Studies of the Synthesis of All Stereoisomers of MG-132 Proteasome Inhibitors in the Tumor Targeting Approach-Reference-Cited by-同舟云学术

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Studies of the Synthesis of All Stereoisomers of MG-132 Proteasome Inhibitors in the Tumor Targeting Approach

Published:2010-01-29 Issue:4 Volume:53 Page:1509-1518
ISSN:0022-2623
Container-title:Journal of Medicinal Chemistry
language:en
Short-container-title:J. Med. Chem.

Author:

Mroczkiewicz Michał¹,Winkler Katarzyna¹²,Nowis Dominika³,Placha Grzegorz⁴,Golab Jakub³,Ostaszewski Ryszard²

Affiliation:

1. Faculty of Chemistry, Warsaw University of Technology, Noakowskiego 3, 00-664 Warsaw, Poland

2. Institute of Organic Chemistry, Polish Academy of Sciences, Kasprzaka 44/52, 01-224 Warsaw, Poland

3. Department of Immunology, Center of Biostructure Research, Medical University of Warsaw, Banacha 1A, 02-097 Warsaw, Poland

4. Department of Internal Diseases, Hypertension, and Vascular Disease, Medical University of Warsaw, Banacha 1A, 02-097 Warsaw, Poland

Publisher

American Chemical Society (ACS)

Subject

Drug Discovery,Molecular Medicine

Link

https://pubs.acs.org/doi/pdf/10.1021/jm901619n

Reference40 articles.

1. Design of novel tripeptides with macrophage migration-enhancing activity

2. Solid-phase synthesis of irreversible human rhinovirus 3C protease inhibitors. Part 1: Optimization of tripeptides incorporating N-terminal amides

3. Glutathione-like tripeptides as inhibitors of glutathionylspermidine synthetase. Part 2: Substitution of the glycine part

4. Peptide inhibitors of IKB protease: Modification of the C-termini of Z-LLF-CHO

5. Tripeptide Aldehyde Inhibitors of Human Rhinovirus 3C Protease: Design, Synthesis, Biological Evaluation, and Cocrystal Structure Solution of P1 Glutamine Isosteric Replacements

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