IN SILICO ADME STUDIES OF POLYAMINE CONJUGATES AS POTENTIAL ANTICANCER DRUGS

Acta Pol Pharm. 2016 Sep;73(5):1191-1200.

Abstract

The ADME properties and drug-likeness of several polyamine derivatives containing dimeric phthalimide, quinoline, cinnoline and chromone moieties with three different polyamines: 1,4-bis(3-aninopropyl)piperazine, 4,9-dioxa-1,12-dodecanediamine and 3,3-diamino-N-methyldipropylamine as linkers were presented. These compounds are structurally related to DNA bisintercalators, a group of agents with anti-cancer activity. Their biological properties were previously assessed in vitio in a highly aggressive melanoma cell line A375. Current studies evaluate their potential to be qualified as drugs by performing in silico ADME screening. The research is carried out using Discovery Studio 3.0 ADMET protocol obtained from Accelrys and might be useful for further developing and optimization of potential anticancer drugs.

MeSH terms

  • Antineoplastic Agents / pharmacokinetics*
  • Antineoplastic Agents / pharmacology
  • Blood-Brain Barrier
  • Cytochrome P-450 CYP2D6 Inhibitors / pharmacology
  • Polyamines / pharmacokinetics*
  • Polyamines / pharmacology
  • Protein Binding
  • Solubility

Substances

  • Antineoplastic Agents
  • Cytochrome P-450 CYP2D6 Inhibitors
  • Polyamines