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Substituted imidazopyridines as potent inhibitors of HCV replication()
BACKGROUND/AIMS: Following lead optimization, a set of substituted imidazopyridines was identified as potent and selective inhibitors of in vitro HCV replication. The particular characteristics of one of the most potent compounds in this series (5-[[3-(4-chlorophenyl)-5-isoxazolyl]methyl]-2-(2,3-dif...
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| Publicado no: | J Hepatol |
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| Main Authors: | , , , , , , , , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
European Association for the Study of the Liver. Published by Elsevier Ireland Ltd.
2009
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7114863/ https://ncbi.nlm.nih.gov/pubmed/19303654 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.jhep.2008.12.028 |
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