Abstract
Herein we describe the optimization of a series of PDE4 inhibitors, with special focus on solubility and pharamcokinetics, to clinical compound 2, 4-(8-(3-fluorophenyl)-1,7-naphthyridin-6-yl)transcyclohexanecarboxylic acid. Although compound 2 produces emesis in humans when given as a single dose, its exemplary pharmacokinetic properties enabled a novel dosing regime comprising multiple escalating doses and the resultant achievement of high plasma drug levels without associated nausea or emesis.
MeSH terms
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Animals
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Cyclohexanecarboxylic Acids / chemistry*
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Cyclohexanecarboxylic Acids / pharmacokinetics
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Cyclohexanecarboxylic Acids / pharmacology
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Dose-Response Relationship, Drug
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Humans
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Naphthyridines / chemistry*
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Naphthyridines / pharmacokinetics
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Naphthyridines / pharmacology
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Nausea / chemically induced
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Phosphodiesterase 4 Inhibitors / chemistry*
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Phosphodiesterase 4 Inhibitors / pharmacokinetics
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Phosphodiesterase 4 Inhibitors / pharmacology
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Pulmonary Disease, Chronic Obstructive / drug therapy*
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Rats
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Solubility
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Structure-Activity Relationship
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Thermodynamics
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Vomiting / chemically induced
Substances
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4-(8-(3-fluorophenyl)-1,7-naphthyridin-6-yl)cyclohexanecarboxylic acid
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Cyclohexanecarboxylic Acids
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Naphthyridines
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Phosphodiesterase 4 Inhibitors