CymitQuimica logo
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 66 prodotti di "CFTR"

Ordinare per

Purezza (%)
0
100
|
0
|
50
|
90
|
95
|
100
prodotti per pagina.
  • CFTR corrector 6

    CAS:
    CFTR corrector 6, a potent CFTR potentiator, aids cystic fibrosis research and related disorders.
    Formula:C22H13F4N9
    Colore e forma:Solid
    Peso molecolare:479.39
  • CP 154526

    CAS:
    <p>CRF1 receptor antagonist</p>
    Formula:C23H33ClN4
    Purezza:98%
    Colore e forma:Solid
    Peso molecolare:400.99
  • CFTR corrector 12

    CAS:
    <p>CFTR corrector 12 is a CFTR corrector that rescues all mutant proteins except M760R ABCA3 and can be used to study cystic fibrosis.</p>
    Formula:C19H21ClN4O2S2
    Purezza:99.47%
    Colore e forma:Solid
    Peso molecolare:436.98
  • DNDS

    CAS:
    DNDS is a channel blocker of voltage-dependent cystic fibrosis transmembrane conductance regulator (CFTR).
    Formula:C14H8N2Na2O10S2
    Purezza:99.92%
    Colore e forma:Physical Description White Powder (Ntp 1992)
    Peso molecolare:474.33
  • (R)-Vanzacaftor

    CAS:
    (R)-Vanzacaftor ((R)-VX-121) is a cystic fibrosis transmembrane conductance regulator (CFTR) modulator [1].
    Formula:C32H39N7O4S
    Colore e forma:Solid
    Peso molecolare:617.76
  • Chromanol 293B

    CAS:
    slow delayed rectifier K+ current (IKs) blocker
    Formula:C15H20N2O4S
    Purezza:98%
    Colore e forma:Solid
    Peso molecolare:324.4
  • BPO-27 racemate

    CAS:
    BPO-27 racemate (BPO-27 (racemate)) is an effective CFTR inhibitor with IC50 of 8 nM.
    Formula:C26H18BrN3O6
    Purezza:97.67% - 98.86%
    Colore e forma:Solid
    Peso molecolare:548.34
  • CRF1 receptor antagonist-1

    CAS:
    CRF1 Receptor Antagonist-1 (Compound 2), a CRF1 receptor antagonist, is utilized in research pertaining to congenital adrenal hyperplasia (CAH) [1].
    Formula:C27H28ClFN2O2S
    Purezza:98%
    Colore e forma:Solid
    Peso molecolare:499.04
  • (R)-Elexacaftor

    CAS:
    (R)-Elexacaftor (compound 37) is the enantiomer of Elexacaftor (compound 1). (R)-Elexacaftor is a CFTR modulator with an EC50 of 0.29 μM for CFTR dF508.
    Formula:C26H34F3N7O4S
    Purezza:98.991%
    Colore e forma:Solid
    Peso molecolare:597.65
  • CFTR corrector 4

    CAS:
    Potent, oral CFTR corrector 4 targets cystic fibrosis, increasing cell surface CFTR levels.
    Formula:C29H27F2NO7
    Purezza:99.32%
    Colore e forma:Solid
    Peso molecolare:539.52
  • CFTR corrector 15

    CAS:
    <p>CFTR Corrector 15 (Compound 4172) serves as a corrector for cystic fibrosis transmembrane conductance regulator (CFTR). When used in combination with VX-809, it addresses the folding defects of F508del-CFTR. CFTR Corrector 15 is also applicable in the research of cystic fibrosis.</p>
    Formula:C24H22ClN5O2S
    Colore e forma:Solid
    Peso molecolare:479.98
  • Crinecerfont tosylate

    CAS:
    Crinecerfont tosylate is an effective oral CRF1 receptor antagonist. It is applicable to studies involving congenital adrenal hyperplasia (CAH).
    Formula:C34H36ClFN2O4S2
    Colore e forma:Solid
    Peso molecolare:655.242
  • CFTR corrector 16

    CAS:
    <p>CFTRcorrector 16 (Compound 39) is a corrector of the cystic fibrosis transmembrane conductance regulator (CFTR), utilized in the research of cystic fibrosis disease.</p>
    Formula:C27H26ClN5O2S
    Colore e forma:Solid
    Peso molecolare:520.05
  • ARN23765

    CAS:
    <p>ARN23765 is an F508del-CFTR corrector with an EC50 of 38 pM in human bronchial epithelial cells. It enhances the maturation and function of F508del-CFTR at the cell membrane, influencing ion transport and secretion, thereby addressing the pathological mechanisms of cystic fibrosis (CF).</p>
    Formula:C30H22F5N3O6
    Colore e forma:Solid
    Peso molecolare:615.504
  • CFTR corrector 18

    CAS:
    CFTRcorrector 18 (Compound I-99) acts as a modulator of the cystic fibrosis transmembrane conductance regulator (CFTR). It enhances the processing and trafficking of CFTR, thereby increasing the amount of CFTR present on the cell surface. CFTRcorrector 18 holds potential for research in cystic fibrosis (CF).
    Formula:C38H40N6O5S
    Colore e forma:Solid
    Peso molecolare:692.826
  • CFTR corrector 17

    CAS:
    CFTRcorrector 17 (example 17) is a regulator of the cystic fibrosis transmembrane conductance regulator (CFTR). It is utilized in the study of diseases mediated by CFTR.
    Formula:C18H15FN2O2
    Colore e forma:Solid
    Peso molecolare:310.32