Literature DB >> 11563043

Design of new mononucleotide prodrugs: aryl (SATE) phosphotriester derivatives.

S Peyrottes1, N Schlienger, T Beltran, I Lefebvre, A Pompon, G Gosselin, A M Aubertin, J L Imbach, C Périgaud.   

Abstract

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 be potent inhibitors of HIV-1 replication in various cell culture experiments. The proposed decomposition process of these mixed phosphotriesters may involve successively an esterase and then a phosphodiesterase activation.

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Year:  2001        PMID: 11563043     DOI: 10.1081/NCN-100002302

Source DB:  PubMed          Journal:  Nucleosides Nucleotides Nucleic Acids        ISSN: 1525-7770            Impact factor:   1.381


  1 in total

1.  Synthesis of 4-thiouridines with prodrug functionalization for RNA metabolic labeling.

Authors:  Sarah Moreno; Melanie Brunner; Isabel Delazer; Dietmar Rieder; Alexandra Lusser; Ronald Micura
Journal:  RSC Chem Biol       Date:  2022-02-25
  1 in total

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