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Ring-substituted 4-Hydroxy-1H-quinolin-2-ones: Preparation and Biological Activity ‡

In the study, a series of twelve ring-substituted 4-hydroxy-1H-quinolin-2-one derivatives were prepared. The procedures for synthesis of the compounds are presented. The compounds were analyzed using RP-HPLC to determine lipophilicity and tested for their photosynthesis-inhibiting activity using spi...

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Detalles Bibliográficos
Autores principales: Jampilek, Josef, Musiol, Robert, Pesko, Matus, Kralova, Katarina, Vejsova, Marcela, Carroll, James, Coffey, Aidan, Finster, Jacek, Tabak, Dominik, Niedbala, Halina, Kozik, Violetta, Polanski, Jaroslaw, Csollei, Jozef, Dohnal, Jiri
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Molecular Diversity Preservation International 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6253998/
https://www.ncbi.nlm.nih.gov/pubmed/19305366
http://dx.doi.org/10.3390/molecules14031145
Descripción
Sumario:In the study, a series of twelve ring-substituted 4-hydroxy-1H-quinolin-2-one derivatives were prepared. The procedures for synthesis of the compounds are presented. The compounds were analyzed using RP-HPLC to determine lipophilicity and tested for their photosynthesis-inhibiting activity using spinach (Spinacia oleracea L.) chloroplasts. All the synthesized compounds were also evaluated for antifungal activity using in vitro screening with eight fungal strains. For all the compounds, the relationships between the lipophilicity and the chemical structure of the studied compounds are discussed, as well as their structure-activity relationships (SAR).