Cargando…
Synthesis of Brominated 2-Phenitidine Derivatives as Valuable Inhibitors of Cholinesterases for the Treatment of Alzheimer’s Disease
The present study reports the synthesis of a series N-substituted derivatives of brominated 2-phenitidine. First, the reaction of 2-phenitidine (1) with benzenesulfonyl chloride (2) in aqueous media yielded N-(2-ethoxyphenyl) benzenesulfonamide (3), which was then subjected to bromination with bromi...
Autores principales: | Abbasi, Muhammad Athar, Saeed, Amna, Aziz-ur-Rehman, Mohmmed Khan, Khalid, Ashraf, Muhammad, Ejaz, Syeda Abida |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Shaheed Beheshti University of Medical Sciences
2014
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3985256/ https://www.ncbi.nlm.nih.gov/pubmed/24734059 |
Ejemplares similares
-
Synthesis, characterization, and in vitro anti-cholinesterase screening of novel indole amines
por: Gondal, Humaira Yasmeen, et al.
Publicado: (2023) -
Microwave-Assisted Synthesis of (Piperidin-1-yl)quinolin-3-yl)methylene)hydrazinecarbothioamides as Potent Inhibitors of Cholinesterases: A Biochemical and In Silico Approach
por: Munir, Rubina, et al.
Publicado: (2021) -
N-(5-Chloro-2-methoxyphenyl)benzenesulfonamide
por: Aziz-ur-Rehman,, et al.
Publicado: (2010) -
HPLC-DAD finger printing, antioxidant, cholinesterase, and α-glucosidase inhibitory potentials of a novel plant Olax nana
por: Ovais, Muhammad, et al.
Publicado: (2018) -
Structure and surface analyses of a newly synthesized acyl thiourea derivative along with its in silico and in vitro investigations for RNR, DNA binding, urease inhibition and radical scavenging activities
por: Khalid, Aqsa, et al.
Publicado: (2022)