6,12-dihydro-1-benzopyrano[3,4-b][1,4]benzothiazin-6-ones: synthesis and mdr reversal in tumor cells

Anticancer Res. 1998 Jul-Aug;18(4C):3001-4.

Abstract

Six 6,12-dihydro-1-benzopyrano[3,4-b][1,4]benzothiazin-6-ones and three coumarins were systematically investigated for reversal of multidrug resistance of bacteria and cancer cells in model experiments. 7-Methylcoumarin was able to eliminate the E. coli plasmid significantly; however, the other derivatives were ineffective. Four of 6,12-dihydro-1-benzopyrano[3,4-b] [1,4]benzothiazin-6-ones had a moderate effect on the multidrug resistance efflux pump of mouse lymphoma cells in vitro. Despite of the similarity of resistance mechanisms of bacteria and tumor cells, the reversal of drug resistance in bacteria and in cancer cells is not uniform because the structure-activity requirements are apparently different.

MeSH terms

  • Animals
  • Antineoplastic Agents / chemical synthesis*
  • Antineoplastic Agents / pharmacology*
  • Coumarins / chemical synthesis
  • Coumarins / pharmacology
  • Drug Resistance, Multiple*
  • Escherichia coli / drug effects
  • Escherichia coli / genetics
  • Lymphoma, T-Cell / drug therapy*
  • Lymphoma, T-Cell / metabolism
  • Mice
  • Plasmids / drug effects
  • Structure-Activity Relationship
  • Thiazines / chemical synthesis*
  • Thiazines / pharmacology*
  • Tumor Cells, Cultured

Substances

  • Antineoplastic Agents
  • Coumarins
  • Thiazines