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dc.contributor.author
Paulino, M.  
dc.contributor.author
Alvareda, E. M.  
dc.contributor.author
Denis, P. A.  
dc.contributor.author
Barreiro, E. J.  
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Sperandio da Silva, G. M.  
dc.contributor.author
Dubin, Marta  
dc.contributor.author
Castellú, C.  
dc.contributor.author
Aguilera, S.  
dc.contributor.author
Tapia, O.  
dc.date.available
2017-07-11T21:48:31Z  
dc.date.issued
2008-10  
dc.identifier.citation
Paulino, M.; Alvareda, E. M.; Denis, P. A.; Barreiro, E. J.; Sperandio da Silva, G. M.; et al.; Studies of trypanocidal (inhibitory) power of naphthoquinones: evaluation of quantum chemical molecular descriptors for structure–activity relationships; Elsevier Masson; European Journal of Medical Chemistry; 43; 10; 10-2008; 2238-2246  
dc.identifier.issn
0223-5234  
dc.identifier.uri
http://hdl.handle.net/11336/20206  
dc.description.abstract
Electronic, lipophilic and steric descriptors included in QSAR-2D and -3D are analyzed for a set of ortho- and para-naphthoquinones that have proved to be powerful oxidative agents with potent trypanocidal activities specially against Leptomonas seymouri and Trypanosoma cruzi. Electronic properties are calculated by means of semiempirical (PM3), ab initio (HF/3-21G) and density functional theory (B3LYP/6-31 + G∗) methodologies. Three different electronic states, neutral quinones, hydroquinones and semiquinones, are studied to investigate if any one of them are statistically related with the biological activities. The best correlations were obtained at the B3LYP level of theory because it includes electronic correlation. The QSAR-2D indicates that the best trypanocidal growth inhibitors are molecules in the semiquinone electronic state, with the following properties: (a) high negative value of EHOMO, (b) high negative charge in the oxygen atoms of the carbonyl groups, (c) high positive charge in the carbon atom of one of carbonyl moieties and (d) high electronegativity (χ). In a complementary way, the QSAR-3D indicates that the electrostatic field correlates with trypanocidal activity and the presence of bulk moieties would increase activity. The idea of comparing the three electronic states may prove to be of most importance in the general strategy to the design of new trypanocidal drugs. In fact, the experimental results showed that semiquinone is the one really statistically relevant indicating a clear connection between biochemical and theoretical aspects. Finally, we demonstrated that to be a good anti-trypanosomatid compound, the molecule must be a good electron acceptor to reach easily the essential semiquinone state. We expect that the present results motivate new experimental as well as theoretical investigations that confirm our findings.  
dc.format
application/pdf  
dc.language.iso
eng  
dc.publisher
Elsevier Masson  
dc.rights
info:eu-repo/semantics/openAccess  
dc.rights.uri
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/  
dc.subject
Quantum Molecular Descriptors  
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B3lyp  
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Qsar  
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Trypanosomatids  
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O-Naphthoquinones  
dc.subject.classification
Biología Celular, Microbiología  
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Ciencias Biológicas  
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CIENCIAS NATURALES Y EXACTAS  
dc.title
Studies of trypanocidal (inhibitory) power of naphthoquinones: evaluation of quantum chemical molecular descriptors for structure–activity relationships  
dc.type
info:eu-repo/semantics/article  
dc.type
info:ar-repo/semantics/artículo  
dc.type
info:eu-repo/semantics/publishedVersion  
dc.date.updated
2017-07-11T19:46:30Z  
dc.journal.volume
43  
dc.journal.number
10  
dc.journal.pagination
2238-2246  
dc.journal.pais
Francia  
dc.journal.ciudad
París  
dc.description.fil
Fil: Paulino, M.. Bioinformatics and Molecular Biomodelling Laboratory ; Uruguay  
dc.description.fil
Fil: Alvareda, E. M.. Bioinformatics and Molecular Biomodelling Laboratory ; Uruguay  
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Fil: Denis, P. A.. Bioinformatics and Molecular Biomodelling Laboratory ; Uruguay  
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Fil: Barreiro, E. J.. Universidade Federal do Rio de Janeiro; Brasil  
dc.description.fil
Fil: Sperandio da Silva, G. M.. Universidade Federal do Rio de Janeiro; Brasil  
dc.description.fil
Fil: Dubin, Marta. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Houssay. Centro de Estudios Farmacológicos y Botánicos. Universidad de Buenos Aires. Facultad de Medicina. Centro de Estudios Farmacológicos y Botánicos; Argentina  
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Fil: Castellú, C.. Laboratorio Horus; Uruguay  
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Fil: Aguilera, S.. Universidad Católica de Chile; Chile  
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Fil: Tapia, O.. Uppsala University. Department of Physical and Analytical Chemistry; Suecia  
dc.journal.title
European Journal of Medical Chemistry  
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/url/http://www.sciencedirect.com/science/article/pii/S0223523407004886  
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/doi/http://dx.doi.org/10.1016/j.ejmech.2007.12.023