A water-soluble, high-output fluorescent sensor, based on a lumazine ligand with a thiophene substituent for Cd(2+), Hg(2+) and Ag(+) metal ions, is reported. The sensor displays fluorescence enhancement upon Cd(2+) binding (log beta = 2.79 +/- 0.08) and fluorescence quenching by chelating with Ag(+) and Hg(2+) (log beta = 4.31 +/- 0.15 and 5.42 +/- 0.1, respectively). The mechanism of quenching is static and occurs by formation of a ground-state non-fluorescent complex followed by rapid intersystem crossing. The value of the Stern-Volmer quenching rate constant (k(q)) by Ag(+) ions is close to 6.71 x 10(12) mol/L/s at 298 K. The thermodynamic parameters (DeltaG, DeltaH and DeltaS) were also evaluated and indicated that the complexation process is spontaneous, exothermic and entropically favourable. The quantitative linear relationship between the softness values of Klopman (sigma(K)) or Ahrland (sigma(A)) and the experimental binding constants (beta) being in the order of Hg(2+) > Ag(+) > Cd(2+) suggests that soft-soft interactions are the key for the observed sensitivity and selectivity in the presence of other metal ions, such as: Pb(2+), Ni(2+), Mn(2+), Cu(2+), Co(2+), Zn(2+) and Mg(2+) ions.