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Molecules ; 28(23)2023 Dec 02.
Artigo em Inglês | MEDLINE | ID: mdl-38067641

RESUMO

Sixteen new 2-substituted quinazolines were synthesized using a straightforward methodology starting from 2-methoxybezoic acid or 3-methoxy-2-naphthoic acid. The anti-proliferative activity of the target compounds was evaluated against nine cancer cell lines. Additionally, all the compounds were screened for their potency and selectivity against a panel of 109 kinases and four bromodomains, using Differential Scanning Fluorimetry (DSF). Compound 17 bearing a 2-methoxyphenyl substitution along with a basic side chain displayed a remarkable profile against the majority of the tested cell lines.


Assuntos
Antineoplásicos , Neoplasias , Humanos , Quinazolinas/farmacologia , Linhagem Celular , Relação Estrutura-Atividade , Antineoplásicos/farmacologia
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