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Discovery of Glycine Hydrazide Pore-occluding CFTR Inhibitors: Mechanism, Structure–Activity Analysis, and In Vivo Efficacy
The cystic fibrosis transmembrane conductance regulator (CFTR) protein is a cAMP-regulated epithelial Cl(−) channel that, when defective, causes cystic fibrosis. Screening of a collection of 100,000 diverse small molecules revealed four novel chemical classes of CFTR inhibitors with K(i) < 10 μM,...
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| Main Authors: | , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
The Rockefeller University Press
2004
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| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2229623/ https://ncbi.nlm.nih.gov/pubmed/15277574 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1085/jgp.200409059 |
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