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˲Ȼ: ½ð±Ò+10, ¡ïÓаïÖú 2015-06-18 19:44:09
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²éѯ½á¹û£º¹²²éµ½218¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . 14,15¦Â-dihydroxyklaineanone ÏàËÆ¶È:70% Chemistry Letters 1990 19 749-752 New Quassinoids from the Roots of Eurycoma longifolia Hiroshi Morita, Etsuko Kishi, Koichi Takeya, Hideji Itokawa and Osamu Tanaka Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 2 . 3¦Â,7¦Â,8¦Â,12¦Æ,17-pentahydroxylabdan-16,15-olide C20H34O7 ÏàËÆ¶È:60% Phytochemistry 2002 60 197-200 Three labdane diterpenoids from Aframomum sceptrum (Zingiberaceae) Christabel Tomla, Pierre Kamnaing, Godfred A. Ayimele, Eric A. Tanifum,Apollinaire Tsopmo, Pierre Tane, Johnson F. Ayafor, Joseph D. Connolly Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 3 . 14,15¦Â-Dihydroxyklnineanone C20H28O8 ÏàËÆ¶È:60% Phytochemistry 1991 30 3138-3141 13¦Â,18-dihydroeurycomanol, a quassinoid from Eurycoma longifolia K.L. Chan, S.P. Lee, T.W. Sam, S.C. Tan, H. Noguchi, U. Sankawa Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 4 . 3¦Â-propionoxy-17¦Á-oxa-14¦Á-androsta-5,15-diene-7,17-dione C22H26O5 ÏàËÆ¶È:59.0% Steroids 1998 63 542-553 Ergosteroids III. syntheses and biological activity of seco-steroids related to dehydroepiandrosterone IevaL Reich, Henry Lardy, Yong Wei, Padma Marwah, Nancy Kneer, DouglasR Powell, HansJ Reich Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 5 . 4-O-Methylbotcinolide C21H36O8 ÏàËÆ¶È:57.1% Phytochemistry 1996 42 1621-1624 Some metabolites of Botrytis cinerea related to botcinolide Isidro G. Collado, Josefina Aleu, Rosario Hern¨¢ndez-Gal¨¢n, James R. Hanson Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 6 . 3¦Â-acetoxy-7-oxo-16,17-secoandrost-5-ene-16,17-dioic acid ÏàËÆ¶È:57.1% Steroids 1998 63 542-553 Ergosteroids III. syntheses and biological activity of seco-steroids related to dehydroepiandrosterone IevaL Reich, Henry Lardy, Yong Wei, Padma Marwah, Nancy Kneer, DouglasR Powell, HansJ Reich Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |
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