CaCC(inh)-A01

CaCC(inh)-A01

CAT N°: 21922
Price:

From 100.00 85.00

CaCC(inh)-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).{37016} CaCC(inh)-A01 (30 µM) induces full vasorelaxation of preconstricted mouse isolated mesenteric arteries in the presence or absence of chloride.{34635} CaCC(inh)-A01 also attenuates CaCC TMEM16-A-induced proliferation in cancer cell lines through targeted degradation of the protein and reduces the activity of large-conductance calcium-activated potassium channels (KCa1.1/BK) in human red blood cells.{37017},{37018}

Territorial Availability: Available through Bertin Technologies only in France

  • Synonyms
    • 6-(1,1-dimethylethyl)-2-[(2-furanylcarbonyl)amino]-4,5,6,7-tetrahydro-benzo[b]thiophene-3-carboxylic acid
  • Correlated keywords
    • CaCC(inh)A01 CaCC-(inh)-A01 ANO1 Anoctamin TMEM16 Blocker I TMEM-16
  • Product Overview:
    CaCC(inh)-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).{37016} CaCC(inh)-A01 (30 µM) induces full vasorelaxation of preconstricted mouse isolated mesenteric arteries in the presence or absence of chloride.{34635} CaCC(inh)-A01 also attenuates CaCC TMEM16-A-induced proliferation in cancer cell lines through targeted degradation of the protein and reduces the activity of large-conductance calcium-activated potassium channels (KCa1.1/BK) in human red blood cells.{37017},{37018}

We also advise you