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「同位素标记抑制剂」Tolcapone-d7

  • 产品货号:E-T202508210001
  • 发布时间:2025-08-21
  • 产品CAS :N/A
  • 产品规格:mg
  • 产品纯度:≥95%
  • 产品货期:现货下单后48小时内发货,定制产品4-8周。
  • 运输条件:顺丰常规运输
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货号:E-T202508210001
CAS:N/A
规格:mg
纯度:≥95%
生产商:试剂家

生物活性:Tolcapone-d7 is a deuterium labeled Tolcapone. Tolcapone is a selective, potent and orally active COMT inhibitor. Tolcapone is also a potent inhibitor of α-syn and Aβ42 oligomerization and fibrillogenesis and protect against extracellular toxicity induced by the aggregation of both proteins in PC12 cells[1][2].
IC50 & Target:COMT[1]
α-syn and Aβ42 oligomerization, fibrillogenesis[2]
分子量:280.28
Formula:C14H4D7NO5
非标记 CAS:134308-13-7
中文名称:托卡朋 d7
运输条件:Room temperature in continental US; may vary elsewhere.
储存方式:Please store the product under the recommended conditions in the Certificate of Analysis.
纯度 & 产品资料
Data Sheet (534 KB)
产品使用指南 (1538 KB)
参考文献
[1]. Paterson NE, et al. Sub-optimal performance in the 5-choice serial reaction time task in rats was sensitive to methylphenidate, atomoxetine and d-amphetamine, but unaffected by the COMT inhibitor tolcapone. Neurosci Res. 2011 Jan;69(1):41-50.
 [Content Brief]
[2]. Di Giovanni S, et al. Entacapone and tolcapone, two catechol O-methyltransferase inhibitors, block fibril formation of alpha-synuclein and beta-amyloid and protect against amyloid-induced toxicity. J Biol Chem. 2010 May 14;285(20):14941-54.
 [Content Brief]

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