Cargando…
Novel Aminoguanidine Hydrazone Analogues: From Potential Antimicrobial Agents to Potent Cholinesterase Inhibitors
A series of thirty-one hydrazones of aminoguanidine, nitroaminoguanidine, 1,3-diaminoguanidine, and (thio)semicarbazide were prepared from various aldehydes, mainly chlorobenzaldehydes, halogenated salicylaldehydes, 5-nitrofurfural, and isatin (yields of 50–99%). They were characterized by spectral...
Autores principales: | Krátký, Martin, Štěpánková, Šárka, Konečná, Klára, Svrčková, Katarína, Maixnerová, Jana, Švarcová, Markéta, Janďourek, Ondřej, Trejtnar, František, Vinšová, Jarmila |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8704707/ https://www.ncbi.nlm.nih.gov/pubmed/34959630 http://dx.doi.org/10.3390/ph14121229 |
Ejemplares similares
-
5-Aryl-1,3,4-oxadiazol-2-amines Decorated with Long Alkyl and Their Analogues: Synthesis, Acetyl- and Butyrylcholinesterase Inhibition and Docking Study
por: Pflégr, Václav, et al.
Publicado: (2022) -
Novel Cholinesterase Inhibitors Based on O-Aromatic N,N-Disubstituted Carbamates and Thiocarbamates
por: Krátký, Martin, et al.
Publicado: (2016) -
Hydrazones of 4-(Trifluoromethyl)benzohydrazide as New Inhibitors of Acetyl- and Butyrylcholinesterase
por: Krátký, Martin, et al.
Publicado: (2021) -
N-Alkyl-2-[4-(trifluoromethyl)benzoyl]hydrazine-1-carboxamides and Their Analogues: Synthesis and Multitarget Biological Activity
por: Krátký, Martin, et al.
Publicado: (2020) -
Novel Inhibitors of Acetyl- and Butyrylcholinesterase Derived from Benzohydrazides: Synthesis, Evaluation and Docking Study
por: Houngbedji, Neto-Honorius, et al.
Publicado: (2023)