Périgaud C - Search Results

1

Decomposition pathways and in vitro HIV inhibitory effects of isoddA pronucleotides: toward a rational approach for intracellular delivery of nucleoside 5'-monophosphates.

Valette G, Pompon A, Girardet JL, Cappellacci L, Franchetti P, Grifantini M, La Colla P, Loi AG, Périgaud C, Gosselin G, Imbach JL. Valette G, et al. Among authors: perigaud c. J Med Chem. 1996 May 10;39(10):1981-90. doi: 10.1021/jm9507338. J Med Chem. 1996. PMID: 8642557

2

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. Among authors: perigaud c. J Med Chem. 1995 Sep 29;38(20):3941-50. doi: 10.1021/jm00020a007. J Med Chem. 1995. PMID: 7562927

3

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: perigaud c. Antiviral Res. 1993 Oct;22(2-3):143-53. doi: 10.1016/0166-3542(93)90092-w. Antiviral Res. 1993. PMID: 8279809

4

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: perigaud c. 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

5

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: perigaud c. 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

6

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: perigaud c. Nucleosides Nucleotides. 1999 Apr-May;18(4-5):973-5. doi: 10.1080/15257779908041617. Nucleosides Nucleotides. 1999. PMID: 10432723

7

Synthesis and anti-HIV activity of some S-acyl-2-thioethyl (SATE) phosphoramidate derivatives of 3'-azido-2',3'-dideoxythymidine.

Egron D, Périgaud C, Gosselin G, Aubertin AM, Imbach JL. Egron D, et al. Among authors: perigaud c. Nucleosides Nucleotides. 1999 Apr-May;18(4-5):981-2. doi: 10.1080/15257779908041620. Nucleosides Nucleotides. 1999. PMID: 10432724

8

New series of mixed pronucleotides. Synthesis and anti-HIV activities of mononucleoside phenyl SATE phosphotriesters.

Schlienger N, Peyrottes S, Aubertin AM, Gosselin G, Imbach JL, Périgaud C. Schlienger N, et al. Among authors: perigaud c. Nucleosides Nucleotides. 1999 Apr-May;18(4-5):1025-6. doi: 10.1080/15257779908041638. Nucleosides Nucleotides. 1999. PMID: 10432735

9

S-Acyl-2-thioethyl aryl phosphotriester derivatives as mononucleotide prodrugs.

Schlienger N, Peyrottes S, Kassem T, Imbach JL, Gosselin G, Aubertin AM, Périgaud C. Schlienger N, et al. Among authors: perigaud c. J Med Chem. 2000 Nov 16;43(23):4570-4. doi: 10.1021/jm000996o. J Med Chem. 2000. PMID: 11087582

10

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: perigaud c. 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

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