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The cell division protein FtsZ as a cellular target to hit cystic fibrosis pathogens.
- Source :
-
European journal of medicinal chemistry [Eur J Med Chem] 2020 Mar 15; Vol. 190, pp. 112132. Date of Electronic Publication: 2020 Feb 08. - Publication Year :
- 2020
-
Abstract
- Cystic fibrosis is a rare genetic disease characterized by the production of dehydrated mucus in the lung able to trap bacteria and rendering their proliferation particularly dangerous, thus leading to chronic infections. Among these bacteria, Staphylococcus aureus and Pseudomonas aeruginosa play a major role while, within emerging pathogens, Stenotrophomonas maltophilia, Achromobacter xylosoxidans, Burkholderia cepacia complex species, as well as non-tuberculous mycobacteria are listed. Since a common feature of these bacteria is the high level of drug resistance, cell division, and in particular FtsZ, has been explored as a novel therapeutic target for the design of new molecules with antibacterial properties. This review summarizes and provides insight into recent advances in the discovery of compounds targeting FtsZ: the majority of them exhibit anti-staphylococcal activity, while a few were directed against the cystic fibrosis Gram negative pathogens.<br />Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.<br /> (Copyright © 2020 Elsevier Masson SAS. All rights reserved.)
- Subjects :
- Anti-Bacterial Agents chemistry
Anti-Bacterial Agents therapeutic use
Cystic Fibrosis microbiology
Enzyme Inhibitors chemistry
Enzyme Inhibitors pharmacology
GTP Phosphohydrolases antagonists & inhibitors
Gram-Negative Bacteria drug effects
Humans
Staphylococcal Infections drug therapy
Staphylococcus aureus drug effects
Anti-Bacterial Agents pharmacology
Bacterial Proteins antagonists & inhibitors
Cytoskeletal Proteins antagonists & inhibitors
Subjects
Details
- Language :
- English
- ISSN :
- 1768-3254
- Volume :
- 190
- Database :
- MEDLINE
- Journal :
- European journal of medicinal chemistry
- Publication Type :
- Academic Journal
- Accession number :
- 32066012
- Full Text :
- https://doi.org/10.1016/j.ejmech.2020.112132