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Acotiamide hydrochloride

CAS No. 773092-05-0

Acotiamide hydrochloride ( —— )

产品货号. M17592 CAS No. 773092-05-0

阿考替胺盐酸盐是阿考替胺的盐酸盐形式,阿考替胺是一种具有胃肠道 (GI) 动力增强活性的促动力剂。

纯度: >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
规格 价格/人民币 库存 数量
100MG ¥340 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
    Acotiamide hydrochloride
  • 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
    阿考替胺盐酸盐是阿考替胺的盐酸盐形式,阿考替胺是一种具有胃肠道 (GI) 动力增强活性的促动力剂。
  • 产品描述
    Acotiamide Hydrochloride is the hydrochloride salt form of acotiamide, a prokinetic agent with gastrointestinal (GI) motility-enhancing activity. Although the exact mechanism by which acotiamide exerts its effect has yet to be fully elucidated, this agent appears to inhibit acetylcholinesterase (AchE), an enzyme responsible for the breakdown of acetylcholine (Ach). Increased Ach concentrations lead to an improvement of gastric emptying and GI motility and eventually to a reduction of dyspepsia symptoms.(In Vivo):Acotiamide monohydrochloride trihydrate (0.3, 1, 3 mg/kg; i.v./3, 10, 30 mg/kg; p.o.) increases the postprandial gastric motility index in a dose-dependent manner.Acotiamide monohydrochloride trihydrate (0.83 mg/kg; i.v.; once) inhibits AChE in rat stomach with IC50 of 1.79 μM.
  • 体外实验
    Acotiamide monohydrochloride trihydrate (10, 30, 100 μM; 1 hour) reduces expression levels of IκB-α phosphorylation in LPS- and MCP-1-stimulated macrophage cell lines. Cell Viability Assay Cell Line:NR8383, macrophage Concentration:10, 30, 100 μM Incubation Time:1 hour Result:Significantly reduced both TNF-α and IL-6 productions in LPS/MCP-1-stimulated NR8383 cells.
  • 体内实验
    Acotiamide monohydrochloride trihydrate (0.3, 1, 3 mg/kg; i.v./3, 10, 30 mg/kg; p.o.) increases the postprandial gastric motility index in a dose-dependent manner.Acotiamide monohydrochloride trihydrate (0.83 mg/kg; i.v.; once) inhibits AChE in rat stomach with IC50 of 1.79 μM. Animal Model:Male mongrel dogs (9-11 kg), Male beagle dogs (9.6-12.9 kg)Dosage:0.3, 1, 3, 10, 30 mg/kg Administration:Intravenous injection; once.Result:Increased the postprandial gastric motility.Animal Model:Male Sprague-Dawley rats (aged 6-7 weeks)Dosage:0.83 mg/kg Administration:Intravenous injection; once.Result:Effectively improved functional dyspepsia by inhibiting AChE in rat stomach.
  • 同义词
    ——
  • 通路
    GPCR/G Protein
  • 靶点
    Melatonin Receptor
  • 受体
    AChE
  • 研究领域
    ——
  • 适应症
    ——

化学信息

  • CAS Number
    773092-05-0
  • 分子量
    541.06
  • 分子式
    C21H37ClN4O8S
  • 纯度
    >98% (HPLC)
  • 溶解度
    In Vitro:?DMSO : 125 mg/mL (231.03 mM)
  • SMILES
    s1c(nc(c1)C(=O)NCCN(C(C)C)C(C)C)NC(=O)c1c(cc(c(c1)OC)OC)O.O.Cl.O.O
  • 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. Kawachi M,et al. Eur J Pharmacol. 2011 Sep;666(1-3):218-25.
产品手册
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