Abstract
Quinolinone-3-carboxamide 1, a novel CFTR potentiator, was discovered using high-throughput screening in NIH-3T3 cells expressing the F508del-CFTR mutation. Extensive medicinal chemistry and iterative structure-activity relationship (SAR) studies to evaluate potency, selectivity, and pharmacokinetic properties resulted in the identification of N-(2,4-di-tert-butyl-5-hydroxyphenyl)-4-oxo-1,4-dihydroquinoline-3-carboxamide (VX-770, 48, ivacaftor), an investigational drug candidate approved by the FDA for the treatment of CF patients 6 years of age and older carrying the G551D mutation.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Aminophenols / chemical synthesis*
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Aminophenols / pharmacokinetics
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Aminophenols / pharmacology
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Animals
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Child
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Cystic Fibrosis / drug therapy*
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Cystic Fibrosis Transmembrane Conductance Regulator / genetics*
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Cystic Fibrosis Transmembrane Conductance Regulator / metabolism*
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Dogs
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Humans
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Macaca fascicularis
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Male
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Mice
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NIH 3T3 Cells
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Quinolones / chemical synthesis*
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Quinolones / pharmacokinetics
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Quinolones / pharmacology
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Rats, Sprague-Dawley
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Structure-Activity Relationship
Substances
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Aminophenols
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Quinolones
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Cystic Fibrosis Transmembrane Conductance Regulator
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ivacaftor