Synthesis and Cytotoxic Activity of Chiral Sulfonamides Based on the 2-Azabicycloalkane Skeleton

A series of chiral sulfonamides containing the 2-azabicycloalkane scaffold were prepared from aza-Diels–Alder cycloadducts through their conversion to amines based on 2-azanorbornane or the bridged azepane skeleton, followed by the reaction with sulfonyl chlorides. The cytotoxic activity of the obta...

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Detalles Bibliográficos
Autores principales: Samadaei, Mahzeiar, Pinter, Matthias, Senfter, Daniel, Madlener, Sibylle, Rohr-Udilova, Nataliya, Iwan, Dominika, Kamińska, Karolina, Wojaczyńska, Elżbieta, Wojaczyński, Jacek, Kochel, Andrzej
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7288168/
https://www.ncbi.nlm.nih.gov/pubmed/32443610
http://dx.doi.org/10.3390/molecules25102355
Descripción
Sumario:A series of chiral sulfonamides containing the 2-azabicycloalkane scaffold were prepared from aza-Diels–Alder cycloadducts through their conversion to amines based on 2-azanorbornane or the bridged azepane skeleton, followed by the reaction with sulfonyl chlorides. The cytotoxic activity of the obtained bicyclic derivatives was evaluated using human hepatocellular carcinoma (HCC), medulloblastoma (MB), and glioblastoma (GBM) cell lines. Chosen compounds were shown to notably reduce cell viability as compared to nonmalignant cells.

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