Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1394174 | European Journal of Medicinal Chemistry | 2014 | 8 Pages |
•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.
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