| Literature DB >> 22532255 |
Adriana Ignat1, Tamas Lovasz, Mihai Vasilescu, Eva Fischer-Fodor, Corina Bianca Tatomir, Castelia Cristea, Luminiţa Silaghi-Dumitrescu, Valentin Zaharia.
Abstract
A series of new phenothiazinyl-thiazolyl-hydrazine derivatives were synthesized by Hantzsch cyclization of 1-(10-ethyl-10H-phenothiazin-3-yl)-methylidene-thiosemicarbazide with α-halocarbonyl derivatives. Comparison between classical and microwave assisted synthesis emphasizes the great advantages induced by microwaves irradiation which afforded high reaction yields in much shorter reaction time. Structural assignments were based on spectroscopic methods (high resolution NMR, FTIR, MS). The new compounds were tested in vitro for their antiproliferative activity against tumor cell lines using spectrometric methods. Most of the compounds exhibit cytotoxicity against hepatic and colon tumor cells in a dose-dependent mode and a relationship between the structure and their biological activity was observed.Entities:
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Year: 2012 PMID: 22532255 DOI: 10.1002/ardp.201100355
Source DB: PubMed Journal: Arch Pharm (Weinheim) ISSN: 0365-6233 Impact factor: 3.751