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Dantrolene sodium hemiheptahydrate

CAS No. 24868-20-0

Dantrolene sodium hemiheptahydrate ( Dantrolene sodium hydrate )

产品货号. M13728 CAS No. 24868-20-0

丹曲林是一种突触后肌肉松弛剂,可减轻肌肉细胞的兴奋-收缩耦合。

纯度: >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
规格 价格/人民币 库存 数量
25MG ¥137 有现货
50MG ¥191 有现货
100MG ¥266 有现货
500MG ¥804 有现货
1G ¥1188 有现货
1 mL x 10 mM in DMSO ¥312 有现货

生物学信息

  • 产品名称
    Dantrolene sodium hemiheptahydrate
  • 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
    丹曲林是一种突触后肌肉松弛剂,可减轻肌肉细胞的兴奋-收缩耦合。
  • 产品描述
    Dantrolene is a postsynaptic muscle relaxant that lessens excitation-contraction coupling in muscle cells, inhibits Ca2+ ions release from sarcoplasmic reticulum stores by antagonizing ryanodine receptors.
  • 体外实验
    RT-PCR Cell Line:Porcine aortic valvular interstitial cells (paVICs) Concentration:60 μM.Incubation Time:At 1 and 3 days Result:Significantly inhibited ACTA2 expression and upregulated RUNX2 expression.
  • 体内实验
    Animal Model:YAC128 transgenic mice (FVBN/NJ background strain) and WT mice Dosage:5 mg/kg Administration:Fed orally twice per week from 2 to 11.5 months of age Result:Resulted in significantly improved performance in the beam-walking and gait-walking assays. Significantly reduced the loss of NeuN-positive striatal neurons and reduced formation of Httexp nuclear aggregates.
  • 同义词
    Dantrolene sodium hydrate
  • 通路
    GPCR/G Protein
  • 靶点
    Calcium Channel
  • 受体
    Others
  • 研究领域
    Other Indications
  • 适应症
    ——

化学信息

  • CAS Number
    24868-20-0
  • 分子量
    400.3
  • 分子式
    C14H17N4NaO8.5
  • 纯度
    >98% (HPLC)
  • 溶解度
    DMSO: ≥ 33 mg/mL
  • SMILES
    C1C(=NC(=O)N1N=CC2=CC=C(O2)C3=CC=C(C=C3)[N+](=O)[O-])[O-].C1C(=NC(=O)N1N=CC2=CC=C(O2)C3=CC=C(C=C3)[N+](=O)[O-])[O-].O.O.O.O.O.O.O.[Na+].[Na+]
  • 化学全称
    2,4-Imidazolidinedione, 1-[[[5-(4-nitrophenyl)-2-furanyl]methylene]amino]-, sodium salt, hydrate (2:2:7)

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. Zucchi R, et al. Pharmacol Rev. 1997 Mar;49(1):1-51. 2. Barker K, et al. Clin Toxicol (Phila). 2006;44(3):351. 3. Ellis KO, et al. J Pharm Sci. 1973 Jun;62(6):948-51.
产品手册
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