| Literature DB >> 15142560 |
Peter Demin1, Olga Rounova, Thomas Grunberger, Lorand Cimpean, Nigel Sharfe, Chaim M Roifman.
Abstract
A series of substituted styryl-acrylonitriles was designed and synthesized. The new compounds, called tyrenes, were tested for the ability to inhibit acute lymphocytic leukemia (ALL) cancer cell growth, as well as on their toxicity to normal bone marrow (NBM) cells. The results showed that 3,4-dihydroxystyryl-acrylonitriles, in particular CR-4, revealed great potency as antitumor agents, and also exhibited low toxicity to normal cells. The effectiveness of these compounds with extended conjugation may be due to their possible functioning as reactive Michael acceptors.Entities:
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Year: 2004 PMID: 15142560 DOI: 10.1016/j.bmc.2004.03.043
Source DB: PubMed Journal: Bioorg Med Chem ISSN: 0968-0896 Impact factor: 3.641