Cargando…
Synthesis and Biological Activity of 3-(Heteroaryl)quinolin-2(1H)-ones Bis-Heterocycles as Potential Inhibitors of the Protein Folding Machinery Hsp90
In the context of our SAR study concerning 6BrCaQ analogues as C-terminal Hsp90 inhibitors, we designed and synthesized a novel series of 3-(heteroaryl)quinolin-2(1H), of types 3, 4, and 5, as a novel class of analogues. A Pd-catalyzed Liebeskind–Srogl cross-coupling was developed as a convenient ap...
Autores principales: | Larghi, Enrique L., Bruneau, Alexandre, Sauvage, Félix, Alami, Mouad, Vergnaud-Gauduchon, Juliette, Messaoudi, Samir |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8778022/ https://www.ncbi.nlm.nih.gov/pubmed/35056725 http://dx.doi.org/10.3390/molecules27020412 |
Ejemplares similares
-
Cancer drug resistance: rationale for drug delivery systems and targeted inhibition of HSP90 family proteins
por: Mathieu, Clélia, et al.
Publicado: (2019) -
The Hsp70/Hsp90 Chaperone Machinery in Neurodegenerative Diseases
por: Lackie, Rachel E., et al.
Publicado: (2017) -
Imbalances in the Hsp90 Chaperone Machinery: Implications for Tauopathies
por: Shelton, Lindsey B., et al.
Publicado: (2017) -
Targeting the Hsp90-Cdc37-client protein interaction to disrupt Hsp90 chaperone machinery
por: Li, Ting, et al.
Publicado: (2018) -
Cruentaren A Binds F(1)F(0) ATP
Synthase To Modulate the Hsp90 Protein Folding Machinery
por: Hall, Jessica A., et al.
Publicado: (2014)