Identification of thienopyridine carboxamides as selective binders of HIV-1 trans Activation Response (TAR) and Rev Response Element (RRE) RNAs

Org Biomol Chem. 2018 Dec 5;16(47):9191-9196. doi: 10.1039/c8ob02753f.

Abstract

Small organic molecules that can selectively bind to RNA with specificity are relatively rare. Here we report the synthesis, biochemical and structural studies of thienopyridine carboxamide derivatives with the capacity of selectively recognizing and binding with HIV-1 TAR and RRE RNAs that are essential elements for viral replication.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Base Sequence
  • Binding Sites
  • Drug Discovery
  • HIV Infections / drug therapy
  • HIV Infections / virology*
  • HIV-1 / chemistry
  • HIV-1 / metabolism*
  • Humans
  • Ligands
  • RNA, Viral / chemistry
  • RNA, Viral / metabolism*
  • Response Elements
  • Small Molecule Libraries / chemical synthesis
  • Small Molecule Libraries / chemistry
  • Small Molecule Libraries / metabolism*
  • Thienopyridines / chemical synthesis
  • Thienopyridines / chemistry
  • Thienopyridines / metabolism*

Substances

  • Ligands
  • RNA, Viral
  • Small Molecule Libraries
  • Thienopyridines