• 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

CaCCinh-A01

CAS No. 407587-33-1

CaCCinh-A01 ( CaCCinh-A01; CaCC(inh)-A01, TMEM16 Blocker I )

产品货号. M17503 CAS No. 407587-33-1

CaCCinh-A01 is an inhibitor of the calcium-activated chloride channel (CaCC, 10 μM) and TMEM16A (IC50: 2.1 μM).

纯度: 98%

COA Datasheet HNMR HPLC MSDS Handing Instructions
规格 价格/人民币 库存 数量
5MG ¥421 有现货
10MG ¥680 有现货
25MG ¥1531 有现货
50MG ¥2535 有现货
100MG ¥4277 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
    CaCCinh-A01
  • 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
    CaCCinh-A01 is an inhibitor of the calcium-activated chloride channel (CaCC, 10 μM) and TMEM16A (IC50: 2.1 μM).
  • 产品描述
    CaCCinh-A01, also known as TMEM16 Blocker I, is a TMEM16 Blocker. CaCCinh-A01 is a non-selective inhibitor of calcium-activated chloride channels (CaCCs) that blocks ATP-stimulated chloride conductance in human salivary gland, intestinal, and bronchial epithelium (mean IC50 = 10 μM).
  • 同义词
    CaCCinh-A01; CaCC(inh)-A01, TMEM16 Blocker I
  • 通路
    Endocrinology/Hormones
  • 靶点
    5-HT Receptor
  • 受体
    TMEM16A;CaCC
  • 研究领域
    ——
  • 适应症
    ——

化学信息

  • CAS Number
    407587-33-1
  • 分子量
    347.43
  • 分子式
    C18H21NO4S
  • 纯度
    98%
  • 溶解度
    DMSO : ≥ 50 mg/mL; 143.91 mM
  • SMILES
    CC(C)(C)C1CCC2=C(C1)SC(=C2C(=O)O)NC(=O)C3=CC=CO3
  • 化学全称
    6-(1,1-dimethylethyl)-2-[(2-furanylcarbonyl)amino]-4,5,6,7-tetrahydro-benzo[b]thiophene-3-carboxylic acid

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.Namkung W,etal. J Biol Chem. 2011 Jan 21;286(3):2365-74.
产品手册
关联产品
  • Vidofludimus

    Vidofludimus (4SC-101, SC12267) is a novel small molecule inhibitor of dihydroorotate dehydrogenase (DHODH).

  • Cerlapirdine

    Cerlapirdine is a selective, potent, full antagonist of the 5-hydroxytryptamine 6 (5-HT6) receptor. Cerlapirdine is already in clinical development for the treatment of cognitive disorders related to Alzheimer's disease and schizophrenia. It works by acting as a selective 5-HT6 receptor antagonist.

  • Bromperidol

    Bromperidol is a butyrophenone derivative and it is a potent and long-acting neuroleptic.