312750-63-3Relevant 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
Rational design of a new series of mixed anti-HIV pronucleotides
Schlienger, Nathalie,Beltran, Thierry,Perigaud, Christian,Lefebvre, Isabelle,Pompon, Alain,Aubertin, Anne-Marie,Gosselin, Gilles,Imbach, Jean-Louis
, p. 3003 - 3006 (2007/10/03)
MonoSATE aryl phosphotriesters of AZT are able to deliver intracellularly the corresponding 5'-mononucleotide. This process requires activation by an esterase followed by a phosphodiesterase. This finding opens the way to the design of new pronucleotide s