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Ã÷Ìì¹ýºó1014: ½ð±Ò+10, ¡ï¡ï¡ïºÜÓаïÖú, ллàÞ 2015-05-27 11:13:34
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1 . cerevisterol C28H46O3 ÏàËÆ¶È:78.5% Chinese Traditional and Herbal Drugs 2012 43 2356-2360 Chemical constituents from sporophore of Hericium coralloides (¢ñ) ZHANG Peng; BAO Hai-ying; Tolgor Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . halistanol sulfate A ÏàËÆ¶È:75% Tetrahedron 1992 48 5467-5472 Halistanol Sulfates A-E, New Steroid Sulfates, from a Marine Sponge, Epipolasis sp. Satoshi Kanazawa, Nobuhiro Fusetani, Shigeki Matsunaga Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . halicrasterol C C28H48O4 ÏàËÆ¶È:75% Steroids 2013 78 1353-1358 Bioactive polyhydroxylated sterols from the marine sponge Haliclona crassiloba Zhong-Bin Cheng, Han Xiao, Cheng-Qi Fan, Ya-Nan Lu, Ge Zhang, Sheng Yin Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . cerevisterol ÏàËÆ¶È:75% Chinese Joumal of Experimental Traditional Medical Fomulae 2014 20 42-46 Chemical Constituents of Laetiporus montanus LI Wei, BAO Hai-ying, BAU Tolgor Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . 6¦Â-Methoxy-3¦Á,5-cyclo-24¦Á-methyl-5¦Á-cholesta-22,25-diene ÏàËÆ¶È:67.8% Steroids 2002 67 597-603 [3,3]-Claisen rearrangements in 24¦Á-methyl steroid synthesis: Application to campesterol, crinosterol, and ¦¤25-crinosterol side chain construction Vladimir A. Khripach, Vladimir N. Zhabinskii, Olga V. Konstantinova, Natalya B. Khripach, Andrey P. Antonchick, Bernd Schneider Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . (22E,24R)-ergosta-7,22-diene-3¦Â,5¦Á,6¦Á,9¦Á-tetraol C32H52O4 ÏàËÆ¶È:67.8% 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 Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . (3¦Â)-3,20-dihydroxyergosta-5,24(28)-dien-7-one C28H44O3 ÏàËÆ¶È:67.8% Helvetica Chimica Acta 2013 96 2245-2250 Ergostane Steroids from Dysoxylum lukii Jiang Hu, Yan Song, Xiao-Dong Shi, Xia Mao, Jian-Gang Chen and Lei Zhu Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . 5-Hydroxy-5¦Á-cholest-2-en-6-one ÏàËÆ¶È:66.6% Steroids 2012 77 461-466 Synthesis and plant growth promoting activity of polyhydroxylated ketones bearing the 5a-hydroxy-6-oxo moiety and cholestane side chain Anielka Rosado-Ab¨®n, Guadalupe de Dios-Bravo ,Rogelio Rodr¨ªguez-Sotres ,Mart¨ªn A. Iglesias-Arteaga Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |
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