• 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

Spiradoline mesylate

CAS No. 87173-97-5

Spiradoline mesylate ( U 62066 )

产品货号. M16337 CAS No. 87173-97-5

Spiradoline (U 62066) 是一种强效、高选择性 κ-阿片受体激动剂,具有镇痛、利尿和镇咳作用。

纯度: >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
规格 价格/人民币 库存 数量
100MG 获取报价 有现货
200MG 获取报价 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
    Spiradoline mesylate
  • 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
    Spiradoline (U 62066) 是一种强效、高选择性 κ-阿片受体激动剂,具有镇痛、利尿和镇咳作用。
  • 产品描述
    Spiradoline (U 62066) is a potent, highly selective κ-opioid agonist that has analgesic diuretic and antitussive effects.Pain Phase 2 Discontinued.
  • 体外实验
    Using the patch-clamp method in isolated rat cardiac myocytes, indicated that Spiradoline mesylate (15 to 500 μM) produces its antiarrythmic effect via blockade of sodium channels (and at the higher doses also of potassium currents) in myocardial tissue. Thus, Spiradoline mesylate reduces the peak sodium current, increased the decay rate of the transient outward potassium current, and reduced the sustained plateau potassium amplitude.
  • 体内实验
    Spiradoline mesylate (U-62066; 0.1-0.4 mg/kg; subcutaneous injection; once; Sprague-Dawley rats) treatment dose-dependently reduces social behaviors in non-stressed adults, producing social avoidance at the highest dose tested, while younger animals displays reduced sensitivity to this socially suppressing effect of Spiradoline mesylate. In stressed animals, the socially suppressing effects of the Spiradoline mesylate are blunted at all ages, with juveniles and adolescents exhibiting increased social preference in response to certain doses of U-62066. Animal Model:Juvenile, adolescent and adult Sprague-Dawley male and female rats exposured to repeated restraint Dosage:0.1 mg/kg, 0.2 mg/kg, 0.3 mg/kg, and 0.4?mg/kg Administration:Subcutaneous injection; once Result:Dose-dependently reduced social behaviors in non-stressed adults, producing social avoidance at the highest dose tested.
  • 同义词
    U 62066
  • 通路
    Endocrinology/Hormones
  • 靶点
    Opioid Receptor
  • 受体
    Opioid Receptor
  • 研究领域
    Neurological Disease
  • 适应症
    Pain

化学信息

  • CAS Number
    87173-97-5
  • 分子量
    521.494
  • 分子式
    C23H34Cl2N2O5S
  • 纯度
    >98% (HPLC)
  • 溶解度
    ——
  • SMILES
    ClC1=C(Cl)C=CC(CC(N(C)[C@H]2CC[C@]3(OCCC3)C[C@@H]2N4CCCC4)=O)=C1.CS(O)(=O)=O
  • 化学全称
    2-(3,4-dichlorophenyl)-N-methyl-N-[(5R,7S,8S)-7-pyrrolidin-1-yl-1-oxaspiro[4.5]decan-8-yl]acetamide mesylate

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. Peters GR, et al. J Pharmacol Exp Ther. 1987 Jan;240(1):128-31. 2. Kamei J, et al. Eur J Pharmacol. 1990 Oct 9;187(2):281-6. 3. Kunihara M, et al. Life Sci. 1989;45(13):1191-8.
产品手册
关联产品
  • Ac-RYYRWK-NH2

    Potent, selective partial agonist peptide for the NOP receptor (Ki = 0.71 nM). Selective over μ, δ and κ opioid receptors (IC50 > 4000 nM). Increases food intake in vivo.

  • Bevenopran

    贝诺普兰 (Bevenopran) 是一种 μ-阿片受体外周拮抗剂,可用于治疗阿片类化合物引起的肠功能障碍的研究。

  • Endomorphin 2?

    Endomorphins-2 (EM-2) 可以降低 IX 层运动神经元 sEPSC 的频率和振幅,而 MOR 拮抗剂 CTOP 可逆转这一现象。