Literature DB >> 8894108

Quiescent affinity inactivators of protein tyrosine phosphatases.

W P Taylor1, Z Y Zhang, T S Widlanski.   

Abstract

alpha-Halobenzylphosphonates were investigated as possible inactivators of protein tyrosine phosphatases (PTPases). These compounds inactivate the Yersinia PTPase (Yop51*delta 162) in a time- and concentration-dependent fashion. This inactivation is active-site directed and irreversible, and is surprisingly rapid in light of the stability of the alpha-halobenzylphosphonates toward nucleophiles in solution. The potential of these molecules for probing the stereochemistry of PTPase inactivation, as well as for providing a useful paradigm for the design of more potent PTPase inhibitors is discussed.

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Year:  1996        PMID: 8894108     DOI: 10.1016/0968-0896(96)00144-7

Source DB:  PubMed          Journal:  Bioorg Med Chem        ISSN: 0968-0896            Impact factor:   3.641


  5 in total

1.  Activity-based probes for protein tyrosine phosphatases.

Authors:  Sanjai Kumar; Bo Zhou; Fubo Liang; Wei-Qing Wang; Zhonghui Huang; Zhong-Yin Zhang
Journal:  Proc Natl Acad Sci U S A       Date:  2004-05-17       Impact factor: 11.205

Review 2.  Covalent inhibition of protein tyrosine phosphatases.

Authors:  Kasi Viswanatharaju Ruddraraju; Zhong-Yin Zhang
Journal:  Mol Biosyst       Date:  2017-06-27

3.  Activity-based protein profiling of protein tyrosine phosphatases.

Authors:  Chad Walls; Bo Zhou; Zhong-Yin Zhang
Journal:  Methods Mol Biol       Date:  2009

4.  Asymmetric epoxidation of fluoroolefins by chiral dioxirane. Fluorine effect on enantioselectivity.

Authors:  O Andrea Wong; Yian Shi
Journal:  J Org Chem       Date:  2009-11-06       Impact factor: 4.354

Review 5.  Synthesis and Reactions of α-Hydroxyphosphonates.

Authors:  Zita Rádai; György Keglevich
Journal:  Molecules       Date:  2018-06-20       Impact factor: 4.411

  5 in total

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