An Original Strategy for Gln Containing Peptide Synthesis Using SPPS and Glu(OH)-1-OAll
Author:
Publisher
Springer Science and Business Media LLC
Subject
Drug Discovery,Molecular Medicine,Biochemistry,Bioengineering,Analytical Chemistry
Link
http://link.springer.com/content/pdf/10.1007/s10989-010-9213-0.pdf
Reference18 articles.
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3. Dragovich PS, Prins TJ (2003) Structure-based design, synthesis, and biological evaluation of irreversible human rhinovirus 3C protease inhibitor 8. Pharmacological optimization of orally bioavailable 2-pyridone-containing peptidomimetics. J Med Chem 46:4572–4585
4. Dragovich PS, Webber SE, Babine RE et al (1998a) Structure-based design, synthesis, and biological evaluation of irreversible human rhinovirus 3C protease inhibitors. 1. Michael acceptor structure-activity studies. J Med Chem 41:2806–2818
5. Dragovich PS, Webber SE, Babine RE et al (1998b) Structure-based design, synthesis, and biological evaluation of irreversible human rhinovirus 3C protease inhibitors. 2. Peptide structure-activity studies. J Med Chem 41:2819–2834
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