Literature DB >> 6552188

Aminoalkylphosphonofluoridate derivatives: rapid and potentially selective inactivators of serine peptidases.

L A Lamden, P A Bartlett.   

Abstract

Phosphonic acid analogs of N-Cbz-alanine and N-Cbz-phenylalanine have been converted to the ester and amide fluoridates and evaluated as inactivators of elastase (EC 3.4.21.11) and chymotrypsin (EC 3.4.21.1). These inhibitors, which mimic the natural peptide substrates, are the most potent inactivators of elastase and chymotrypsin yet reported, showing a modest selectivity which correlates with the substrate specificity of the two enzymes.

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Year:  1983        PMID: 6552188     DOI: 10.1016/0006-291x(83)91729-1

Source DB:  PubMed          Journal:  Biochem Biophys Res Commun        ISSN: 0006-291X            Impact factor:   3.575


  4 in total

1.  Late-Stage Conversion of Diphenylphosphonate to Fluorophosphonate Probes for the Investigation of Serine Hydrolases.

Authors:  Felipe B d'Andrea; Craig A Townsend
Journal:  Cell Chem Biol       Date:  2019-04-11       Impact factor: 8.116

2.  Exploration of fluorine chemistry at the multidisciplinary interface of chemistry and biology.

Authors:  Iwao Ojima
Journal:  J Org Chem       Date:  2013-05-06       Impact factor: 4.354

3.  Chemical reactivity at an antibody binding site elicited by mechanistic design of a synthetic antigen.

Authors:  A Tramontano; K D Janda; R A Lerner
Journal:  Proc Natl Acad Sci U S A       Date:  1986-09       Impact factor: 11.205

Review 4.  ClpP Protease, a Promising Antimicrobial Target.

Authors:  Carlos Moreno-Cinos; Kenneth Goossens; Irene G Salado; Pieter Van Der Veken; Hans De Winter; Koen Augustyns
Journal:  Int J Mol Sci       Date:  2019-05-07       Impact factor: 5.923

  4 in total

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