Literature DB >> 28504895

Progress toward inhibitors of metallo-β-lactamases.

Ross P McGeary1, Daniel Tc Tan1, Gerhard Schenk1.   

Abstract

The global overuse of antibiotics has led to the emergence of drug-resistant pathogenic bacteria. Bacteria can combat β-lactams by expressing β-lactamases. Inhibitors of one class of β-lactamase, the serine-β-lactamases, are used clinically to prevent degradation of β-lactam antibiotics. However, a second class of β-lactamase, the metallo-β-lactamases (MBLs), function by a different mechanism to serine-β-lactamases and no inhibitors of MBLs have progressed to be used in the clinic. Bacteria that express MBLs are an increasingly important threat to human health. This review outlines various approaches taken to discover MBL inhibitors, with an emphasis on the different chemical classes of inhibitors. Recent progress, particularly new screening methods and the rational design of potent MBL inhibitors are discussed.

Entities:  

Keywords:  antibiotics; bacterial resistance; metalloenzymes

Mesh:

Substances:

Year:  2017        PMID: 28504895     DOI: 10.4155/fmc-2017-0007

Source DB:  PubMed          Journal:  Future Med Chem        ISSN: 1756-8919            Impact factor:   3.808


  12 in total

1.  1,4,7-Triazacyclononane Restores the Activity of β-Lactam Antibiotics against Metallo-β-Lactamase-Producing Enterobacteriaceae: Exploration of Potential Metallo-β-Lactamase Inhibitors.

Authors:  Anou M Somboro; Daniel G Amoako; John Osei Sekyere; Hezekiel M Kumalo; René Khan; Linda A Bester; Sabiha Y Essack
Journal:  Appl Environ Microbiol       Date:  2019-01-23       Impact factor: 4.792

Review 2.  The Continuing Challenge of Metallo-β-Lactamase Inhibition: Mechanism Matters.

Authors:  Lin-Cheng Ju; Zishuo Cheng; Walter Fast; Robert A Bonomo; Michael W Crowder
Journal:  Trends Pharmacol Sci       Date:  2018-04-18       Impact factor: 14.819

3.  Synthesis and biological evaluation of zinc chelating compounds as metallo-β-lactamase inhibitors.

Authors:  Geir Kildahl-Andersen; Christian Schnaars; Anthony Prandina; Sylvie Radix; Marc Le Borgne; Lars Petter Jordheim; Tor Gjøen; Adriana Magalhães Santos Andresen; Silje Lauksund; Christopher Fröhlich; Ørjan Samuelsen; Pål Rongved; Ove Alexander Høgmoen Åstrand
Journal:  Medchemcomm       Date:  2019-03-08       Impact factor: 3.597

Review 4.  β-lactam/β-lactamase inhibitor combinations: an update.

Authors:  Kamaleddin H M E Tehrani; Nathaniel I Martin
Journal:  Medchemcomm       Date:  2018-08-17       Impact factor: 3.597

Review 5.  Diversity and Proliferation of Metallo-β-Lactamases: a Clarion Call for Clinically Effective Metallo-β-Lactamase Inhibitors.

Authors:  Anou M Somboro; John Osei Sekyere; Daniel G Amoako; Sabiha Y Essack; Linda A Bester
Journal:  Appl Environ Microbiol       Date:  2018-08-31       Impact factor: 4.792

6.  Kinetic and Structural Characterization of the First B3 Metallo-β-Lactamase with an Active-Site Glutamic Acid.

Authors:  Liam A Wilson; Esmée G Knaven; Marc T Morris; Marcelo Monteiro Pedroso; Christopher J Schofield; Thomas B Brück; Mikael Boden; David W Waite; Philip Hugenholtz; Luke Guddat; Gerhard Schenk
Journal:  Antimicrob Agents Chemother       Date:  2021-07-26       Impact factor: 5.191

7.  Thiol-Containing Metallo-β-Lactamase Inhibitors Resensitize Resistant Gram-Negative Bacteria to Meropenem.

Authors:  Kamaleddin Haj Mohammad Ebrahim Tehrani; Nathaniel I Martin
Journal:  ACS Infect Dis       Date:  2017-08-28       Impact factor: 5.084

8.  Small Molecule Carboxylates Inhibit Metallo-β-lactamases and Resensitize Carbapenem-Resistant Bacteria to Meropenem.

Authors:  Kamaleddin H M E Tehrani; Nora C Brüchle; Nicola Wade; Vida Mashayekhi; Diego Pesce; Matthijs J van Haren; Nathaniel I Martin
Journal:  ACS Infect Dis       Date:  2020-04-03       Impact factor: 5.084

9.  Broad spectrum antibiotic-degrading metallo-β-lactamases are phylogenetically diverse.

Authors:  Marcelo Monteiro Pedroso; David W Waite; Okke Melse; Liam Wilson; Nataša Mitić; Ross P McGeary; Iris Antes; Luke W Guddat; Philip Hugenholtz; Gerhard Schenk
Journal:  Protein Cell       Date:  2020-08       Impact factor: 14.870

10.  Differential active site requirements for NDM-1 β-lactamase hydrolysis of carbapenem versus penicillin and cephalosporin antibiotics.

Authors:  Zhizeng Sun; Liya Hu; Banumathi Sankaran; B V Venkataram Prasad; Timothy Palzkill
Journal:  Nat Commun       Date:  2018-10-30       Impact factor: 14.919

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