Cargando…
Novel Lipophilic Acetohydroxamic Acid Derivatives Based on Conformationally Constrained Spiro Carbocyclic 2,6-Diketopiperazine Scaffolds with Potent Trypanocidal Activity
[Image: see text] We describe novel acetohydroxamic acid derivatives with potent activity against cultured bloodstream-form Trypanosoma brucei and selectivity indices of >1000. These analogues were derived from conformationally constrained, lipophilic, spiro carbocyclic 2,6-diketopiperazine (2,6-...
Autores principales: | Fytas, Christos, Zoidis, Grigoris, Tzoutzas, Nikolaos, Taylor, Martin C., Fytas, George, Kelly, John M. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2011
|
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3140774/ https://www.ncbi.nlm.nih.gov/pubmed/21542562 http://dx.doi.org/10.1021/jm200217m |
Ejemplares similares
-
An E/Z conformational behaviour study on the trypanocidal action of lipophilic spiro carbocyclic 2,6-diketopiperazine-1-acetohydroxamic acids
por: Tsatsaroni, Alexandra, et al.
Publicado: (2013) -
Novel Lipophilic Hydroxamates Based on Spirocarbocyclic Hydantoin Scaffolds with Potent Antiviral and Trypanocidal Activity
por: Pardali, Vasiliki, et al.
Publicado: (2023) -
Multiscale modelling of the radical-induced chemistry of acetohydroxamic acid in aqueous solution
por: Conrad, Jacy K., et al.
Publicado: (2022) -
Synthesis and Effect of Conformationally Locked Carbocyclic Guanine Nucleotides on Dynamin
por: Toti, Kiran S., et al.
Publicado: (2022) -
Antiglycation, radical scavenging, and semicarbazide-sensitive amine oxidase inhibitory activities of acetohydroxamic acid in vitro
por: Liu, Yuh-Hwa, et al.
Publicado: (2017)