Abstract
Synthesis and SAR are described for a structurally distinct class of DPP-IV inhibitors based on aminobenzo[a]quinolizines bearing (hetero-)aromatic substituents in the S1 specificity pocket. The m-(fluoromethyl)-phenyl derivative (S,S,S)-2g possesses the best fit in the S1 pocket. However, (S,S,S)-2i, bearing a more hydrophilic 5-methyl-pyridin-2-yl residue as substituent for the S1 pocket, displays excellent in vivo activity and superior drug-like properties.
Copyright (c) 2009 Elsevier Ltd. All rights reserved.
MeSH terms
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Animals
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Crystallography, X-Ray
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Dipeptidyl Peptidase 4 / metabolism
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Dipeptidyl-Peptidase IV Inhibitors* / chemistry*
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Dipeptidyl-Peptidase IV Inhibitors* / metabolism
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Dipeptidyl-Peptidase IV Inhibitors* / pharmacology
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Humans
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Protease Inhibitors / chemistry
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Protease Inhibitors / metabolism
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Protease Inhibitors / pharmacology
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Quinolizines / chemistry*
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Quinolizines / metabolism
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Quinolizines / pharmacology
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Rats
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Rats, Zucker
Substances
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Dipeptidyl-Peptidase IV Inhibitors
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Protease Inhibitors
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Quinolizines
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DPP4 protein, human
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Dipeptidyl Peptidase 4