEROL DERIVATIVES WITH OXIDIZED RINGS A AND B N. V. Kovganko, Zh. N. Kashkan,E. V. Borisov, and E. V. Batura Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 17 . Stylisterol C C28H46O3 ÏàËÆ¶È:71.4% Steroids 2005 70 63-70 New polyhydroxylated sterols stylisterols A¨CC and a novel 5,19-cyclosterol hatomasterol from the Okinawan marine sponge Stylissa sp. Hidemichi Mitome, Nao Shirato, Ayako Hoshino, Hiroaki Miyaoka, Yasuji Yamada, Rob W.M. Van Soest Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 18 . Hatomastero C28H46O3 ÏàËÆ¶È:71.4% Steroids 2005 70 63-70 New polyhydroxylated sterols stylisterols A¨CC and a novel 5,19-cyclosterol hatomasterol from the Okinawan marine sponge Stylissa sp. Hidemichi Mitome, Nao Shirato, Ayako Hoshino, Hiroaki Miyaoka, Yasuji Yamada, Rob W.M. Van Soest Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |

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