-
1
-
-
0026605647
-
Nucleoside analogues as chemotherapeutic agents: A review
-
Périgaud, C., Gosselin, G. & Imbach, J.-L. (1992) Nucleoside analogues as chemotherapeutic agents: a review. Nucleosides & Nucleotides 11, 903-945.
-
(1992)
Nucleosides & Nucleotides
, vol.11
, pp. 903-945
-
-
Périgaud, C.1
Gosselin, G.2
Imbach, J.-L.3
-
2
-
-
0028932336
-
Current antiviral agents. Part 1 - Herpes viruses, hepatitis viruses and respiratory viruses
-
Kinchington, D. & Golfdthorpe, S. (1995) Current antiviral agents. Part 1 - Herpes viruses, hepatitis viruses and respiratory viruses. Int. Antiviral News 3, 57-61.
-
(1995)
Int. Antiviral News
, vol.3
, pp. 57-61
-
-
Kinchington, D.1
Golfdthorpe, S.2
-
3
-
-
1542479869
-
Current antiviral agents. Part 2 - Human immunodeficiency viruses
-
Goldthorpe, S., Kinchington, D. & Lovelidge, L. (1995) Current antiviral agents. Part 2 - Human immunodeficiency viruses. Int. Antiviral News 3, 92-98.
-
(1995)
Int. Antiviral News
, vol.3
, pp. 92-98
-
-
Goldthorpe, S.1
Kinchington, D.2
Lovelidge, L.3
-
4
-
-
0027407484
-
Nucleoside analogs: Similarities and differences
-
Sommadossi, J.-P. (1993) Nucleoside analogs: similarities and differences. Clin. Infec. Dis. 16 (Suppl 1), S7-S15.
-
(1993)
Clin. Infec. Dis.
, vol.16
, Issue.1 SUPPL.
-
-
Sommadossi, J.-P.1
-
5
-
-
0027156952
-
Inhibition of HIV-1 replication in cultured cells with phosphorylatcd dideoxyuridine derivatives encapsulated in immunoliposomes
-
Zelphati, O., Degols, G., Loughrey, H., Leserman, L., Pompon, A., Puech, F., Maggio, A.-F., Imbach, J.-L. & Gosselin, G. (1993) Inhibition of HIV-1 replication in cultured cells with phosphorylatcd dideoxyuridine derivatives encapsulated in immunoliposomes. Antiviral Res. 21, 181-195.
-
(1993)
Antiviral Res.
, vol.21
, pp. 181-195
-
-
Zelphati, O.1
Degols, G.2
Loughrey, H.3
Leserman, L.4
Pompon, A.5
Puech, F.6
Maggio, A.-F.7
Imbach, J.-L.8
Gosselin, G.9
-
6
-
-
21844523601
-
Prodrugs of analogs of nucleic acid components
-
Alexander, P. & Holy, A. (1994) Prodrugs of analogs of nucleic acid components. Collect. Czech. Chem. Commun. 59, 2127-2165.
-
(1994)
Collect. Czech. Chem. Commun.
, vol.59
, pp. 2127-2165
-
-
Alexander, P.1
Holy, A.2
-
8
-
-
77956802548
-
Comments on nucleotide delivery forms
-
De Clercq, E. ed.
-
Périgaud, C., Girardet, J.-L., Gosselin, G. & Imbach, J.-L. (1995) Comments on nucleotide delivery forms; in Advances in Antiviral Drug Design (De Clercq, E. ed.) vol. 2, pp. 142-172.
-
(1995)
Advances in Antiviral Drug Design
, vol.2
, pp. 142-172
-
-
Périgaud, C.1
Girardet, J.-L.2
Gosselin, G.3
Imbach, J.-L.4
-
9
-
-
0027943194
-
Synthesis and antitumor evaluation of bis[(pivaloyloxy)metliyl] 2′-deoxy-5-fluorouridine 5′-monophosphate (FdUMP): A strategy to introduce nucleotides into cells
-
and references cited therein
-
Farquhar, D., Khan, S., Srivastva, D.N. & Saunders, P.P. (1994) Synthesis and antitumor evaluation of bis[(pivaloyloxy)metliyl] 2′-deoxy-5-fluorouridine 5′-monophosphate (FdUMP): A strategy to introduce nucleotides into cells. J. Med. Chem. 37, 3902-3909, and references cited therein.
-
(1994)
J. Med. Chem.
, vol.37
, pp. 3902-3909
-
-
Farquhar, D.1
Khan, S.2
Srivastva, D.N.3
Saunders, P.P.4
-
10
-
-
0028290089
-
Decomposition pathways of the mono- and bis(pivaloyloxymethyl) esters of azidothymidine 5-monophosphate in cell extract and in tissue culture medium: An application of the "on-line ISRP-cleaning" HPLC technique
-
Pompon, A., Lefebvre, I., Imbach, J.-L., Kahn, S. & Farquhar, D. (1994) Decomposition pathways of the mono- and bis(pivaloyloxymethyl) esters of azidothymidine 5-monophosphate in cell extract and in tissue culture medium: an application of the "on-line ISRP-cleaning" HPLC technique. Antiviral Chem. Chemother. 5, 91-98.
-
(1994)
Antiviral Chem. Chemother.
, vol.5
, pp. 91-98
-
-
Pompon, A.1
Lefebvre, I.2
Imbach, J.-L.3
Kahn, S.4
Farquhar, D.5
-
11
-
-
0027722026
-
Rational design for cytosolic delivery of nucleoside monophosphates: "SATE" and "DTE" as enzyme-labile transient phosphate protecting groups
-
Périgaud, C., Gosselin, G., Lefebvre, I., Girardet, J.-L., Benzaria, S., Barber, I. & Imbach, J.-L. (1993) Rational design for cytosolic delivery of nucleoside monophosphates: "SATE" and "DTE" as enzyme-labile transient phosphate protecting groups. Bioorg. Med. Chem. Lett. 3, 2521-2526.
-
(1993)
Bioorg. Med. Chem. Lett.
, vol.3
, pp. 2521-2526
-
-
Périgaud, C.1
Gosselin, G.2
Lefebvre, I.3
Girardet, J.-L.4
Benzaria, S.5
Barber, I.6
Imbach, J.-L.7
-
12
-
-
0026524003
-
A new strategy for the chemotherapy of acquired immunodeficiency syndrome: Membrane permeable dideoxyuridine monophosphate analogues as potent inhibitors of human immunodeficiency virus infection
-
Sastry, K.J., Nehete, P.N., Khan, S., Plunkett, W., Arlinghaus, R.B. & Farquhar, D. (1992) A new strategy for the chemotherapy of acquired immunodeficiency syndrome: membrane permeable dideoxyuridine monophosphate analogues as potent inhibitors of human immunodeficiency virus infection. Mol. Pharmacol. 41, 441-445.
-
(1992)
Mol. Pharmacol.
, vol.41
, pp. 441-445
-
-
Sastry, K.J.1
Nehete, P.N.2
Khan, S.3
Plunkett, W.4
Arlinghaus, R.B.5
Farquhar, D.6
-
13
-
-
0343507395
-
The anti-HIV nucleoside phosphotriester approach: Controversial comments and complementary data
-
Gosselin, G. & Imbach, J.-L. (1993) The anti-HIV nucleoside phosphotriester approach: controversial comments and complementary data. Int. Antiviral News 1, 100-102.
-
(1993)
Int. Antiviral News
, vol.1
, pp. 100-102
-
-
Gosselin, G.1
Imbach, J.-L.2
-
14
-
-
0027433373
-
Intracellular delivery of nucleoside monophosphates through a reductase-mediated activation process
-
Puech, F., Gosselin, G., Lefebvre, I., Pompon, A., Aubertin, A.-M., Kirn, A. & Imbach, J.-L. (1993) Intracellular delivery of nucleoside monophosphates through a reductase-mediated activation process. Antiviral Res. 22, 155-174.
-
(1993)
Antiviral Res.
, vol.22
, pp. 155-174
-
-
Puech, F.1
Gosselin, G.2
Lefebvre, I.3
Pompon, A.4
Aubertin, A.-M.5
Kirn, A.6
Imbach, J.-L.7
-
15
-
-
0028819889
-
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, A.-M., Girardet, J.-L., Kirn, A., Gosselin, G. & Imbach, J.-L. (1995) Mononucleoside phosphotriester derivatives with S-acyl-2-thioethyl bioreversible phosphate-protecting groups: intracellular delivery of 3′-azido-2′,3′-dideoxythymidine 5′-monophosphate. J. Med. Chem. 38, 3941-3950.
-
(1995)
J. Med. Chem.
, vol.38
, pp. 3941-3950
-
-
Lefebvre, I.1
Périgaud, C.2
Pompon, A.3
Aubertin, A.-M.4
Girardet, J.-L.5
Kirn, A.6
Gosselin, G.7
Imbach, J.-L.8
-
16
-
-
0026739035
-
Synthesis and in vitro evaluation of a phosphonate prodrug: Bis(pivaloyloxymethyl) 9-(2-phosphonylmethoxyethyl)adenine
-
Starrett, J.E., Jr., Tortolani, D.R., Hitchcock, M.J.M., Martin, J.C. & Mansuri, M.M. (1992) Synthesis and in vitro evaluation of a phosphonate prodrug: bis(pivaloyloxymethyl) 9-(2-phosphonylmethoxyethyl)adenine. Antiviral Res. 19, 267-273.
-
(1992)
Antiviral Res.
, vol.19
, pp. 267-273
-
-
Starrett Jr., J.E.1
Tortolani, D.R.2
Hitchcock, M.J.M.3
Martin, J.C.4
Mansuri, M.M.5
-
17
-
-
0027440278
-
Metabolism and in vitro antiretroviral activities of bis(pivaloyloxymethyl) prodrugs of acyclic nucleoside phosphonates
-
Srinivas, R.V., Robbins, B.L, Connelly, M.C., Gong, Y.-F., Bischofberger, N. & Friedland, A. (1993) Metabolism and in vitro antiretroviral activities of bis(pivaloyloxymethyl) prodrugs of acyclic nucleoside phosphonates. Antimicrob. Agents Chemother. 37, 2247-2250.
-
(1993)
Antimicrob. Agents Chemother.
, vol.37
, pp. 2247-2250
-
-
Srinivas, R.V.1
Robbins, B.L.2
Connelly, M.C.3
Gong, Y.-F.4
Bischofberger, N.5
Friedland, A.6
-
18
-
-
0028273851
-
Pivaloyloxymethyl esters of acyclic nucleoside phosphonates
-
Srinivas, R.V., Robbins, B.L., Connelly, M.C., Gong, Y.-F., Bischofberger, N. & Friedland, A. (1994) Pivaloyloxymethyl esters of acyclic nucleoside phosphonates. Int. Antiviral News 2, 53-55.
-
(1994)
Int. Antiviral News
, vol.2
, pp. 53-55
-
-
Srinivas, R.V.1
Robbins, B.L.2
Connelly, M.C.3
Gong, Y.-F.4
Bischofberger, N.5
Friedland, A.6
-
19
-
-
0028306517
-
Synthesis, oral bioavailability determination, and in vitro evaluation of prodrugs of the antiviral agent 9-[2-(phosphonylmethoxy)ethyl]adenine (PMEA)
-
Starrett, J.E., Jr., Tortolani, D.R., Russell, J., Hitchcock, M.J.M., Whiterock, V, Martin, J.C. & Mansuri, M.M. (1994) Synthesis, oral bioavailability determination, and in vitro evaluation of prodrugs of the antiviral agent 9-[2-(phosphonylmethoxy)ethyl]adenine (PMEA). J. Med. Chem. 37, 1857-1864.
-
(1994)
J. Med. Chem.
, vol.37
, pp. 1857-1864
-
-
Starrett Jr., J.E.1
Tortolani, D.R.2
Russell, J.3
Hitchcock, M.J.M.4
Whiterock, V.5
Martin, J.C.6
Mansuri, M.M.7
-
20
-
-
0028286804
-
Oral bioavailability of the antiretroviral agent 9-(2-phosphonylmethoxyethyl)adenine (PMEA) from three formulations of the prodrug bis(pivaloyloxymethyl)-PMEA in fasted male cynomolgus monkeys
-
Cundy, K.C., Fishback, J.A., Shaw, J.-P., Lee, M.L., Soike, K.F., Visor, G.C. & Lee, W.A. (1994) Oral bioavailability of the antiretroviral agent 9-(2-phosphonylmethoxyethyl)adenine (PMEA) from three formulations of the prodrug bis(pivaloyloxymethyl)-PMEA in fasted male cynomolgus monkeys. Pharmaceut. Res. 11, 839-843.
-
(1994)
Pharmaceut. Res.
, vol.11
, pp. 839-843
-
-
Cundy, K.C.1
Fishback, J.A.2
Shaw, J.-P.3
Lee, M.L.4
Soike, K.F.5
Visor, G.C.6
Lee, W.A.7
-
21
-
-
0029086438
-
Antiretroviral activity of stavudine (2′,3′-didehydro-3-deoxythymidine, D4T)
-
Riddler, S.A., Anderson, R.E. & Mellors, J.W. (1995) Antiretroviral activity of stavudine (2′,3′-didehydro-3-deoxythymidine, D4T). Antiviral Res. 27, 189-203.
-
(1995)
Antiviral Res.
, vol.27
, pp. 189-203
-
-
Riddler, S.A.1
Anderson, R.E.2
Mellors, J.W.3
-
22
-
-
0028843908
-
Increase of the anti-HIV activity of D4T in human T-cell cultures by the use of the SATE pronucleotide approach
-
Girardet, J.-L., Périgaud, C., Aubertin, A.-M., Gosselin, G., Kirn, A. & Imbach, J.-L. (1995) Increase of the anti-HIV activity of D4T in human T-cell cultures by the use of the SATE pronucleotide approach. Bioorg. Med. Chem. Lett. 5, 2981-2984.
-
(1995)
Bioorg. Med. Chem. Lett.
, vol.5
, pp. 2981-2984
-
-
Girardet, J.-L.1
Périgaud, C.2
Aubertin, A.-M.3
Gosselin, G.4
Kirn, A.5
Imbach, J.-L.6
-
23
-
-
0023808097
-
Metabolic pathways for the activation of the antiretroviral agent 2′,3′-dideoxyadenosine in human lymphoid cells
-
Johnson, M.A., Ahluwalia, G., Connelly, M.C., Cooney, D.A., Broder, S., Johns, D.G. & Fridland, A. (1988) Metabolic pathways for the activation of the antiretroviral agent 2′,3′-dideoxyadenosine in human lymphoid cells. J. Biol. Chem. 263, 15354-15357.
-
(1988)
J. Biol. Chem.
, vol.263
, pp. 15354-15357
-
-
Johnson, M.A.1
Ahluwalia, G.2
Connelly, M.C.3
Cooney, D.A.4
Broder, S.5
Johns, D.G.6
Fridland, A.7
-
25
-
-
0026561089
-
Interpretation of the roles of adenylosuccinate Iyase and of AMP deaminase in the anti-HIV activity of 2′,3′-dideoxyadenosine and 2′,3′-dideoxyinosine
-
Nair, V. & Sells, T.B. (1992) Interpretation of the roles of adenylosuccinate Iyase and of AMP deaminase in the anti-HIV activity of 2′,3′-dideoxyadenosine and 2′,3′-dideoxyinosine. Biochim. Biophys. Acta 1119, 201-204.
-
(1992)
Biochim. Biophys. Acta
, vol.1119
, pp. 201-204
-
-
Nair, V.1
Sells, T.B.2
-
26
-
-
0344093211
-
The SATE pronucleotide derivative of dd A: A more potent HIV inhibitor than AZT
-
Benzaria, S., Girardet, J.-L., Périgaud, C., Aubertin, A.-M., Pélicano, H., Maury, G., Gosselin, G., Kirn, A. & Imbach, J.-L. (1994) The SATE pronucleotide derivative of dd A: a more potent HIV inhibitor than AZT. Nucleic Acids Symp. Series 31, 129-130.
-
(1994)
Nucleic Acids Symp. Series
, vol.31
, pp. 129-130
-
-
Benzaria, S.1
Girardet, J.-L.2
Périgaud, C.3
Aubertin, A.-M.4
Pélicano, H.5
Maury, G.6
Gosselin, G.7
Kirn, A.8
Imbach, J.-L.9
-
27
-
-
0027980948
-
Equal inhibition of the replication of human immunodeficiency virus in human T-cell culture by ddA bis(SATE)phosphotriester and 3′-azido-2′,3′-dideoxythymidine
-
Périgaud, C., Aubertin, A.-M., Benzaria, S., Pélicano, H., Girardet, J.-L., Maury, G., Gosselin, G., Kirn, A. & Imbach, J.-L. (1994) Equal inhibition of the replication of human immunodeficiency virus in human T-cell culture by ddA bis(SATE)phosphotriester and 3′-azido-2′,3′-dideoxythymidine. Biochem. Pharmacol. 48, 11-14.
-
(1994)
Biochem. Pharmacol.
, vol.48
, pp. 11-14
-
-
Périgaud, C.1
Aubertin, A.-M.2
Benzaria, S.3
Pélicano, H.4
Girardet, J.-L.5
Maury, G.6
Gosselin, G.7
Kirn, A.8
Imbach, J.-L.9
-
29
-
-
0028006272
-
Aciclovir. A reappraisal of its antiviral activity, pharmacokinetic properties and therapeutic efficacy
-
Wagstaff, A.J., Faulds, D. & Goa, K.L. (1994) Aciclovir. A reappraisal of its antiviral activity, pharmacokinetic properties and therapeutic efficacy. Drugs 47, 153-205.
-
(1994)
Drugs
, vol.47
, pp. 153-205
-
-
Wagstaff, A.J.1
Faulds, D.2
Goa, K.L.3
-
30
-
-
0022483442
-
Synthesis and anti-herpes-virus activity of acyclic 2′-deoxyguanosine analogues related to 9-(1,3-dihydroxy-2-propoxy)methyllguanine
-
Martin, J.C., McGee, D.P.C., Jeffrey, G.A., Hobbs, D.W., Smee, D.F., Matthews, T.R. & Verheyden, J.P.H. (1986) Synthesis and anti-herpes-virus activity of acyclic 2′-deoxyguanosine analogues related to 9-[(1,3-dihydroxy-2-propoxy)methyllguanine. J. Med. Chem. 29, 1384-1389.
-
(1986)
J. Med. Chem.
, vol.29
, pp. 1384-1389
-
-
Martin, J.C.1
McGee, D.P.C.2
Jeffrey, G.A.3
Hobbs, D.W.4
Smee, D.F.5
Matthews, T.R.6
Verheyden, J.P.H.7
-
31
-
-
0028815254
-
Development of zidovudine (AZT) resistance in Jurkat T cells is associated with decreased expression of the thymidine kinase (TK) gene and hypermethylation of the 5′ end of human TK gene
-
Wu, S., Liu, X., Solorzano, M.M., Kwock, R. & Avramis, V.I. (1995) Development of zidovudine (AZT) resistance in Jurkat T cells is associated with decreased expression of the thymidine kinase (TK) gene and hypermethylation of the 5′ end of human TK gene. J. Acquired Immune-Defic. Syndromes Hum. Retrovirol. 8, 1-9.
-
(1995)
J. Acquired Immune-Defic. Syndromes Hum. Retrovirol.
, vol.8
, pp. 1-9
-
-
Wu, S.1
Liu, X.2
Solorzano, M.M.3
Kwock, R.4
Avramis, V.I.5
|