Synthesis of 5-substituted-2,3-dihydro-1,4-benzoxathiins: biological evaluation as melatonin receptors ligands

J Enzyme Inhib Med Chem. 2003 Apr;18(2):187-93. doi: 10.1080/1475636032000096855.

Abstract

The synthesis of benzoxathiins bearing a retroamide function is described from 8-hydroxythiochroman, the key step involving the synthesis of the benzoxathiin ring through a sulfonium salt. These new melatonin analogues were evaluated on human receptors MT1 and MT2 and have a similar affinity to that of melatonin itself.

MeSH terms

  • Animals
  • Binding, Competitive
  • Cell Line
  • Humans
  • Ligands
  • Melatonin / analogs & derivatives*
  • Melatonin / metabolism
  • Molecular Structure
  • Oxathiins / chemical synthesis*
  • Oxathiins / pharmacology*
  • Receptor, Melatonin, MT1 / metabolism*
  • Receptor, Melatonin, MT2 / metabolism*
  • Structure-Activity Relationship

Substances

  • Ligands
  • Oxathiins
  • Receptor, Melatonin, MT1
  • Receptor, Melatonin, MT2
  • Melatonin