Cargando…
In Silico Discovery and Optimisation of a Novel Structural Class of Hsp90 C-Terminal Domain Inhibitors
Hsp90 is a promising target for the development of novel agents for cancer treatment. The N-terminal Hsp90 inhibitors have several therapeutic limitations, the most important of which is the induction of heat shock response, which can be circumvented by targeting the allosteric binding site on the C...
Autores principales: | Zajec, Živa, Dernovšek, Jaka, Gobec, Martina, Tomašič, Tihomir |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9312846/ https://www.ncbi.nlm.nih.gov/pubmed/35883440 http://dx.doi.org/10.3390/biom12070884 |
Ejemplares similares
-
Structure-Activity Relationships of Benzothiazole-Based Hsp90 C-Terminal-Domain Inhibitors
por: Dernovšek, Jaka, et al.
Publicado: (2021) -
Discovery of Novel Hsp90 C-Terminal Inhibitors Using 3D-Pharmacophores Derived from Molecular Dynamics Simulations
por: Tomašič, Tihomir, et al.
Publicado: (2020) -
Catalytic Stereoconvergent Synthesis of Homochiral
β-CF(3), β-SCF(3), and
β-OCF(3) Benzylic Alcohols
por: Cotman, Andrej Emanuel, et al.
Publicado: (2022) -
Design and synthesis of novel 3-triazolyl-1-thiogalactosides as galectin-1, -3 and -8 inhibitors
por: van Klaveren, Sjors, et al.
Publicado: (2022) -
Discovery of new molecular entities able to strongly interfere with Hsp90 C-terminal domain
por: Terracciano, Stefania, et al.
Publicado: (2018)