Improved guanide compounds which bind the CXCR4 co-receptor and inhibit HIV-1 infection

Bioorg Med Chem Lett. 2013 Apr 1;23(7):2197-201. doi: 10.1016/j.bmcl.2013.01.107. Epub 2013 Jan 30.

Abstract

The G-protein coupled receptor CXCR4 is a co-receptor for HIV-1 infection and is involved in signaling cell migration and proliferation. In a previous study of non-peptide, guanide-based CXCR4-binding compounds, spermine and spermidine phenylguanides inhibited HIV-1 entry at low micromolar concentrations. Subsequently, crystal structures of CXCR4 were used to dock a series of naphthylguanide derivatives of the polyamines spermidine and spermine. Synthesis and evaluation of the naphthylguanide compounds identified our best compound, spermine tris-1-naphthylguanide, which bound CXCR4 with an IC(50) of 40 nM and inhibited the infection of TZM-bl cells with X4, but not R5, strains of HIV-1 with an IC(50) of 50-100 nM.

Publication types

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

MeSH terms

  • Anti-HIV Agents / chemical synthesis
  • Anti-HIV Agents / chemistry
  • Anti-HIV Agents / pharmacology*
  • Biguanides / chemical synthesis
  • Biguanides / chemistry*
  • Biguanides / pharmacology*
  • Cell Line
  • Cell Proliferation / drug effects
  • Dose-Response Relationship, Drug
  • HIV Infections / drug therapy*
  • HIV-1 / drug effects
  • Humans
  • Microbial Sensitivity Tests
  • Molecular Structure
  • Receptors, CXCR4 / antagonists & inhibitors*
  • Receptors, CXCR4 / chemistry
  • Structure-Activity Relationship

Substances

  • Anti-HIV Agents
  • Biguanides
  • Receptors, CXCR4