634178-99-7

Upstream product

• 634178-95-3 C₃₃H₃₁N₃O₇S 

Downstream Products

• 1246677-09-7 5'-(N-α,ω-di-Boc-L-lysyl)-C-(2'-deoxy-β-D-ribofuranosyl-1')-N-[3-(2-acetylaminothiazole-4-yl)phenyl]carboxamide 
• 1246677-10-0 3',5'-di-(N-α,ω-di-Boc-L-lysyl)-C-(2'-deoxy-β-D-ribofuranosyl-1')-N-[3-(2-acetylaminothiazole-4-yl)phenyl]carboxamide 
• 1246677-11-1 5'-(N-α,δ,ω-tri-Z-L-arginyl)-C-(2'-deoxy-β-D-ribofuranosyl-1')-N-[3-(2-acetylaminothiazole-4-yl)phenyl]carboxamide 
• 1246677-12-2 3',5'-di-(N-α,δ,ω-tri-Z-L-arginyl)-C-(2'-deoxy-β-D-ribofuranosyl-1')-N-[3-(2-acetylaminothiazole-4-yl)phenyl]carboxamide 

Relevant academic research and scientific papers

Design of novel RNA ligands that bind stem-bulge HIV-1 TAR RNA

We report here the rational design and the synthesis of a new series of RNA ligands. These molecules are constituted of various binding motifs that interact cooperatively with HIV-1 TAR RNA, used as a model.

Design of artificial nucleobases for the recognition of the AT inversion by triple-helix forming oligonucleotides: A structure-stability relationship study and neighbour bases effect

We report herein on the synthesis, the incorporation into triplex forming oligonucleotides (TFO) and the recognition properties of a series of synthetic nucleosides designed for the specific recognition of an inverted A·T base pair in a pyrimidine triple