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

Citation
M. Dupuy 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, CHEM PHARM, 49(9), 2001, pp. 1061-1065
Citations number
17
Categorie Soggetti
Chemistry & Analysis
Journal title
CHEMICAL & PHARMACEUTICAL BULLETIN
ISSN journal
00092363 → ACNP
Volume
49
Issue
9
Year of publication
2001
Pages
1061 - 1065
Database
ISI
SICI code
0009-2363(200109)49:9<1061:SAIVCE>2.0.ZU;2-5
Abstract
Access to the original series of pyrido[1 ' ,2 ' :1,2]imidazo[4,5-h]quinazo line was developed from a 1,3-dicarbonyl unit with some "N-C-N" bisnucleoph ilic reagents and the derivatives obtained were evaluated for in vitro cyto toxic activities against HL60 and A2780 cells. All compounds exhibited cyto toxic activities on resistant cell lines (MDR+; HL60R and A2780R) with no r esistance phenomena.