| Literature DB >> 27677735 |
Martina Tireli1, Kristina Starčević2, Tamara Martinović3, Sandra Kraljević Pavelić3, Grace Karminski-Zamola4, Marijana Hranjec5.
Abstract
A series of pyrido[1,2-a]benzimidazoles has been designed, and novel examples are synthesized and evaluated for their potential antiproliferative activity against four human tumour cell lines-cervical (HeLa), colorectal (SW620), breast (MCF-7) and hepatocellular carcinoma (HepG2). In addition, their antioxidative potency has been evaluated by in vitro spectrophotometric assays. Preliminary structure-activity relationships among the synthesized compounds are discussed. Evaluation of their antioxidative capacity has shown that two compounds (25 and 26) possess promising reducing characteristics and free radical scavenging activity. Selective antiproliferative effect in the single-digit micromolar range was observed for compound 25 on MCF-7 [Formula: see text] and HeLa [Formula: see text] cell lines, comparable to the standards 5-fluorouracil and cisplatin. The combination of the radical scavenging activity and antiproliferative activity of compound 25 positions this compound as a potential lead candidate for further optimization.Entities:
Keywords: Amides; Antioxidative activity; Antiproliferative activity; Cyclization; Pyrido[1, 2-a]benzimidazoles
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Year: 2016 PMID: 27677735 DOI: 10.1007/s11030-016-9702-y
Source DB: PubMed Journal: Mol Divers ISSN: 1381-1991 Impact factor: 2.943