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S87295

Opicapone

源叶(MedMol) 98%
  • 英文名:
  • Opicapone
  • 别名:
  • CAS号:
  • 923287-50-7
  • 分子式:
  • C15H10Cl2N4O6
  • 分子量:
  • 413.17
  • 核磁/质谱:
品牌货号产品规格价格(RMB) 库存(上海) 北京 武汉 南京 数量计量单位 加入购物车...
源叶(MedMol) S87295-5mg 98% ¥780.00元 6 - - - EA 加入购物车
源叶(MedMol) S87295-10mg 98% ¥1180.00元 5 - - - EA 加入购物车
源叶(MedMol) S87295-25mg 98% ¥1980.00元 6 - - - EA 加入购物车
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  • 提示:详情请下载说明书。
  • 产品描述: Opicapone (BIA 9-1067) is a potent third-generation catechol-O-methyltransferase (COMT) inhibitor for the research of Parkinson's disease and motor fluctuations. Opicapone decreases the ATP content of the cells with an IC50 of 98 μM
  • 靶点: COMT;Transferase
  • 体内研究:
    Opicapone inhibits rat peripheral COMT with ED50 values below 1.4 mg/kg up to 6 h post-administration. The effect is sustained over the first 8 h and by 24 h COMT had not returned to control values. A single administration of Opicapone resulted in increased and sustained plasma L-DOPA levels with a concomitant reduction in 3-OMD from 2 h up to 24 h post-administration, while Ro 40-7592 produces significant effects only at 2 h post-administration. The effects of Opicapone on brain catecholamines after L-DOPA administration are sustained up to 24 h post-administration. Opicapone is also the least potent compound in decreasing both the mitochondrial membrane potential and the ATP content in human primary hepatocytes after a 24 h incubation period
  • 参考文献:
    1. Bonifácio MJ, et al. Pharmacological profile of Opicapone, a third-generation nitrocatechol catechol-O-methyl transferase inhibitor, in the rat. Br J Pharmacol. 2015 Apr;172(7):1739-52. 2. Ferreira JJ, et al. Opicapone as an adjunct to L-DOPA in patients with Parkinson's disease and end-of-dose motor fluctuations: a randomised, double-blind, controlled trial. Lancet Neurol. 2016 Feb;15(2):154-165.
  • 溶解性: Soluble  in  DMSO
  • 保存条件: -20℃
  • 配置溶液浓度参考:
    1mg 5mg 10mg
    1 mM 2.42 ml 12.102 ml 24.203 ml
    5 mM 0.484 ml 2.42 ml 4.841 ml
    10 mM 0.242 ml 1.21 ml 2.42 ml
    50 mM 0.048 ml 0.242 ml 0.484 ml
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