期刊文献+

Fluoxetine Hydrochloride的NMR数据解析 被引量:1

NMR Study of Fluoxetine Hydrochloride
在线阅读 下载PDF
导出
摘要 由美国Lilly公司开发的第二代抗抑郁症药物盐酸氟西汀(Fluoxetine hydrochloride),属于选择性5-羟色胺再摄取抑制剂(SSRI),除了用于治疗各类抑郁症,包括轻性或重性抑郁症,尤宜用于老年性抑郁症之外,对于强迫症、惊恐发作、贪食症、经前期焦虑等亦有很好疗效.Fluoxetine hydrochloride是一种双环化合物,与传统的三环类、杂环类或单胺氧化酶抑制剂抗抑郁药相比,具有疗效好、不良反应轻而少,安全性高、耐受性好等特点,目前已作为一线的抗抑郁药得到广泛应用.本文对Fluoxetine hydrochloride进行了1H NMR和13C NMR检测,并通过DEPT和1H-1HCOSY、HMBC、HSQC等2D NMR技术对其1H NMR和13C NMR数据进行了较为详细的解析和比文献[1]更为全面的NMR归属,为以后的分析鉴定提供更完善的依据. Fluoxetine hydrochloride is a novel type of antidepressant that was developed by Eli Lilly and other companies in the United States. It has been used as a first line drug in clinical practice for treating depression, especially gerontal depression. In addi- tion, the compound is also used for treatments of anxiety, chronic pain and eating disorders such as obesity and bulimia. Compared to the traditional tricyclic antidepressants, fluoxetine also exhibits tolerability and safety advantages. The chemical structure of fluoxetine hydrochloride is a bicyclic compound belonging to a class of selective serotonin reuptake inhibitors. In this study, the 1H and 13C NMR spectra of fluoxetine were acquired, completely assigned and analyzed by a combination of 1D (1H, 13C NMR and DEPT) and 2D NMR (1H_1H COSY, HSQC and HMBC) techniques. The results obtained in this study will provide a reference for characterization of similar compounds in the future.
出处 《波谱学杂志》 CAS CSCD 北大核心 2007年第3期297-301,共5页 Chinese Journal of Magnetic Resonance
关键词 NMR 归属 2D NMR FLUOXETINE HYDROCHLORIDE NMR, assignment, 2D NMR, fluoxetine hydrochloride
  • 相关文献

参考文献10

二级参考文献55

  • 1胡琛.5-羟色胺再吸收抑制剂氟西汀[J].国外医药(合成药.生化药.制剂分册),1996,17(1):32-34. 被引量:10
  • 2黄彦合,王礼琛,黄嘉梓.抗抑郁药氟西汀的合成[J].中国药物化学杂志,1996,6(1):56-58. 被引量:10
  • 3[12]Sica D A. Pharmacotherapy in congestive heart failure: Metolazone and its role in edema management[J]. Congest Heart Fail, 2003,9(2):100-5.
  • 4[1]Shetty B V, Rochester N Y, Belleville N J. Tetrahydro-halo-sulfamyl-quinazolinones[P]. US: 3 360 518,1967-12-26.
  • 5[2]Shetty B V, Rochester N Y. N and N, N-alkyl, acyl and aryl-sulfamyl-tetrahydroquinazones[P]. US: 3 557111,1971-01-19.
  • 6[3]Shetty B V, Campanella L A, Thomas T L, et al. Synthesis and activity of some 3-aryl and 3-aralkyl-1,2,3,4-tetrahydyo-4-oxo-6-quinazolinesulfonamides[J]. J Med Chem, 1970,13 : 886-895.
  • 7[4]Belair E J, Kaiser F, Van Denburgh B, et al. Pharmacology of SR 720-22[J]. Arch Int Pharmacodyn Ther,1969,177:71-87.
  • 8[5]Belair E J. The renal pharmacology of metolazone, 2-methyl-3-O-tolyl-6-sulfamyl-7-chloro-1,2, 3,4-tetrahydro-4-quinazolinone[J]. Res Comm Chem Pathol Pharmacol, 1971,2(1) : 98-117.
  • 9[6]Schoonees R, Mostert J W, Moore R H. Evaluation of metolazone. New diuretic in chronic renal disease[J].New York State Journal of Medicine, 1971,71 :566-569 .
  • 10[7]Shetty B V. A review on a quinozolone diuretic zaroxolyn (metolazone) [J]. Ind J Pharmac, 1974,6(1) :40-53.

共引文献23

同被引文献7

引证文献1

二级引证文献11

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