• 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

Tetrodotoxin citrate

CAS No. 18660-81-6

Tetrodotoxin citrate ( TTx citrate )

产品货号. M12881 CAS No. 18660-81-6

Tetrodotoxin (TTx) 是一种有效的、高选择性的钠通道阻滞剂,对于 Nav1.6 的 IC50 为 33 nM。

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
    Tetrodotoxin citrate
  • 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
    Tetrodotoxin (TTx) 是一种有效的、高选择性的钠通道阻滞剂,对于 Nav1.6 的 IC50 为 33 nM。
  • 产品描述
    Tetrodotoxin (TTx) is a potent, highly selective sodium channel blocker with IC50 of 33 nM for Nav1.6; Tetrodotoxin-sensitive sodium channel (Nav) family includes Nav1.1, Nav1.2, Nav1.3, Nav1.4, Nav1.6, and Nav1.7, the Nav1.5, Nav1.8, and Nav1.9 channels are TTX-resistant; inhibits the firing of action potentials in neurons by binding to the voltage-gated sodium channels in nerve cell membranes and blocking the passage of sodium ions into the neuron.Pain Phase 3 Clinical.
  • 体外实验
    ——
  • 体内实验
    ——
  • 同义词
    TTx citrate
  • 通路
    Membrane Transporter/Ion Channel
  • 靶点
    Sodium Channel
  • 受体
    Sodium Channel
  • 研究领域
    Neurological Disease
  • 适应症
    Pain

化学信息

  • CAS Number
    18660-81-6
  • 分子量
    511.3915
  • 分子式
    C17H25N3O15
  • 纯度
    >98% (HPLC)
  • 溶解度
    H2O
  • SMILES
    C(C(=O)O)C(CC(=O)O)(C(=O)O)O.C(C1(C2C3C(N=C(NC34C(C1OC(C4O)(O2)O)O)N)O)O)O
  • 化学全称
    5,9:7,10a-Dimethano-10aH-[1,3]dioxocino[6,5-d]pyrimidine-4,7,10,11,12-pentol, 2-amino-1,4,4a,5,9,10-hexahydro-12-(hydroxymethyl)-, 2-hydroxy-1,2,3-propanetricarboxylate (1:1), [C(S),C(S),C(S),3S,4S,5R,9R,10R,11R]-

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. Rogers M, et al. Assay Drug Dev Technol. 2016 Mar;14(2):109-30. 2. Frelin C, et al. J Biol Chem. 1983 Jun 25;258(12):7256-9. 3. Reiser G, et al. Brain Res. 1983 Feb 21;261(2):335-40.
产品手册
关联产品
  • Silperisone HCl

    Silperisone HCl (RGH-5002) blocks sodium and calcium channels in cells, decreases excitability and contractility of muscle cells, reduces peripheral tone, and acts as a muscle relaxant and peripheral vasodilator. Silperisone HCl is used to treat recurrent painful myoclonus due to spinal cord injury, abnormal hypertonia due to cerebrovascular disease, dystonia symptoms, cone tension syndrome, multiple sclerosis myospasm and myelitis. silperisone is a sodium channel protein type 2 alpha channel blocker. silperisone is an organosilicon similar to tolperisone, an organosilicon compound with centrally acting muscle relaxant properties.

  • BI 01383298

    BI 01383298 是柠檬酸钠协同转运蛋白 (SLC13A5) 的选择性抑制剂。

  • Ropivacaine hydrochl...

    Ropivacaine hydrochloride 是一种有效的钠通道 (sodium channel) 阻断剂。Ropivacaine 通过可逆地抑制钠离子内流 (sodium ion influx) 从而引起神经纤维脉冲传导阻滞。Ropivacaine 也是一种 K2P (双孔钾通道) TREK-1 的抑制剂,在 COS-7 细胞膜上的 IC50 值为 402.7 μM。