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΢Æ×ÇóÖú s-2-5-1 ÒÑÓÐ1È˲ÎÓë
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17.2,18.47,18.93,19.03,19.11,19.3,20.11,21.24,22.92,23.05,23.47,24.44,25.37,26.13,26.44,27.57,28.61,29.47,29.59,29.73,29.9,30.04,30.1,30.68,31.79,32.23,32.32,32.75,32.92,34.01,34.23,34.39,34.5,34.63,35.61,35.95,36.2,36.5,36.87,37.24,38.73,39.13,39.91,42.62,46.11,50.25,53.97,56.05,56.54,56.75,60.3,63.41,65.79,67.06,72.89,128.46,128.5,130.46,130.53,158.24,170.8,173.4,173.53,198.49 |
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ÖÁ×ðľ³æ (ÖªÃû×÷¼Ò)
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¸¡ÔÆpuppy: ½ð±Ò+10, ¡ï¡ï¡ïºÜÓаïÖú 2015-05-20 13:51:24
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¸¡ÔÆpuppy: ½ð±Ò+10, ¡ï¡ï¡ïºÜÓаïÖú 2015-05-20 13:51:24
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1 . (¦Ã-hydroxylmethylleucine(4))-cyclosporin A ÏàËÆ¶È:65.6% Chinese Journal of Antibiotics 2013 38 512-515 Purifi cation and identifi cation of (¦Ã-hydroxylmethylleucine4)-cyclosporin A Ren Feng-zhi, Zhang Xue-xia, Chen Shu-hong, Li Li-hong and Duan Bao-ling Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 2 . Benzyl (+/-)-7¦Á,12¦Á-dihydroxy-3¦Á-(3-{[2,5,7,8-tetramethyl-2-(4,8,12-trimethyltridecyl)chroman-6-yl]oxycarbonyl}propanoyloxy)-5¦Â-cholan-24-oate ÏàËÆ¶È:65.6% Steroids 2013 78 435-453 New propanoyloxy derivatives of 5¦Â-cholan-24-oic acid as drug absorption modifiers Lenka Coufalov¨¢, Lech Mr¨®zek, Lucie R¨¢rov¨¢, Luk¨¢š Plaček, Radka Opatřilov¨¢, Jiř¨ª Dohnal, Katar¨ªna Kr¨¢l¡¯ov¨¢, Oldřich Paleta, Vladim¨ªr Kr¨¢l, Pavel Drašar, Josef Jamp¨ªlek Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 3 . CsA ÏàËÆ¶È:62.5% Journal of the American Chemical Society 1992 114 2676-2686 Novel backbone conformation of cyclosporin A: the complex with lithium chloride Matthias Koeck, Horst Kessler, Dieter Seebach, Adrian Thaler Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 4 . Cyclosporine D ÏàËÆ¶È:62.5% Helvetica Chimica Acta 1982 65 1655-1677 Isolierung und Strukturermittlung der neuen Cyclosporine E, F, G, H und I Ren¨¦ Traber, Hans-Rudolf Loosli, Hans Hofmann, Max Kuhn and Albert Von Wartburg Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 5 . Compound 3 C65H96N8O17 ÏàËÆ¶È:61.1% Bioorganic & Medicinal Chemistry Letters 2001 11 13-16 [Lys3]didemnins as potential affinity ligands Matthew D. Vera, Amy J. Pfizenmayer, Xiaobin Ding, Dong Xiao, Madeleine M. Joulli¨¦ Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 6 . 7¦Â-tert-Butyldimethylsilyloxysitosteryl-9,10-ditert-butyldimethylsilyloxystearate C65H126O5Si3 ÏàËÆ¶È:60.9% Steroids 2008 73 1098-1109 Synthesis of highly pure oxyphytosterols and (oxy)phytosterol esters: Part II. (Oxy)-sitosterol esters derived from oleic acid and from 9,10-dihydroxystearic acid [1] Diane Julien-David, Philippe Geoffroy, Eric Marchioni, Françis Raul, Dalal Aoud¨¦-Werner, Michel Miesch Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 7 . N(2.8)-[ (tert-Butoxy)carbonyl][5-[4,4,4,4',4',4'-hexafluoro-N-(2-hydroxyethyoxy)-L-valine]]-7,8-secocyclosporin tert-Butyl Ester ÏàËÆ¶È:60.9% Helvetica Chimica Acta 2010 93 1583-1601 Stereoselective Synthesis of [5-[4,4,4,4¡ä,4¡ä,4¡ä-Hexafluoro-N-(2-hydroxyethoxy)-D-valine]]- and [5-[4,4,4,4¡ä,4¡ä,4¡ä-Hexafluoro-N-(2-hydroxyethoxy)-L-valine]cyclosporin A Marcel K. Eberle and Reinhart Keese Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 8 . ¦Â-sitosteryl acetate ÏàËÆ¶È:60.9% Chemical Communications 1978 319-320 Biosynthesis of ¦Â-sitosterol from [4-13C]mevalonic acid and sodium [1, 2-13C]acetate in tissue cultures of Isodon japonicus hara Shujiro Seo, Yutaka Tomita and Kazuo Tori Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |

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