| Literature DB >> 29329071 |
Temístocles Italo de Santana1, Miria de Oliveira Barbosa2, Paulo André Teixeira de Moraes Gomes2, Anne Cecília Nascimento da Cruz1, Teresinha Gonçalves da Silva1, Ana Cristina Lima Leite3.
Abstract
Thiazole derivatives are recognized to possess various biological activities as antiparasitic, antifungal, antimicrobial and antiproliferative. The present work reports the synthesis of 22 new substances belonging to two classes of compounds: thiosemicarbazones and thiazoles, with the purpose of developing new drugs that present high specificity for tumor cells and low toxicity to the organism. A cytotoxic screening was performed to evaluate the performance of the new derivatives in five tumor cell lines. Eight compounds were shown to be promising in at least three tumor cell lines. These compounds had their IC50 determined within 72 h and the activity structure ratio was assessed. The effect of the best compounds on PBMC and hemolytic activity assay was then evaluated. The compound 1d was considered the most promising among the samples tested and its influence on cell cycle, DNA fragmentation and mitochondrial depolarization was evaluated.Entities:
Keywords: Cancer; Cell cycle; DNA fragmentation; Mitochondrial depolarization; Thiazoles
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Year: 2017 PMID: 29329071 DOI: 10.1016/j.ejmech.2017.12.040
Source DB: PubMed Journal: Eur J Med Chem ISSN: 0223-5234 Impact factor: 6.514