Synthesis and anti-HIV-1 activity of 4-[4-(4,6-bisphenylamino-triazin-2-ylamino)-5-methoxy-2-methylphenylazo]-5-hydroxynaphthalene-2,7-disulfonic acid and its derivatives

Bioorg Med Chem. 2004 Mar 1;12(5):1215-20. doi: 10.1016/j.bmc.2003.11.006.

Abstract

A structure-based design approach has been used to optimize a lead HIV-1 entry inhibitor targeted to the envelope glycoprotein gp41. The docking study on this lead compound revealed important structural requirements that need to be preserved as well as structural non-requirements that could be eliminated to substantially reduce the molecular size of the lead compound. Based on the results from docking study, a limited number of analogues were designed and synthesized. This approach yielded a new analogue (compound 4) that retained the anti-HIV-1 activity with reduced molecular size approaching towards more drug-like character.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Anti-HIV Agents / chemical synthesis*
  • Anti-HIV Agents / pharmacology
  • Computer Simulation
  • Drug Design
  • HIV-1 / drug effects
  • Humans
  • Molecular Weight
  • Naphthalenesulfonates* / chemical synthesis
  • Naphthalenesulfonates* / pharmacology
  • Structure-Activity Relationship
  • Triazines / chemical synthesis
  • Triazines / pharmacology

Substances

  • Anti-HIV Agents
  • Naphthalenesulfonates
  • Triazines
  • ADS J1