-
1
-
-
0027534661
-
Differential antiherpesvirus and antiretrovirus effects of the (S) and (R) enantiomers of acyclic nucleoside phos-phonates: Potent and selective in vitro and in vivo antiretrovirus activities of (R)-9-(2-phosphonomethoxypropyl)-2,6-diaminopurine
-
Balzarini J, Holy A, Jindrich J, Naesens L, Snoeck R, Schols D & De Clercq E (1993) Differential antiherpesvirus and antiretrovirus effects of the (S) and (R) enantiomers of acyclic nucleoside phos-phonates: potent and selective in vitro and in vivo antiretrovirus activities of (R)-9-(2-phosphonomethoxypropyl)-2,6-diaminopurine. Antimicrobial Agents & Chemotherapy 37:332-338.
-
(1993)
Antimicrobial Agents & Chemotherapy
, vol.37
, pp. 332-338
-
-
Balzarini, J.1
Holy, A.2
Jindrich, J.3
Naesens, L.4
Snoeck, R.5
Schols, D.6
De Clercq, E.7
-
2
-
-
0029852052
-
Anti-retrovirus specificity and intracellular metabolism of 2′,3′-didehydro-2′,3′-dideoxythymidine (Stavudine) and its 5′-monophosphate triester prodrug So324
-
Balzarini J, Egberink H, Hartmann K, Cahard D, Thormar H, De Clercq E & McGuigan C (1996a) Anti-retrovirus specificity and intracellular metabolism of 2′,3′-didehydro-2′,3′-dideoxythymidine (Stavudine) and its 5′-monophosphate triester prodrug So324. Molecular Pharmacology 50:1207-1213.
-
(1996)
Molecular Pharmacology
, vol.50
, pp. 1207-1213
-
-
Balzarini, J.1
Egberink, H.2
Hartmann, K.3
Cahard, D.4
Thormar, H.5
De Clercq, E.6
McGuigan, C.7
-
3
-
-
0029946597
-
Mechanism of anti-HIV action of masked alaninyl d4TMP derivatives
-
Balzarini J, Karlsson A, Aquaro S, Perno C-F, Cahard D, Naesens L, De Clercq E & McGuigan C (1996b) Mechanism of anti-HIV action of masked alaninyl d4TMP derivatives. Proceedings of the National Academy of Sciences, USA 93:7295-7299.
-
(1996)
Proceedings of the National Academy of Sciences, USA
, vol.93
, pp. 7295-7299
-
-
Balzarini, J.1
Karlsson, A.2
Aquaro, S.3
Perno, C.-F.4
Cahard, D.5
Naesens, L.6
De Clercq, E.7
McGuigan, C.8
-
4
-
-
0025350764
-
Synthesis and biological properties of novel phos-photriesters: A new approach to the introduction of biologically active nucleotides into cells
-
Farrow SN, Jones AS, Kumar A, Walker RT, Balzarini J & De Clercq E (1990) Synthesis and biological properties of novel phos-photriesters: a new approach to the introduction of biologically active nucleotides into cells. Journal of Medicinal Chemistry 33:1400-1406.
-
(1990)
Journal of Medicinal Chemistry
, vol.33
, pp. 1400-1406
-
-
Farrow, S.N.1
Jones, A.S.2
Kumar, A.3
Walker, R.T.4
Balzarini, J.5
De Clercq, E.6
-
6
-
-
0025091612
-
Synthesis and biological evaluation of some cyclic phosphoramidate nucleoside derivatives
-
Kumar A, Coe PL, Jones AS, Walker RT, Balzarini J & De Clercq E (1990) Synthesis and biological evaluation of some cyclic phosphoramidate nucleoside derivatives. Journal of Medicinal Chemistry 33:2368-2375.
-
(1990)
Journal of Medicinal Chemistry
, vol.33
, pp. 2368-2375
-
-
Kumar, A.1
Coe, P.L.2
Jones, A.S.3
Walker, R.T.4
Balzarini, J.5
De Clercq, E.6
-
9
-
-
0025801734
-
Synthesis and anti-HIV activity of some haloalkyl phosphoramidate derivatives of 3′-azido-3′-deoxythymidine (AZT): Potent activity of the trichloroethyl methoxyalaninyl compound
-
McGuigan C, Devine KG, O'Connor TJ & Kinchington D (1991) Synthesis and anti-HIV activity of some haloalkyl phosphoramidate derivatives of 3′-azido-3′-deoxythymidine (AZT): potent activity of the trichloroethyl methoxyalaninyl compound. Antiviral Research 15:255-263.
-
(1991)
Antiviral Research
, vol.15
, pp. 255-263
-
-
McGuigan, C.1
Devine, K.G.2
O'Connor, T.J.3
Kinchington, D.4
-
11
-
-
0029975897
-
Aryl phosphoramidate derivatives of d4T have improved anti-HIV efficacy in tissue culture and may act by the generation of a novel intracellular metabolite
-
McGuigan C, Cahard D, Sheeka HM, De Clercq E & Balzarini J (1996a) Aryl phosphoramidate derivatives of d4T have improved anti-HIV efficacy in tissue culture and may act by the generation of a novel intracellular metabolite. Journal of Medicinal Chemistry 39:1748-1753.
-
(1996)
Journal of Medicinal Chemistry
, vol.39
, pp. 1748-1753
-
-
McGuigan, C.1
Cahard, D.2
Sheeka, H.M.3
De Clercq, E.4
Balzarini, J.5
-
12
-
-
0029998158
-
Novel nucleoside phosphoramidates as inhibitors of HIV: Studies on the stereochemical requirements of the phosphoramidate amino acid
-
McGuigan C, Salgado A, Yarnold C, Harries TY, De Clercq E & Balzarini J (1996b) Novel nucleoside phosphoramidates as inhibitors of HIV: studies on the stereochemical requirements of the phosphoramidate amino acid. Antiviral Chemistry Chemotherapy 7:184-188.
-
(1996)
Antiviral Chemistry Chemotherapy
, vol.7
, pp. 184-188
-
-
McGuigan, C.1
Salgado, A.2
Yarnold, C.3
Harries, T.Y.4
De Clercq, E.5
Balzarini, J.6
-
13
-
-
0030044583
-
Phosphoramidates as potent pro-drugs of anti-HIV nucleotides: Studies in the amino region
-
McGuigan C, Cahard D, Salgado A, De Clercq E & Balzarini J (1996c) Phosphoramidates as potent pro-drugs of anti-HIV nucleotides: studies in the amino region. Antiviral Chemistry & Chemotherapy 7:31-36.
-
(1996)
Antiviral Chemistry & Chemotherapy
, vol.7
, pp. 31-36
-
-
McGuigan, C.1
Cahard, D.2
Salgado, A.3
De Clercq, E.4
Balzarini, J.5
-
14
-
-
0030872397
-
Phosphoramidate derivatives of d4T as inhibitors of HIV: The effect of amino acid variation
-
McGuigan C.Tsang HW, Cahard D, Turner K, Velázquez S, Salgado A, Bidois L, Naesens L, De Clercq E & Balzarini J (1997) Phosphoramidate derivatives of d4T as inhibitors of HIV: the effect of amino acid variation. Antiviral Research 35:195-204.
-
(1997)
Antiviral Research
, vol.35
, pp. 195-204
-
-
McGuigan, C.1
Tsang, H.W.2
Cahard, D.3
Turner, K.4
Velázquez, S.5
Salgado, A.6
Bidois, L.7
Naesens, L.8
De Clercq, E.9
Balzarini, J.10
-
15
-
-
0030927126
-
ADA-bypass by lipophilic cycloSAL-ddAMP pro-nucleotides. A second example of the efficiency of the cycloSAL-concept
-
Meier C, Knispel T, De Clercq E & Balzarini J (1997) ADA-bypass by lipophilic cycloSAL-ddAMP pro-nucleotides. A second example of the efficiency of the cycloSAL-concept. Bioorganic and Medicinal Chemistry Letters 7:1577-1582.
-
(1997)
Bioorganic and Medicinal Chemistry Letters
, vol.7
, pp. 1577-1582
-
-
Meier, C.1
Knispel, T.2
De Clercq, E.3
Balzarini, J.4
-
16
-
-
0027722026
-
Rational design for cytosolic delivery of nucleoside monophosphates: 'SATE' and 'DTE' as enzyme-labile transient phosphate protecting groups
-
Perigaud C, Gosselin G, Lefebvre I, Girardet JL, Benzaria S, Barber I & Imbach JL (1993) Rational design for cytosolic delivery of nucleoside monophosphates: 'SATE' and 'DTE' as enzyme-labile transient phosphate protecting groups. Bioorganic and Medicinal Chemistry Letters 3:2521-2526.
-
(1993)
Bioorganic and Medicinal Chemistry Letters
, vol.3
, pp. 2521-2526
-
-
Perigaud, C.1
Gosselin, G.2
Lefebvre, I.3
Girardet, J.L.4
Benzaria, S.5
Barber, I.6
Imbach, J.L.7
-
17
-
-
0029953984
-
Decomposition pathways in in vitro HIV inhibitory effects of IsoddA pronucleotides: Towards a rational approach for intracellular delivery of nucleoside 5′-monophosphates
-
Valette G, Pompon A, Girardet J-L, Cappellaci L, Franchetti P, Grifantimi M, Colla PL, Loi AG, Perigaud C, Gosselin G Se Imbach J-L (1996) Decomposition pathways in in vitro HIV inhibitory effects of IsoddA pronucleotides: towards a rational approach for intracellular delivery of nucleoside 5′-monophosphates. Journal of Medicinal Chemistry 39:1981-1990.
-
(1996)
Journal of Medicinal Chemistry
, vol.39
, pp. 1981-1990
-
-
Valette, G.1
Pompon, A.2
Girardet, J.-L.3
Cappellaci, L.4
Franchetti, P.5
Grifantimi, M.6
Colla, P.L.7
Loi, A.G.8
Perigaud, C.9
Gosselin, G.10
Se Imbach, J.-L.11
|