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CFTR

CFTR

CFTR è una proteina canale del cloruro che regola il trasporto di ioni cloruro e bicarbonato attraverso le membrane delle cellule epiteliali, svolgendo un ruolo cruciale nel mantenimento dell'equilibrio dei fluidi nei tessuti. Le mutazioni nel gene CFTR portano alla fibrosi cistica, un disturbo genetico caratterizzato dalla produzione di muco denso che può ostruire le vie respiratorie e causare gravi problemi respiratori e digestivi. Presso CymitQuimica, offriamo una selezione di modulatori CFTR per supportare la tua ricerca sulla fibrosi cistica, sul trasporto ionico e sui disturbi genetici.

Trovati 67 prodotti per "CFTR".

prodotti per pagina.
  • Glibenclamide

    CAS:
    Glibenclamide (Glyburide) is an antidiabetic sulfonylurea derivative with actions similar to those of chlorpropamide.
    Formula:C23H28ClN3O5S
    Purezza:99.05% - 99.75%
    Colore e forma:White Solid
    Peso molecolare:494.004
  • Elexacaftor

    CAS:
    Elexacaftor (VX-445) is a cystic fibrosis transmembrane conductance regulator (CFTR) corrector.Cost-effective and quality-assured.
    Formula:C26H34F3N7O4S
    Purezza:98.87% - 99.87%
    Colore e forma:Solid
    Peso molecolare: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
    Purezza:99.70%
    Colore e forma:Solid
    Peso molecolare:441.52
  • H2-Gamendazole

    CAS:
    H2-Gamendazole: inhibits spermatogenesis, cancer therapy, targets heat shock proteins & EF1α, regulates Hsp90.
    Formula:C18H13Cl2F3N2O2
    Purezza:97.39%
    Colore e forma:Solid
    Peso molecolare:417.209
  • Cavosonstat

    CAS:
    Cavosonstat (N91115) is an oral GSNOR inhibitor aiding CFTR in cystic fibrosis.
    Formula:C16H10ClNO3
    Purezza:99.64%
    Colore e forma:Yellow Solid
    Peso molecolare: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.
    Colore e forma:Solid
  • Astressin 2B

    CAS:
    CRF2 antagonist with IC50 of 1.3 nM; >500 nM for CRF1. Aids gastric emptying.
    Formula:C183H307N49O53
    Purezza:98%
    Colore e forma:Solid
    Peso molecolare: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
    Peso molecolare:4171.26
  • Zatonacaftor

    CAS:
    Zatonacaftor, a cystic fibrosis transmembrane regulator (CFTR) modulator, is utilized in the research of cystic fibrosis [1] [2].
    Formula:C24H27N3O4S
    Colore e forma:Solid
    Peso molecolare: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
    Purezza:98.51%
    Colore e forma:Orange Solid
    Peso molecolare: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
    Colore e forma:Solid
    Peso molecolare: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
    Purezza:99.14%
    Colore e forma:White Solid
    Peso molecolare:617.76
  • (Rac)-Tezacaftor

    CAS:
    (Rac)-Tezacaftor, a racemate, corrects F508del CFTR for cystic fibrosis research.
    Formula:C26H27F3N2O6
    Colore e forma:Solid
    Peso molecolare: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
    Colore e forma:Solid
    Peso molecolare: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
    Purezza:99.87%
    Colore e forma:Solid
    Peso molecolare:397.4244
  • Crinecerfont hydrochloride

    CAS:
    SSR-125543, a potent CRF1 receptor non-peptide antagonist, effective in CAH research, taken orally.
    Formula:C27H29Cl2FN2OS
    Colore e forma:Solid
    Peso molecolare: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
    Purezza:98.84% - >99.99%
    Colore e forma:Solid
    Peso molecolare: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
    Purezza:99.08%
    Colore e forma:Solid
    Peso molecolare:422.328
  • PPQ-102

    CAS:
    PPQ-102 (CFTR Inhibitor), an effective CFTR inhibitor, can completely inhibit CFTR chloride current (IC50: 90 nM).
    Formula:C26H22N4O3
    Purezza:98.80% - ≥95%
    Colore e forma:Yellow Solid
    Peso molecolare: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
    Purezza:99% - >99.99%
    Colore e forma:Solid
    Peso molecolare:545.18