29706-85-2Relevant articles and documents
Design of new mononucleotide prodrugs: Aryl (SATE) phosphotriester derivatives
Peyrottes,Schlienger,Beltran,Lefebvre,Pompon,Gosselin,Aubertin,Imbach,Perigaud
, p. 315 - 321 (2007/10/03)
Synthesis, biological activities and decomposition kinetics of novel phosphotriester derivatives of 3′-azido-2′,3′-dideoxythymidine (AZT) bearing a S-tButyl-2-thioethyl (tBuSATE) group and L-tyrosinyl residues are reported. All the derivatives appeared to
As
Meier, Chris,De Clercq, Eric,Balzarini, Jan
, p. 793 - 796 (2007/10/03)
The synthesis of cycloSal-AZTMPs 3a-h as new pro-nucleotides of AZTMP 2 is described. Phosphotriesters 3 selectively release AZTMP 2 by a controlled, chemically induced tandem reaction. Cyc/oSal-AZTMPs 3 exhibited high biological activity in HIVl/HIV-2 infected CEM/O cells but lost their activity nearly completely in CEM/TK cells. Copyright