Literature DB >> 34299555

Oxazolidinone Antibiotics: Chemical, Biological and Analytical Aspects.

Claudia Foti1, Anna Piperno1, Angela Scala1, Ottavia Giuffrè1.   

Abstract

This review covers the main aspects concerning the chemistry, the biological activity and the analytical determination of oxazolidinones, the only new class of synthetic antibiotics advanced in clinical use over the past 50 years. They are characterized by a chemical structure including the oxazolidone ring with the S configuration of substituent at C5, the acylaminomethyl group linked to C5 and the N-aryl substituent. The synthesis of oxazolidinones has gained increasing interest due to their unique mechanism of action that assures high antibiotic efficiency and low susceptibility to resistance mechanisms. Here, the main features of oxazolidinone antibiotics licensed or under development, such as Linezolid, Sutezolid, Eperezolid, Radezolid, Contezolid, Posizolid, Tedizolid, Delpazolid and TBI-223, are discussed. As they are protein synthesis inhibitors active against a wide spectrum of multidrug-resistant Gram-positive bacteria, their biological activity is carefully analyzed, together with the drug delivery systems recently developed to overcome the poor oxazolidinone water solubility. Finally, the most employed analytical techniques for oxazolidinone determination in different matrices, such as biological fluids, tissues, drugs and natural waters, are reviewed. Most are based on HPLC (High Performance Liquid Chromatography) coupled with UV-Vis or mass spectrometer detectors, but, to a lesser extent are also based on spectrofluorimetry or voltammetry.

Entities:  

Keywords:  Linezolid; TBI-233; analytical determination; antibiotic resistance; oxazolidinone antibiotics

Year:  2021        PMID: 34299555     DOI: 10.3390/molecules26144280

Source DB:  PubMed          Journal:  Molecules        ISSN: 1420-3049            Impact factor:   4.411


  4 in total

1.  The asymmetric Henry reaction as synthetic tool for the preparation of the drugs linezolid and rivaroxaban.

Authors:  Martin Vrbický; Karel Macek; Jaroslav Pochobradský; Jan Svoboda; Miloš Sedlák; Pavel Drabina
Journal:  Beilstein J Org Chem       Date:  2022-04-14       Impact factor: 2.544

Review 2.  Synthesis of Thiomorpholine via a Telescoped Photochemical Thiol-Ene/Cyclization Sequence in Continuous Flow.

Authors:  Alexander Steiner; Ryan C Nelson; Doris Dallinger; C Oliver Kappe
Journal:  Org Process Res Dev       Date:  2022-08-04       Impact factor: 3.858

Review 3.  Strategies to Improve the Potency of Oxazolidinones towards Bacterial Biofilms.

Authors:  Audrey R N Ndukwe; Sandra Wiedbrauk; Nathan R B Boase; Kathryn E Fairfull-Smith
Journal:  Chem Asian J       Date:  2022-04-13

Review 4.  Overcoming Mycobacterium tuberculosis through small molecule inhibitors to break down cell wall synthesis.

Authors:  Wenbin Kuang; Haolin Zhang; Xiao Wang; Peng Yang
Journal:  Acta Pharm Sin B       Date:  2022-04-27       Impact factor: 14.903

  4 in total

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