Please use this identifier to cite or link to this item: http://bura.brunel.ac.uk/handle/2438/11782
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dc.contributor.authorWilliams, K-
dc.contributor.authorBilsland, E-
dc.contributor.authorSparkes, A-
dc.contributor.authorAubrey, W-
dc.contributor.authorYoung, M-
dc.contributor.authorSoldatova, LN-
dc.contributor.authorDe Grave, K-
dc.contributor.authorRamon, J-
dc.contributor.authorDe Clare, M-
dc.contributor.authorSirawaraporn, W-
dc.contributor.authorOliver, SG-
dc.contributor.authorKing, RD-
dc.date.accessioned2015-12-22T14:04:49Z-
dc.date.available2015-02-04-
dc.date.available2015-12-22T14:04:49Z-
dc.date.issued2015-
dc.identifier.citationJournal of The Royal Society Interface, 12 (104): (2015)en_US
dc.identifier.issn1742-5689-
dc.identifier.issn1742-5662-
dc.identifier.urihttp://rsif.royalsocietypublishing.org/content/12/104/20141289-
dc.identifier.urihttp://bura.brunel.ac.uk/handle/2438/11782-
dc.description.abstractThere is an urgent need to make drug discovery cheaper and faster. This will enable the development of treatments for diseases currently neglected for economic reasons, such as tropical and orphan diseases, and generally increase the supply of new drugs. Here,we report the Robot Scientist ‘Eve’ designed to make drug discovery more economical. A Robot Scientist is a laboratory automation system that uses artificial intelligence (AI) techniques to discover scientific knowledge through cycles of experimentation. Eve integrates and automates library-screening, hit-confirmation, and lead generation through cycles of quantitative structure activity relationship learning and testing. Using econometric modelling we demonstrate that the use of AI to select compounds economically outperforms standard drug screening. For further efficiency Eve uses a standardized form of assay to compute Boolean functions of compound properties. These assays can be quickly and cheaply engineered using synthetic biology, enabling more targets to be assayed for a given budget. Eve has repositioned several drugs against specific targets in parasites that cause tropical diseases. One validated discovery is that the anti-cancer compound TNP-470 is a potent inhibitor of dihydrofolate reductase from the malaria-causing parasite Plasmodium vivax.en_US
dc.description.sponsorshipMehedi Nahianen_US
dc.format.extent20141289 - 20141289-
dc.language.isoenen_US
dc.publisherRoyal Societyen_US
dc.subjectDrug designen_US
dc.subjectArtificial intelligenceen_US
dc.subjectQuantitative structure activity relationshipen_US
dc.titleCheaper faster drug development validated by the repositioning of drugs against neglected tropical diseasesen_US
dc.typeArticleen_US
dc.identifier.doihttp://dx.doi.org/10.1098/rsif.2014.1289-
dc.relation.isPartOfJournal of The Royal Society Interface-
pubs.issue104-
pubs.publication-statusPublished-
pubs.publication-statusPublished-
pubs.volume12-
Appears in Collections:Institute for the Environment

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