| Literature DB >> 16944545 |
Gianluca Sbardella1, Sara Bartolini, Sabrina Castellano, Marino Artico, Nicola Paesano, Dante Rotili, Corrado Spadafora, Antonello Mai.
Abstract
Novel triazine analogues of 5-alkyl-2-alkylthio-6-[1-(2,6-difluorophenyl)alkyl]-3,4-dihydropyrimidin-4(3H)-ones (F(2)-DABOs), previously described by us as nonnucleoside HIV-1 reverse transcriptase inhibitors (NNRTIs), were tested for their antiproliferative and cytodifferentiating activity on the A-375 human melanoma cell line. Most of the tested derivatives were effective in decreasing cell proliferation, facilitating morphological differentiation, and reprogramming gene expression. All these effects were reversible upon withdrawal of RT inhibitors. Among the compounds tested, 3 f showed the highest antiproliferative effect, whereas compound 6 c, although not affecting cell proliferation, is endowed with a strong cytodifferentiating effect, which is probably related to a marked upregulation of the e-cad gene. These results support the potential of NNRTIs as valuable antitumor agents.Entities:
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Year: 2006 PMID: 16944545 DOI: 10.1002/cmdc.200600139
Source DB: PubMed Journal: ChemMedChem ISSN: 1860-7179 Impact factor: 3.466