“…As a consequence of these characteristics, oxadiazoles have impacted drug discovery programs in numerous areas including muscarinic agonists [8,9], benzodiazepine receptor partial agonists [10,11], dopamine transporters [12], anti-rhinovirals [13], growth hormone secretogogues [14], 5-HT agonists[15], antispasmodics [16], nematocidal, fungicidal and microbicides [17], analgesics [18], anti-inflammatory agents [19,20], Fab I inhibitors as antibacterial agents [21], immnosuppressants [22], and also antiplatelet and antithrombotic agents [23], 5-HT antagonists [24], human NK 1 antagonists [25], They have been used as peptide mimetics due to their particular geometric and electrostatic properties [26,27]. Accordingly, in continuation of our work [28,29,30,31,32,33,34], a variety of heterocyclic derivatives involving some new oxadiazoles have been prepared from saccharide derivatives, and their chemistry and the effect of these derivatives on tyrosinase enzyme [35,36,37,38], which is the rate limiting step in melanine biosynthesis [39] as well as different biological actions were studied [40].…”