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Oxotremorine sesquifumarate

CAS No. 17360-35-9

Oxotremorine sesquifumarate ( —— )

产品货号. M27678 CAS No. 17360-35-9

Oxotremorine sesquifumarate 是一种毒蕈碱受体激动剂。

纯度: >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
规格 价格/人民币 库存 数量
5MG ¥352 有现货
10MG ¥528 有现货
25MG ¥884 有现货
50MG ¥1200 有现货
100MG ¥1737 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
    Oxotremorine sesquifumarate
  • 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
    Oxotremorine sesquifumarate 是一种毒蕈碱受体激动剂。
  • 产品描述
    Oxotremorine sesquifumarate is a muscarinic receptor agonist.(In Vitro):Oxotremorine (10.5 micron) produced a paralytic effect on twitch responses of rat diaphragm in vitro to direct and indirect stimulation.(In Vivo):Rats with signs of neuropathy were subjected to SCS applied in awake, freely moving condition. Oxotremorine was administered intrathecally. Tactile, cold and heat sensitivities were assessed by using von Frey filaments, cold spray and focused radiant heat, respectively. Oxotremorine i.t. dose-dependently suppressed the tactile hypersensitivity. SCS markedly increased withdrawal thresholds (WTs), withdrawal latencies and cold scores.
  • 体外实验
    Oxotremorine (10.5 μM) produces a paralytic effect on twitch responses of rat diaphragm in vitro to direct and indirect stimulation.
  • 体内实验
    In rats with sciatic nerve injuries, Oxotremorine (10, 5, 21 μg; 10 μL) i.t. dose-dependently suppresses the tactile hypersensitivity.
  • 同义词
    ——
  • 通路
    Cell Cycle/DNA Damage
  • 靶点
    AChR
  • 受体
    ——
  • 研究领域
    ——
  • 适应症
    ——

化学信息

  • CAS Number
    17360-35-9
  • 分子量
    760.794
  • 分子式
    C36H48N4O14
  • 纯度
    >98% (HPLC)
  • 溶解度
    In Vitro:?DMSO : 125 mg/mL (328.60 mM)
  • SMILES
    OC(=O)\C=C\C(O)=O.OC(=O)\C=C\C(O)=O.OC(=O)\C=C\C(O)=O.O=C1CCCN1CC#CCN1CCCC1.O=C1CCCN1CC#CCN1CCCC1
  • 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.Extractives of jack pine bark: Occurrence of cis- and trans-pinosylvin dimethyl ether and ferulic acid esters. J.W.Rowe, et al. Phytochemistry. 1969 Jan, 8 (1): 235-241.
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