Abstract
Drug transporters mediate the uptake and elimination of drugs in various organs; therefore, having knowledge of how a transporter functions in the body would play a key role in ensuring drug efficacy in in vivo systems. In this context, we designed and synthesized [(11)C]dehydropravastatin, a novel PET probe that would be potentially useful for evaluation of the functions of the OATP1B1 and MRP2 transporters, based on the use of palladium(0)-mediated rapid C-[(11)C]methylation (viz., the rapid cross-coupling between [(11)C]methyl iodide and a boron intermediate).
Copyright © 2012 Elsevier Ltd. All rights reserved.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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ATP-Binding Cassette Transporters / analysis*
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ATP-Binding Cassette Transporters / metabolism
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Animals
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Liver / chemistry*
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Liver / metabolism
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Liver-Specific Organic Anion Transporter 1
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Male
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Organic Anion Transporters / analysis*
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Organic Anion Transporters / metabolism
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Positron-Emission Tomography*
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Pravastatin / analogs & derivatives*
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Pravastatin / chemical synthesis
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Pravastatin / chemistry
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Radiopharmaceuticals / chemical synthesis*
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Radiopharmaceuticals / chemistry
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Rats
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Rats, Sprague-Dawley
Substances
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((11)C)dehydropravastatin
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ATP-Binding Cassette Transporters
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Abcc2 protein, rat
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Liver-Specific Organic Anion Transporter 1
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Organic Anion Transporters
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Radiopharmaceuticals
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SLCO1B1 protein, human
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Pravastatin