Synthesis and in Vitro Cytotoxic Evaluation of New Derivatives of Pyrido[1,2-a]benzimidazolic Ring System: The Pyrido[1,2:1,2]imidazo[4,5-h]quinazolines - Archive ouverte HAL
Article Dans Une Revue Chemical and Pharmaceutical Bulletin Année : 2001

Synthesis and in Vitro Cytotoxic Evaluation of New Derivatives of Pyrido[1,2-a]benzimidazolic Ring System: The Pyrido[1,2:1,2]imidazo[4,5-h]quinazolines

Résumé

Access to the original series of pyrido[1',2':1,2]imidazo[4,5-h]quinazoline was developed from a 1,3-dicarbonyl unit with some “N-C-N” bisnucleophilic reagents and the derivatives obtained were evaluated for in vitro cytotoxic activities against HL60 and A2780 cells. All compounds exhibited cytotoxic activitise on resistant cell lines (MDR+; HL60R and A2780R) with no resistance phenomena.
Fichier principal
Vignette du fichier
Dupuy M et al Chem Pharm Bull 2001.pdf (80.65 Ko) Télécharger le fichier
Origine Fichiers éditeurs autorisés sur une archive ouverte
Loading...

Dates et versions

hal-02384513 , version 1 (28-11-2019)

Identifiants

Citer

Marianne Dupuy, Frédéric Pinguet, Olivier Chavignon, Jean-Michel Chezal, Jean-Claude Teulade, et al.. Synthesis and in Vitro Cytotoxic Evaluation of New Derivatives of Pyrido[1,2-a]benzimidazolic Ring System: The Pyrido[1,2:1,2]imidazo[4,5-h]quinazolines. Chemical and Pharmaceutical Bulletin, 2001, 49, pp.1061 - 1065. ⟨10.1248/cpb.49.1061⟩. ⟨hal-02384513⟩
72 Consultations
68 Téléchargements

Altmetric

Partager

More