Synthesis and biological evaluation of novel quinazolin-4(3H)-one Schiff base derivatives as nitric oxide synthase inhibitors
Synthesis of new Schiff base derivatives bearing a 6-nitro-2-ibuprofenyl-4(3H)-quinazolin-4-one skeleton, as well as their in vitro biological evaluation as inhibitors of nitric oxide synthase (iNOS and nNOS) isoforms, is defined. Structures of these novel heterocycles were confirmed based on their...
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doaj-2d701c31846d48a998cf31f49ece31852021-09-19T04:55:41ZengElsevierArabian Journal of Chemistry1878-53522021-10-011410103362Synthesis and biological evaluation of novel quinazolin-4(3H)-one Schiff base derivatives as nitric oxide synthase inhibitorsAyman M. Algohary0Mohamed M. Hassan1Department of Chemistry, College of Science Al-zulfi, Majmaah University, P.O. 66, Al-Majmaah 11952, Saudi Arabia; Egyption Drug Authority (EDA), P.O. 29, Giza, EgyptChemistry Department, Faculty of Education, Ain Shams University, Roxy, 11711 Cairo, EgyptSynthesis of new Schiff base derivatives bearing a 6-nitro-2-ibuprofenyl-4(3H)-quinazolin-4-one skeleton, as well as their in vitro biological evaluation as inhibitors of nitric oxide synthase (iNOS and nNOS) isoforms, is defined. Structures of these novel heterocycles were confirmed based on their spectral, (IR, 1H NMR, 13C NMR and MS) and elemental analyses. In general, the assayed compounds behave as better iNOS than nNOS inhibitors. Quinazolinyl Schiff bases 9a-e are the most active inhibitors of all tested compounds and the most iNOS/nNOS selective of all studied compounds, with expected potential as anti-stroke agents.http://www.sciencedirect.com/science/article/pii/S1878535221003774QuinazolinoneIbuprofenArginineInhibitionSchiff Base |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Ayman M. Algohary Mohamed M. Hassan |
spellingShingle |
Ayman M. Algohary Mohamed M. Hassan Synthesis and biological evaluation of novel quinazolin-4(3H)-one Schiff base derivatives as nitric oxide synthase inhibitors Arabian Journal of Chemistry Quinazolinone Ibuprofen Arginine Inhibition Schiff Base |
author_facet |
Ayman M. Algohary Mohamed M. Hassan |
author_sort |
Ayman M. Algohary |
title |
Synthesis and biological evaluation of novel quinazolin-4(3H)-one Schiff base derivatives as nitric oxide synthase inhibitors |
title_short |
Synthesis and biological evaluation of novel quinazolin-4(3H)-one Schiff base derivatives as nitric oxide synthase inhibitors |
title_full |
Synthesis and biological evaluation of novel quinazolin-4(3H)-one Schiff base derivatives as nitric oxide synthase inhibitors |
title_fullStr |
Synthesis and biological evaluation of novel quinazolin-4(3H)-one Schiff base derivatives as nitric oxide synthase inhibitors |
title_full_unstemmed |
Synthesis and biological evaluation of novel quinazolin-4(3H)-one Schiff base derivatives as nitric oxide synthase inhibitors |
title_sort |
synthesis and biological evaluation of novel quinazolin-4(3h)-one schiff base derivatives as nitric oxide synthase inhibitors |
publisher |
Elsevier |
series |
Arabian Journal of Chemistry |
issn |
1878-5352 |
publishDate |
2021-10-01 |
description |
Synthesis of new Schiff base derivatives bearing a 6-nitro-2-ibuprofenyl-4(3H)-quinazolin-4-one skeleton, as well as their in vitro biological evaluation as inhibitors of nitric oxide synthase (iNOS and nNOS) isoforms, is defined. Structures of these novel heterocycles were confirmed based on their spectral, (IR, 1H NMR, 13C NMR and MS) and elemental analyses. In general, the assayed compounds behave as better iNOS than nNOS inhibitors. Quinazolinyl Schiff bases 9a-e are the most active inhibitors of all tested compounds and the most iNOS/nNOS selective of all studied compounds, with expected potential as anti-stroke agents. |
topic |
Quinazolinone Ibuprofen Arginine Inhibition Schiff Base |
url |
http://www.sciencedirect.com/science/article/pii/S1878535221003774 |
work_keys_str_mv |
AT aymanmalgohary synthesisandbiologicalevaluationofnovelquinazolin43honeschiffbasederivativesasnitricoxidesynthaseinhibitors AT mohamedmhassan synthesisandbiologicalevaluationofnovelquinazolin43honeschiffbasederivativesasnitricoxidesynthaseinhibitors |
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