Discovery of a new class of potent prolylcarboxypeptidase inhibitors derived from alanine.

Bioorganic & Medicinal Chemistry Letters(2012)

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摘要
Efforts to modify the central proline portion of lead compound 4 lead to the discovery of novel prolylcarboxypeptidase (PrCP) inhibitors. Especially, replacement with alanine afforded compound 19 displaying more potent human and mouse PrCP inhibitory activity than 4 and an overall comparable profile.
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关键词
Prolylcarboxypeptidase (PrCP),Obesity,Inhibitor
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