Cargando…
Optimization and Evaluation of 5-Styryl-Oxathiazol-2-one Mycobacterium tuberculosis Proteasome Inhibitors as Potential Antitubercular Agents
This is the first report of 5-styryl-oxathiazol-2-ones as inhibitors of the Mycobacterium tuberculosis (Mtb) proteasome. As part of the study, the structure–activity relationship of oxathiazolones as Mtb proteasome inhibitors has been investigated. Furthermore, the prepared compounds displayed a goo...
Autores principales: | Russo, Francesco, Gising, Johan, Åkerbladh, Linda, Roos, Annette K, Naworyta, Agata, Mowbray, Sherry L, Sokolowski, Anders, Henderson, Ian, Alling, Torey, Bailey, Mai A, Files, Megan, Parish, Tanya, Karlén, Anders, Larhed, Mats |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley & Sons, Ltd
2015
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4522185/ https://www.ncbi.nlm.nih.gov/pubmed/26246997 http://dx.doi.org/10.1002/open.201500001 |
Ejemplares similares
-
Trisubstituted Imidazoles
as Mycobacterium tuberculosis Glutamine Synthetase
Inhibitors†
por: Gising, Johan, et al.
Publicado: (2012) -
Synthesis and In Vitro Biological
Evaluation of Quinolinyl Pyrimidines Targeting Type II NADH-Dehydrogenase
(NDH-2)
por: Lu, Lu, et al.
Publicado: (2022) -
Synthesis of Functionalized Cinnamaldehyde Derivatives by an Oxidative Heck Reaction and Their Use as Starting Materials for Preparation of Mycobacterium tuberculosis 1-Deoxy-d-xylulose-5-phosphate Reductoisomerase Inhibitors
por: Nordqvist, Anneli, et al.
Publicado: (2011) -
Crystal structure determination as part of an ongoing undergraduate organic laboratory project: 5-[(E)-styryl]-1,3,4-oxathiazol-2-one
por: Nason, Trevor R., et al.
Publicado: (2017) -
Synthesis and anti-tubercular activity of 3-substituted benzo[b]thiophene-1,1-dioxides
por: Chandrasekera, N. Susantha, et al.
Publicado: (2014)