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carolyn_yang: ½ð±Ò+30, ¡ï¡ï¡ïºÜÓаïÖú 2013-09-04 17:24:40
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carolyn_yang: ½ð±Ò+30, ¡ï¡ï¡ïºÜÓаïÖú 2013-09-04 17:24:40
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²éѯ½á¹û£º¹²²éµ½12478¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . compound 15 ÏàËÆ¶È:88.8% Steroids 2007 72 643-652 Atypical regioselective biohydrolysis on steroidal oxiranes by Aspergillus niger whole cells: Some stereochemical features Fabricio R. Bisogno, Alejandro A. Orden, Celeste Aguirre Pranzoni, Diego A. Cifuente, Oscar S. Giordano, Marcela Kurina Sanz Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . cholest-3¦Â,5¦Á,6¦Â-triol ÏàËÆ¶È:88.8% Journal of Shenyang Pharmaceutical University 2010 27 711-714 Steroids from marine spongeSpheciospongia sp. from the South China Sea LIU Dong, LIN Wen-han, DENG Zhi-wei, WU Li-jun Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . 5¦Á-Cholestane-3¦Â,5,6¦Â-triol 3-acetate C28H50O4 ÏàËÆ¶È:85.7% 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 4 . compound 8 ÏàËÆ¶È:85.7% Australian Journal of Chemistry 1975 28 1017-1021 Carbon-13 N.M.R. spectra of 6¦Â-Substituted-5¦Á-cholestane-3¦Â,5-diols: ¦Ã- and ¦Ä-effects JW Blunt Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . bebryceoid A C26H44O3 ÏàËÆ¶È:85.1% Chemical & Pharmaceutical Bulletin 2010 58 1240-1242 New 3¦Â,5¦Á,6¦Â-Trihydroxysteroids from the Octocorals Bebryce sp. (Plexauridae) and Carijoa sp. (Clavulariidae) Ping-Jyun Sung and Chih-Yang Liu Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . chelestane-3¦Â,5¦Á,6¦Â-triol ÏàËÆ¶È:85.1% Pharmazie 2006 61 645-647 New polyoxygenated steroids from the South China Sea gorgonian Echinogorgia aurantiaca Yunqi Qiu, Shuhua Qi, Si Zhang, Jin Yang and Zhihui Xiao Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . compound 7b ÏàËÆ¶È:85.1% Australian Journal of Chemistry 1981 34 1451-1465 Carbon-13 N.M.R. studies of 5¦Á- and 5¦Â-Cholestan-5-ols and analogous 8a-Methyl-trans- and cis-decahydronaphthalen-4a-ols JM Coxon and JR Gibson Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . (24S)-24-ethylcholesta-3¦Â,5¦Á,6¦Â-triol ÏàËÆ¶È:82.7% Journal of Natural Products 1992 Vol 55 1310 Studies on Marine Chemicals, Part IV. Isolation of Cholesterol Derivatives from the Marine Sponge Spirastrella inconstans B. Das, K. V. N. S. Srinivas Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . 24R-methylcholesta-3¦Â,5¦Á,6¦Â-triol ÏàËÆ¶È:82.1% Natural Product Research 1997 10 231-237 Two 11¦Á-Acetoxysterols from the Palauan Soft Coral lobophytum cf. Pauciflorum Qing Lu; D. John Faulkner Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . 24S-methylcholestan-1¦Á,3¦Â-diol C28H50O2 ÏàËÆ¶È:82.1% Steroids 2012 77 433-440 Polyhydroxylated sterols from the Indonesian soft coral Sinularia sp.and their effect on farnesoid X-activated receptor Masteria Yunovilsa Putra,Giorgio Bavestrello,Carlo Cerrano,Barbara Renga,Claudio D¡¯Amore ,Stefano Fiorucci,Ernesto Fattorusso,Orazio Taglialatela-Scafati Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . muriflasteroid A C28H46O4 ÏàËÆ¶È:82.1% Steroids 2013 78 108-114 3¦Â,5¦Á,6¦Â-Oxygenated sterols from the South China Sea gorgonian Muriceopsis flavida and their tumor cell growth inhibitory activity and apoptosis-inducing function Tao-Fang Liu, Xin Lu, Hua Tang, Min-Min Zhang, Pan Wang, Peng Sun, Zhi-Yong Liu, Zeng-Lei Wang, Ling Li, Yao-Cheng Rui, Tie-Jun Li, Wen Zhang Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . ergost-3¦Â,5¦Á,6¦Â-triol ÏàËÆ¶È:82.1% Acta Scientiarum Naturalium Universitatis Sunyatseni 2007 46(4) 116-118 The Secondary Metabolite of the Soft Coral Cespitularia cocerulea May(¢ò) HE Xi-xin, YAN Su-jun, SU Jing-yu, ZENG Long-mei Structure 13C NMR ̼Æ×Ä£Äâͼ |
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