Synthesis and biological evaluation of 3-aromatic Shiff base-5-fluoroindol-2-one derivatives / 药学学报
Acta Pharmaceutica Sinica
; (12): 1338-1343, 2011.
Article
em Zh
| WPRIM
| ID: wpr-232988
Biblioteca responsável:
WPRO
ABSTRACT
Based on the structure of 5-fluoroindol-2-one and fragments from thirteen multi-target tyrosine kinase inhibitors which have been marketed or in the phase of clinical research, eleven 3-aromatic Shiff base-5-fluoroindol-2-one derivatives were designed and synthesized. Their structures were identified by 1H NMR, MS and elemental analysis. In vitro antitumor bioactivities evaluation was done by MTT method. It was shown that most of synthesized compounds had antitumor activities and compounds 1b, 1g, 1i and 1h were better than or equal to the antitumor activity of positive control.
Texto completo:
1
Índice:
WPRIM
Assunto principal:
Farmacologia
/
Ensaios de Seleção de Medicamentos Antitumorais
/
Química
/
Linhagem Celular Tumoral
/
Proliferação de Células
/
Indóis
/
Antineoplásicos
Limite:
Humans
Idioma:
Zh
Revista:
Acta Pharmaceutica Sinica
Ano de publicação:
2011
Tipo de documento:
Article