• 咨询热线
    客服服务热线 13671568941/15317326293
  • 在线咨询
  • 微信客服
    微信客服
  • 公众号
    扫码关注公众号

Quinupramine

CAS No. 31721-17-2

Quinupramine ( —— )

产品货号. M35460 CAS No. 31721-17-2

Quinupramine 是一种口服有效的抗抑郁剂。Quinupramine 可透过中枢神经系统,影响神经传递的一些过程。Quinupramine 的抗抑郁活性与中枢血清素系统有关,但与 β- 肾上腺素能系统无关。

纯度: >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
规格 价格/人民币 库存 数量
5MG ¥7059 有现货
25MG ¥13857 有现货
50MG ¥17949 有现货
500MG 获取报价 有现货
1G 获取报价 有现货

生物学信息

  • 产品名称
    Quinupramine
  • 注意事项
    本公司产品仅用于科研实验,不得用于人体或动物的临床与诊断
  • 产品简述
    Quinupramine 是一种口服有效的抗抑郁剂。Quinupramine 可透过中枢神经系统,影响神经传递的一些过程。Quinupramine 的抗抑郁活性与中枢血清素系统有关,但与 β- 肾上腺素能系统无关。
  • 产品描述
    Quinupramine is an orally active antidepressant. Quinupramine can penetrate into the CNS and affect some of the processes of neurotransmission. The antidepressant activity of quinupramine is associated with the central serotonin system, but not with the β-adrenergic system.
  • 体外实验
    ——
  • 体内实验
    Quinupramine (10 mg/kg, PO, twice daily for 10 days) causes a down-regulation of serotonin S2 receptors in the frontal cortex of the rat.Quinupramine-EVA matrix containing a permeation enhancer can be a good transdermal delivery system for providing sustained plasma concentrations.Animal Model:Sprague-Dawley rats (Male, 220-270 g)Dosage:10 mg/kg Administration:PO, twice daily for 10 days Result:Caused a down-requlation of serotonin S2 receptors in the frontal cortex of the rat, did not alter the binding populations of Q-adrenergic, muscarinic cholinergic and a2-adrenergic receptors in the rat brain.
  • 同义词
    ——
  • 通路
    GPCR/G Protein
  • 靶点
    5-HT Receptor
  • 受体
    5-HT Receptor
  • 研究领域
    ——
  • 适应症
    ——

化学信息

  • CAS Number
    31721-17-2
  • 分子量
    304.43
  • 分子式
    C21H24N2
  • 纯度
    >98% (HPLC)
  • 溶解度
    ——
  • SMILES
    C=1C=CC2=C(C1)N(C=3C=CC=CC3CC2)C4CN5CCC4CC5
  • 化学全称
    ——

运输与储存

  • 储存条件
    (-20℃)
  • 运输条件
    With Ice Pack
  • 稳定性
    ≥ 2 years

参考文献

1. Sakamoto H, et al. Effects of quinupramine on the central monoamine uptake systems and involvement of pharmacokinetics in its pharmacological activities. Jpn J Pharmacol. 1987;45(2):169-175.?
产品手册
关联产品
  • Relenopride

    Relenopride (YKP 10811) is a selective 5-HT4 receptor agonist that promotes intestinal motility and is used in the study of intestinal disorders.

  • E-3620

    E-3620 是一种有效的 5-HT3 受体拮抗剂。E-3620 可用于运动障碍和胃肠动力障碍研究。

  • Naluzotan hydrochlor...

    Naluzotan hydrochloride (PRX 00023 hydrochloride) is a hERG K+ channel blocker with an IC50 value of 3800 nM and is commonly used in the study of anxiety and depression.Naluzotan hydrochloride is also a novel, potent, and selective 5-HT1A agonist, with an IC50 value of about 20 nM and a Ki value of about 5.1 Naluzotan hydrochloride is also a novel, potent and selective 5-HT1A agonist with an IC50 of approximately 20 nM and a Ki of approximately 5.1 nM.