136 Results for "

CFTR

" in MedChemExpress (MCE) Product Catalog:
Products (136)

136 Results for "CFTR" in MCE Product Catalog:

  • Targets Recommended:
51
51 Publications Verification
Cat. No.: HY-111772
CAS No.: 2216712-66-0
Purity:  99.74%
Synonyms: VX-445
Target:  

CFTR Autophagy

Research Areas:  

Inflammation/Immunology

Elexacaftor (VX-445, Compound 1) is a modulator of cystic fibrosis transmembrane conductance regulator (CFTR). Elexacaftor (VX-445, Compound 1) facilitates the processing and trafficking of CFTR to increase the amount of CFTR at the cell surface .
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29
29 Cited Publications
Cat. No.: HY-13017
CAS No.: 873054-44-5
Purity:  99.97%
Synonyms: VX-770
Target:  

CFTR Autophagy

Research Areas:  

Endocrinology

Ivacaftor (VX-770) is a potent and orally bioavailable CFTR potentiator, targeting G551D-CFTR and F508del-CFTR with EC50s of 100 nM and 25 nM, respectively.
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28
28 Cited Publications
Cat. No.: HY-15448
CAS No.: 1152311-62-0
Purity:  99.85%
Synonyms: VX-661
Target:  

CFTR

Research Areas:  

Cancer

Tezacaftor (VX-661) is a F508del CFTR corrector. It helps CFTR protein reach the cell surface. However, Ivacaftor (VX-770, HY-13017), a CFTR potentiator, helps to prolong the opening time of cell surface CFTR protein channels. Tezacaftor combining with Ivacaftor, shows potent efficacy against cystic fibrosis and diseases with homozygous for the CFTR Phe508del mutation. Moreover, Elexacaftor (VX-445, HY-111772) is also a CFTR corrector. Elexacaftor-Tezacaftor-Ivacaftor aims at with cystic fibrosis (CF) with at least one Phe508del mutation, often avoids the indication for lung transplantation .
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28
28 Cited Publications
Cat. No.: HY-15206
CAS No.: 10238-21-8
Purity:  99.94%
Synonyms: Glyburide
Glibenclamide (Glyburide) is an orally active ATP-sensitive K + channel (KATP) inhibitor and can be used for the research of diabetes and obesity . Glibenclamide inhibits P-glycoprotein. Glibenclamide directly binds and blocks the SUR1 subunits of KATP and inhibits the cystic fibrosis transmembrane conductance regulator protein (CFTR) . Glibenclamide interferes with mitochondrial bioenergetics by inducing changes on membrane ion permeability . Glibenclamide can induce autophagy .
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25
25 Cited Publications
Cat. No.: HY-16671
CAS No.: 307510-92-5
Target:  

CFTR Autophagy

Research Areas:  

Others

CFTR(inh)-172 is a potent and selective blocker of the CFTR chloride channel; reversibly inhibits CFTR short-circuit current in less than 2 minutes with a Ki of 300 nM.
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21
21 Cited Publications
Cat. No.: HY-13262
CAS No.: 936727-05-8
Purity:  99.85%
Synonyms: VX-809; VRT 826809
Target:  

CFTR Autophagy

Research Areas:  

Inflammation/Immunology

Lumacaftor (VX-809; VRT 826809) is a CFTR modulator that corrects the folding and trafficking of CFTR protein.
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8
8 Cited Publications
Cat. No.: HY-14832
CAS No.: 775304-57-9
Purity:  99.82%
Synonyms: PTC124
Target:  

CFTR Autophagy

Research Areas:  

Metabolic Disease Cancer

Ataluren (PTC124) is an orally available CFTR-G542X nonsense allele inhibitor.
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8
8 Cited Publications
Cat. No.: HY-D1297
CAS No.: 730931-46-1
ER-Tracker dye is a derivative of BODIPY series dyes coupled with Glibenclamide (HY-15206), highly selective binding to the endoplasmic reticulum, non-toxic to cells at low concentrations, this type of dye is an environmentally sensitive probe, and formaldehyde treatment can still retain part of the fluorescence, with high fluorescence life, good extinction coefficient and other characteristics. Glibenclamide is an atp-dependent K + channel blocker (Kir6, KATP) and CFTR Cl-channel blocker that binds in the endoplasmic reticulum. ER-Tracker is not suitable for staining cells after fixation .
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5
5 Cited Publications
Cat. No.: HY-145603
CAS No.: 2374124-49-7
Purity:  98.19%
Synonyms: VX-121
Target:  

CFTR Chloride Channel

Research Areas:  

Neurological Disease

Vanzacaftor (VX-121) is an orally active noval corrector of Cystic fibrosis transmembrane conductance regulator (CFTR). Vanzacaftor improves processing and trafficking of CFTR protein as well as increases chloride transport in triple combined with Tezacaftor (HY-15448) and Deutivacaftor. Vanzacaftor-Tezacaftor-Deutivacaftor is safe and well tolerated, improving lung function, respiratory symptoms, and CFTR function with cystic fibrosis, which is promising for research in the field of cystic fibrosis diseases .
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5
5 Cited Publications
Cat. No.: HY-18336
CAS No.: 328541-79-3
Target:  

CFTR

Research Areas:  

Cardiovascular Disease

GlyH-101 is a potent CFTR inhibitor. GlyH-101 also is a potent and reversible inhibitor of the VSORC conductance. GlyH-101 shows antiproliferative activity. GlyH-101 inhibits CFTR-like current and VSORC current .
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5
5 Cited Publications
Cat. No.: HY-D1431
ER-Tracker dye is a derivative of BODIPY series dyes coupled with Glibenclamide (HY-15206), highly selective binding to the endoplasmic reticulum, non-toxic to cells at low concentrations, this type of dye is an environmentally sensitive probe, and formaldehyde treatment can still retain part of the fluorescence, with high fluorescence life, good extinction coefficient and other characteristics. Glibenclamide is an atp-dependent K + channel blocker (Kir6, KATP) and CFTR Cl-channel blocker that binds in the endoplasmic reticulum. ER-Tracker is not suitable for staining cells after fixation. Ex/Em=587/615 nm .
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4
4 Cited Publications
Cat. No.: HY-18337
CAS No.: 1191252-49-9
Target:  

CFTR SARS-CoV

Research Areas:  

Infection Metabolic Disease

IOWH-032 is a a synthetic anti-secretory molecule, is a potent CFTR inhibitor with an IC50 value of 8 μM. IOWH-032 also is a anti-diarrheal agent .
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4
4 Cited Publications
Cat. No.: HY-14179
CAS No.: 931706-15-9
Purity:  99.73%
Synonyms: CFTR Inhibitor
Target:  

CFTR

Research Areas:  

Others

PPQ-102 (CFTR Inhibitor) is a reversible CFTR inhibitor that completely inhibits CFTR chloride currents (IC50 ~90 nM). PPQ-102 is not affected by membrane potential-dependent cell allocation or blocking efficiency (uncharged at physiological pH) and effectively prevents cyst enlargement in polycystic kidney disease .
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3
3 Cited Publications
Cat. No.: HY-19778
CAS No.: 1415390-47-4
Target:  

CFTR Autophagy

Research Areas:  

Inflammation/Immunology

(R)-BPO-27, the R enantiomer of BPO-27, is a potent, orally active and ATP-competitive CFTR inhibitor with an IC50 of 4 nM.
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3
3 Cited Publications
Cat. No.: HY-108457
CAS No.: 484-17-3
Purity:  99.61%
Synonyms: 9-Hydroxyphenanthrene; NSC 50554
Target:  

TRP Channel

Research Areas:  

Cardiovascular Disease

9-Phenanthrol (9-Hydroxyphenanthrene) is a selective TRPM4 inhibitor with an IC50 of 17 μM. 9-Phenanthrol has no inhibitory activity on TRPM5, TRPC6, and CFTR. 9-Phenanthrol can be used for the research of ischemia-reperfusion injury .
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2
2 Cited Publications
Cat. No.: HY-N6818
CAS No.: 5631-70-9
Synonyms: TMF
5,7,4’-Trimethoxyflavone can be isolated from the medicinal plant Kaempferia parviflora (KP). 5,7,4’-Trimethoxyflavone is a CFTR activator and EC50 is 64 μM. 5,7,4’-Trimethoxyflavone induces apoptosis, increases proteolytic activation of caspase-3, and degradation of ADP-ribose polymerase (PARP) protein. 5,7,4’-Trimethoxyflavone has antitumor activity. 5,7,4’-Trimethoxyflavone can be used to prevent skin aging and oxidative stress .
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2
2 Cited Publications
Cat. No.: HY-111099
CAS No.: 1654725-02-6
Purity:  99.86%
Synonyms: ABBV-974
Target:  

CFTR Autophagy

Research Areas:  

Others

GLPG1837 is a potent and reversible CFTR potentiator, with EC50s of 3 nM and 339 nM for F508del and G551D CFTR, respectively.
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2
2 Cited Publications
Cat. No.: HY-111680
CAS No.: 1953130-87-4
Purity:  99.37%
Synonyms: PTI-428
Target:  

CFTR Autophagy

Research Areas:  

Endocrinology

Nesolicaftor (PTI-428) is a specific cystic fibrosis transmembrane conductance regulator (CFTR) amplifier .
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2
2 Cited Publications
Cat. No.: HY-19970
CAS No.: 774549-97-2
Target:  

CFTR Autophagy

Research Areas:  

Endocrinology

KM11060 is a corrector of the F508 deletion (F508del)-cystic fibrosis transmembrane conductance regulator (CFTR) trafficking defect. KM11060 can be used for the research of F508del-CFTR processing defect and development of cystic fibrosis research .
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1
1 Cited Publications
Cat. No.: HY-13017S
CAS No.: 1413431-07-8
Purity:  99.83%
Synonyms: VX-770-d9
Ivacaftor-d9 is a potent CFTR modulator and exhibits an EC50 value of 255 nM for CFTR potentiation in G551D/F508del HBE Cells. Ivacaftor-D9 acts as an orally active and improved deuterated Ivacaftor analog for cystic fibrosis research .
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