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Suppression of the breakthrough of human immunodeficiency virus type 1 (HIV-1) in cell culture by thiocarboxanilide derivatives when used individually or in combination with other HIV-1-specific inhibitors (i.e., TSAO derivatives).

Five structurally related thiophene and furane analogues of the oxathiin carboxanilide derivative NSC 615985 (UC84) (designated UC10, UC68, UC81, UC42, and UC16) were identified as potent inhibitors of HIV-1 replication in cell culture and HIV-1 reverse transcriptase activity. These compounds were m...

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Detalhes bibliográficos
Publicado no:Proc Natl Acad Sci U S A
Principais autores: Balzarini, J, Pérez-Pérez, M J, Vélazquez, S, San-Félix, A, Camarasa, M J, De Clercq, E, Karlsson, A
Formato: Artigo
Idioma:Inglês
Publicado em: National Academy of Sciences 1995
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC41716/
https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/7539917/
https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.92.12.5470
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