“…The incorporation of recognition domains such as intercalating moieties ( phen, bipy, and dpqz) as a component of drug is known to impart superior binding to target DNA/RNAs and more potent cytotoxic response in resistant cancer cells. 19,20 In this work, bilastine was coordinated to a metal center via the deprotonation of a carboxylic acid functionality in the presence of triethylamine (TEA), a base, to achieve tailored metalbased anticancer drug formulation of the type [BLA( phen) 2 M (II)] + •X − , where X − = NO 3 − and ClO 4 − , and M(II) = Co(II), 1, Cu (II), 2 and Zn(II), 3. The synthesized metal-based chemotherapeutics derived from the bilastine ligand act as potent anticancer drug candidates, and to the best of our knowledge, this is the first demonstration reported in the literature.…”