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Design and synthesis of diaminopyrrolidinone inhibitors of human osteoclast cathepsin K.
Authors:K J Duffy  L H Ridgers  R L DesJarlais  T A Tomaszek  M J Bossard  S K Thompson  R M Keenan  D F Veber
Institution:Department of Medicinal Chemistry, SmithKline Beecham Pharmaceuticals, Collegeville, PA 19246, USA.
Abstract:The structure-based design and synthesis of lactam-constrained azapeptide inhibitors of human cathepsin K are described. Enhanced stability to proteolytic cleavage over acyclic analogues is discussed.
Keywords:
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