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Repurposing the Antihistamine Terfenadine for Antimicrobial Activity against Staphylococcus aureus
[Image: see text] Staphylococcus aureus is a rapidly growing health threat in the U.S., with resistance to several commonly prescribed treatments. A high-throughput screen identified the antihistamine terfenadine to possess, previously unreported, antimicrobial activity against S. aureus and other G...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical
Society
2014
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4207543/ https://www.ncbi.nlm.nih.gov/pubmed/25238555 http://dx.doi.org/10.1021/jm5010682 |
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author | Perlmutter, Jessamyn I. Forbes, Lauren T. Krysan, Damian J. Ebsworth-Mojica, Katherine Colquhoun, Jennifer M. Wang, Jenna L. Dunman, Paul M. Flaherty, Daniel P. |
author_facet | Perlmutter, Jessamyn I. Forbes, Lauren T. Krysan, Damian J. Ebsworth-Mojica, Katherine Colquhoun, Jennifer M. Wang, Jenna L. Dunman, Paul M. Flaherty, Daniel P. |
author_sort | Perlmutter, Jessamyn I. |
collection | PubMed |
description | [Image: see text] Staphylococcus aureus is a rapidly growing health threat in the U.S., with resistance to several commonly prescribed treatments. A high-throughput screen identified the antihistamine terfenadine to possess, previously unreported, antimicrobial activity against S. aureus and other Gram-positive bacteria. In an effort to repurpose this drug, structure–activity relationship studies yielded 84 terfenadine-based analogues with several modifications providing increased activity versus S. aureus and other bacterial pathogens, including Mycobacterium tuberculosis. Mechanism of action studies revealed these compounds to exert their antibacterial effects, at least in part, through inhibition of the bacterial type II topoisomerases. This scaffold suffers from hERG liabilities which were not remedied through this round of optimization; however, given the overall improvement in activity of the set, terfenadine-based analogues provide a novel structural class of antimicrobial compounds with potential for further characterization as part of the continuing process to meet the current need for new antibiotics. |
format | Online Article Text |
id | pubmed-4207543 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | American Chemical
Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-42075432015-09-19 Repurposing the Antihistamine Terfenadine for Antimicrobial Activity against Staphylococcus aureus Perlmutter, Jessamyn I. Forbes, Lauren T. Krysan, Damian J. Ebsworth-Mojica, Katherine Colquhoun, Jennifer M. Wang, Jenna L. Dunman, Paul M. Flaherty, Daniel P. J Med Chem [Image: see text] Staphylococcus aureus is a rapidly growing health threat in the U.S., with resistance to several commonly prescribed treatments. A high-throughput screen identified the antihistamine terfenadine to possess, previously unreported, antimicrobial activity against S. aureus and other Gram-positive bacteria. In an effort to repurpose this drug, structure–activity relationship studies yielded 84 terfenadine-based analogues with several modifications providing increased activity versus S. aureus and other bacterial pathogens, including Mycobacterium tuberculosis. Mechanism of action studies revealed these compounds to exert their antibacterial effects, at least in part, through inhibition of the bacterial type II topoisomerases. This scaffold suffers from hERG liabilities which were not remedied through this round of optimization; however, given the overall improvement in activity of the set, terfenadine-based analogues provide a novel structural class of antimicrobial compounds with potential for further characterization as part of the continuing process to meet the current need for new antibiotics. American Chemical Society 2014-09-19 2014-10-23 /pmc/articles/PMC4207543/ /pubmed/25238555 http://dx.doi.org/10.1021/jm5010682 Text en Copyright © 2014 American Chemical Society Terms of Use (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) |
spellingShingle | Perlmutter, Jessamyn I. Forbes, Lauren T. Krysan, Damian J. Ebsworth-Mojica, Katherine Colquhoun, Jennifer M. Wang, Jenna L. Dunman, Paul M. Flaherty, Daniel P. Repurposing the Antihistamine Terfenadine for Antimicrobial Activity against Staphylococcus aureus |
title | Repurposing the Antihistamine Terfenadine for Antimicrobial
Activity against Staphylococcus aureus |
title_full | Repurposing the Antihistamine Terfenadine for Antimicrobial
Activity against Staphylococcus aureus |
title_fullStr | Repurposing the Antihistamine Terfenadine for Antimicrobial
Activity against Staphylococcus aureus |
title_full_unstemmed | Repurposing the Antihistamine Terfenadine for Antimicrobial
Activity against Staphylococcus aureus |
title_short | Repurposing the Antihistamine Terfenadine for Antimicrobial
Activity against Staphylococcus aureus |
title_sort | repurposing the antihistamine terfenadine for antimicrobial
activity against staphylococcus aureus |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4207543/ https://www.ncbi.nlm.nih.gov/pubmed/25238555 http://dx.doi.org/10.1021/jm5010682 |
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