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Bioorg Med Chem Lett ; 25(11): 2401-4, 2015 Jun 01.
Artículo en Inglés | MEDLINE | ID: mdl-25913116

RESUMEN

A series of N-((1,3-diphenyl-1H-pyrazol-4-yl)methyl)anilines were synthesized and evaluated in vitro for cytotoxicity and antiviral activity against a large panel of viruses. Most of the tested compounds interfered with RSV replication in the micromolar concentrations (EC50s ranging from 5 µM to 28 µM). SAR studies suggested that the presence of a trifluoromethyl group in R(1) abolished the anti-RSV activity and enhanced the cytotoxicity while the best results in term of both anti-RSV activity and selectivity were obtained by the introduction in R(1) of a chlorine or a bromine atom.


Asunto(s)
Compuestos de Anilina/química , Antivirales/farmacología , Pirazoles/química , Virus Sincitiales Respiratorios/efectos de los fármacos , Antivirales/síntesis química , Antivirales/química , Línea Celular , Humanos , Replicación Viral/efectos de los fármacos
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