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cftr inhibitor  (MedChemExpress)


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    Structured Review

    MedChemExpress cftr inhibitor
    Cftr Inhibitor, supplied by MedChemExpress, used in various techniques. Bioz Stars score: 93/100, based on 6 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/cftr inhibitor/product/MedChemExpress
    Average 93 stars, based on 6 article reviews
    cftr inhibitor - by Bioz Stars, 2026-02
    93/100 stars

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    TargetMol cftr function
    ( ETI) treatment on cystic fibrosis transmembrane conductance protein <t>(CFTR)</t> <t>function</t> and infection pattern in cystic fibrosis (CF) cultures. A) Fold change in TEER measurements after 24 hours of ETI treatement (+ ETI) or no treatement (-ETI) in ALI cultures from three CF donors homozygous for ΔF508 mutation. B) TEEC after CFTR stimulation in treated (+ ETI) and untreated (-ETI) cells. Each dot represents one independent donor. C) TEER change after 14 h of infection with PAO1 laboratory strain in treated (+ ETI) and untreated (-ETI). D) Bacterial growth (CFU) after 14 h of infection in the apical (non attached / free bacteria), attached to the epithelium, and basolateral compartment, along with the total number of bacteria. In A,C-D, each dot represents one independent experiment and the mean ± SD is included. Statistical significance was calculated by paired two-sided t-test where **p<0.01 and ****p<0.0001. E) Three-dimensional reconstruction of confocal microscopy images of immunofluorescent staining of CFTR protein in ALI cultures from the CF donors treated (+ ETI) and untreated (-ETI). Green: Anti-CFTR 570 (CFTR protein), Red: Phalloidin (F-actin), Blue: DAPI (nuclei). ALI: air-liquid interface; TEER: transepithelial electrical resistance; TEEC: transepithelial electrical conductance; CFU: colony-forming units.
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    TargetMol cftr inhibitor ppq
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    MedChemExpress cftr inhibitor 172
    ( ETI) treatment on cystic fibrosis transmembrane conductance protein <t>(CFTR)</t> <t>function</t> and infection pattern in cystic fibrosis (CF) cultures. A) Fold change in TEER measurements after 24 hours of ETI treatement (+ ETI) or no treatement (-ETI) in ALI cultures from three CF donors homozygous for ΔF508 mutation. B) TEEC after CFTR stimulation in treated (+ ETI) and untreated (-ETI) cells. Each dot represents one independent donor. C) TEER change after 14 h of infection with PAO1 laboratory strain in treated (+ ETI) and untreated (-ETI). D) Bacterial growth (CFU) after 14 h of infection in the apical (non attached / free bacteria), attached to the epithelium, and basolateral compartment, along with the total number of bacteria. In A,C-D, each dot represents one independent experiment and the mean ± SD is included. Statistical significance was calculated by paired two-sided t-test where **p<0.01 and ****p<0.0001. E) Three-dimensional reconstruction of confocal microscopy images of immunofluorescent staining of CFTR protein in ALI cultures from the CF donors treated (+ ETI) and untreated (-ETI). Green: Anti-CFTR 570 (CFTR protein), Red: Phalloidin (F-actin), Blue: DAPI (nuclei). ALI: air-liquid interface; TEER: transepithelial electrical resistance; TEEC: transepithelial electrical conductance; CFU: colony-forming units.
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    Cayman Chemical cftr inhibitor cayman chemical (15545)
    Pharmacological inhibitors and activators used in this study.
    Cftr Inhibitor Cayman Chemical (15545), supplied by Cayman Chemical, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Image Search Results


    ( ETI) treatment on cystic fibrosis transmembrane conductance protein (CFTR) function and infection pattern in cystic fibrosis (CF) cultures. A) Fold change in TEER measurements after 24 hours of ETI treatement (+ ETI) or no treatement (-ETI) in ALI cultures from three CF donors homozygous for ΔF508 mutation. B) TEEC after CFTR stimulation in treated (+ ETI) and untreated (-ETI) cells. Each dot represents one independent donor. C) TEER change after 14 h of infection with PAO1 laboratory strain in treated (+ ETI) and untreated (-ETI). D) Bacterial growth (CFU) after 14 h of infection in the apical (non attached / free bacteria), attached to the epithelium, and basolateral compartment, along with the total number of bacteria. In A,C-D, each dot represents one independent experiment and the mean ± SD is included. Statistical significance was calculated by paired two-sided t-test where **p<0.01 and ****p<0.0001. E) Three-dimensional reconstruction of confocal microscopy images of immunofluorescent staining of CFTR protein in ALI cultures from the CF donors treated (+ ETI) and untreated (-ETI). Green: Anti-CFTR 570 (CFTR protein), Red: Phalloidin (F-actin), Blue: DAPI (nuclei). ALI: air-liquid interface; TEER: transepithelial electrical resistance; TEEC: transepithelial electrical conductance; CFU: colony-forming units.

    Journal: bioRxiv

    Article Title: Infection dynamics and virulence potential of clinical Pseudomonas aeruginosa isolates in a human airway epithelium model system

    doi: 10.1101/2025.04.11.644308

    Figure Lengend Snippet: ( ETI) treatment on cystic fibrosis transmembrane conductance protein (CFTR) function and infection pattern in cystic fibrosis (CF) cultures. A) Fold change in TEER measurements after 24 hours of ETI treatement (+ ETI) or no treatement (-ETI) in ALI cultures from three CF donors homozygous for ΔF508 mutation. B) TEEC after CFTR stimulation in treated (+ ETI) and untreated (-ETI) cells. Each dot represents one independent donor. C) TEER change after 14 h of infection with PAO1 laboratory strain in treated (+ ETI) and untreated (-ETI). D) Bacterial growth (CFU) after 14 h of infection in the apical (non attached / free bacteria), attached to the epithelium, and basolateral compartment, along with the total number of bacteria. In A,C-D, each dot represents one independent experiment and the mean ± SD is included. Statistical significance was calculated by paired two-sided t-test where **p<0.01 and ****p<0.0001. E) Three-dimensional reconstruction of confocal microscopy images of immunofluorescent staining of CFTR protein in ALI cultures from the CF donors treated (+ ETI) and untreated (-ETI). Green: Anti-CFTR 570 (CFTR protein), Red: Phalloidin (F-actin), Blue: DAPI (nuclei). ALI: air-liquid interface; TEER: transepithelial electrical resistance; TEEC: transepithelial electrical conductance; CFU: colony-forming units.

    Article Snippet: To subsequently inhibit CFTR function, a solution containing CFTR inhibitor PPQ-102 30 μM (TargetMol) was added to the apical side.

    Techniques: Infection, Mutagenesis, Bacteria, Confocal Microscopy, Staining

    Pharmacological inhibitors and activators used in this study.

    Journal: Cells

    Article Title: Effects of Akt Activator SC79 on Human M0 Macrophage Phagocytosis and Cytokine Production

    doi: 10.3390/cells13110902

    Figure Lengend Snippet: Pharmacological inhibitors and activators used in this study.

    Article Snippet: CFTR inh 172 , CFTR inhibitor , Cayman Chemical (15545).

    Techniques:

    SC79 activates NO production via Akt. ( A ) Bar graph of endpoint DAF-FM fluorescence from 5 independent experiments using macrophages from different donors. Responses were tested with 0.1–10 µg/mL SC79 ± Akt inhibitors MK2206 (10 µg/mL) or GSK690693 (10 µM), PKC inhibitor Gö6983 (10 µM), PKA inhibitor H89 (10 µM), NOS inhibitor L-NAME (10 µM), or inactive D-NAME (10 µM). Significance was determined via one-way ANOVA with Dunnett’s post-test, comparing values to those for HBSS alone; * p < 0.05. ( B ) DAF-FM fluorescence data with 1 and 10 µg/mL SC79 ± 10 µM CFTR inh 172 pretreatment. No significant differences were determined via one-way ANOVA. ( C ) Representative real-time traces of DAF-FM fluorescence, ± L-NAME or D-NAME. Time of addition of the indicated drugs is denoted by the arrow. ( D ) Data from 5 independent experiments done similarly as in ( C ). Significance was determined via one-way ANOVA with Dunnett’s post-test, comparing values to those for SC79 alone; * p < 0.05.

    Journal: Cells

    Article Title: Effects of Akt Activator SC79 on Human M0 Macrophage Phagocytosis and Cytokine Production

    doi: 10.3390/cells13110902

    Figure Lengend Snippet: SC79 activates NO production via Akt. ( A ) Bar graph of endpoint DAF-FM fluorescence from 5 independent experiments using macrophages from different donors. Responses were tested with 0.1–10 µg/mL SC79 ± Akt inhibitors MK2206 (10 µg/mL) or GSK690693 (10 µM), PKC inhibitor Gö6983 (10 µM), PKA inhibitor H89 (10 µM), NOS inhibitor L-NAME (10 µM), or inactive D-NAME (10 µM). Significance was determined via one-way ANOVA with Dunnett’s post-test, comparing values to those for HBSS alone; * p < 0.05. ( B ) DAF-FM fluorescence data with 1 and 10 µg/mL SC79 ± 10 µM CFTR inh 172 pretreatment. No significant differences were determined via one-way ANOVA. ( C ) Representative real-time traces of DAF-FM fluorescence, ± L-NAME or D-NAME. Time of addition of the indicated drugs is denoted by the arrow. ( D ) Data from 5 independent experiments done similarly as in ( C ). Significance was determined via one-way ANOVA with Dunnett’s post-test, comparing values to those for SC79 alone; * p < 0.05.

    Article Snippet: CFTR inh 172 , CFTR inhibitor , Cayman Chemical (15545).

    Techniques: Fluorescence

    SC79 enhancement of phagocytosis is not altered by CFTR inh 172. ( A ) The same type of FITC E. coli phagocytosis experiments as in , testing the SC79 ± CFTR inh 172 pretreatment. ( B ) The same type of phagocytosis experiments of pHrodo S. aureus as in , but testing SC79 ± CFTR inh 172 pretreatment. Significance was determined via one-way ANOVA with Bonferroni’s post-test with paired comparisons; * p < 0.05 vs. 0 µg/mL SC79 (HBSS + 0.1% DMSO vehicle control); n.s. means there was no statistical significance between bracketed groups. Data from 5–6 independent experiments per condition with macrophages from different donors.

    Journal: Cells

    Article Title: Effects of Akt Activator SC79 on Human M0 Macrophage Phagocytosis and Cytokine Production

    doi: 10.3390/cells13110902

    Figure Lengend Snippet: SC79 enhancement of phagocytosis is not altered by CFTR inh 172. ( A ) The same type of FITC E. coli phagocytosis experiments as in , testing the SC79 ± CFTR inh 172 pretreatment. ( B ) The same type of phagocytosis experiments of pHrodo S. aureus as in , but testing SC79 ± CFTR inh 172 pretreatment. Significance was determined via one-way ANOVA with Bonferroni’s post-test with paired comparisons; * p < 0.05 vs. 0 µg/mL SC79 (HBSS + 0.1% DMSO vehicle control); n.s. means there was no statistical significance between bracketed groups. Data from 5–6 independent experiments per condition with macrophages from different donors.

    Article Snippet: CFTR inh 172 , CFTR inhibitor , Cayman Chemical (15545).

    Techniques: Control