Abstract
Structures containing the (R)-3-amino-3-methyl piperidine unit as a new pharmacophore moiety have been shown to possess moderate inhibitory activity for DPP-4 with good pharmacokinetics profile. One of these compounds was found to have good oral bioavailability and PK/PD profile in ZF-rat.
Copyright © 2010 Elsevier Ltd. All rights reserved.
MeSH terms
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Animals
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Dipeptidyl Peptidase 4 / chemistry*
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Dipeptidyl Peptidase 4 / metabolism
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Dipeptidyl-Peptidase IV Inhibitors / chemical synthesis
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Dipeptidyl-Peptidase IV Inhibitors / chemistry*
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Dipeptidyl-Peptidase IV Inhibitors / pharmacokinetics
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Drug Evaluation, Preclinical
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Humans
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Microsomes, Liver / metabolism
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Piperidines / chemical synthesis
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Piperidines / chemistry*
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Piperidines / pharmacokinetics
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Pyrimidinones / chemical synthesis
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Pyrimidinones / chemistry*
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Pyrimidinones / pharmacokinetics
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Rats
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Stereoisomerism
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Structure-Activity Relationship
Substances
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(R)-3-amino-3-methylpiperidine
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Dipeptidyl-Peptidase IV Inhibitors
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Piperidines
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Pyrimidinones
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Dipeptidyl Peptidase 4