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These three compounds also exhibited more potent or comparable inhibitory activities to that of 1 toward cathepsins L and K, demonstrating that these act as pan-cathepsin inhibitors rather than selective inhibitors (Supplementary Fig

By Emily Rodriguez, RDN, CSSD|Source reviewed by FormBlends Medical Team|| Source Reviewed Written by Emily Rodriguez, RDN, CSSD Checked against primary sources by FormBlends Medical Team In This Article This article is part of our Peptide Therapy collection

The Lancet Global Health 2014;2:323-33