5-(Haloalkyl)-2'-deoxyuridines: a novel type of potent antiviral nucleoside analogue

J Med Chem. 1985 Nov;28(11):1679-84. doi: 10.1021/jm00149a024.

Abstract

Syntheses of 5-(2-haloethyl)-2'-deoxyuridines, 5-(3-chloropropyl)-2'-deoxyuridines, and 5-(2-chloroethyl)-2'-deoxycytidine are described. The antiviral activities of these compounds were determined in cell culture against herpes simplex virus types 1 and 2. All compounds were shown to possess significant and selective antiviral activity. The most potent derivative, 5-(2-chloroethyl)-2'-deoxyuridine (CEDU), inhibited HSV-1 at concentrations below 0.1 microgram/mL. It exerted measurable inhibitory effects on cell proliferation only at concentrations higher than 100 micrograms/mL. In vivo CEDU reduced the mortality rate of HSV-1-infected mice at concentrations lower than 5 mg/kg per day when given intraperitoneally and orally. Thus, it proved to be more effective in this in vivo model than the reference compounds (E)-5-(2-bromovinyl)-2'-deoxyuridine (BVDU) and 9-[(2-hydroxyethoxy)methyl]guanine (ACV).

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Bromodeoxyuridine / analogs & derivatives
  • Bromodeoxyuridine / therapeutic use
  • Chemical Phenomena
  • Chemistry
  • Deoxyuridine / analogs & derivatives*
  • Deoxyuridine / chemical synthesis
  • Deoxyuridine / therapeutic use*
  • Dose-Response Relationship, Drug
  • Halogens / chemical synthesis
  • Halogens / therapeutic use
  • Herpes Simplex / drug therapy*
  • Mice
  • Rats

Substances

  • Halogens
  • brivudine
  • Bromodeoxyuridine
  • Deoxyuridine