santa cruz biotechnology, inc.
SCBT Logo

Willkommen!        Produkt(e) im Warenkorb.     Bestellen
 

Chloride Channel Modulators

  • 9-AC
    Cl- transport inhibitor with a moderate to strong inhibitory action on PKA activated cardiac IcI.
    Katalog #CAS NummerSummenformelMenge
    sc-203483723-62-6C15H10O2100 mg
  • DPC
    A potent, non-specific blocker of Cl channel and chloride-bicarbonate exchange. Also inhibits cystic fibrosis transmembrane regulator (CFTR) ATPase activity.
    Katalog #CAS NummerSummenformelMenge
    sc-20259091-40-7C13H11NO21 g
  • DCPIB
    Selective blocker of VSAC/ICl, swell in various CV tissues; inhibits glucose-stimulated insulin release. In vitro, reverses cell swelling-induced action potential duration shortening in atrial myocytes and inhibits astroglial swelling.
    Katalog #CAS NummerSummenformelMenge
    sc-20391382749-70-0C22H28Cl2O410 mg/50 mg
  • DCEBIO
    Stimulates the secretion of Cl- via activation of hIK1 K+ channels and the activation of an apical Cl- conductance. Is more potent than its analog 1-EBIO
    Katalog #CAS NummerSummenformelMenge
    sc-20356160563-36-2C9H8Cl2N2O10 mg/50 mg
  • DIDS, Disodium Salt
    Binds covalently and irreversibly to the outer surface of human erythrocyte membranes. Inhibits ATP transport into endoplasmic reticulum vesicles. Anion transport inhibitor that inhibits Cl– uptake (IC50 = 150 nM) in neuroblastoma cells. Has anti-ulcerous properties.
    Katalog #CAS NummerSummenformelMenge
    sc-20391967483-13-0C16H8Na2N2O6S4250 mg/25 mg/100 mg
  • Fipronil
    A channel blocker that blocks GABA-gated chloride channels and glutamate-activated chloride channels (GluCls).
    Katalog #CAS NummerSummenformelMenge
    sc-201546120068-37-3C12H4Cl2F6N4OS20 mg/100 mg
  • IAA-94
    A potent mammalian skeletal muscle and epithelial Cl- channel blocker (Ki=1µM in bovine kidney cortex microsomes).
    Katalog #CAS NummerSummenformelMenge
    sc-20154454197-31-8C17H18Cl2O410 mg/50 mg
  • Lonidamine
    An indazole compound that has been reported to inhibit angiogenic-related endothelial cell functions. Also been shown to cause a decrease in proliferation, migration, and morphogenesis of cells.
    Katalog #CAS NummerSummenformelMenge
    sc-20311550264-69-2C15H10Cl2N2O25 mg/25 mg
  • 5-Nitro-2-(3-phenylpropylamino)benzoic Acid (NPPB)
    A potent chloride channel blocker. Shown to suppress prostaglandin E2 release.
    Katalog #CAS NummerSummenformelMenge
    sc-201542107254-86-4C16H16N2O410 mg/50 mg
  • PG 01
    A cystic fibrosis transmembrane conductance regulator (CFTR) potentiator which is reported to correct gating defects of several CFTR mutants.
    Katalog #CAS NummerSummenformelMenge
    sc-358839853138-65-5C28H29N3O210 mg/50 mg
  • Picrotoxin
    A noncompetitive inhibitor of GABA Cl--current which affects neuronal firing activity. Shown to increase noradrenaline levels and turnover in the hypothalamus.
    Katalog #CAS NummerSummenformelMenge
    sc-202765124-87-8C30H34O131 g/5 g
  • SFK1
    A cell permeable suppressor of FK506 1, which, in high salt media, reverses the inhibition of cell growth by FK506. It interacts with Por1p (YVDAC1) channel protein in the outer mitochondrial membrane. The compound perturbs ion homeostasis and induces hyperpolarization of the inner mitochondrial membrane and mitochondria-dependent cell death with ROS (reactive oxygen species) production in a low NaCl growth media. It also induces expression of calcineurin targeted genes.
    Katalog #CAS NummerSummenformelMenge
    sc-215849678997-25-6C23H36N2O2•HCl10 mg
  • Talniflumate
    Calcium-activated chloride channel (hCLCA1/mCLCA3) blocker that reduces mucin synthesis and release in animal models and cell culture. Possesses anti-inflammatory actions via inhibition of cyclooxygenases and inhibits Cl-/HCO3- exchanger activity. Increases survival in a cystic fibrosis mouse model of distal intestinal obstructive syndrome.
    Katalog #CAS NummerSummenformelMenge
    sc-20370666898-62-2C21H13F3N2O410 mg/50 mg
  • VRT-532
    A mutated G551D CFTR corrector. VRT-532 mediates G551D-CFTR by enhancing ATP affinity of the mutant. VRT-532 also potentiates F508del mutated CFTR and works specifically on mutant CFTR rather than other membrane proteins.
    Katalog #CAS NummerSummenformelMenge
    sc-25383238214-71-0C16H14N2O5 mg