Synthesis, molecular docking analysis and carbonic anhydrase I-II inhibitory evaluation of new sulfonamide derivatives.
ADME
Carbonic anhydrase
Cytotoxicity
Molecular docking
Sulfonamide
Journal
Bioorganic chemistry
ISSN: 1090-2120
Titre abrégé: Bioorg Chem
Pays: United States
ID NLM: 1303703
Informations de publication
Date de publication:
10 2019
10 2019
Historique:
received:
26
12
2018
revised:
23
05
2019
accepted:
24
07
2019
pubmed:
6
8
2019
medline:
21
10
2020
entrez:
6
8
2019
Statut:
ppublish
Résumé
New sulfonamide-hydrazone derivatives (3a-3n) were synthesized to evaluate their inhibitory effects on purified human carbonic anhydrase (hCA) I and II. The inhibition profiles of the synthesized compounds on hCA I-II isoenzyme were investigated by comparing their IC
Identifiants
pubmed: 31382057
pii: S0045-2068(18)31535-9
doi: 10.1016/j.bioorg.2019.103153
pii:
doi:
Substances chimiques
Acetamides
0
Carbonic Anhydrase Inhibitors
0
Carbonic Anhydrase I
EC 4.2.1.-
Carbonic Anhydrase II
EC 4.2.1.-
Types de publication
Evaluation Study
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
103153Informations de copyright
Copyright © 2019 Elsevier Inc. All rights reserved.