Design and synthesis of novel 2-pyridone peptidomimetic falcipain 2/3 inhibitors
The structure-based design, chemical synthesis and in vitro activity evaluation of various falcipain inhibitors derived from 2-pyridone are reported. These compounds contain a peptidomimetic binding determinant and a Michael acceptor terminal moiety capable of deactivating the cysteine protease acti...
Main Author: | |
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Other Authors: | , , , , , , |
Format: | article |
Language: | eng |
Published: |
2014
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Subjects: | |
Online Access: | http://hdl.handle.net/10400.1/4221 |
Country: | Portugal |
Oai: | oai:sapientia.ualg.pt:10400.1/4221 |