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dc.contributor.author
Urán Landaburu, Héctor Lionel
dc.contributor.author
Garnham, Mercedes Didier
dc.contributor.author
Agüero, Fernan Gonzalo
dc.date.available
2024-02-28T12:53:33Z
dc.date.issued
2023-02
dc.identifier.citation
Urán Landaburu, Héctor Lionel; Garnham, Mercedes Didier; Agüero, Fernan Gonzalo; Targeting trypanosomes: how chemogenomics and artificial intelligence can guide drug discovery; Journal of the Serbian Chemical Society; Biochemical Society Transactions; 51; 1; 2-2023; 195-206
dc.identifier.issn
0300-5127
dc.identifier.uri
http://hdl.handle.net/11336/228757
dc.description.abstract
Trypanosomatids are protozoan parasites that cause human and animal neglected diseases. Despite global efforts, effective treatments are still much needed. Phenotypic screens have provided several chemical leads for drug discovery, but the mechanism of action for many of these chemicals is currently unknown. Recently, chemogenomic screens assessing the susceptibility or resistance of parasites carrying genome-wide modifications started to define the mechanism of action of drugs at large scale. In this review, we discuss how genomics is being used for drug discovery in trypanosomatids, how integration of chemical and genomics data from these and other organisms has guided prioritisations of candidate therapeutic targets and additional chemical starting points, and how these data can fuel the expansion of drug discovery pipelines into the era of artificial intelligence.
dc.format
application/pdf
dc.language.iso
eng
dc.publisher
Journal of the Serbian Chemical Society
dc.rights
info:eu-repo/semantics/restrictedAccess
dc.rights.uri
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
dc.subject
Chagas
dc.subject
Quimioinformática
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Bioinformática
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Trypanosoma cruzi
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Ciencias de la Información y Bioinformática
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Ciencias de la Computación e Información
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CIENCIAS NATURALES Y EXACTAS
dc.title
Targeting trypanosomes: how chemogenomics and artificial intelligence can guide drug discovery
dc.type
info:eu-repo/semantics/article
dc.type
info:ar-repo/semantics/artículo
dc.type
info:eu-repo/semantics/publishedVersion
dc.date.updated
2024-02-28T10:24:41Z
dc.journal.volume
51
dc.journal.number
1
dc.journal.pagination
195-206
dc.journal.pais
Reino Unido
dc.journal.ciudad
Londres
dc.description.fil
Fil: Urán Landaburu, Héctor Lionel. Universidad Nacional de San Martín; Argentina. Universidad Nacional de San Martín. Instituto de Investigaciones Biotecnológicas. - Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Parque Centenario. Instituto de Investigaciones Biotecnológicas; Argentina
dc.description.fil
Fil: Garnham, Mercedes Didier. Universidad Nacional de San Martín; Argentina. Universidad Nacional de San Martín. Instituto de Investigaciones Biotecnológicas. - Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Parque Centenario. Instituto de Investigaciones Biotecnológicas; Argentina
dc.description.fil
Fil: Agüero, Fernan Gonzalo. Universidad Nacional de San Martín. Instituto de Investigaciones Biotecnológicas. - Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Parque Centenario. Instituto de Investigaciones Biotecnológicas; Argentina. Universidad Nacional de San Martín; Argentina
dc.journal.title
Biochemical Society Transactions
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/url/https://portlandpress.com/biochemsoctrans/article/doi/10.1042/BST20220618/232416/Targeting-trypanosomes-how-chemogenomics-and
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/doi/https://doi.org/10.1042/BST20220618
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