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Atipamezole (hydrochloride)
品牌： Cayman
产品货号： 9001181-5 mg
规格： 5 mg

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数量： - +
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  • 产品名称:
    Atipamezole (hydrochloride)
  • 别名:
  • 产品描述:
    Atipamezole is an antagonist of α2A-adrenergic receptors (α2A-ARs; Ki = 1.86 nM).{25705,25706} It is selective for α2A-ARs over α2B- and α1-ARs (Kis = 1,949.83 and 13,300 nM, respectively), as well as over 40 receptors, ion channels, and transporters (IC50s = 540->10,000 nM). Atipamezole (0.04, 0.08, and 1.2 mg/kg) reverses bradycardia and sedation induced by the α2-AR agonist medetomidine in dogs.{60727} It also prevents hypoalgesia induced by the non-steroidal anti-inflammatory drug (NSAID) ketoprofen in sheep.{60728} Atipamezole (0.3 mg/kg) enhances contralateral circling behavior induced by apomorphine or L-DOPA (Item No. 13248) and prolongs the duration of action of L-DOPA in a rat model of Parkinson’s disease.{25704} Formulations containing atipamezole have been used to reverse the sedative and analgesic effects of dexmedetomidine or medetomidine in dogs. Atipamezole is an imidazole that potently antagonizes the α2-adrenoceptor (Ki = 1.6 nM).{25705,25706} It shows selectivity over the α1-adrenoceptor (Ki = 13,300 nM) and is a poor antagonist at a wide variety of other receptors and channels.{25706} Through its effects at the α2-adrenoceptor, atipamezole reverses the sedative and analgesic effects of α2-adrenoceptor agonists, alters cognitive functions and sexual behavior, and has neuroprotective effects.{25706} It may also potentiate the effects of dopaminergic drugs used in Parkinson’s disease.{25706,25704}
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  • 阳性对照:
  • 保存温度:
    -20
  • 运输温度:
    -20
  • 细胞定位:
  • 预期分子量:
    248.8
  • 产品形式:
    A crystalline solid
  • 存储溶液:
  • 有效期:
    1460
  • 产地:
    美国
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  • 纯度:
    ≥98%
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  • CAS号:
    104075-48-1
  • 分子式:
    C14H16N2 • HCl
  • 溶解度:
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