221665-12-9Relevant academic research and scientific papers
Synthesis and antiviral activity of ethidium-arginine conjugates directed against the TAR RNA of HIV-1
Peytou, Valérie,Condom, Roger,Patino, Nadia,Guedj, Roger,Aubertin, Anne-Marie,Gelus, Nathalie,Bailly, Christian,Terreux, Rapha?l,Cabrol-Bass, Daniel
, p. 4042 - 4053 (2007/10/03)
The regulatory protein Tat is essential for viral gene expression and replication of the human immunodeficiency virus type 1 (HIV-1). Tat transactivates the HIV-1 long terminal repeat (LTR) via its binding to the transactivation responsive element (TAR) and increases the viral transcription. Studies have shown that the binding of arginine and arginine derivatives induces a conformational change of the TAR RNA at the Tat-binding site. The unpaired A17 residue delimits a small cavity which constitutes a receptor site for small molecules, especially for ethidium bromide. These binding characteristics have prompted us to design a series of ethidium- arginine conjugates capable of interacting with the TAR RNA. Here we report the synthesis of six ethidium derivatives equipped with arginine side chains. These molecules were biologically evaluated, and two compounds (17 and 20) exhibited in vitro anti-HIV-1 activity at micromolar concentration, without toxicity (up to 100 μM concentration). Melting temperature studies indicated that the most active molecule (20) bound strongly to TAR in vitro. RNase protection experiments agreed with the molecular modeling studies which suggested that the ethidium moiety of 20 was inserted next to the A17 residue while the arginine side chain occupied the pyrimidine bulge.
Synthesis of a new class of HIV-1 inhibitors
Di Giorgio, Audrey Farese,Pairot, Sandrine,Patino, Nadia,Condom, Roger,Di Giorgio, Christophe,Aumelas, Andre,Aubertin, Anne-Marie,Guedj, Roger
, p. 263 - 275 (2007/10/03)
A new family of molecules potentially inhibitors of the HIV-1 Tat-TAR complex was prepared. These compounds are constituted by dinucleotide analogs (PNA dimer) bound, through a linker, to an arginine residue. In this series, several molecules inhibit vira
