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BacPROTAC approach for tuberculosis drug discovery

dc.contributor.authorBonjorno, Andressa Francielli [UNESP]
dc.contributor.authorPavan, Aline Renata
dc.contributor.authorLopes, Juliana Romano [UNESP]
dc.contributor.authorPrates, João Lucas Bruno [UNESP]
dc.contributor.authorde Souza, Mateus Mello [UNESP]
dc.contributor.authorScarim, Cauê Benito [UNESP]
dc.contributor.authordos Santos, Jean Leandro [UNESP]
dc.date.accessioned2026-05-07T14:49:24Z
dc.date.issued2024-01-01
dc.description.abstractAccording to the World Health Organization, tuberculosis (TB) continued to be a significant health burden in 2023, affecting an estimated 10 million individuals and resulting in 1.3 million deaths globally. One of the greatest challenges in combating TB is the rise of Multi-Drug Resistant (MDR) strains, which complicate and diminish the effectiveness of treatment. The PROteolysis Targeting Chimeras (PROTAC) strategy has emerged as a promising alternative in the quest for anti-Mycobacterium tuberculosis (Mtb) agents. The application of PROTACs in addressing MDR-TB represents an innovative and potentially effective approach, opening new avenues for the discovery of therapeutic agents against this disease. In this chapter, we discussed the challenges encountered in developing compounds to combat TB, particularly MDR-TB. Additionally, we explored the mechanisms underpinning this novel strategy and present the most recent advancements in this field.
dc.description.affiliationSchool of Pharmaceutical Sciences, University of São Paulo State Julio de Mesquita Filho (UNESP), Araraquara, Brazil
dc.description.affiliationCenter for Hematology and Hemotherapy at the Universidade Estadual de Campinas (Unicamp), Campinas, Brazil
dc.description.affiliationUnespSchool of Pharmaceutical Sciences, University of São Paulo State Julio de Mesquita Filho (UNESP), Araraquara, Brazil
dc.identifierhttps://app.dimensions.ai/details/publication/pub.1182140592
dc.identifier.dimensionspub.1182140592
dc.identifier.doi10.1016/bs.armc.2024.10.004
dc.identifier.isbn9780443295843
dc.identifier.issn0065-7743
dc.identifier.issn1557-8437
dc.identifier.orcid0000-0002-8666-008X
dc.identifier.orcid0000-0002-4932-7720
dc.identifier.orcid0000-0002-3141-501X
dc.identifier.orcid0000-0003-0187-4626
dc.identifier.orcid0000-0003-0840-0183
dc.identifier.orcid0000-0002-2540-6395
dc.identifier.orcid0000-0002-2460-2829
dc.identifier.urihttps://hdl.handle.net/11449/323444
dc.publisherElsevier
dc.relation.ispartofAnnual Reports in Medicinal Chemistry; v. 63; p. 93-112
dc.relation.ispartofPROTAC and Similar Technologies
dc.relation.ispartofseriesAnnual Reports in Medicinal Chemistry
dc.rights.accessRightsAcesso restritopt
dc.rights.sourceRightsclosed
dc.sourceDimensions
dc.titleBacPROTAC approach for tuberculosis drug discovery
dc.typeCapítulo de livropt
dspace.entity.typePublication
relation.isOrgUnitOfPublication95697b0b-8977-4af6-88d5-c29c80b5ee92
relation.isOrgUnitOfPublication.latestForDiscovery95697b0b-8977-4af6-88d5-c29c80b5ee92
unesp.campusUniversidade Estadual Paulista (UNESP), Faculdade de Ciências Farmacêuticas, Araraquarapt

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