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Author(s)
1Núcleo de Estudos e Seleção de Moléculas Bioativas, Instituto de Ciências da Saúde, Universidade Federal do Pará, Belém, Brazil.
1Núcleo de Estudos e Seleção de Moléculas Bioativas, Instituto de Ciências da Saúde, Universidade Federal do Pará, Belém, Brazil.
2Laboratório de Farmacologia e Toxicologia de Produtos Naturais, Instituto de Ciências da Saúde, Universidade Federal do Pará, Belém, Brazil.
3Instituto de Química de São Carlos, Universidade de São Paulo, São Carlos, Brazil.
1Núcleo de Estudos e Seleção de Moléculas Bioativas, Instituto de Ciências da Saúde, Universidade Federal do Pará, Belém, Brazil.
2Laboratório de Farmacologia e Toxicologia de Produtos Naturais, Instituto de Ciências da Saúde, Universidade Federal do Pará, Belém, Brazil.
3Instituto de Química de São Carlos, Universidade de São Paulo, São Carlos, Brazil.
The paracetamol has more antioxidant properties than
the salicylic acid on the several oxidative stress-forced models and
one possible mechanism is due to electron or hydrogen transfer by the
evaluated hydroxyl radicals. The antioxidant mechanism for the compounds
studied here was performed by molecular modeling using quantum chemical
calculations at the B3LYP level of theory. Our results show that the
paracetamol has more antioxidant properties than the salicylic acid in
experimental and theoretical studies. The theoretical mechanism show
that the hydrogen transfer is more favorable than the electron transfer.
From the study it was concluded that the electron abstraction for
paracetamol is more favored than salicylic acid.
KEYWORDS
Cite this paper
Borges, R. , Barros, T. , Pereira, G. , Batista Jr.,
J. , Beleza Filho, R. , Veiga, A. , Hamoy, M. , Mello, V. , Silva, A.
and Barros, C. (2014) A Structure and Antioxidant Activity Study of
Paracetamol and Salicylic Acid. Pharmacology & Pharmacy, 5, 1185-1191. doi: 10.4236/pp.2014.513130.
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