Literature DB >> 32786279

ANT2681: SAR Studies Leading to the Identification of a Metallo-β-lactamase Inhibitor with Potential for Clinical Use in Combination with Meropenem for the Treatment of Infections Caused by NDM-Producing Enterobacteriaceae.

David T Davies1, Simon Leiris1, Nicolas Sprynski1, Jérôme Castandet1, Clarisse Lozano1, Justine Bousquet1, Magdalena Zalacain1, Srinivas Vasa2, Praveen K Dasari2, Ramesh Pattipati2, Naresh Vempala2, Swetha Gujjewar2, SyamKumar Godi2, Raju Jallala2, Rajashekar Reddy Sathyap2, Narasimha A Darshanoju2, Vengala R Ravu2, Ramakrishna R Juventhala2, Narender Pottabathini2, Somesh Sharma2, Srinivasu Pothukanuri2, Kirsty Holden3, Peter Warn3, Francesca Marcoccia4, Manuela Benvenuti5, Cecilia Pozzi5, Stefano Mangani5, Jean-Denis Docquier4, Marc Lemonnier1, Martin Everett1.   

Abstract

The clinical effectiveness of the important β-lactam class of antibiotics is under threat by the emergence of resistance, mostly due to the production of acquired serine- (SBL) and metallo-β-lactamase (MBL) enzymes. To address this resistance issue, multiple β-lactam/β-lactamase inhibitor combinations have been successfully introduced into the clinic over the past several decades. However, all of those combinations contain SBL inhibitors and, as yet, there are no MBL inhibitors in clinical use. Consequently, there exists an unaddressed yet growing healthcare problem due to the rise in recent years of highly resistant strains which produce New Delhi metallo (NDM)-type metallo-carbapenemases. Previously, we reported the characterization of an advanced MBL inhibitor lead compound, ANT431. Herein, we discuss the completion of a lead optimization campaign culminating in the discovery of the preclinical candidate ANT2681, a potent NDM inhibitor with strong potential for clinical development.

Entities:  

Keywords:  ANT2681; New Delhi metallo-β-lactamase (NDM); antibiotic resistance; carbapenem-resistant Enterobacteriaceae; meropenem; metallo-β-lactamase inhibitor

Mesh:

Substances:

Year:  2020        PMID: 32786279     DOI: 10.1021/acsinfecdis.0c00207

Source DB:  PubMed          Journal:  ACS Infect Dis        ISSN: 2373-8227            Impact factor:   5.084


  10 in total

1.  Compound Uptake into E. coli Can Be Facilitated by N-Alkyl Guanidiniums and Pyridiniums.

Authors:  Sarah J Perlmutter; Emily J Geddes; Bryon S Drown; Stephen E Motika; Myung Ryul Lee; Paul J Hergenrother
Journal:  ACS Infect Dis       Date:  2020-11-23       Impact factor: 5.084

2.  Imitation of β-lactam binding enables broad-spectrum metallo-β-lactamase inhibitors.

Authors:  Jürgen Brem; Tharindi Panduwawala; Jon Ulf Hansen; Joanne Hewitt; Edgars Liepins; Pawel Donets; Laura Espina; Alistair J M Farley; Kirill Shubin; Gonzalo Gomez Campillos; Paula Kiuru; Shifali Shishodia; Daniel Krahn; Robert K Leśniak; Juliane Schmidt Adrian; Karina Calvopiña; María-Carmen Turrientes; Madeline E Kavanagh; Dmitrijs Lubriks; Philip Hinchliffe; Gareth W Langley; Ali F Aboklaish; Anders Eneroth; Maria Backlund; Andrei G Baran; Elisabet I Nielsen; Michael Speake; Janis Kuka; John Robinson; Solveiga Grinberga; Lindsay Robinson; Michael A McDonough; Anna M Rydzik; Thomas M Leissing; Juan Carlos Jimenez-Castellanos; Matthew B Avison; Solange Da Silva Pinto; Andrew D Pannifer; Marina Martjuga; Emma Widlake; Martins Priede; Iva Hopkins Navratilova; Marek Gniadkowski; Anna Karin Belfrage; Peter Brandt; Jari Yli-Kauhaluoma; Eric Bacque; Malcolm G P Page; Fredrik Björkling; Jonathan M Tyrrell; James Spencer; Pauline A Lang; Pawel Baranczewski; Rafael Cantón; Stuart P McElroy; Philip S Jones; Fernando Baquero; Edgars Suna; Angus Morrison; Timothy R Walsh; Christopher J Schofield
Journal:  Nat Chem       Date:  2021-12-13       Impact factor: 24.427

Review 3.  Recent Developments to Cope the Antibacterial Resistance via β-Lactamase Inhibition.

Authors:  Zafar Iqbal; Jian Sun; Haikang Yang; Jingwen Ji; Lili He; Lijuan Zhai; Jinbo Ji; Pengjuan Zhou; Dong Tang; Yangxiu Mu; Lin Wang; Zhixiang Yang
Journal:  Molecules       Date:  2022-06-14       Impact factor: 4.927

Review 4.  β-Lactam Antibiotics and β-Lactamase Enzymes Inhibitors, Part 2: Our Limited Resources.

Authors:  Silvana Alfei; Anna Maria Schito
Journal:  Pharmaceuticals (Basel)       Date:  2022-04-13

5.  Structural Basis of Metallo-β-lactamase Inhibition by N-Sulfamoylpyrrole-2-carboxylates.

Authors:  Alistair J M Farley; Yuri Ermolovich; Karina Calvopiña; Patrick Rabe; Tharindi Panduwawala; Jürgen Brem; Fredrik Björkling; Christopher J Schofield
Journal:  ACS Infect Dis       Date:  2021-05-18       Impact factor: 5.084

Review 6.  New Carbapenemase Inhibitors: Clearing the Way for the β-Lactams.

Authors:  Juan C Vázquez-Ucha; Jorge Arca-Suárez; Germán Bou; Alejandro Beceiro
Journal:  Int J Mol Sci       Date:  2020-12-06       Impact factor: 5.923

Review 7.  Drug development concerning metallo-β-lactamases in gram-negative bacteria.

Authors:  Xiuyun Li; Jing Zhao; Bin Zhang; Xuexia Duan; Jin Jiao; Weiwei Wu; Yuxia Zhou; Hefeng Wang
Journal:  Front Microbiol       Date:  2022-09-15       Impact factor: 6.064

Review 8.  β-lactam Resistance in Pseudomonas aeruginosa: Current Status, Future Prospects.

Authors:  Karl A Glen; Iain L Lamont
Journal:  Pathogens       Date:  2021-12-18

Review 9.  Recommendations to Synthetize Old and New β-Lactamases Inhibitors: A Review to Encourage Further Production.

Authors:  Silvana Alfei; Guendalina Zuccari
Journal:  Pharmaceuticals (Basel)       Date:  2022-03-21

10.  Studies on the Reactions of Biapenem with VIM Metallo β-Lactamases and the Serine β-Lactamase KPC-2.

Authors:  Anka Lucic; Tika R Malla; Karina Calvopiña; Catherine L Tooke; Jürgen Brem; Michael A McDonough; James Spencer; Christopher J Schofield
Journal:  Antibiotics (Basel)       Date:  2022-03-16
  10 in total

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