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How to Cite 1. For In-Text Citation (Materials & Methods): 2. For Key Resources Table: |
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| Formula | C26H34F3N7O4S |
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| Molecular Weight | 597.65 | CAS No. | 2216712-66-0 | ||||||||||||
| Solubility (25°C)* | In vitro | DMSO | 100 mg/mL (167.32 mM) | ||||||||||||
| Water | Insoluble | ||||||||||||||
| Ethanol | Insoluble | ||||||||||||||
| In vivo (Add solvents to the product individually and in order) |
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* <1 mg/ml means slightly soluble or insoluble. * Please note that Selleck tests the solubility of all compounds in-house, and the actual solubility may differ slightly from published values. This is normal and is due to slight batch-to-batch variations. * Room temperature shipping (Stability testing shows this product can be shipped without any cooling measures.) |
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| Description | Elexacaftor (VX-445) is a next-generation cystic fibrosis transmembrane conductance regulator (CFTR) corrector.This is a compound which is not chiral purity. | |
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| In vitro | The pendrin-dependent increase in cystic fibrosis transmembrane conductance regulator (CFTR) current is additive with the CFTR modulator elexacaftor. |
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| Uncovering Cystic Fibrosis Carrier: Insights From a Heterozygous CFTR-F508del Rabbit Model [ Int Forum Allergy Rhinol, 2026, 10.1002/alr.70128] | PubMed: 41758072 |
| Identification of small molecules that enhance aminoglycoside-mediated suppression of CFTR and NF1 nonsense mutations [ Mol Ther Oncol, 2026, 34(2):201173] | PubMed: 41939791 |
| Altered functional interactions between CFTR disease mutants ΔF508 and G551D and the protein kinase A catalytic subunit [ J Physiol, 2026, 604(8):3344-3362] | PubMed: 41920076 |
| Investigation of HE4 expression concerning epithelial-mesenchymal transition (EMT) in cystic fibrosis epithelial cells [ J Cyst Fibros, 2026, S1569-1993(26)00086-X] | PubMed: 41936498 |
| CFTR rescue in W1282X cystic fibrosis patient-derived intestinal organoids (PDIOs) mediated by translational readthrough-inducing drugs (TRIDs) [ Genet Med Open, 2026, 4:103472] | PubMed: 41492359 |
| ACE-tRNAs are a platform technology for suppressing nonsense mutations that cause cystic fibrosis [ Nucleic Acids Res, 2025, 53(13)gkaf675] | PubMed: 40650978 |
| Antisense oligonucleotide targeting the E3 ligase RFFL potentiates CFTR modulator efficacy in CF primary bronchial epithelial cells [ Mol Ther Nucleic Acids, 2025, 36(4):102756] | PubMed: 41323797 |
| Transcriptomic and functional responses of the cystic fibrosis airway epithelium to CFTR modulator therapy [ JCI Insight, 2025, 10(21)e196018] | PubMed: 41212059 |
| Endometrium-derived organoids from cystic fibrosis patients and mice as new models to study disease-associated endometrial pathobiology [ Cell Mol Life Sci, 2025, 82(1):109] | PubMed: 40074868 |
| CFTR negatively reprograms Th2 cell responses, and CFTR potentiation restrains allergic airway inflammation [ JCI Insight, 2025, 10(9)e191098] | PubMed: 40131363 |
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