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ACS Med Chem Lett ; 2(2): 142-7, 2011 Feb 10.
Artículo en Inglés | MEDLINE | ID: mdl-24900293

RESUMEN

The discovery of potent and selective cyanamide-based inhibitors of the cysteine protease cathepsin C is detailed. Optimization of the template with regard to plasma stability led to the identification of compound 17, a potent cathepsin C inhibitor with excellent selectivity over other cathepsins and potent in vivo activity in a cigarette smoke mouse model.

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