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• W2168447130 abstract "The search for compounds active against Mycobacterium tuberculosis is reliant upon high-throughput screening (HTS) in whole cells. We have used Bayesian machine learning models which can predict anti-tubercular activity to filter an internal library of over 150,000 compounds prior to in vitro testing. We used this to select and test 48 compounds in vitro; 11 were active with MIC values ranging from 0.4 μM to 10.2 μM, giving a high hit rate of 22.9%. Among the hits, we identified several compounds belonging to the same series including five quinolones (including ciprofloxacin), three molecules with long aliphatic linkers and three singletons. This approach represents a rapid method to prioritize compounds for testing that can be used alongside medicinal chemistry insight and other filters to identify active molecules. Such models can significantly increase the hit rate of HTS, above the usual 1% or lower rates seen. In addition, the potential targets for the 11 molecules were predicted using TB Mobile and clustering alongside a set of over 740 molecules with known M. tuberculosis target annotations. These predictions may serve as a mechanism for prioritizing compounds for further optimization." @default.
• W2168447130 created "2016-06-24" @default.
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• W2168447130 date "2014-03-01" @default.
• W2168447130 modified "2023-10-16" @default.
• W2168447130 title "Bayesian models for screening and TB Mobile for target inference with Mycobacterium tuberculosis" @default.
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• W2168447130 doi "https://doi.org/10.1016/j.tube.2013.12.001" @default.
• W2168447130 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/4394018" @default.
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