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CFTR

CFTR

CFTR is a chloride channel protein that regulates the transport of chloride and bicarbonate ions across epithelial cell membranes, playing a crucial role in maintaining fluid balance in tissues. Mutations in the CFTR gene lead to cystic fibrosis, a genetic disorder characterized by the production of thick mucus that can clog airways and lead to severe respiratory and digestive problems. At CymitQuimica, we provide a selection of CFTR modulators to support your research in cystic fibrosis, ion transport, and genetic disorders.

Found 67 products for "CFTR".

products per page.
  • Glibenclamide

    CAS:
    Glibenclamide (Glyburide) is an antidiabetic sulfonylurea derivative with actions similar to those of chlorpropamide.
    Formula:C23H28ClN3O5S
    Purity:99.05% - 99.75%
    Color and Shape:White Solid
    Molecular weight:494.004
  • Elexacaftor

    CAS:
    Elexacaftor (VX-445) is a cystic fibrosis transmembrane conductance regulator (CFTR) corrector.Cost-effective and quality-assured.
    Formula:C26H34F3N7O4S
    Purity:98.87% - 99.87%
    Color and Shape:Solid
    Molecular weight:597.653
  • CFTR activator 2

    CAS:
    CFTR activator 2 (WAY-326769) is an activator of mutant CFTR (cystic fibrosis transmembrane conductance regulator), which increases ion transport activity and can be used for research into cystic fibrosis (CF).
    Formula:C27H27N3O3
    Purity:99.70%
    Color and Shape:Solid
    Molecular weight:441.52
  • H2-Gamendazole

    CAS:
    H2-Gamendazole: inhibits spermatogenesis, cancer therapy, targets heat shock proteins & EF1α, regulates Hsp90.
    Formula:C18H13Cl2F3N2O2
    Purity:97.39%
    Color and Shape:Solid
    Molecular weight:417.209
  • Cavosonstat

    CAS:
    Cavosonstat (N91115) is an oral GSNOR inhibitor aiding CFTR in cystic fibrosis.
    Formula:C16H10ClNO3
    Purity:99.64%
    Color and Shape:Yellow Solid
    Molecular weight:299.708
  • Crofelemer

    CAS:
    Crofelemer (Provir) is an orally active antidiarrheal agent. It targets the cystic fibrosis transmembrane conductance regulator (CFTR) and calcium-activated chloride channels (CACC), which are responsible for chloride and fluid secretion in the gastrointestinal tract. Crofelemer is applicable for research in diarrhea-related conditions.
    Color and Shape:Solid
  • Astressin 2B

    CAS:
    CRF2 antagonist with IC50 of 1.3 nM; >500 nM for CRF1. Aids gastric emptying.
    Formula:C183H307N49O53
    Purity:98%
    Color and Shape:Solid
    Molecular weight:4041.69
  • Urocortin III, mouse (free acid)


    Urocortin III (mouse) is a CRF2 receptor agonist that slows gastric emptying without affecting colonic transit.
    Formula:C186H311N51S2
    Molecular weight:4171.26
  • Zatonacaftor

    CAS:
    Zatonacaftor, a cystic fibrosis transmembrane regulator (CFTR) modulator, is utilized in the research of cystic fibrosis [1] [2].
    Formula:C24H27N3O4S
    Color and Shape:Solid
    Molecular weight:453.55
  • (R)-Crinecerfont

    CAS:
    4-(2-chloro-4-methoxy-5-methylphenyl)-N-[(1A)-2-cyclopropyl-1-(3-fluoro-4-methylphenyl)ethyl]-5-methyl-N-(2-propyn-1-yl)-2-thiazolamine is an enantiomeric
    Formula:C27H28ClFN2OS
    Purity:98.51%
    Color and Shape:Orange Solid
    Molecular weight:483.04
  • kCAL01

    CAS:
    kCAL01 is a CAL inhibitor with a Ki value of 2.3 μM and holds potential for research in cystic fibrosis (CF).
    Formula:C36H57N11O9
    Color and Shape:Solid
    Molecular weight:787.91
  • Vanzacaftor

    CAS:
    Vanzacaftor is a CFTR modulator improving protein processing and surface trafficking, restoring chloride transport and aiding cystic fibrosis therapy research.
    Formula:C32H39N7O4S
    Purity:99.14%
    Color and Shape:White Solid
    Molecular weight:617.76
  • (Rac)-Tezacaftor

    CAS:
    (Rac)-Tezacaftor, a racemate, corrects F508del CFTR for cystic fibrosis research.
    Formula:C26H27F3N2O6
    Color and Shape:Solid
    Molecular weight:520.5
  • CP-628006

    CAS:
    CP-628006 is a small molecule CFTR potentiator that effectively restores ATP-dependent channel gating to G551D-CFTR, the mutant form found in cystic fibrosis.
    Formula:C32H35F3N2O2
    Color and Shape:Solid
    Molecular weight:536.639
  • WAY-326766

    CAS:
    WAY-326766 increases ion transport through mutant CFTR and can be used to alter the lifespan of eukaryotes.WAY-326766 can be used to treat cystic fibrosis (CF).
    Formula:C21H23N3O5
    Purity:99.87%
    Color and Shape:Solid
    Molecular weight:397.4244
  • Crinecerfont hydrochloride

    CAS:
    SSR-125543, a potent CRF1 receptor non-peptide antagonist, effective in CAH research, taken orally.
    Formula:C27H29Cl2FN2OS
    Color and Shape:Solid
    Molecular weight:519.501
  • Tezacaftor

    CAS:
    Tezacaftor (VX661) is a small molecule that can be used as a corrector of the cystic fibrosis transmembrane conductance regulator (CFTR) gene function.
    Formula:C26H27F3N2O6
    Purity:98.84% - >99.99%
    Color and Shape:Solid
    Molecular weight:520.4976
  • KM11060

    CAS:
    KM11060 is a novel corrector of the F508del-CFTR trafficking defect, Correcting F508del-CFTR trafficking, increasing the amount of functional CFTR at the plasma
    Formula:C19H17Cl2N3O2S
    Purity:99.08%
    Color and Shape:Solid
    Molecular weight:422.328
  • PPQ-102

    CAS:
    PPQ-102 (CFTR Inhibitor), an effective CFTR inhibitor, can completely inhibit CFTR chloride current (IC50: 90 nM).
    Formula:C26H22N4O3
    Purity:98.80% - ≥95%
    Color and Shape:Yellow Solid
    Molecular weight:438.4779
  • IOWH-032

    CAS:
    IOWH-032 (IOWH032) , a synthetic CFTR inhibitor, has been investigated for the treatment of cholera, diarrhea, and secretory diarrhea.
    Formula:C22H15Br2N3O4
    Purity:99% - >99.99%
    Color and Shape:Solid
    Molecular weight:545.18