Estudio computacional de la reactividad y propiedades fisicoquímicas del eugenol, 2-metoxi-4-oxiranilmetilfenol y quinona metilada
Computational study of the reactivity and physicochemical properties of eugenol, 2-methoxy-4-oxiranylmethylphenol and methylated quinone
DOI:
https://doi.org/10.15446/rcciquifa.v48n2.82695Palavras-chave:
Eugenol, potencial farmacológico, propiedades fisicoquímicas, reactividad (es)Eugenol, pharmacological potential, physicochemical properties, reactivity (en)
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Referências
J.P. Noel, M.B. Austin, E.K. Bomati, Structure-function relationships in plant phenylpropanoid biosynthesis, Curr. Opin. Plant. Biol., 8, 249-253 (2005).
U.K. Sharma, A.K. Sharma, A.K. Pandey, Medicinal attributes of major phenylpropanoids present in cinnamon, BMC Complement. Altern. Med., 16, 156 (2016).
A.K. Pandey, A.K. Mishra, A. Mishra, Antifungal and antioxidative potential of oil and extracts derived from leaves of Indian spice plant Cinnamomum tamala, Cell Mol. Biol., 58, 142-147 (2012).
M.R. Charan-Raja, V. Srinivasan, S. Selvaraj, S.K. Mahapatra, Versatile and synergistc potential of eugenol: A Review, Pharm. Anal. Acta, 6, 367-372 (2015).
X. Kong, X. Liu, J. Li, Y. Yang, Advances in pharmacological research of eugenol, Curr. Opin. Complement. Alternat. Med., 1, 8-11 (2014).
A. Cherkasov, E.N. Muratov, D. Fourches et al., QSAR Modeling: Where have you been? Where are you going to? J. Med. Chem., 57, 4977-5010 (2014).
A. Absalan, S.A. Mesbah-Namin, T. Tiraihi, T. Taheri, The effects of cinnamaldehyde and eugenol on human adipose-derived mesenchymal stem cells viability, growth and differentiation: a cheminformatics and in vitro study, Avicenna J. Phytomed., 6, 643-657 (2016).
J.L. Bolton, Quinone methide bioactivation Pathway: Contribution to toxicity and/or cytoprotection? Curr. Org. Chem., 18, 61-69 (2014).
G. Luo, T.M. Guenthner, Investigation of the role of the 2,3-epoxidation pathway in the bioactivation and genotoxicity of dietary allylbenzene analogs, Toxicology, 160, 47-58 (2001).
C. Southan, A. Stracz, Extracting and connecting chemical structures from text sources using chemicalize.org, J. Cheminform., 5, 20 (2013).
D. Fourches, E. Muratov, A. Tropsha, Trust, but verify: On the importance of chemical structure curation in cheminformatics and QSAR modeling research, J. Chem. Inf. Model., 50, 1189-1204 (2010).
D. Banfi, L. Patiny, Resurrecting and Processing NMR Spectra On-line, Chimia, 62, 280-281(2008).
L.N. Fierro, C.A. Faúndez, J.O. Valderrama, Método de contribución de grupos: una herramienta fundamental en cursos avanzados de termodinámica y física de fluidos para la estimación de propiedades de sustancias, Formación Universitaria, 9, 99-108 (2016).
L. Constantinou, R. Gani, New group contribution method for estimating properties of pure compounds, AIChE J., 40, 1697-1710 (1994).
J.L. Kingsley, G.L. Wilson, E.M. Essex, A.L. Markus, Combining structure and ligand based approaches to improve site of metabolism prediction in CYP2C9 substrates, Pharm. Res., 32, 986-1001 (2015).
S. Sivakumar, P. Anitha, B. Ramesh, G. Suresh, Analysis of EAWAG-BBD pathway prediction system for the identification of malathion degrading microbes, Bioinformation, 13, 73-77 (2017).
R. Chang, Fisicoquímica, México, Mc Graw Hill, 3a ed., 2008.
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