Allosteric Noncompetitive Small Molecule Selective Inhibitors of CD45 Tyrosine Phosphatase Suppress T-Cell Receptor Signals and Inflammation In Vivo-Reference-Cited by-同舟云学术

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Allosteric Noncompetitive Small Molecule Selective Inhibitors of CD45 Tyrosine Phosphatase Suppress T-Cell Receptor Signals and Inflammation In Vivo

Published:2014-01-28 Issue:4 Volume:85 Page:553-563
ISSN:0026-895X
Container-title:Molecular Pharmacology
language:en
Short-container-title:Mol Pharmacol

Author:

Perron Michael D.,Chowdhury Shafinaz,Aubry Isabelle,Purisima Enrico,Tremblay Michel L.,Saragovi H. Uri

Publisher

American Society for Pharmacology & Experimental Therapeutics (ASPET)

Subject

Pharmacology,Molecular Medicine

Reference41 articles.

1. The CD45 tyrosine phosphatase: a positive and negative regulator of immune cell function

2. The Src homology 2 domain of the protein-tyrosine kinase p56lck mediates both intermolecular and intramolecular interactions.

3. Delayed-type hypersensitivity: activation of mast cells by antigen-specific T-cell factors initiates the cascade of cellular interactions

4. Nitroarylhydroxymethylphosphonic acids as inhibitors of CD45

5. Molecular surface generation using a variable-radius solvent probe

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2. A novel binding pocket in the D2 domain of protein tyrosine phosphatase mu (PTPmu) guides AI screen to identify small molecules that modulate tumour cell adhesion, growth and migration;Journal of Cellular and Molecular Medicine;2023-10-20

3. Shikonin and Juglone Inhibit Mycobacterium tuberculosis Low-Molecular-Weight Protein Tyrosine Phosphatase a (Mt-PTPa);BioTech;2023-09-20

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