AdoHcy hydrolase of Trichomonas vaginalis: studies of the effects of 5'-modified adenosine analogues and related 6-N-cyclopropyl derivatives

Bioorg Med Chem Lett. 2010 Dec 15;20(24):7466-8. doi: 10.1016/j.bmcl.2010.10.014. Epub 2010 Oct 31.

Abstract

Trypanosoma brucei and Trichomonas vaginalis are both parasitic protozoans that are known to share many similar biochemical pathways. Aristeromycin, as well as 5'-iodovinyl and 5'-oxime analogues of adenosine, are potent inhibitors of AdoHcy hydrolase in T. brucei, an enzyme that catalyses the hydrolysis of AdoHcy to adenosine and L-homocysteine. To help determine the role of this enzyme in T. vaginalis, we have tested a library of 5'-modified adenosine derivatives, including 5'-deoxy-5'-(iodomethylene)-adenosine and related 6-N-cyclopropyl analogues. Our results indicate that these inhibitors are effective at inhibiting the growth of T. vaginalis, by as much as 95%.

Publication types

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

MeSH terms

  • Adenosine / analogs & derivatives*
  • Adenosine / chemical synthesis
  • Adenosine / chemistry
  • Adenosine / pharmacology
  • Adenosylhomocysteinase / antagonists & inhibitors*
  • Adenosylhomocysteinase / metabolism
  • Amino Acid Sequence
  • Antiprotozoal Agents / chemical synthesis
  • Antiprotozoal Agents / chemistry*
  • Antiprotozoal Agents / pharmacology
  • Cyclopropanes / chemistry*
  • Molecular Sequence Data
  • Sequence Alignment
  • Structure-Activity Relationship
  • Trichomonas vaginalis / enzymology*

Substances

  • Antiprotozoal Agents
  • Cyclopropanes
  • aristeromycin
  • cyclopropene
  • Adenosylhomocysteinase
  • Adenosine