Publicação: Oxazolidinones as versatile scaffolds in medicinal chemistry
dc.contributor.author | Fernandes, Guilherme Felipe Santos | |
dc.contributor.author | Scarim, Cauê Benito [UNESP] | |
dc.contributor.author | Kim, Seong-Heun | |
dc.contributor.author | Wu, Jingyue | |
dc.contributor.author | Castagnolo, Daniele | |
dc.contributor.institution | University College London | |
dc.contributor.institution | Universidade Estadual Paulista (UNESP) | |
dc.contributor.institution | King's College London | |
dc.date.accessioned | 2023-07-29T13:48:32Z | |
dc.date.available | 2023-07-29T13:48:32Z | |
dc.date.issued | 2023-02-08 | |
dc.description.abstract | Oxazolidinone is a five-member heterocyclic ring with several biological applications in medicinal chemistry. Among the three possible isomers, 2-oxazolidinone is the most investigated in drug discovery. Linezolid was pioneered as the first approved drug containing an oxazolidinone ring as the pharmacophore group. Numerous analogues have been developed since its arrival on the market in 2000. Some have succeeded in reaching the advanced stages of clinical studies. However, most oxazolidinone derivatives reported in recent decades have not reached the initial stages of drug development, despite their promising pharmacological applications in a variety of therapeutic areas, including antibacterial, antituberculosis, anticancer, anti-inflammatory, neurologic, and metabolic diseases, among other areas. Therefore, this review article aims to compile the efforts of medicinal chemists who have explored this scaffold over the past decades and highlight the potential of the class for medicinal chemistry. | en |
dc.description.affiliation | Department of Chemistry University College London, 20 Gordon Street | |
dc.description.affiliation | Department of Drugs and Medicines School of Pharmaceutical Sciences São Paulo State University | |
dc.description.affiliation | School of Cancer and Pharmaceutical Sciences King's College London, 150 Stamford Street | |
dc.description.affiliationUnesp | Department of Drugs and Medicines School of Pharmaceutical Sciences São Paulo State University | |
dc.description.sponsorship | Horizon 2020 | |
dc.format.extent | 823-847 | |
dc.identifier | http://dx.doi.org/10.1039/d2md00415a | |
dc.identifier.citation | RSC Medicinal Chemistry, v. 14, n. 5, p. 823-847, 2023. | |
dc.identifier.doi | 10.1039/d2md00415a | |
dc.identifier.issn | 2632-8682 | |
dc.identifier.scopus | 2-s2.0-85151326755 | |
dc.identifier.uri | http://hdl.handle.net/11449/248603 | |
dc.language.iso | eng | |
dc.relation.ispartof | RSC Medicinal Chemistry | |
dc.source | Scopus | |
dc.title | Oxazolidinones as versatile scaffolds in medicinal chemistry | en |
dc.type | Resenha | pt |
dspace.entity.type | Publication | |
relation.isDepartmentOfPublication | e214da1b-9929-4ae9-b8fd-655e9bfeda4b | |
relation.isDepartmentOfPublication.latestForDiscovery | e214da1b-9929-4ae9-b8fd-655e9bfeda4b | |
unesp.author.orcid | 0000-0002-7644-5466[1] | |
unesp.author.orcid | 0000-0002-2540-6395[2] | |
unesp.author.orcid | 0000-0002-9774-9311 0000-0002-9774-9311[3] | |
unesp.author.orcid | 0000-0002-9289-5109[4] | |
unesp.author.orcid | 0000-0002-7517-5732[5] | |
unesp.department | Fármacos e Medicamentos - FCF | pt |