195304-72-4Relevant academic research and scientific papers
Synthesis and biological activity of modified (2'-5')triadenylates containing 2'-terminal 2',3'-dideoxy-3'-fluoroadenosine derivatives
Kvasyuk,Kulak,Tkachenko,Sentyureva,Mikhailopulo,Suhadolnik,Heoderson,Horvath,Guan,Pfleiderer
, p. 1278 - 1284 (2007/10/03)
Some new (2'-5')triadenylates 13-16, containing at the 2'-terminal end 3'-fluoro-2',3'-dideoxyadenosine derivatives, have been synthesized by the phosphotriester method. The selectively blocked nucleosides 2, 4, 5, and 7 were synthesized from the corresponding unprotected 'nucleosides 1, 3, and 6. The synthesized trimers 13 and 14 were 4- and 8-fold, respectively, more stable towards phosphodiesterase from Crotalus durissus than the natural trimer 17. In comparison to trimer 17 the new compounds 13-15 inhibit HIV-1 reverse transcriptase (RT) activity, and 15 and 16 the HIV-1 induced syncytia formation 2-3 fold whereas none of 13-16 can improve RNase L activity.
Synthesis and biological activity of new sugar modified 2',5'- oligoadenylate trimers
Kvasyuk,Kulak,Tkachenko,Sentyureva,Mikhailopulo,Suhadolnik,Henderson,Horvath,Guan,Pfleiderer
, p. 773 - 776 (2007/10/03)
New 2',5'-oligonucleotide trimers containing 2',3'-dideoxy-3'-fluoro derivatives of adenosine at the 2'-terminal end of oligomers have been synthesized. Some of the synthesized trimers showed biological inhibitions of HIV-1 reverse transcriptase and HIV-1 induced syncytia formation.
