期刊文献+

牛磺熊去氧胆酸有关物质的合成及高效液相分析

Synthesis and HPLC Analysis of Related Substances of Tauroursodeoxycholic Acid
下载PDF
导出
摘要 为加强对牛磺熊去氧胆酸原料药和制剂产品的质量控制,合成了可能存在的两个有关物质:牛磺鹅去氧胆酸和牛磺石胆酸,结构经1HNMR和MS确证,并通过高效液相色谱仪建立了牛磺熊去氧胆酸有关物质的分析方法,可为化学药的仿制研究及其原料药与制剂的质量控制提供依据和参考。 To perform the quality control of raw material and medicinal preparation of tauroursodeoxycholic acid,two possible related substances were prepared,and the structures were confirmed by1 HNMR and MS. The analytical method of related substance of tauroursodeoxycholic acid was established by HPLC,and a basis and reference for the research and quality control of generic drugs was supplied.
出处 《化学试剂》 CAS 北大核心 2016年第1期63-66,共4页 Chemical Reagents
基金 贵州省普通高等学校药物化学工程研究中心项目(黔教合KY字[2014]219) 贵州医科大学药物化学重点实验室项目(GYZD[2014]001) 贵州省科技厅-贵州医科大学联合基金(黔科合LH字[2015]7340)
关键词 牛磺熊去氧胆酸 有关物质 合成 结构确证 tauroursodeoxycholic acid related substance synthesis structure identification
  • 相关文献

参考文献9

  • 1卓超,冯炜,吴达俊,熊志刚.牛磺熊去氧胆酸的合成研究[J].合成化学,2002,10(5):444-446. 被引量:6
  • 2王海龙,吴成龙,邓勇.牛磺熊去氧胆酸的合成[J].中国医药工业杂志,2009,40(2):88-89. 被引量:6
  • 3VENTURONI F, GIOIELLO A, SARDELLA R, et al. Con- tinuous flow synthesis and scale-up of glycine- and tau- rine-conjugated bile salts[ J]. Org. Biomol. Chem. ,2012, 10:4 109-4 115.
  • 4邓勇,王海龙,沈怡.用于制备胆酸偶联物的化合物及其制备方法和用途:中国专利,101503454[P].2009-08-12.
  • 5邓勇,沈怡,王海龙.胆酸类偶合物及其制备方法和用途:中国专利,101798332[P].2010-08-11.
  • 6ANELLI P L,LATTUADA L,LORUSSO V,et al. Conju- gates of gadolinium complexes to bile acids as hepatocyte- directed contrast agents for magnetic resonance imaging [ J]. J. Med. Chem. ,2004,47(14) :3 629-3 641.
  • 7黄凌,张和平,秦和平.一种牛磺酸熊去氧胆酸水合物的制备方法:中国专利,102558268[P].2012-07-11.
  • 8ROBERTO A,VITTORLO R. Process for the preparation of taurocholic acids : EP ,0 629 634 [ P ]. 1994-12-21.
  • 9ARNE N. Preparation of conjugated bile acids using mixed carboxylic acid anhydrides[ J]. Ark. Kemi. , 1955,8 (3) :331-342.

二级参考文献12

  • 1傅贤波,林三仁,范竹萍,邱德凯.牛磺熊去氧胆酸溶解胆囊胆固醇结石有效性和安全性——随机、双盲、安慰剂对照、多中心临床研究[J].中国微创外科杂志,2007,7(12):1159-1163. 被引量:28
  • 2李继珩,许东,牟晓虹.牛磺熊去氧胆酸结构及性质的研究[J].中国药科大学学报,1993,24(3):145-149. 被引量:10
  • 3Arosio R, Rossetti V. Process for the preparation of taurocholanic acids: US, 5565587 [P]. 1995-10-15. (CA 1994, 122: 265776).
  • 4Dayal B, Bhojawala J, Rapole KR, et al. Chemical synthesis, structural analysis, and decomposition of N-nitroso bile acid conjugates [J]. Bioorg Ailed Chem, 1996, 4 (6) : 885-890.
  • 5Momose T, Tsubaki T, lida T, et al. An improved synthesis of taurine- and glycine-conjugated bile acids [J]. Lipids, 1997, 32 (7) : 775-778,
  • 6Bonaldi A, Molinari E. Process for the preparation of taurine-conjugated bile acids: US, 5362891 [P]. 1994-11-08. (CA 1993, 121: 9815)
  • 7Furlenmeier A, Hofheinz W, Hubschwerlen CN, et al. Process for the manufacture of 1-sulpho-2-oxoazetidine carboxylic acid intermediates via catalytic ester cleavage: US, 4652651 [P]. 1987-03-24. (CA 1987, 107: 154164)
  • 8Massimn Darenti, Novi Ligute.Purification of Tauroursodesoxycholic Acid Dihydrate[P],US 5 260 462,1993.
  • 9Kou-Yi Tserng, David L.Hachey, Peter D.Klein.An Improved Procedure for the Synthesis of Glycine and Taurine Conjugate of Bile Acids[J].ournal of Lipid Research,1977,18:404-407.
  • 10Toshiaki Momose,Takayuki Tsubaki,Takashi lida.Toshio Nambara an improved Synthesis of Taurine and Glycine-Conjugated Bile Acids[J].Lipids,1997,32(7):775-778.

共引文献9

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部