(Hungary grant 20391-3/2018/FEKUSTRAT) Támogató: EMMI
(TKP2021-EGA-32) Támogató: NKFIH
(Open access funding provided by University of Szeged)
Szakterületek:
Farmakológia és gyógyszerészet
Kémiai tudományok
Szerveskémia
Szintetikus szerveskémia
A series of novel heterocyclic structures, namely 1,3-oxazines, 1,3-thiazines and
2,4-diaminopyrimidines, were designed and synthesised. The bioassay tests demonstrated
that, among these analogues, 2,4-diaminopyridine derivatives showed significant antiproliferative
activity against different human cancer cell lines (A2780, SiHa, HeLa, MCF-7 and MDA-MB-231).
Pyrimidines substituted with N-2-(p-trifluoromethyl)aniline, in particular, displayed
a potent inhibitory effect on the growth of cancer cells. Structure-activity relationships
were also studied from the aspects of stereochemistry on the aminodiol moiety as well
as exploring the effects of substituents on the pyrimidine scaffold.