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Synthesis of novel 6-seleno-dihydropyrimidinones: Potentially bioactive compounds
Synthesis of novel 6-seleno-dihydropyrimidinones: Potentially bioactive compounds
Barbosa, Flavio A. R.; Canto, Rômulo F. S.; Braga, Antonio L.
Abstract:
Organoselenium compounds and dihydropyrimidinones (DHPMs) are biologically privileged classes of compounds due to its interactions with a wide range of molecular targets what leads to distinct pharmacological activities. Recent studies have shown that DHPMs are capable to act as anti-inflammatory and antitumoral agents.The same activities are described for organoselenium compounds, however, the mechanism of action of both classes are not supposed to be the same. Exploring the versatility of the Biginelli scaffold and the biological activities presented by organochalcogens, a series of novel potentially bioactive 6-seleno-dihydropyrimidinones was synthesized in this work.This new hybrid compounds are potential drug candidates, and we can also expect a possible synergism between the different pharmacophores
Organoselenium compounds and dihydropyrimidinones (DHPMs) are biologically privileged classes of compounds due to its interactions with a wide range of molecular targets what leads to distinct pharmacological activities. Recent studies have shown that DHPMs are capable to act as anti-inflammatory and antitumoral agents.The same activities are described for organoselenium compounds, however, the mechanism of action of both classes are not supposed to be the same. Exploring the versatility of the Biginelli scaffold and the biological activities presented by organochalcogens, a series of novel potentially bioactive 6-seleno-dihydropyrimidinones was synthesized in this work.This new hybrid compounds are potential drug candidates, and we can also expect a possible synergism between the different pharmacophores
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DOI: 10.5151/chempro-15bmos-BMOS2013_2013819222620
Referências bibliográficas
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Como citar:
Barbosa, Flavio A. R.; Canto, Rômulo F. S.; Braga, Antonio L.; "Synthesis of novel 6-seleno-dihydropyrimidinones: Potentially bioactive compounds", p-182-182.
In: In Blucher Chemistry Proceedings, São Paulo, v. 1, n. 2, Dezembro.2013.
São Paulo: Blucher,
2013.
ISSN 23184043,
DOI 10.5151/chempro-15bmos-BMOS2013_2013819222620
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TY - CONF T1 - Synthesis of novel 6-seleno-dihydropyrimidinones: Potentially bioactive compounds JO - Blucher Chemistry Proceedings VL - 1 IS - 2 SP - 182 EP - 182 PY - 2013 T2 - Brazilian Meeting on Organic Synthesis 2013 AU - , , SN - 23184043 DO - http://dx.doi.org/10.5151/chempro-15bmos-BMOS2013_2013819222620 UR - www.proceedings.blucher.com.br/article-details/synthesis-of-novel-6-seleno-dihydropyrimidinones-potentially-bioactive-compounds-8402 KW - ER -
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@article{Barbosa20144,
title="Synthesis of novel 6-seleno-dihydropyrimidinones: Potentially bioactive compounds",
journal="Blucher Chemistry Proceedings",
volume="1",
number="2",
pages="182 - 182",
year="2013",
note="",
issn="23184043",
doi="http://dx.doi.org/10.5151/chempro-15bmos-BMOS2013_2013819222620",
url="www.proceedings.blucher.com.br/article-details/synthesis-of-novel-6-seleno-dihydropyrimidinones-potentially-bioactive-compounds-8402",
author="Flavio A. R. Barbosa", "Rômulo F. S. Canto", "Antonio L. Braga",
keywords="",
}
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Flavio A. R. Barbosa, Rômulo F. S. Canto, Antonio L. Braga, Synthesis of novel 6-seleno-dihydropyrimidinones: Potentially bioactive compounds, Blucher Chemistry Proceedings, Volume 1, 2013, Pages 182-182, ISSN 23184043, http://dx.doi.org/10.5151/chempro-15bmos-BMOS2013_2013819222620 (www.proceedings.blucher.com.br/article-details/synthesis-of-novel-6-seleno-dihydropyrimidinones-potentially-bioactive-compounds-8402) Palavras-chave:: ;