Synthesis, stability, and implications of phosphothioate agonists of sphingosine-1-phosphate receptors

Bioorg Med Chem Lett. 2005 Oct 15;15(20):4470-4. doi: 10.1016/j.bmcl.2005.07.057.

Abstract

Phosphothioates may provide metabolic stability when compared to their phosphate counterparts, while retaining the potency and efficacy as agonists at sphingosine-1-phosphate (S1P) G-protein coupled receptors. Unlike their phosphate precursors, phosphothioate compounds with S1P-receptor profiles similar to that of FTY720, an emerging immunomodulator, were shown to evoke prolonged lymphopenia in vivo. Analysis of mouse plasma concentrations for a series of related alcohol/phosphate/phosphothioate compounds showed the conversion of the phosphate to alcohol. These preliminary data highlight the importance of metabolic regulation of S1P receptor ligands.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Magnetic Resonance Spectroscopy
  • Receptors, Lysosphingolipid / agonists*
  • Thionucleotides / chemical synthesis*
  • Thionucleotides / chemistry
  • Thionucleotides / pharmacology*

Substances

  • Receptors, Lysosphingolipid
  • Thionucleotides