Resumen
A facile and metal-free one-pot protocol for the synthesis of fused imidazopyridine scaffolds has been developed. This novel protocol combines the Groebke-Blackburn-Bienaymé reaction (GBBR) with a sequential TBAB-mediated cyclization cascade. Biological evaluation demonstrated that compound 6a inhibits human prostate cancer cell DU-145 proliferation with an IC50 of 1.6 μM. The molecular mechanism study indicates that 6a significantly suppresses the oncogenic Erk kinase phosphorylation at 3 μM.
Idioma original | English (US) |
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Páginas (desde-hasta) | 12632-12638 |
Número de páginas | 7 |
Publicación | Journal of Organic Chemistry |
Volumen | 84 |
N.º | 19 |
DOI | |
Estado | Published - oct 4 2019 |
Publicado de forma externa | Sí |
ASJC Scopus subject areas
- Organic Chemistry