The biological activities, molecular docking studies, and anticancer effects of 1-arylsuphonylpyrazole derivatives.
Pyrazolpiridines
anticancer
enzyme inhibition
molecular docking
pyridazole pyridines
Journal
Journal of biomolecular structure & dynamics
ISSN: 1538-0254
Titre abrégé: J Biomol Struct Dyn
Pays: England
ID NLM: 8404176
Informations de publication
Date de publication:
Jun 2021
Jun 2021
Historique:
pubmed:
5
5
2020
medline:
3
7
2021
entrez:
5
5
2020
Statut:
ppublish
Résumé
This work is devoted to definition of the direction of reaction between 1-benzenesulfonylimino pyridinium chloride and α- or β-halo-containing sulfamides, chloroacetic acid, 1-chloro-2,3-dihydroxypropane, etc. The optimal conditions for the synchronous reaction of heterocyclization are determined. Benzenesulfonyliminopyridinium chloride was obtained to form pyrazolopyridines with 1,2-polarophiles, and pyridazine pyridines with 1,3-polarophiles. These novel derivatives were found as effective inhibitors of the α-glycosidase with K
Identifiants
pubmed: 32364008
doi: 10.1080/07391102.2020.1763838
doi:
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM