| Literature DB >> 24681983 |
Camilla D Buarque1, Eduardo J Salustiano2, Kevin C Fraga3, Bruna R M Alves3, Paulo R R Costa4.
Abstract
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.Entities:
Keywords: Antileukemic activity; Aza-arylation; Aza-heck; Sulfonamide
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Year: 2014 PMID: 24681983 DOI: 10.1016/j.ejmech.2014.03.039
Source DB: PubMed Journal: Eur J Med Chem ISSN: 0223-5234 Impact factor: 6.514