Synthesis and evaluation of arylaminoethyl amides as noncovalent inhibitors of cathepsin S. Part 3: Heterocyclic P3-Reference-Cited by-同舟云学术

Synthesis and evaluation of arylaminoethyl amides as noncovalent inhibitors of cathepsin S. Part 3: Heterocyclic P3

Published:2006-04 Issue:7 Volume:16 Page:1975-1980
ISSN:0960-894X
Container-title:Bioorganic & Medicinal Chemistry Letters
language:en
Short-container-title:Bioorganic & Medicinal Chemistry Letters

Author:

Tully David C.,Liu Hong,Alper Phil B.,Chatterjee Arnab K.,Epple Robert,Roberts Michael J.,Williams Jennifer A.,Nguyen KhanhLinh T.,Woodmansee David H.,Tumanut Christine,Li Jun,Spraggon Glen,Chang Jonathan,Tuntland Tove,Harris Jennifer L.,Karanewsky Donald S.

Publisher

Elsevier BV

Subject

Organic Chemistry,Clinical Biochemistry,Drug Discovery,Pharmaceutical Science,Molecular Biology,Molecular Medicine,Biochemistry

Reference17 articles.

1. Cathepsin S inhibitors

2. Impaired Invariant Chain Degradation and Antigen Presentation and Diminished Collagen-Induced Arthritis in Cathepsin S Null Mice

3. Cathepsin S Is Required for Murine Autoimmune Myasthenia Gravis Pathogenesis

4. Cysteine protease cathepsin S as a key step in antigen presentation

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