Abstract
The design of drugs with selective tissue distribution can be an effective strategy for enhancing efficacy and safety, but understanding the translation of preclinical tissue distribution data to the clinic remains an important challenge. As part of a discovery program to identify next generation liver selective HMG-CoA reductase inhibitors we report the identification of (3R,5R)-7-(4-((3-fluorobenzyl)carbamoyl)-5-cyclopropyl-2-(4-fluorophenyl)-1H-imidazol-1-yl)-3,5-dihydroxyheptanoic acid (26) as a candidate for treating hypercholesterlemia. Clinical evaluation of 26 (PF-03491165), as well as the previously reported 2 (PF-03052334), provided an opportunity for a case study comparison of the preclinical and clinical pharmacokinetics as well as pharmacodynamics of tissue targeted HMG-CoA reductase inhibitors.
Copyright © 2010 Elsevier Ltd. All rights reserved.
MeSH terms
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Animals
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Cells, Cultured
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Dogs
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Dose-Response Relationship, Drug
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Drug Discovery*
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Hepatocytes / drug effects
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Heptanoic Acids / chemical synthesis*
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Heptanoic Acids / chemistry
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Heptanoic Acids / pharmacokinetics
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Heptanoic Acids / pharmacology
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Humans
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Hydroxymethylglutaryl-CoA Reductase Inhibitors / chemical synthesis*
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Hydroxymethylglutaryl-CoA Reductase Inhibitors / pharmacokinetics
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Hydroxymethylglutaryl-CoA Reductase Inhibitors / therapeutic use
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Hypercholesterolemia / drug therapy*
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Imidazoles / chemical synthesis*
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Imidazoles / chemistry
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Imidazoles / pharmacokinetics
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Imidazoles / pharmacology
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Inhibitory Concentration 50
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Liver / drug effects*
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Molecular Structure
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Pyrazoles / chemical synthesis
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Pyrazoles / chemistry
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Pyrazoles / pharmacokinetics
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Pyrazoles / pharmacology
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Rats
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Tissue Distribution
Substances
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7-(2-(4-fluorophenyl)-4-isopropyl-5-(4-methylbenzylcarbamoyl)-2H-pyrazol-3-yl)-3,5-dihydroxyheptanoic acid
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7-(4-((3-fluorobenzyl)carbamoyl)-5-cyclopropyl-2-(4-fluorophenyl)-1H-imidazol-1-yl)-3,5-dihydroxyheptanoic acid
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Heptanoic Acids
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Hydroxymethylglutaryl-CoA Reductase Inhibitors
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Imidazoles
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Pyrazoles