854389-42-7Relevant articles and documents
Inhibition of human thymidine phosphorylase by conformationally constrained pyrimidine nucleoside phosphonic acids and their "open-structure" isosteres
Ko?iová, Ivana,?imák, Ond?ej,Panova, Natalya,Budě?ínsky, Milo?,Petrová, Magdalena,Rejman, Dominik,Liboska, Radek,Páv, Ond?ej,Rosenberg, Ivan
, p. 145 - 168 (2014/02/14)
A series of conformationally constrained uridine-based nucleoside phosphonic acids containing annealed 1,3-dioxolane and 1,4-dioxane rings and their "open-structure" isosteres were synthesized and evaluated as potential multisubstrate-like inhibitors of t
Nucleosidyl-O-methylphosphonates: A pool of monomers for modified oligonucleotides
Rejman, Dominik,Masojidkova, Milena,Rosenberg, Ivan
, p. 1683 - 1705 (2007/10/03)
An unique set of 5′-O- and 3′-O-phosphonomethyl derivatives of four natural 2′-deoxyribonucleosides, 1-(2-deoxy-β-D-threo- pentofuranosyl)thymine, 5′-O- and 2′-O-phosphonomethyl derivatives of 1-(3-deoxy-β-D-erythro-pentofuranosyl)thymine, and 1-(3-deoxy-β-D- threo-pentofuranosyl)thymine has been synthesized as a pool of monomers for the synthesis of modified oligonucleotides. The phosphonate moiety was protected with 4-methoxy-1-oxido-2-pyridylmethyl ester group, serving also as an intramolecular catalyst in the coupling step.