Synthesis and preliminary evaluation of N-oxide derivatives for the prevention of atherothrombotic events


Autoria(s): Rosseto, Leandro Augusto; Pires, Maria Elisa Lopes; Melchior, Aylime Castanho Bolognesi; Bosquesi, Priscila Longhin; Pavan, Aline Renata; Marcondes, Sisi; Chin, Chung Man; Santos, Jean Leandro dos
Contribuinte(s)

Universidade Estadual Paulista (UNESP)

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