Article ID Journal Published Year Pages File Type
1394174 European Journal of Medicinal Chemistry 2014 8 Pages PDF
Abstract

•Aza-deoxi-pterocarpans exhibited antineoplastic effect on MDR leukemia cell lines.•LQB-223 is the most promising prototype for targeting these cells.•LQB-223 is a candidate for treatment of unresponsive leukemias with a lower chance of side effects.•The tosyl group (a sulfonamide) is very important for the biological activity.

Aza-deoxi-pterocarpans (1) were synthesized through palladium-catalyzed aza-arylation of dihydronaphtalen, and showed antineoplastic effect on MDR leukemic cell lines (K562, Lucena-1 and FEPS). Compounds 1c–d were prepared to identify the pharmacophoric group responsible for the activity as well as compounds 2a–c were prepared to evaluate the structural requirements in the D-ring. LQB-223 (1b) is the most promising antileukemic agent since it was the most active on MDR cells without detectable toxicity to normal immune system cells.

Graphical abstractFigure optionsDownload full-size imageDownload as PowerPoint slide

Related Topics
Physical Sciences and Engineering Chemistry Organic Chemistry
Authors
, , , , ,