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Next-generation antimicrobials: from chemical biology to first-in-class drugs

The global emergence of multi-drug resistant bacteria invokes an urgent and imperative necessity for the identification of novel antimicrobials. The general lack of success in progressing novel chemical entities from target-based drug screens have prompted calls for radical and innovative approaches...

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Detalles Bibliográficos
Autores principales: Ang, Michelle Lay Teng, Murima, Paul, Pethe, Kevin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Pharmaceutical Society of Korea 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4567591/
https://www.ncbi.nlm.nih.gov/pubmed/26259630
http://dx.doi.org/10.1007/s12272-015-0645-0
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author Ang, Michelle Lay Teng
Murima, Paul
Pethe, Kevin
author_facet Ang, Michelle Lay Teng
Murima, Paul
Pethe, Kevin
author_sort Ang, Michelle Lay Teng
collection PubMed
description The global emergence of multi-drug resistant bacteria invokes an urgent and imperative necessity for the identification of novel antimicrobials. The general lack of success in progressing novel chemical entities from target-based drug screens have prompted calls for radical and innovative approaches for drug discovery. Recent developments in chemical biology and target deconvolution strategies have revived interests in the utilization of whole-cell phenotypic screens and resulted in several success stories for the discovery and development novel drug candidates and target pathways. In this review, we present and discuss recent chemical biology approaches focusing on the discovery of novel targets and new lead molecules for the treatment of human bacterial and protozoan infections.
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spelling pubmed-45675912015-09-15 Next-generation antimicrobials: from chemical biology to first-in-class drugs Ang, Michelle Lay Teng Murima, Paul Pethe, Kevin Arch Pharm Res Review The global emergence of multi-drug resistant bacteria invokes an urgent and imperative necessity for the identification of novel antimicrobials. The general lack of success in progressing novel chemical entities from target-based drug screens have prompted calls for radical and innovative approaches for drug discovery. Recent developments in chemical biology and target deconvolution strategies have revived interests in the utilization of whole-cell phenotypic screens and resulted in several success stories for the discovery and development novel drug candidates and target pathways. In this review, we present and discuss recent chemical biology approaches focusing on the discovery of novel targets and new lead molecules for the treatment of human bacterial and protozoan infections. Pharmaceutical Society of Korea 2015-08-11 2015 /pmc/articles/PMC4567591/ /pubmed/26259630 http://dx.doi.org/10.1007/s12272-015-0645-0 Text en © The Author(s) 2015 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Review
Ang, Michelle Lay Teng
Murima, Paul
Pethe, Kevin
Next-generation antimicrobials: from chemical biology to first-in-class drugs
title Next-generation antimicrobials: from chemical biology to first-in-class drugs
title_full Next-generation antimicrobials: from chemical biology to first-in-class drugs
title_fullStr Next-generation antimicrobials: from chemical biology to first-in-class drugs
title_full_unstemmed Next-generation antimicrobials: from chemical biology to first-in-class drugs
title_short Next-generation antimicrobials: from chemical biology to first-in-class drugs
title_sort next-generation antimicrobials: from chemical biology to first-in-class drugs
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4567591/
https://www.ncbi.nlm.nih.gov/pubmed/26259630
http://dx.doi.org/10.1007/s12272-015-0645-0
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