Novel PIKK inhibitor antibody-drug conjugates: Synthesis and anti-tumor activity

Bioorg Med Chem Lett. 2019 Apr 1;29(7):943-947. doi: 10.1016/j.bmcl.2019.01.009. Epub 2019 Jan 11.

Abstract

Novel neolymphostin-based antibody-drug conjugate (ADC) precursors were synthesized either through amide couplings between both cleavable and non-cleavable linkers and neolymphostin derivatives, or through Cu(I)-catalyzed acetylene-azide click cycloadditon between non-cleavable linkers and neolymphostin acetal derivatives. These precursors were site-specifically conjugated to cysteine mutant trastuzumab-A114C to provide neolymphostin-based ADCs. Preliminary in vitro data indicated that the corresponding ADCs were active against HER2-expressing tumor cell lines, thus providing a proof-of-concept for using neolymphostin as ADC-based anticancer agents.

Keywords: ADC; Antitumor; HER2-expressing tumor cell lines; Neolymphostin; PIKK inhibitor; Trastuzumab conjugates.

MeSH terms

  • Aminoquinolines / chemical synthesis
  • Aminoquinolines / pharmacology*
  • Antineoplastic Agents / chemical synthesis
  • Antineoplastic Agents / pharmacology*
  • Cell Line, Tumor
  • Drug Screening Assays, Antitumor
  • Humans
  • Immunoconjugates / pharmacology*
  • Mutation
  • Phosphoinositide-3 Kinase Inhibitors / chemical synthesis
  • Phosphoinositide-3 Kinase Inhibitors / pharmacology*
  • Proof of Concept Study
  • Pyrroles / chemical synthesis
  • Pyrroles / pharmacology*
  • Trastuzumab / genetics
  • Trastuzumab / pharmacology*

Substances

  • Aminoquinolines
  • Antineoplastic Agents
  • Immunoconjugates
  • Phosphoinositide-3 Kinase Inhibitors
  • Pyrroles
  • Trastuzumab