Literature DB >> 25278235

Oxo- and thiooxo-imidazo[1,5-c]pyrimidine molecule library: beyond their interest in inhibition of Brucella suis histidinol dehydrogenase, a powerful protection tool in the synthesis of histidine analogues.

François Turtaut1, Marie Lopez1, Safia Ouahrani-Bettache2, Stephan Köhler2, Jean-Yves Winum3.   

Abstract

Histidinol dehydrogenase (HDH) has been established as a virulence factor for the human pathogen bacterium Brucella suis. Targeting such a virulence factor is a relevant anti-infectious approach as it could decrease the frequency of antibiotic resistance appearance. In this paper, we describe the synthesis of a family of oxo- and thioxo-imidazo[1,5-c]pyrimidines, potential enzyme inhibitors. Beyond their anti-HDH activity, the synthesis approach of these molecules, never described before, is highly original and these oxo- and thioxo- derivatives can improve dramatically the efficiency of the histidine protection pathway for the synthesis of histidine analogues.
Copyright © 2014 Elsevier Ltd. All rights reserved.

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Keywords:  Anti-infectious agents; Brucella suis; Enzyme inhibitors; Histidinol dehydrogenase; Oxo-imidazopyrimidines

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Year:  2014        PMID: 25278235     DOI: 10.1016/j.bmcl.2014.09.020

Source DB:  PubMed          Journal:  Bioorg Med Chem Lett        ISSN: 0960-894X            Impact factor:   2.823


  1 in total

1.  A novel synthetic approach to hydroimidazo[1,5-b]pyridazines by the recyclization of itaconimides and HPLC-HRMS monitoring of the reaction pathway.

Authors:  Dmitry Yu Vandyshev; Khidmet S Shikhaliev; Andrey Yu Potapov; Michael Yu Krysin; Fedor I Zubkov; Lyudmila V Sapronova
Journal:  Beilstein J Org Chem       Date:  2017-11-30       Impact factor: 2.883

  1 in total

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