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Medicinal Hypervalent Tellurium Prodrugs Bearing Different Ligands: A Comparative Study of the Chemical Profiles of AS101 and Its Halido Replaced Analogues.

Lorenzo ChiaveriniDamiano CirriIogann TolbatovFrancesca CorsiIlaria PianoAlessandro MarroneAlessandro PratesiTiziano MarzoDiego La Mendola
Published in: International journal of molecular sciences (2022)
Ammonium trichloro (dioxoethylene-O,O') tellurate (AS101) is a potent immunomodulator prodrug that, in recent years, entered various clinical trials and was tested for a variety of potential therapeutic applications. It has been demonstrated that AS101 quickly activates in aqueous milieu, producing TeOCl 3 - , which likely represents the pharmacologically active species. Here we report on the study of the activation process of AS101 and of two its analogues. After the synthesis and characterization of AS101 and its derivatives, we have carried out a comparative study through a combined experimental and computational analysis. Based on the obtained results, we describe here, for the first time, the detailed reaction that AS101 and its bromido- and iodido-replaced analogues undergo in presence of water, allowing the conversion of the original molecule to the likely true pharmacophore. Interestingly, moving down in the halogens' group we observed a higher tendency to react, attributable to the ligands' effect. The chemical and mechanistic implications of these meaningful differences are discussed.
Keyphrases
  • molecular docking
  • structure activity relationship
  • clinical trial
  • ionic liquid
  • randomized controlled trial
  • anti inflammatory
  • drug release
  • drug delivery
  • double blind
  • phase iii
  • drug discovery