Generic placeholder image

Combinatorial Chemistry & High Throughput Screening


ISSN (Print): 1386-2073
ISSN (Online): 1875-5402

Virtual High Throughput Screening of Carbapenem Derivatives as New Generation Carbapenemase and Penicillin Binding Protein Inhibitors: A Hunt to Save Drug of Last Resort

Author(s): Abhishek Chowdhury, Paulomi Paul, Amitabha Bhattacharjee, Anupam Das Talukdar and Manabendra Dutta Choudhury

Volume 18, Issue 1, 2015

Page: [18 - 23] Pages: 6

DOI: 10.2174/1386207317666141226131709

Price: $65


The advent of carbapenem resistance by the production of β-lectamases and mutated penicillin binding proteins (PBPs) has challenged the treatment of Enterobacteriaceae. Hence there is an urgent need to establish drugs that can fit in the pipeline by overcoming those situations.

The working hypothesis of the work is based on two facts, i.e., i) design of inhibitors against mutated PBPs to which present drugs cannot bind efficiently to kill pathogen by inhibiting cell wall formation, ii) design of molecules that can bind with β-lectamases with high affinity, so that they can supplement available drugs preventing their unwanted hydrolysis.

In this work, over thousands of thienamycin (first natural carbapenem) derivatives were generated and out of which non-toxic 273 molecules were used for further study. Out of which, only few followed the first hypothesis and rest obeyed the second. Ligand L5 strictly followed the first hypothesis and L1-L4 followed to a satisfactory level. Molecular dynamic simulation was performed to check post-docking stability of the pharmacophores.

Keywords: Beta lactamase, carbapenem resistance, computer aided drug design, molecular docking, penicillin binding proteins, thienamycin.

Rights & Permissions Print Export Cite as
© 2023 Bentham Science Publishers | Privacy Policy