Article (Scientific journals)
Assessment of anti-inflammatory-like, antioxidant activities and molecular docking of three alkynyl-substituted 3-ylidene-dihydrobenzo[d]isothiazole 1,1-dioxide derivatives.
Etse, Koffi Senam; Etsè, Kodjo Djidjolé; Nyssen, Pauline et al.
2021In Chemico-Biological Interactions, 344, p. 109513
Peer Reviewed verified by ORBi
 

Files


Full Text
1-s2.0-S0009279721001496-main.pdf
Publisher postprint (6.09 MB)
Request a copy

All documents in ORBi are protected by a user license.

Send to



Details



Keywords :
Benzoisothiazoles; DPPH assay; Docking; HL-60 cells; MPO; MTS viability; Reactive oxygen species
Abstract :
[en] The presence of enyne and benzoisothiazole functions in the molecular architecture of compounds 1, 2 and 3 were expected to provide biochemical activities. In the present work, we first examined the molecular surface contact of three alkynyl-substituted 3-ylidenedihydrobenzo[d] isothiazole 1,1-dioxides. The analysis of the Hirshfeld surfaces reveals that only compound 3 exhibited a well-defined red spots, indicating intermolecular interactions identified as S-O⋯H, C-H⋯O and C-O⋯H contacts. Comparative fingerprint histograms of the three compounds show that close pair interactions are dominated by C-H⋯H-C contact. By UV-visible analysis, compound 1 showed the most intense absorbances at 407 and 441 nm, respectively. The radical scavenging activity explored in the DPPH test, shows that only 1 exhibited low anti-radical activity. Furthermore, cellular antioxidant capacity of benzoisothiazoles 1-3 was investigated with PMA-activated HL-60 cells using chemiluminescence and fluorescence techniques in the presence of L-012 and Amplex Red probe, respectively. Results highlight that compound 1 exhibited moderate anti-ROS capacity while compounds 2 and 3 enhanced ROS production. The cytotoxicity test performed on HL-60 cells, using the MTS assay, confirmed the lack of toxicity of the tested benzoisothiazole 1 compared to 2 and 3 which show low cytotoxicity (≤30%). Anti-catalytic activity was evaluated by following the inhibitory potential of the benzoisothiazoles on MPO activity and depicted benzoisothiazoles-MPO interactions by docking. Both SIEFED and docking studies demonstrated an anti-catalytic activity of the tested benzoisothiazoles towards MPO with the best activity for compound 2.
Disciplines :
Chemistry
Author, co-author :
Etse, Koffi Senam ;  Université de Liège - ULiège > Département de pharmacie > Chimie analytique
Etsè, Kodjo Djidjolé;  Université de Lomé > Faculté des Sciences (FDS) > Laboratoire de Physiologie et Biotechnologie Végétales
Nyssen, Pauline ;  Université de Liège - ULiège > Département de physique > Spectroscopie biomédicale
Mouithys-Mickalad, Ange ;  Université de Liège - ULiège > Centre de l'oxygène : Recherche et développement (C.O.R.D.)
Language :
English
Title :
Assessment of anti-inflammatory-like, antioxidant activities and molecular docking of three alkynyl-substituted 3-ylidene-dihydrobenzo[d]isothiazole 1,1-dioxide derivatives.
Publication date :
2021
Journal title :
Chemico-Biological Interactions
ISSN :
0009-2797
eISSN :
1872-7786
Publisher :
Elsevier, Amsterdam, Netherlands
Volume :
344
Pages :
109513
Peer reviewed :
Peer Reviewed verified by ORBi
Commentary :
Copyright © 2021 Elsevier B.V. All rights reserved.
Available on ORBi :
since 24 August 2021

Statistics


Number of views
67 (1 by ULiège)
Number of downloads
1 (1 by ULiège)

Scopus citations®
 
8
Scopus citations®
without self-citations
3
OpenCitations
 
8
OpenAlex citations
 
10

Bibliography


Similar publications



Contact ORBi