Synthesis and preliminary evaluation of N-oxide derivatives for the prevention of atherothrombotic events
Contribuinte(s) |
Universidade Estadual Paulista (UNESP) |
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Data(s) |
07/12/2015
07/12/2015
2015
|
Resumo |
Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP) Processo FAPESP: 2010/02774-5 Thrombosis is the main outcome of many cardiovascular diseases. Current treatments to prevent thrombotic events involve the long-term use of antiplatelet drugs. However, this therapy has several limitations, thereby justifying the development of new drugs. A series of N-oxide derivatives (furoxan and benzofuroxan) were synthesized and characterized as potential antiplatelet/antithrombotic compounds. All compounds (3a,b, 4a,b, 8a,b, 9a,b, 13a,b and 14a,b) inhibited platelet aggregation induced by adenosine-5-diphosphate, collagen, and arachidonic acid. All compounds protected mice from pulmonary thromboembolism induced by a mixture of collagen and epinephrine; however, benzofuroxan derivatives (13a,b and 14a,b) were the most active compounds, reducing thromboembolic events by up to 80%. N-oxide derivative 14a did not induce genotoxicity in vivo. In conclusion, 14a has emerged as a new antiplatelet/antithrombotic prototype useful for the prevention of atherothrombotic events. |
Formato |
18185-200 |
Identificador |
http://dx.doi.org/10.3390/molecules201018185 Molecules (basel, Switzerland), v. 20, n. 10, p. 18185-18200, 2015. 1420-3049 http://hdl.handle.net/11449/131455 10.3390/molecules201018185 PM26457696.pdf 26457696 |
Idioma(s) |
eng |
Publicador |
Molecules |
Relação |
Molecules (basel, Switzerland) |
Direitos |
openAccess |
Palavras-Chave | #N-oxide #Antiplatelet activity #Atherothrombosis #Benzofuroxan #Bleeding time #Furoxan #Genotoxicity |
Tipo |
info:eu-repo/semantics/article |