Imidazole-pyrazole hybrids: Synthesis, characterization and in-vitro bioevaluation against α-glucosidase enzyme with molecular docking studies.
Molecular modeling
Multicomponent reactions
Tetrasubstituted imidazoles
α-Glucosidase inhibitors
Journal
Bioorganic chemistry
ISSN: 1090-2120
Titre abrégé: Bioorg Chem
Pays: United States
ID NLM: 1303703
Informations de publication
Date de publication:
02 2019
02 2019
Historique:
received:
08
07
2018
revised:
27
09
2018
accepted:
23
10
2018
pubmed:
6
11
2018
medline:
31
8
2019
entrez:
6
11
2018
Statut:
ppublish
Résumé
Herein, substituted imidazole-pyrazole hybrids (2a-2n) were prepared via a multi component reaction employing pyrazole-4-carbaldehydes (1a-1d), ammonium acetate, benzil and arylamines as reactants. All the new compounds were characterized through their spectral and elemental analyses. Further these compounds were tested against α-glucosidase enzyme. The compounds 2k, 2l and 2n possessed good inhibition potencies, however, compounds 2f (IC
Identifiants
pubmed: 30396060
pii: S0045-2068(18)30679-5
doi: 10.1016/j.bioorg.2018.10.047
pii:
doi:
Substances chimiques
Glycoside Hydrolase Inhibitors
0
Imidazoles
0
Pyrazoles
0
alpha-Glucosidases
EC 3.2.1.20
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
267-273Informations de copyright
Copyright © 2018 Elsevier Inc. All rights reserved.