Literature DB >> 15028261

Design, synthesis and in vitro antitumor activity of new trans 2-[2-(heteroaryl)vinyl]-1,3-dimethylimidazolium iodides.

Francesco P Ballistreri1, Vincenza Barresi, Paolo Benedetti, Gianluigi Caltabiano, Cosimo G Fortuna, Maria L Longo, Giuseppe Musumarra.   

Abstract

The design, the synthesis, and the in vitro antitumor activities of trans 2-[2-(heteroaryl)vinyl]-1,3-dimethylimidazolium iodides versus MCF7 (human mammary carcinoma) and LNCap (prostate carcinoma) cell lines are reported. The design indicates trans 2-[2-[5-(2-chlorophenyl)furan-2-yl]vinyl]-1, 3-dimethylimidazolium iodide 5 and trans 2-[2-[5-(4-bromophenyl)furan-2-yl]vinyl]-1, 3-dimethylimidazolium iodide 6 as highly active compounds in the series. The synthesis of the above new derivatives and in vitro antitumor tests, confirm their significant antiproliferative and cytotoxic activities.

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Year:  2004        PMID: 15028261     DOI: 10.1016/j.bmc.2004.01.018

Source DB:  PubMed          Journal:  Bioorg Med Chem        ISSN: 0968-0896            Impact factor:   3.641


  1 in total

1.  1-Benzyl-3-(2-methoxy-phen-yl)imidazolium tetra-fluoro-borate.

Authors:  Ping Jiang
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2009-08-19
  1 in total

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