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157 related items for PubMed ID: 15134542
1. SATE pronucleotide approaches: an overview. Peyrottes S, Egron D, Lefebvre I, Gosselin G, Imbach JL, Périgaud C. Mini Rev Med Chem; 2004 May; 4(4):395-408. PubMed ID: 15134542 [Abstract] [Full Text] [Related]
2. New insights regarding the potential of the pronucleotide approach in antiviral chemotherapy. Gosselin G, Girardet JL, Périgaud C, Benzaria S, Lefebvre I, Schlienger N, Pompon A, Imbach JL. Acta Biochim Pol; 1996 May; 43(1):196-208. PubMed ID: 8790724 [Abstract] [Full Text] [Related]
3. Some new acyclic nucleotide analogues as antiviral prodrugs: synthesis and bioactivities in vitro. Tang YB, Peng ZG, Liu ZY, Li YP, Jiang JD, Li ZR. Bioorg Med Chem Lett; 2007 Nov 15; 17(22):6350-3. PubMed ID: 17888662 [Abstract] [Full Text] [Related]
4. The S-acyl-2-thioethyl pronucleotide approach applied to acyclovir: part I. Synthesis and in vitro anti-hepatitis B virus activity of bis(S-acyl-2-thioethyl)phosphotriester derivatives of acyclovir. Périgaud C, Gosselin G, Girardet JL, Korba BE, Imbach JL. Antiviral Res; 1999 Jan 15; 40(3):167-78. PubMed ID: 10027651 [Abstract] [Full Text] [Related]
5. Intracellular trapping of cycloSal-pronucleotides: modification of prodrugs with amino acid esters. Jessen HJ, Balzarini J, Meier C. J Med Chem; 2008 Oct 23; 51(20):6592-8. PubMed ID: 18826203 [Abstract] [Full Text] [Related]
7. Synthesis and study of a new series of phosphoramidate derivatives as mononucleotide prodrugs. Egron D, Périgaud C, Gosselin G, Aubertin AM, Imbach JL. Nucleosides Nucleotides Nucleic Acids; 2001 Jul 18; 20(4-7):751-4. PubMed ID: 11563108 [Abstract] [Full Text] [Related]
8. A step further in the SATE mononucleotide prodrug approach. Peyrottes S, Villard AL, Coussot G, Augustijns P, Lefebvre I, Aubertin AM, Gosselin G, Périgaud C. Nucleic Acids Symp Ser (Oxf); 2008 Jul 18; (52):539-40. PubMed ID: 18776492 [Abstract] [Full Text] [Related]
9. Application of the cycloSal-prodrug approach for improving the biological potential of phosphorylated biomolecules. Meier C, Balzarini J. Antiviral Res; 2006 Sep 18; 71(2-3):282-92. PubMed ID: 16735066 [Abstract] [Full Text] [Related]
10. "Lock-in"-cycloSal-pronucleotides - a new generation of chemical Trojan Horses? Meier C, Ruppel MF, Vukadinovic D, Balzarini J. Mini Rev Med Chem; 2004 May 18; 4(4):383-94. PubMed ID: 15134541 [Abstract] [Full Text] [Related]
11. The SATE pronucleotide approach applied to acyclovir: part II. Effects of bis(SATE)phosphotriester derivatives of acyclovir on duck hepatitis B virus replication in vitro and in vivo. Hantz O, Périgaud C, Borel C, Jamard C, Zoulim F, Trépo C, Imbach JL, Gosselin G. Antiviral Res; 1999 Jan 18; 40(3):179-87. PubMed ID: 10027652 [Abstract] [Full Text] [Related]
12. An original pronucleotide strategy for the simultaneous delivery of two bioactive drugs. Villard AL, Aubertin AM, Peyrottes S, Périgaud C. Eur J Med Chem; 2021 Apr 15; 216():113315. PubMed ID: 33711763 [Abstract] [Full Text] [Related]
13. Mononucleoside SATE glucosyl phosphorothiolates as a new series of pronucleotides. Jochum A, Schlienger N, Gosselin G, Imbach JL, Aubertin AM, Périgaud C. Nucleosides Nucleotides Nucleic Acids; 2003 Apr 15; 22(5-8):899-901. PubMed ID: 14565306 [Abstract] [Full Text] [Related]
14. Bis-S-acyl-2-thioethyl (SATE)-bearing monophosphate prodrug of beta-L-FD4C as potent anti-HBV agent. Li X, Carmichael E, Feng M, King I, Doyle TW, Chen SH. Bioorg Med Chem Lett; 1998 Jan 06; 8(1):57-62. PubMed ID: 9871628 [Abstract] [Full Text] [Related]
15. S-acyl-2-thioethyl (SATE) pronucleotides are potent inhibitors of HIV-1 replication in T-lymphoid cells cross-resistant to deoxycytidine and thymidine analogs. Gröschel B, Cinatl J, Périgaud C, Gosselin G, Imbach JL, Doerr HW, Cinatl J. Antiviral Res; 2002 Feb 06; 53(2):143-52. PubMed ID: 11750940 [Abstract] [Full Text] [Related]
16. S-Acyl-2-thioethyl aryl phosphotriester derivatives as mononucleotide prodrugs. Schlienger N, Peyrottes S, Kassem T, Imbach JL, Gosselin G, Aubertin AM, Périgaud C. J Med Chem; 2000 Nov 16; 43(23):4570-4. PubMed ID: 11087582 [Abstract] [Full Text] [Related]
17. Mononucleoside phosphotriester derivatives with S-acyl-2-thioethyl bioreversible phosphate-protecting groups: intracellular delivery of 3'-azido-2',3'-dideoxythymidine 5'-monophosphate. Lefebvre I, Périgaud C, Pompon A, Aubertin AM, Girardet JL, Kirn A, Gosselin G, Imbach JL. J Med Chem; 1995 Sep 29; 38(20):3941-50. PubMed ID: 7562927 [Abstract] [Full Text] [Related]
18. cycloSal-pronucleotides design of chemical trojan horses. Meier C. Mini Rev Med Chem; 2002 Jun 29; 2(3):219-34. PubMed ID: 12370064 [Abstract] [Full Text] [Related]
19. Synthesis and antiviral evaluation of 2-amino-6-carbamoylpurine dioxolane nucleoside derivatives and their phosphoramidates prodrugs. Cho JH, Bondana L, Detorio MA, Montero C, Bassit LC, Amblard F, Coats SJ, Schinazi RF. Bioorg Med Chem; 2014 Dec 01; 22(23):6665-6671. PubMed ID: 25458500 [Abstract] [Full Text] [Related]
20. Design of new mononucleotide prodrugs: aryl (SATE) phosphotriester derivatives. Peyrottes S, Schlienger N, Beltran T, Lefebvre I, Pompon A, Gosselin G, Aubertin AM, Imbach JL, Périgaud C. Nucleosides Nucleotides Nucleic Acids; 2001 Dec 01; 20(4-7):315-21. PubMed ID: 11563043 [Abstract] [Full Text] [Related] Page: [Next] [New Search]