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Synthesis, Antimicrobial and Antioxidant Activities of 2-Isoxazoline Derivatives
A series of derivatives of trans-3-(2,4,6-trimethoxyphenyl)4,5-dihydroisoxazolo-4,5-bis[carbonyl-(4′phenyl)thiosemicarbazide (9) and of trans-3-(2,4,6-trimethoxyphenyl)-4,5-dihydro isoxazolo-4,5-bis(aroylcarbohydrazide) (10a–c) were synthesized from trans-3-(2,4,6-trimethoxyphenyl)-4,5-dihydro-4,5-b...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7570493/ https://www.ncbi.nlm.nih.gov/pubmed/32961855 http://dx.doi.org/10.3390/molecules25184271 |
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author | Alshamari, Asma Al-Qudah, Mahmoud Hamadeh, Fedaa Al-Momani, Lo’ay Abu-Orabi, Sultan |
author_facet | Alshamari, Asma Al-Qudah, Mahmoud Hamadeh, Fedaa Al-Momani, Lo’ay Abu-Orabi, Sultan |
author_sort | Alshamari, Asma |
collection | PubMed |
description | A series of derivatives of trans-3-(2,4,6-trimethoxyphenyl)4,5-dihydroisoxazolo-4,5-bis[carbonyl-(4′phenyl)thiosemicarbazide (9) and of trans-3-(2,4,6-trimethoxyphenyl)-4,5-dihydro isoxazolo-4,5-bis(aroylcarbohydrazide) (10a–c) were synthesized from trans-3-(2,4,6-trimethoxyphenyl)-4,5-dihydro-4,5-bis(hydrazenocarbonyl)isoxazole (8). The structures of the compounds were elucidated by both elemental and spectral (IR, NMR, and MS) analysis. Compound 9 shows activity against some bacterial species. No antibacterial activities were observed for compounds 10a–c. The antioxidant activity of the new compounds has been screened. Compound 9 showed higher antioxidant activity using the DPPH (1,1-diphenyl-2-picrylhydrazyl) and ABTS (2’-azino–bis(3-ethylbenzoline-6-sulfonic acid) diammonium salt methods. |
format | Online Article Text |
id | pubmed-7570493 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-75704932020-10-28 Synthesis, Antimicrobial and Antioxidant Activities of 2-Isoxazoline Derivatives Alshamari, Asma Al-Qudah, Mahmoud Hamadeh, Fedaa Al-Momani, Lo’ay Abu-Orabi, Sultan Molecules Article A series of derivatives of trans-3-(2,4,6-trimethoxyphenyl)4,5-dihydroisoxazolo-4,5-bis[carbonyl-(4′phenyl)thiosemicarbazide (9) and of trans-3-(2,4,6-trimethoxyphenyl)-4,5-dihydro isoxazolo-4,5-bis(aroylcarbohydrazide) (10a–c) were synthesized from trans-3-(2,4,6-trimethoxyphenyl)-4,5-dihydro-4,5-bis(hydrazenocarbonyl)isoxazole (8). The structures of the compounds were elucidated by both elemental and spectral (IR, NMR, and MS) analysis. Compound 9 shows activity against some bacterial species. No antibacterial activities were observed for compounds 10a–c. The antioxidant activity of the new compounds has been screened. Compound 9 showed higher antioxidant activity using the DPPH (1,1-diphenyl-2-picrylhydrazyl) and ABTS (2’-azino–bis(3-ethylbenzoline-6-sulfonic acid) diammonium salt methods. MDPI 2020-09-18 /pmc/articles/PMC7570493/ /pubmed/32961855 http://dx.doi.org/10.3390/molecules25184271 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Alshamari, Asma Al-Qudah, Mahmoud Hamadeh, Fedaa Al-Momani, Lo’ay Abu-Orabi, Sultan Synthesis, Antimicrobial and Antioxidant Activities of 2-Isoxazoline Derivatives |
title | Synthesis, Antimicrobial and Antioxidant Activities of 2-Isoxazoline Derivatives |
title_full | Synthesis, Antimicrobial and Antioxidant Activities of 2-Isoxazoline Derivatives |
title_fullStr | Synthesis, Antimicrobial and Antioxidant Activities of 2-Isoxazoline Derivatives |
title_full_unstemmed | Synthesis, Antimicrobial and Antioxidant Activities of 2-Isoxazoline Derivatives |
title_short | Synthesis, Antimicrobial and Antioxidant Activities of 2-Isoxazoline Derivatives |
title_sort | synthesis, antimicrobial and antioxidant activities of 2-isoxazoline derivatives |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7570493/ https://www.ncbi.nlm.nih.gov/pubmed/32961855 http://dx.doi.org/10.3390/molecules25184271 |
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