Antioxidant capacity of eugenol derivatives

Toxicity and antioxidant capacity of eugenol derivatives (E2 = 2-Methoxy-4-[1-propenylphenyl]acetate, E3 = 4-Allyl-2-methoxyphenylacetate, E4 = 4-Allyl-2-methoxy-4-nitrophenol, E5 = 5-Allyl-3-nitrobenzene-1,2-diol, E6 = 4-Allyl-2-methoxy-5-nitrophenyl acetate) were evaluated in order to determine th...
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Gespeichert in:

Autor*in:	María E. Hidalgo [verfasserIn] Carlos De la Rosa [verfasserIn] Héctor Carrasco [verfasserIn] Wilson Cardona [verfasserIn] Claudio Gallardo [verfasserIn] Luis Espinoza [verfasserIn]

Format:	E-Artikel
Sprache:	Englisch ; Spanisch ; Portugiesisch

Erschienen:	2009

Schlagwörter:	eugenol derivatives antioxidant capacity

Übergeordnetes Werk:	In: Química Nova - Sociedade Brasileira de Química, 2004, 32(2009), 6, Seite 1467-1470
Übergeordnetes Werk:	volume:32 ; year:2009 ; number:6 ; pages:1467-1470

Links:	Link aufrufen Link aufrufen Link aufrufen Journal toc Journal toc

DOI / URN:	10.1590/S0100-40422009000600020

Katalog-ID:	DOAJ055177492

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language	English Spanish Portuguese
source	In Química Nova 32(2009), 6, Seite 1467-1470 volume:32 year:2009 number:6 pages:1467-1470
sourceStr	In Química Nova 32(2009), 6, Seite 1467-1470 volume:32 year:2009 number:6 pages:1467-1470
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topic_facet	eugenol derivatives antioxidant capacity Chemistry
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authorswithroles_txt_mv	María E. Hidalgo @@aut@@ Carlos De la Rosa @@aut@@ Héctor Carrasco @@aut@@ Wilson Cardona @@aut@@ Claudio Gallardo @@aut@@ Luis Espinoza @@aut@@
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callnumber-first	Q - Science
author	María E. Hidalgo
spellingShingle	María E. Hidalgo misc QD1-999 misc eugenol derivatives misc antioxidant capacity misc Chemistry Antioxidant capacity of eugenol derivatives
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topic_title	QD1-999 Antioxidant capacity of eugenol derivatives eugenol derivatives antioxidant capacity
topic	misc QD1-999 misc eugenol derivatives misc antioxidant capacity misc Chemistry
topic_unstemmed	misc QD1-999 misc eugenol derivatives misc antioxidant capacity misc Chemistry
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title	Antioxidant capacity of eugenol derivatives
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title_full	Antioxidant capacity of eugenol derivatives
author_sort	María E. Hidalgo
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author_browse	María E. Hidalgo Carlos De la Rosa Héctor Carrasco Wilson Cardona Claudio Gallardo Luis Espinoza
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class	QD1-999
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author-letter	María E. Hidalgo
doi_str_mv	10.1590/S0100-40422009000600020
author2-role	verfasserin
title_sort	antioxidant capacity of eugenol derivatives
callnumber	QD1-999
title_auth	Antioxidant capacity of eugenol derivatives
abstract	Toxicity and antioxidant capacity of eugenol derivatives (E2 = 2-Methoxy-4-[1-propenylphenyl]acetate, E3 = 4-Allyl-2-methoxyphenylacetate, E4 = 4-Allyl-2-methoxy-4-nitrophenol, E5 = 5-Allyl-3-nitrobenzene-1,2-diol, E6 = 4-Allyl-2-methoxy-5-nitrophenyl acetate) were evaluated in order to determine the influence of the sustituents. E2-E6 were synthesized from eugenol (E1). E1 was extracted from cloves oil, and E2-E6 were obtained through acetylation and nitration reactions. Antioxidant capacity evaluated by DPPH (1, 1-Diphenyl-2-picrylhydrazil) and ORAC fluorescein demonstrated that E1 and E5 have a higher capacity and the minor toxicity evaluated by red blood cells haemolysis and the Artemia saline test. In accordance with our results, the compound's (E1-E5) use in the pharmaceutical, cosmetic and or food industries could be suggested.
abstractGer	Toxicity and antioxidant capacity of eugenol derivatives (E2 = 2-Methoxy-4-[1-propenylphenyl]acetate, E3 = 4-Allyl-2-methoxyphenylacetate, E4 = 4-Allyl-2-methoxy-4-nitrophenol, E5 = 5-Allyl-3-nitrobenzene-1,2-diol, E6 = 4-Allyl-2-methoxy-5-nitrophenyl acetate) were evaluated in order to determine the influence of the sustituents. E2-E6 were synthesized from eugenol (E1). E1 was extracted from cloves oil, and E2-E6 were obtained through acetylation and nitration reactions. Antioxidant capacity evaluated by DPPH (1, 1-Diphenyl-2-picrylhydrazil) and ORAC fluorescein demonstrated that E1 and E5 have a higher capacity and the minor toxicity evaluated by red blood cells haemolysis and the Artemia saline test. In accordance with our results, the compound's (E1-E5) use in the pharmaceutical, cosmetic and or food industries could be suggested.
abstract_unstemmed	Toxicity and antioxidant capacity of eugenol derivatives (E2 = 2-Methoxy-4-[1-propenylphenyl]acetate, E3 = 4-Allyl-2-methoxyphenylacetate, E4 = 4-Allyl-2-methoxy-4-nitrophenol, E5 = 5-Allyl-3-nitrobenzene-1,2-diol, E6 = 4-Allyl-2-methoxy-5-nitrophenyl acetate) were evaluated in order to determine the influence of the sustituents. E2-E6 were synthesized from eugenol (E1). E1 was extracted from cloves oil, and E2-E6 were obtained through acetylation and nitration reactions. Antioxidant capacity evaluated by DPPH (1, 1-Diphenyl-2-picrylhydrazil) and ORAC fluorescein demonstrated that E1 and E5 have a higher capacity and the minor toxicity evaluated by red blood cells haemolysis and the Artemia saline test. In accordance with our results, the compound's (E1-E5) use in the pharmaceutical, cosmetic and or food industries could be suggested.
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container_issue	6
title_short	Antioxidant capacity of eugenol derivatives
url	https://doi.org/10.1590/S0100-40422009000600020 https://doaj.org/article/b6a7f54159ea45a9862805c595dd82f3 http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0100-40422009000600020 https://doaj.org/toc/0100-4042 https://doaj.org/toc/1678-7064
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author2	Carlos De la Rosa Héctor Carrasco Wilson Cardona Claudio Gallardo Luis Espinoza
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up_date	2024-07-03T13:26:47.771Z
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