Antitumour benzothiazoles. Part 15: The synthesis and physico-chemical properties of 2-(4-aminophenyl)benzothiazole sulfamate salt derivatives

Bioorg Med Chem Lett. 2001 Apr 23;11(8):1093-5. doi: 10.1016/s0960-894x(01)00142-1.

Abstract

A series of sulfamate salt derivatives of the potent and selective 2-(4-aminophenyl)benzothiazole antitumour agents has been prepared and their evaluation as potential prodrugs for parenteral administration carried out. The salts were sparingly soluble under aqueous conditions (pH 4-9), and degradation to the active free amine was shown to occur under strongly acidic conditions. The salts were found to be markedly less active than their parent amines against sensitive human tumour cell lines in vitro.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amines / chemistry
  • Antineoplastic Agents / chemical synthesis*
  • Antineoplastic Agents / chemistry
  • Antineoplastic Agents / pharmacology*
  • Benzothiazoles
  • Breast Neoplasms / drug therapy
  • Drug Stability
  • Enzyme Activators / chemical synthesis
  • Enzyme Activators / chemistry
  • Enzyme Activators / pharmacology
  • Female
  • Guanylate Cyclase / drug effects
  • Guanylate Cyclase / metabolism
  • Humans
  • Hydrogen-Ion Concentration
  • Inhibitory Concentration 50
  • Platelet Aggregation Inhibitors / chemical synthesis
  • Platelet Aggregation Inhibitors / chemistry
  • Platelet Aggregation Inhibitors / pharmacology
  • Prodrugs / chemistry*
  • Prodrugs / pharmacology
  • Solubility
  • Sulfonic Acids / chemical synthesis*
  • Thiazoles / chemistry*
  • Thiazoles / pharmacology
  • Tumor Cells, Cultured / drug effects

Substances

  • 2-(4-aminophenyl)benzothiazole
  • Amines
  • Antineoplastic Agents
  • Benzothiazoles
  • Enzyme Activators
  • Platelet Aggregation Inhibitors
  • Prodrugs
  • Sulfonic Acids
  • Thiazoles
  • sulfamic acid
  • Guanylate Cyclase
  • benzothiazole