Locking the two ends of tetrapeptidic HTLV-I protease inhibitors inside the enzyme

Bioorg Med Chem. 2008 Jul 15;16(14):6880-90. doi: 10.1016/j.bmc.2008.05.052. Epub 2008 May 28.

Abstract

Adult T-cell leukemia and tropical spastic paraparesis/HTLV-I-associated myelopathy are only some of the more common end results of an infection with a human T-cell leukemia virus type 1 (HTLV-I). Expanding from our previous reports, we synthesized all different permutations of tetrapeptidic HTLV-I protease inhibitors using at least eight P(3)-cap and five P(1)(')-cap moieties. The inhibitors exhibited over 97% inhibition against HIV-1 protease and a wide range of inhibitory activity against HTLV-I protease.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • HTLV-I Infections / drug therapy
  • Human T-lymphotropic virus 1 / enzymology*
  • Humans
  • Peptides / chemical synthesis
  • Peptides / pharmacology*
  • Protease Inhibitors / chemistry*
  • Protease Inhibitors / pharmacology
  • Structure-Activity Relationship

Substances

  • Peptides
  • Protease Inhibitors