Cargando…
Synthesis and Biological Evaluation of 1,3-Dideazapurine-Like 7-Amino-5-Hydroxymethyl-Benzimidazole Ribonucleoside Analogues as Aminoacyl-tRNA Synthetase Inhibitors
Aminoacyl-tRNA synthetases (aaRSs) have become viable targets for the development of antimicrobial agents due to their crucial role in protein translation. A series of six amino acids were coupled to the purine-like 7-amino-5-hydroxymethylbenzimidazole nucleoside analogue following an optimized synt...
Autores principales: | Zhang, Baole, Pang, Luping, Nautiyal, Manesh, De Graef, Steff, Gadakh, Bharat, Lescrinier, Eveline, Rozenski, Jef, Strelkov, Sergei V., Weeks, Stephen D., Van Aerschot, Arthur |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7587597/ https://www.ncbi.nlm.nih.gov/pubmed/33081246 http://dx.doi.org/10.3390/molecules25204751 |
Ejemplares similares
-
Synthesis and Biological Evaluation of Lipophilic Nucleoside Analogues as Inhibitors of Aminoacyl-tRNA Synthetases
por: Nautiyal, Manesh, et al.
Publicado: (2019) -
N-Alkylated Aminoacyl sulfamoyladenosines as Potential Inhibitors of Aminoacylation Reactions and Microcin C Analogues Containing D-Amino Acids
por: Vondenhoff, Gaston H., et al.
Publicado: (2013) -
Aminoacyl-tRNA Synthetases as Valuable Targets for Antimicrobial Drug Discovery
por: Pang, Luping, et al.
Publicado: (2021) -
Structural Basis of Cysteine Ligase MshC Inhibition by Cysteinyl-Sulfonamides
por: Pang, Luping, et al.
Publicado: (2022) -
Partitioning of the initial catalytic steps of leucyl-tRNA synthetase is driven by an active site peptide-plane flip
por: Pang, Luping, et al.
Publicado: (2022)