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. 5¦Á-Ergosta-7,9(11),22-trien-3¦Â-ol C26H44O ÏàËÆ¶È:82.1% Organic Magnetic Resonance 1977 9 439-464 13C N.m.r. Spectra of steroids¡ªA Survey and Commentary J.W.Blunt and J.B.Stothers Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . 5¦Á-Ergosta-7,9(11),22-triene-3¦Â,5-diol C29H44O2 ÏàËÆ¶È:82.1% Organic Magnetic Resonance 1977 9 439-464 13C N.m.r. Spectra of steroids¡ªA Survey and Commentary J.W.Blunt and J.B.Stothers Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . cerevisterol C28H46O3 ÏàËÆ¶È:78.5% Chinese Joumal of Experimental Traditional Medical Fomulae 2012 18 125-128 Isolation and Biological Evaluation of Secondary Metabolites of EndophyticFungus Aspergillus sp.from Astragalus membranaceus ZHOU Feng, ZHANG Hong-chi, LIU Rui, ZHANG Yong-fang Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . 5¦Á-Ergosta-7,9(11),22-trien-3¦Â-yl acetate C30H46O2 ÏàËÆ¶È:76.6% Organic Magnetic Resonance 1977 9 439-464 13C N.m.r. Spectra of steroids¡ªA Survey and Commentary J.W.Blunt and J.B.Stothers Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . cerevisterol ÏàËÆ¶È:75% Phytochemistry 1997 44 1443-1448 Cytochalasins and phytotoxins from the fungus Xylaria obovata Dawit Abate, Wolf-Rainer Abraham, Holger Meyer Structure 13C NMR ̼Æ×Ä£Äâͼ |
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