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Novel N-methylsulfonyl-indole derivatives: biological activity and COX-2/5-LOX inhibitory effect with improved gastro protective profile and reduced cardio vascular risks

Three novel series of N-methylsulfonylindole derivatives 3a&b, 4a–e, and 5a–e were synthesised. Different biological activities of the synthesised compounds were studied. Antimicrobial activity showed that, compounds 4b, 4e and 5d had selective antibacterial activity against the Gram-negative ba...

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Autores principales: Philoppes, John N., Abdelgawad, Mohamed A., Abourehab, Mohammed A. S., Sebak, Mohamed, A. Darwish, Mostafa, Lamie, Phoebe F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9721424/
https://www.ncbi.nlm.nih.gov/pubmed/36458373
http://dx.doi.org/10.1080/14756366.2022.2145283
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author Philoppes, John N.
Abdelgawad, Mohamed A.
Abourehab, Mohammed A. S.
Sebak, Mohamed
A. Darwish, Mostafa
Lamie, Phoebe F.
author_facet Philoppes, John N.
Abdelgawad, Mohamed A.
Abourehab, Mohammed A. S.
Sebak, Mohamed
A. Darwish, Mostafa
Lamie, Phoebe F.
author_sort Philoppes, John N.
collection PubMed
description Three novel series of N-methylsulfonylindole derivatives 3a&b, 4a–e, and 5a–e were synthesised. Different biological activities of the synthesised compounds were studied. Antimicrobial activity showed that, compounds 4b, 4e and 5d had selective antibacterial activity against the Gram-negative bacteria, Salmonella enterica and/or E. coli. The anti-oxidant activity of the synthesised compounds was evaluated by DPPH radical scavenging activity. In vitro anti-inflammatory activity was estimated. Compounds 4d, 4e, 5b, and 5d showed the highest anti-inflammatory activity. The COX-1, COX-2 and 5-LOX inhibitory activities were measured using enzyme immune assay (EIA) kits. Due to the dual COX-2/5-LOX inhibitory activity of compound 5d, its cardiovascular profile was determined by measuring cardiac biomarkers (LDH, CK-MB, and Tn-I). Besides, the histopathological study of the heart muscle and stomach were examined for the most active COX-2 inhibitors 4e and 5d. Finally, a molecular modelling study and pharmacokinetic properties were obtained using different computational methods.
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spelling pubmed-97214242022-12-06 Novel N-methylsulfonyl-indole derivatives: biological activity and COX-2/5-LOX inhibitory effect with improved gastro protective profile and reduced cardio vascular risks Philoppes, John N. Abdelgawad, Mohamed A. Abourehab, Mohammed A. S. Sebak, Mohamed A. Darwish, Mostafa Lamie, Phoebe F. J Enzyme Inhib Med Chem Research Paper Three novel series of N-methylsulfonylindole derivatives 3a&b, 4a–e, and 5a–e were synthesised. Different biological activities of the synthesised compounds were studied. Antimicrobial activity showed that, compounds 4b, 4e and 5d had selective antibacterial activity against the Gram-negative bacteria, Salmonella enterica and/or E. coli. The anti-oxidant activity of the synthesised compounds was evaluated by DPPH radical scavenging activity. In vitro anti-inflammatory activity was estimated. Compounds 4d, 4e, 5b, and 5d showed the highest anti-inflammatory activity. The COX-1, COX-2 and 5-LOX inhibitory activities were measured using enzyme immune assay (EIA) kits. Due to the dual COX-2/5-LOX inhibitory activity of compound 5d, its cardiovascular profile was determined by measuring cardiac biomarkers (LDH, CK-MB, and Tn-I). Besides, the histopathological study of the heart muscle and stomach were examined for the most active COX-2 inhibitors 4e and 5d. Finally, a molecular modelling study and pharmacokinetic properties were obtained using different computational methods. Taylor & Francis 2022-12-01 /pmc/articles/PMC9721424/ /pubmed/36458373 http://dx.doi.org/10.1080/14756366.2022.2145283 Text en © 2022 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Paper
Philoppes, John N.
Abdelgawad, Mohamed A.
Abourehab, Mohammed A. S.
Sebak, Mohamed
A. Darwish, Mostafa
Lamie, Phoebe F.
Novel N-methylsulfonyl-indole derivatives: biological activity and COX-2/5-LOX inhibitory effect with improved gastro protective profile and reduced cardio vascular risks
title Novel N-methylsulfonyl-indole derivatives: biological activity and COX-2/5-LOX inhibitory effect with improved gastro protective profile and reduced cardio vascular risks
title_full Novel N-methylsulfonyl-indole derivatives: biological activity and COX-2/5-LOX inhibitory effect with improved gastro protective profile and reduced cardio vascular risks
title_fullStr Novel N-methylsulfonyl-indole derivatives: biological activity and COX-2/5-LOX inhibitory effect with improved gastro protective profile and reduced cardio vascular risks
title_full_unstemmed Novel N-methylsulfonyl-indole derivatives: biological activity and COX-2/5-LOX inhibitory effect with improved gastro protective profile and reduced cardio vascular risks
title_short Novel N-methylsulfonyl-indole derivatives: biological activity and COX-2/5-LOX inhibitory effect with improved gastro protective profile and reduced cardio vascular risks
title_sort novel n-methylsulfonyl-indole derivatives: biological activity and cox-2/5-lox inhibitory effect with improved gastro protective profile and reduced cardio vascular risks
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9721424/
https://www.ncbi.nlm.nih.gov/pubmed/36458373
http://dx.doi.org/10.1080/14756366.2022.2145283
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