Synthesis of new indazole based dual inhibitors of α-glucosidase and α-amylase enzymes, their in vitro, in silico and kinetics studies.
Computer Simulation
Enzyme Inhibitors
/ chemical synthesis
Glycoside Hydrolase Inhibitors
/ chemical synthesis
In Vitro Techniques
Indazoles
/ chemistry
Kinetics
Magnetic Resonance Spectroscopy
Molecular Docking Simulation
Molecular Structure
Structure-Activity Relationship
alpha-Amylases
/ antagonists & inhibitors
Carbothioamide
Hyperglycemia
Indazole
α-amylase
α-glucosidase
Journal
Bioorganic chemistry
ISSN: 1090-2120
Titre abrégé: Bioorg Chem
Pays: United States
ID NLM: 1303703
Informations de publication
Date de publication:
01 2020
01 2020
Historique:
received:
02
04
2019
revised:
01
07
2019
accepted:
11
08
2019
pubmed:
28
8
2019
medline:
20
2
2021
entrez:
28
8
2019
Statut:
ppublish
Résumé
The current study describes the discovery of novel inhibitors of α-glucosidase and α-amylase enzymes. For that purpose, new hybrid analogs of N-hydrazinecarbothioamide substituted indazoles 4-18 were synthesized and fully characterized by EI-MS, FAB-MS, HRFAB-MS,
Identifiants
pubmed: 31451297
pii: S0045-2068(19)30513-9
doi: 10.1016/j.bioorg.2019.103195
pii:
doi:
Substances chimiques
Enzyme Inhibitors
0
Glycoside Hydrolase Inhibitors
0
Indazoles
0
alpha-Amylases
EC 3.2.1.1
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
103195Informations de copyright
Copyright © 2019 Elsevier Inc. All rights reserved.