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Curr Pharm Des ; 15(11): 1187-90, 2009.
Artigo em Inglês | MEDLINE | ID: mdl-19355959

RESUMO

In vitro screening of 307 drugs with various clinical indications (cardiotropic, neurotropic, antibacterial, etc.) has revealed 6 compounds which displayed remarkable antiretroviral activity. Three of these drugs had a tendency to have undesirable side effects and were thus excluded from further consideration. Remaining three, i.e., Xantinol Nicotinate, Tardiferon, and Trental may become valid candidates for inclusion into antiviral regimens such as HAART. In vitro tests have shown that xantinol and trental display synergistic effect with azidothymidine, inhibit the replication AZT-resistant strains of HIV, and have no competing undesirable activities. These compounds should be evaluated in safety studies to determine optimal doses for patients with HIV. If these studies confirm in vitro results these compounds may become valid candidates as safe and affordable means to be added into the arsenal of antiretroviral drugs.


Assuntos
Fármacos Anti-HIV/farmacologia , Compostos Ferrosos , Mucinas , Pentoxifilina , Vasodilatadores/farmacologia , Niacinato de Xantinol , Animais , Fármacos Anti-HIV/uso terapêutico , Combinação de Medicamentos , Infecções por HIV/tratamento farmacológico , Humanos , Vasodilatadores/uso terapêutico
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