Synthesis and biological activities of a pH-dependently activated water-soluble prodrug of a novel hexacyclic camptothecin analog

Bioorg Med Chem Lett. 2009 May 15;19(10):2772-6. doi: 10.1016/j.bmcl.2009.03.123. Epub 2009 Mar 28.

Abstract

CH0793076 (1) is a novel hexacyclic camptothecin analog showing potent antitumor activity in various human caner xenograft models. To improve the water solubility of 1, water-soluble prodrugs were designed to generate an active drug 1 nonenzymatically, thus expected to show less interpatient PK variability than CPT-11. Among the prodrugs synthesized, 4c (TP300, hydrochloride) having a glycylsarcosyl ester at the C-20 position of 1 is highly water-soluble (>10mg/ml), stable below pH 4 and rapidly generates 1 at physiological pH in vitro. The rapid (ca. <1min) generation of 1 after incubation of TP300 with plasma (mouse, rat, dog and monkey) was also demonstrated. TP300 showed a broader antitumor spectrum and more potent antitumor activity than CPT-11 in various human cancer xenograft models.

MeSH terms

  • Animals
  • Antineoplastic Agents / blood
  • Antineoplastic Agents / chemical synthesis*
  • Antineoplastic Agents / pharmacokinetics
  • Camptothecin / analogs & derivatives*
  • Camptothecin / blood
  • Camptothecin / chemical synthesis
  • Camptothecin / chemistry
  • Camptothecin / pharmacokinetics
  • DNA Topoisomerases, Type I / metabolism
  • Dogs
  • Haplorhini
  • Humans
  • Hydrogen-Ion Concentration
  • Irinotecan
  • Mice
  • Mice, Nude
  • Prodrugs / chemical synthesis*
  • Prodrugs / chemistry
  • Prodrugs / pharmacokinetics
  • Rats
  • Topoisomerase I Inhibitors
  • Transplantation, Heterologous
  • Water / chemistry

Substances

  • Antineoplastic Agents
  • CH 0793076
  • Prodrugs
  • Topoisomerase I Inhibitors
  • Water
  • Irinotecan
  • DNA Topoisomerases, Type I
  • Camptothecin