| Literature DB >> 20056519 |
Marina O Shibinskaya1, Sergey A Lyakhov, Alexander V Mazepa, Sergey A Andronati, Alexander V Turov, Nadezhda M Zholobak, Nikolay Ya Spivak.
Abstract
New 6-(2-aminoethyl)-6H-indolo[2,3-b]quinoxalines were synthesized with high yields using bromoethylisatin and 6-(2-bromoethyl)-6H-indolo[2,3-b]quinoxaline as intermediates. These compounds were screened for the cytotoxicity, antiviral activity and interferon inducing ability. It was shown, that tested 6-(2-aminoethyl)-6H-indolo[2,3-b]quinoxalines are low toxic potent interferon inducers and antivirals. Morpholine and 4-methyl-piperidine derivatives appeared as the most active antivirals and the least cytotoxic in the investigated series. Copyright (c) 2009 Elsevier Masson SAS. All rights reserved.Entities:
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Year: 2009 PMID: 20056519 DOI: 10.1016/j.ejmech.2009.12.014
Source DB: PubMed Journal: Eur J Med Chem ISSN: 0223-5234 Impact factor: 6.514