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酒石酸托特罗定合成路线图解 被引量:3

Graphical Synthetic Routes of Tolterodine Tartrate
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摘要 酒石酸托特罗定(tolterodine tartrate,1),化学名为2-[(1R)-3-[二(1-甲基乙基)氨基]-1-苯基丙基]-4-甲基苯酚L-(+)酒石酸盐,是美国Pharmacia & Upjohn公司研发的新型毒蕈碱受体拮抗剂,1998年首次在瑞士上市,临床主要用于由膀胱过动症引起的尿频、尿急和急迫性尿失禁等症状。本品能竞争性阻断神经递质乙酰胆碱与毒蕈碱受体的结合,有效抑制逼尿肌的收缩,
出处 《中国医药工业杂志》 CAS CSCD 北大核心 2009年第4期314-316,共3页 Chinese Journal of Pharmaceuticals
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参考文献11

  • 1Appell RA, Norton PA, Kawabe K. Clinical efficacy and safety of tolterodine in the treatment of overactive bladder: apoolad analysis [J]. Urology, 1997, 50(6A) : 90-99. 被引量:1
  • 2袁宁.治疗膀胱过度活动症的新药托特罗定[J].药学进展,2001,25(1):52-56. 被引量:15
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二级参考文献13

  • 1[1]Yarker YE, Goa KG, Fittin A. Oxybutynin, a review of its pharmacodynamic and pharmacokinetic properties and its therapeutic use in detrusor instability [J]. Drug Aging, 1995, 6(3): 243-262. 被引量:1
  • 2[2]Nilvebrant L, Sundquist S, Gillberg P-G. Tolterodine is not subtype (ml - m5 ) selective but exhibits functional bladder selectivity in vivo [J]. Neurourol Urodyn, 1996, 15: 310-311. 被引量:1
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