Our computational studies suggest that 3-substituted xanthines are good candidates for tetrad and quadruplex structures. 3-Methylxanthine (3MX) has been synthesized from 7-benzylxanthine, and the existence of tetrameric and octameric aggregates of 3MX with NH 4 + , Na + and K + ions in the gas phase (MS) and in DMSO-d 6 solution (NMR) has been observed. The ''internal'' H-bonds (N1HÁ Á ÁO6) are stronger than the ''external'' ones (N7HÁ Á ÁO2) in these clusters (NMR). Fig. 1 Tetrads composed of 7H-3-methylxanthine (3MX) and different cations [cat + = none, Na + , K + , NH 4 + ; purine atom and spectroscopic (underlined) numbering shown in upper left ring].