| Literature DB >> 27717850 |
Katarína Mikušová1, Sean Ekins2.
Abstract
Tuberculosis drug discovery has shifted in recent years from a primarily target-based approach to one that uses phenotypic high-throughput screens. As examples of this, through our EU-funded FP7 collaborations, New Medicines for Tuberculosis was target-based and our more-recent More Medicines for Tuberculosis project predominantly used phenotypic screening. From these projects we have examples of success (DprE1) and failure (PimA) going from drug to target and from target to drug, respectively. It is clear that we still have much to learn about the drug targets and the complex effects of the drugs on Mycobacterium tuberculosis. We propose a more integrated approach that learns from earlier drug discovery efforts that could help to move drug discovery forward.Entities:
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Year: 2016 PMID: 27717850 PMCID: PMC5362327 DOI: 10.1016/j.drudis.2016.09.025
Source DB: PubMed Journal: Drug Discov Today ISSN: 1359-6446 Impact factor: 7.851