Potent and Highly Selective Inhibitors of the Proteasome Trypsin-like Site by Incorporation of Basic Side Chain Containing Amino Acid Derived Sulfonyl Fluorides-Reference-Cited by-同舟云学术

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Potent and Highly Selective Inhibitors of the Proteasome Trypsin-like Site by Incorporation of Basic Side Chain Containing Amino Acid Derived Sulfonyl Fluorides

Published:2018-05-21 Issue:12 Volume:61 Page:5395-5411
ISSN:0022-2623
Container-title:Journal of Medicinal Chemistry
language:en
Short-container-title:J. Med. Chem.

Author:

Artschwager Raik¹,Ward David J.¹,Gannon Susan¹,Brouwer Arwin J.²,van de Langemheen Helmus¹,Kowalski Hubert¹,Liskamp Rob M. J.¹²^ORCID

Affiliation:

1. School of Chemistry, University of Glasgow, Joseph Black Building, University Avenue, Glasgow G12 8QQ, United Kingdom

2. Chemical Biology and Drug Discovery, Department of Pharmaceutical Sciences, Faculty of Science, Utrecht University, P.O. Box 80082, NL-3508 TB Utrecht, The Netherlands

Funder

University of Glasgow

Publisher

American Chemical Society (ACS)

Subject

Drug Discovery,Molecular Medicine

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.jmedchem.8b00685

Reference26 articles.

1. The predator becomes the prey: regulating the ubiquitin system by ubiquitylation and degradation

2. Immunoproteasomes

3. Proteasomes in immune cells: more than peptide producers?

4. Structure- and function-based design of Plasmodium-selective proteasome inhibitors

5. COVALENT DRUGS FORM LONG-LIVED TIES

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