41107-55-5Relevant academic research and scientific papers
3'-Fluoro-2',3'-dideoxy-5-chlorouridine: most selective anti-HIV-1 agent among a series of new 2'- and 3'-fluorinated 2',3'-dideoxynucleoside analogues.
Van Aerschot,Herdewijn,Balzarini,Pauwels,De Clercq
, p. 1743 - 1749 (2007/10/02)
A series of 2'- and 3'-fluorinated 2',3'-dideoxynucleosides and 3'-azido-2',3'-dideoxynucleosides were synthesized and evaluated for their inhibitory activity against human immunodeficiency virus-1 (HIV-1) replication in MT-4 cells. Neither conversion of
Synthesis and Biological Activity of 5-Fluoro-2',3'-dideoxy-3'-fluorouridine and Its 5'-Phosphate
Ajmera, Sudhir,Bapat, Ashok R.,Danenberg, Kathleen,Danenberg, Peter V.
, p. 11 - 14 (2007/10/02)
5-Fluoro-2',3'-dideoxy-3'-fluorouridine (3'-FFdUrd) and 5-fluoro-2',3'-dideoxy-3'-fluorouridine 5'-phosphate (3'-FFdUMP) have been synthesized, and their interactions with thymidine (dThd) phosphorylase and thymidylate (dTMP) synthetase, respectively, have been examined. 3'-FFdUrd is not a substrate for dThd phosphorylase, but is a weak, noncompetitive inhibitor (Ki = 1.7 mM). 3'-FFdUMP inhibits dTMP synthetase competitively with deoxyuridylate (Ki = 0.13 mM) when both the substrate and inhibitor are present simultaneously.However, in the presence of 5,10-methylenete trahydrofolate, the inhibition increases with time in a first-order manner (konobsd = 0.029 s-1).A complex is formed between 3'-FFdUMP and dTMP synthetase, which is isolable on nitrocellulose filters, and has a dissociation rate (koffobsd = 1.4*10-2 min-1) similar to that of the potent inhibitor 5-fluoro-2'-deoxyuridilate (koffobsd = 1.3*10-2 min-1) from its ternary complex with dTMP synthetase.These results are explained in terms of a two-stage model involving the initial formation of a revesible adsorption complex, followed by a slow conversion to a tight-binding catalytic complex.
