Literature DB >> 21282057

Targeting bacterial biofilms: design of a terpenoid-like library as non-toxic anti-biofilm compounds.

Cheikh Sall1, Linda Dombrowsky, Olivier Bottzeck, Annie Praud-Tabariès, Yves Blache.   

Abstract

A new class of anti-biofilm compounds possessing 1,4-disubstituted-(1H)-1,2,3-triazolic cores was designed. Their efficient synthesis was performed by means of click chemistry through 1,3-dipolar cycloadditions. Two compounds were found to act as specific anti-biofilm agents against a gram negative species.
Copyright © 2011 Elsevier Ltd. All rights reserved.

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Year:  2011        PMID: 21282057     DOI: 10.1016/j.bmcl.2010.12.134

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


  3 in total

1.  Preparation of azidoaryl- and azidoalkyloxazoles for click chemistry.

Authors:  Catherine M Loner; Frederick A Luzzio; Donald R Demuth
Journal:  Tetrahedron Lett       Date:  2012-10-17       Impact factor: 2.415

2.  Antitrypanosomal and antileishmanial activity of prenyl-1,2,3-triazoles.

Authors:  Exequiel O J Porta; Sebastián N Jäger; Isabel Nocito; Galina I Lepesheva; Esteban C Serra; Babu L Tekwani; Guillermo R Labadie
Journal:  Medchemcomm       Date:  2017-03-10       Impact factor: 3.597

3.  Leveraging phytochemicals: the plant phylogeny predicts sources of novel antibacterial compounds.

Authors:  Malini A Prasad; Christine P Zolnik; Jeanmaire Molina
Journal:  Future Sci OA       Date:  2019-07-25
  3 in total

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