Antitumor agents. 5. Synthesis, structure-activity relationships, and biological evaluation of dimethyl-5 H-pyridophenoxazin-5-ones, tetrahydro-5 H- …

…, M Manfra, A Lavecchia, E Novellino…

Index: Bolognese, Adele; Correale, Gaetano; Manfra, Michele; Lavecchia, Antonio; Novellino, Ettore; Pepe, Stefano Journal of Medicinal Chemistry, 2006 , vol. 49, # 17 p. 5110 - 5118

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Citation Number: 24

Abstract

New antiproliferative compounds, dimethyl-5 H-pyrido [3, 2-a] phenoxazin-5-ones (1-6), tetrahydro-5 H-benzopyrido [2, 3-j] phenoxazin-5-ones (7-9), and 5 H-benzopyrido [3, 2-a] phenoxazin-5-ones (10-12) were synthesized and evaluated against representative human neoplastic cell lines. Dimethyl derivatives 1-6 were more active against carcinoma than leukemia cell lines. The tetrahydrobenzo derivatives 7-9 were scarcely active, whereas ...