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ACS Comb Sci ; 17(8): 442-51, 2015 Aug 10.
Artigo em Inglês | MEDLINE | ID: mdl-26161720

RESUMO

A sequential single-flask multicomponent reactions is highly effective for the synthesis of 1,2-dihydroisoquinolines through amidealkylation from intermediate N-acylisoquinolinium salts under mild conditions. N-Acylisoquinolinium ions and trichloromethyl-1-(1H-indol-3-yl)isoquinoline-2(1H)-carboxylate have demonstrated their reactivity toward aromatic and aliphatic π-nucleophiles. One of the 1,2-dihydroisoquinoline derivatives was found to be a potent inhibitor for transcription factor NF-κB by blocking IκBα degradation, p65 nuclear translocation, and NF-κB DNA binding in TNF-α-induced NIH 3T3 cells.


Assuntos
Isoquinolinas/síntese química , Isoquinolinas/farmacologia , NF-kappa B/antagonistas & inibidores , Animais , Células Cultivadas , Humanos , Isoquinolinas/química , Camundongos , Estrutura Molecular , NF-kappa B/metabolismo , Células NIH 3T3 , Relação Estrutura-Atividade , Fator de Necrose Tumoral alfa/antagonistas & inibidores , Fator de Necrose Tumoral alfa/metabolismo
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