A novel series of C-nucleosides, featuring the presence of a 1,2,3-triazole ring linked to an isoxazolidine system, has been designed as mimetics of the pyrimidine nucleobases. An antiproliferative effect was observed for compounds 17a and 17b: the growth inhibitory effect reaches the 50% in HepG2 and HT-29 cells and increases up to 56% in the SH-SY5Y cell line after 72 h of incubation at a 100 μM concentration.

Synthesis and biological properties of 5-(1H-1,2,3-triazol-4-yl)isoxazolidines: A new class of C-nucleosides

Mancuso, Raffaella;
2015-01-01

Abstract

A novel series of C-nucleosides, featuring the presence of a 1,2,3-triazole ring linked to an isoxazolidine system, has been designed as mimetics of the pyrimidine nucleobases. An antiproliferative effect was observed for compounds 17a and 17b: the growth inhibitory effect reaches the 50% in HepG2 and HT-29 cells and increases up to 56% in the SH-SY5Y cell line after 72 h of incubation at a 100 μM concentration.
2015
1,3-dipolar cycloaddition; Antiproliferative activity; C-Nucleosides; Microwave; Vinyl triazoles; Antineoplastic Agents; Cell Proliferation; Drug Screening Assays, Antitumor; HT29 Cells; Hep G2 Cells; Humans; Isoxazoles; Molecular Mimicry; Molecular Structure; Nucleosides; Pyrimidines; Structure-Activity Relationship; Medicine (all); Organic Chemistry
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.11770/264940
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