Lefebvre I - Search Results

1

Anti-HIV pronucleotides: SATE versus phenyl as a protecting group of AZT phosphoramidate derivatives.

Beltran T, Egron D, Lefebvre I, Périgaud C, Pompon A, Gosselin G, Aubertin AM, Imbach JL. Beltran T, et al. Among authors: lefebvre i. Nucleosides Nucleotides. 1999 Apr-May;18(4-5):973-5. doi: 10.1080/15257779908041617. Nucleosides Nucleotides. 1999. PMID: 10432723

2

S-acyl-2-thioethyl aryl phosphotriester derivatives of AZT: synthesis, antiviral activity, and stability study.

Peyrottes S, Coussot G, Lefebvre I, Imbach JL, Gosselin G, Aubertin AM, Périgaud C. Peyrottes S, et al. Among authors: lefebvre i. J Med Chem. 2003 Feb 27;46(5):782-93. doi: 10.1021/jm021016y. J Med Chem. 2003. PMID: 12593658

3

Phenyl phosphotriester derivatives of AZT: variations upon the SATE moiety.

Villard AL, Coussot G, Lefebvre I, Augustijns P, Aubertin AM, Gosselin G, Peyrottes S, Périgaud C. Villard AL, et al. Among authors: lefebvre i. Bioorg Med Chem. 2008 Aug 1;16(15):7321-9. doi: 10.1016/j.bmc.2008.06.024. Epub 2008 Jun 18. Bioorg Med Chem. 2008. PMID: 18585917

4

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. Lefebvre I, et al. J Med Chem. 1995 Sep 29;38(20):3941-50. doi: 10.1021/jm00020a007. J Med Chem. 1995. PMID: 7562927

5

5'-Hydrogenphosphonates of anti-HIV nucleoside analogues revisited: controversial mode of action.

Gosselin G, Périgaud C, Lefebvre I, Pompon A, Aubertin AM, Kirn A, Szabo T, Stawinski J, Imbach JL. Gosselin G, et al. Among authors: lefebvre i. Antiviral Res. 1993 Oct;22(2-3):143-53. doi: 10.1016/0166-3542(93)90092-w. Antiviral Res. 1993. PMID: 8279809

6

Intracellular delivery of nucleoside monophosphates through a reductase-mediated activation process.

Puech F, Gosselin G, Lefebvre I, Pompon A, Aubertin AM, Kirn A, Imbach JL. Puech F, et al. Among authors: lefebvre i. Antiviral Res. 1993 Oct;22(2-3):155-74. doi: 10.1016/0166-3542(93)90093-x. Antiviral Res. 1993. PMID: 8279810

7

Anti-HIV pronucleotides: decomposition pathways and correlation with biological activities.

Egron D, Lefebvre I, Périgaud C, Beltran T, Pompon A, Gosselin G, Aubertin AM, Imbach JL. Egron D, et al. Among authors: lefebvre i. Bioorg Med Chem Lett. 1998 May 5;8(9):1045-50. doi: 10.1016/s0960-894x(98)00158-9. Bioorg Med Chem Lett. 1998. PMID: 9871705

8

Rational design of a new series of mixed anti-HIV pronucleotides.

Schlienger N, Beltran T, Périgaud C, Lefebvre I, Pompon A, Aubertin AM, Gosselin G, Imbach JL. Schlienger N, et al. Among authors: lefebvre i. Bioorg Med Chem Lett. 1998 Nov 3;8(21):3003-6. doi: 10.1016/S0960-894X(98)00535-6. Bioorg Med Chem Lett. 1998. PMID: 9873664

9

Rational design of a new series of pronucleotide.

Beltran T, Egron D, Pompon A, Lefebvre I, Périgaud C, Gosselin G, Aubertin A, Imbach J. Beltran T, et al. Among authors: lefebvre i. Bioorg Med Chem Lett. 2001 Jul 9;11(13):1775-7. doi: 10.1016/s0960-894x(01)00299-2. Bioorg Med Chem Lett. 2001. PMID: 11425558

10

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. Peyrottes S, et al. Among authors: lefebvre i. Nucleosides Nucleotides Nucleic Acids. 2001 Apr-Jul;20(4-7):315-21. doi: 10.1081/NCN-100002302. Nucleosides Nucleotides Nucleic Acids. 2001. PMID: 11563043

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