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13C NMR (101 MHz, CDCl3) ¦Ä 199.84, 171.90, 138.26, 129.61, 123.87, 77.48, 77.16, 76.85, 56.16, 56.03, 53.97, 51.38, 45.98, 42.54, 42.42, 40.60, 39.77, 39.67, 38.97, 38.76, 36.26, 35.99, 35.83, 35.77, 34.12, 34.03, 33.79, 33.10, 32.56, 32.20, 32.01, 31.62, 31.05, 30.42, 29.84, 29.30, 29.00, 28.33, 26.23, 25.54, 24.39, 24.33, 23.22, 22.83, 21.30, 21.22, 21.18, 20.34, 19.96, 19.17, 19.13, 18.85, 18.77, 18.40, 17.53, 15.52, 14.25, 12.38, 12.29, 12.12, 12.09, 0.13.
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yangyinhe

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3Â¥: Originally posted by 874643370 at 2015-05-07 19:24:21
ÅźÃÁË£º0.13,12.09,12.12,12.29,12.38,14.25,15.52,17.53,18.40,18.77,  18.85,19.13,19.17,19.96,20.34,21.18,21.22,21.30,22.83,23.22,  24.33,24.39,25.54,26.23,28.33,29.00,29.30,29.84,30.42, 31.05, 31.62 ...

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2Â¥2015-05-07 15:48:04
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874643370

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2Â¥: Originally posted by yangyinhe at 2015-05-07 15:48:04
´ÓСµ½´ó˳ÐòÊäÈ룬Êý×Ö¼äÓÃÓ¢Îİë½Ç¶ººÅ(,)·Ö¸ôÀýÈ磺
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ÅźÃÁË£º0.13,12.09,12.12,12.29,12.38,14.25,15.52,17.53,18.40,18.77,  18.85,19.13,19.17,19.96,20.34,21.18,21.22,21.30,22.83,23.22,  24.33,24.39,25.54,26.23,28.33,29.00,29.30,29.84,30.42, 31.05, 31.62,32.01,32.20,32.56,33.10,33.79,34.03,34.12, 35.77, 35.83, 35.99,36.26,38.76,38.97, 39.67,39.77,40.60,42.42, 42.54,45.98, 51.38,53.97, 56.03,56.16,76.85,77.16,  77.48,123.87,129.61, 138.26,171.90,199.84,
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3Â¥2015-05-07 19:24:21
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874643370: ½ð±Ò+10, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸, ллÄú 2015-05-08 12:04:26
1 .     4-Ethylcholesta-4,24(28)-dien-3-one
C29H46O     ÏàËÆ¶È:72.1%
Chemistry of Natural Compounds          2011          Vol. 47, No. 3          465-466
POLYSACCHARIDES OF Fabaceae. VI. GALACTOMANNANS FROM SEEDS OF Astragalus alpinus AND A. tibetanus
D. N. Olennikov and A. V. Rokhin
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




2 .     ¦Â-sitosteryl acetate
    ÏàËÆ¶È:69.3%
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     Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




3 .     ¦Â-sitosterol and stigmasterol
    ÏàËÆ¶È:68.8%
China Journal of Chinese Materia Medica          2001          26          692-694
Chemical Constituents of loxocalyx urticifolius Hemsl
ZHANG Xiaorong, WANG Ming'an, ZHANG Yong, WANG Mingkui, IDNG Lisheng
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




4 .     sitosterol
    ÏàËÆ¶È:67.2%
Chemical Communications          1986                   1139-1140
Biosynthesis of Sitosterol in Tissue Cultures of Rabdosia japonica Hara and Ergosterol in Yeast from [2-13C, 2-2H3]Acetate
Shujiro Seo, * Ushio Sankawa, Haruo Seto, Atsuko Uomori, Yohko Yoshimura, Yutaka Ebizuka, Hiroshi Noguchi, and Ken'ichi Takeda
Structure      13C NMR   Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




5 .     7¦Â-tert-Butyldimethylsilyloxysitosteryl-9,10-ditert-butyldimethylsilyloxystearate
C65H126O5Si3     ÏàËÆ¶È:65.5%
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     Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




6 .     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:63.4%
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     Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




7 .     Cyclosporine D
    ÏàËÆ¶È:63.4%
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     Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




8 .     Cyclosporine G
C63H113N11O12     ÏàËÆ¶È:63.4%
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     Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




9 .     Cyclosporin D
    ÏàËÆ¶È:63.4%
Helvetica Chimica Acta          1987          70          13-36
Neue Cyclosporine aus Tolypocladium inflatum. Die Cyclosporine K¨CZ
Ren¨¦ Traber, Hans Hofmann, Hans-Rudolf Loosli, Monique Ponelle and Albert von Wartburg
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




10 .     3¦Á-Hydroxy-7¦Á,12¦Á-bis(3-{[2,5,7,8-tetramethyl-2-(4,8,12-trimethyltridecyl)chroman-6-yl]oxycarbonyl}propanoyloxy)-5¦Â-cholan-24-oic acid
C90H144O13     ÏàËÆ¶È:63.0%
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     Ì¼Æ×Ä£Äâͼ
5Â¥2015-05-08 08:22:20
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