-
1
-
-
28044454891
-
-
U.S Food and drug Administration: Silver Spring, MD, accessed 5 March 2009
-
Drugs Used in the Treatment of HIV Infection; U.S Food and drug Administration: Silver Spring, MD, 2008; http://www.fda.gov/oashi/aids/virals. html (accessed 5 March 2009).
-
(2008)
Drugs Used in the Treatment of HIV Infection
-
-
-
3
-
-
50849109191
-
Acyclovir is activated into a HIV-1 reverse transcriptase inhibitor in herpesvirus-infected human tissues
-
Lisco, A.; Vanpouille, C.; Tchesnokov, E. P.; Grivel, J.-C.; Biancotto, A.; Brichacek, B.; Elliott, J.; Fromentin, E.; Shattock, R.; Anton, P.; Gorelick, R.; Balzarini, J.; McGuigan, C.; Derudas, M.; Gotte, M.; Schinazi, R. F.; Margolis, L. Acyclovir is activated into a HIV-1 reverse transcriptase inhibitor in herpesvirus-infected human tissues. Cell Host Microbe 2008, 4, 260-270.
-
(2008)
Cell Host Microbe
, vol.4
, pp. 260-270
-
-
Lisco, A.1
Vanpouille, C.2
Tchesnokov, E.P.3
Grivel, J.-C.4
Biancotto, A.5
Brichacek, B.6
Elliott, J.7
Fromentin, E.8
Shattock, R.9
Anton, P.10
Gorelick, R.11
Balzarini, J.12
McGuigan, C.13
Derudas, M.14
Gotte, M.15
Schinazi, R.F.16
Margolis, L.17
-
4
-
-
0019321437
-
Phosphorylation of acyclovir monophosphate by GMP kinase
-
Miller, W. H.; Miller, R. L. Phosphorylation of acyclovir monophosphate by GMP kinase. J. Biol. Chem. 1980, 255, 7204-7207.
-
(1980)
J. Biol. Chem.
, vol.255
, pp. 7204-7207
-
-
Miller, W.H.1
Miller, R.L.2
-
5
-
-
0020408238
-
Phosphorylation of acyclovir diphosphate by cellular enzyme
-
Miller, W. H.; Miller, R. L. Phosphorylation of acyclovir diphosphate by cellular enzyme. Biochem. Phamacol. 1982, 31, 3879-3884.
-
(1982)
Biochem. Phamacol.
, vol.31
, pp. 3879-3884
-
-
Miller, W.H.1
Miller, R.L.2
-
6
-
-
26644461226
-
Naphthyl phosphoramidate derivatives of BVdU as potential anticancer agents: Design, synthesis and biological evaluation
-
DOI 10.1081/NCN-200061774
-
Congiatu, C.; McGuigan, C.; Jiang, W. G.; Davies, G.; Mason, M. D. Naphthyl phosphoramidate derivatives of BVdU as potential anticancer agents: design, synthesis and biological evaluation. Nucleosides, Nucleotides Nucleic Acids 2005, 24, 485-489. (Pubitemid 41440634)
-
(2005)
Nucleosides, Nucleotides and Nucleic Acids
, vol.24
, Issue.5-7
, pp. 485-489
-
-
Congiatu, C.1
McGuigan, C.2
Jiang, W.G.3
Davies, G.4
Mason, M.D.5
-
7
-
-
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, H. M.; De Clercq, E.; Balzarini, J. Aryl phosphoramidate derivatives of d4T have improved anti-HIV efficacy in tissue culture and may act by the generation of a novel intracellular metabolite. J. Med. Chem. 1996, 39, 1748-1753.
-
(1996)
J. Med. Chem.
, vol.39
, pp. 1748-1753
-
-
McGuigan, C.1
Cahard, D.2
Sheeka, H.M.3
De Clercq, E.4
Balzarini, J.5
-
8
-
-
20844434037
-
Application of phosphoramidate pronucleotide technology to abacavir leads to a significant enhancement of antiviral potency
-
McGuigan, C.; Harris, S. A.; Daluge, S. M.; Gudmundsson, K. S.; McLean, E. W.; Burnette, T. C.; Marr, H.; Hazen, R.; Condreay, L. D.; Johnson, L.; De Clercq, E.; Balzarini, J. Application of phosphoramidate pronucleotide technology to abacavir leads to a significant enhancement of antiviral potency. J. Med. Chem. 2005, 48, 3504-3515.
-
(2005)
J. Med. Chem.
, vol.48
, pp. 3504-3515
-
-
McGuigan, C.1
Harris, S.A.2
Daluge, S.M.3
Gudmundsson, K.S.4
McLean, E.W.5
Burnette, T.C.6
Marr, H.7
Hazen, R.8
Condreay, L.D.9
Johnson, L.10
De Clercq, E.11
Balzarini, J.12
-
9
-
-
34247259962
-
Application of the phosphoramidate ProTide approach to 4′-azidouridine confers submicromolar potency versus hepatitis C virus on an inactive nucleoside
-
Perrone, P.; Luoni, G. M.; Kelleher, M. R.; Daverio, F.; Angell, A.; Mulready, S.; Congiatu, C.; Rajyaguru, S.; Martin, J. A.; Levêque, V.; Le Pogam, S.; Najera, I.; Klumpp, K.; Smith, D. B.; McGuigan, C. Application of the phosphoramidate ProTide approach to 4′-azidouridine confers submicromolar potency versus hepatitis C virus on an inactive nucleoside. J. Med. Chem. 2007, 50, 1840-1849.
-
(2007)
J. Med. Chem.
, vol.50
, pp. 1840-1849
-
-
Perrone, P.1
Luoni, G.M.2
Kelleher, M.R.3
Daverio, F.4
Angell, A.5
Mulready, S.6
Congiatu, C.7
Rajyaguru, S.8
Martin, J.A.9
Levêque, V.10
Le Pogam, S.11
Najera, I.12
Klumpp, K.13
Smith, D.B.14
McGuigan, C.15
-
10
-
-
0032834955
-
Characterization of the activation pathway of phosphoramidate triester prodrugs of stavudine and zidovudine
-
Saboulard, D.; Naesens, L.; Cahard, D.; Salgado, A.; Pathirana, R.; Velazquez, S.; McGuigan, C.; De Clercq, E.; Balzarini, J. Characterization of the activation pathway of phosphoramidate triester prodrugs of stavudine (d4T) and Zidovudine (AZT). Mol. Pharmacol. 1999, 56, 693-704. (Pubitemid 29491170)
-
(1999)
Molecular Pharmacology
, vol.56
, Issue.4
, pp. 693-704
-
-
Saboulard, D.1
Naesens, L.2
Cahard, D.3
Salgado, A.4
Pathirana, R.5
Velazquez, S.6
Mcguigan, C.7
De Clercq, E.8
Balzarini, J.9
-
11
-
-
47749152548
-
Successful kinase bypass with new acyclovir phosphoramidate prodrugs
-
McGuigan, C.; Derudas, M.; Bugert, J. J.; Andrei, G.; Snoeck, R.; Balzarini, J. Successful kinase bypass with new acyclovir phosphoramidate prodrugs. Bioorg. Med. Chem. Lett. 2008, 18, 4364-4367.
-
(2008)
Bioorg. Med. Chem. Lett.
, vol.18
, pp. 4364-4367
-
-
McGuigan, C.1
Derudas, M.2
Bugert, J.J.3
Andrei, G.4
Snoeck, R.5
Balzarini, J.6
-
12
-
-
0030872397
-
Phosphoramidate derivatives of d4T as inhibitors of HIV: The effect of amino acid variation
-
DOI 10.1016/S0166-3542(97)00029-6, PII S0166354297000296
-
McGuigan, C.; Tsang, H. -W.; Cahard, D.; Turner, K.; Velazquez, S.; Salgado, A.; Bidois, L.; Naesens, L.; De Clercq, E.; Balzarini, J. Phosphoramidate derivatives of d4T as inhibitors of HIV: the effect of amino acid variation. Antiviral Res. 1997, 35, 195-204. (Pubitemid 27351420)
-
(1997)
Antiviral Research
, vol.35
, Issue.3
, pp. 195-204
-
-
McGuigan, C.1
Tsang, H.-W.2
Cahard, D.3
Turner, K.4
Velazquez, S.5
Salgado, A.6
Bidois, L.7
Naesens, L.8
De Clercq, E.9
Balzarini, J.10
-
13
-
-
0027463852
-
O-Selective phosphorylation of nucleosides without N-protection
-
Uchiyama, M.; Aso, Y.; Noyori, R.; Hayakawa, Y. O-Selective phosphorylation of nucleosides without N-protection. J. Org. Chem. 1993, 58, 373-379.
-
(1993)
J. Org. Chem.
, vol.58
, pp. 373-379
-
-
Uchiyama, M.1
Aso, Y.2
Noyori, R.3
Hayakawa, Y.4
-
14
-
-
0000484160
-
Phosphorylation of nucleoside derivatives with aryl phosphoramidochloridates
-
Van Boom, J. H.; Burgers, P. M. J.; Crea, R.; Luyten, W. C. M. M.; Vink, A. B. J.; Reese, C. B. Phosphorylation of nucleoside derivatives with aryl phosphoramidochloridates. Tetrahedron 1975, 31, 2953-2959.
-
(1975)
Tetrahedron
, vol.31
, pp. 2953-2959
-
-
Van Boom, J.H.1
Burgers, P.M.J.2
Crea, R.3
Luyten, W.C.M.M.4
Vink, A.B.J.5
Reese, C.B.6
-
15
-
-
0030872397
-
Phosphoramidate derivatives of d4T as inhibitors of HIV: The effect of amino acid variation
-
DOI 10.1016/S0166-3542(97)00029-6, PII S0166354297000296
-
McGuigan, C.; Tsang, H.-W.; Cahard, D.; Turner, K.; Velazquez, S.; Salgado, A.; Bidois, L.; Naesens, L.; De Clercq, E.; Balzarini, J. Phosphoramidate derivatives of d4T as inhibitors of HIV: the effect of amino acid variation. Antiviral Res. 1997, 35, 195-204. (Pubitemid 27351420)
-
(1997)
Antiviral Research
, vol.35
, Issue.3
, pp. 195-204
-
-
McGuigan, C.1
Tsang, H.-W.2
Cahard, D.3
Turner, K.4
Velazquez, S.5
Salgado, A.6
Bidois, L.7
Naesens, L.8
De Clercq, E.9
Balzarini, J.10
-
16
-
-
2542610580
-
Aryloxy Phosphoramidate Triesters as Pro-Tides
-
Cahard, D.; McGuigan, C.; Balzarini, J. Aryloxy Phosphoramidate Triesters as Pro-Tides. Mini-Rev. Med. Chem. 2004, 4, 371-382.
-
(2004)
Mini-Rev. Med. Chem.
, vol.4
, pp. 371-382
-
-
Cahard, D.1
McGuigan, C.2
Balzarini, J.3
-
17
-
-
0028010544
-
2.8 Å Structure of yeast serine carboxypeptidase
-
Endrizzi, J. A.; Breddam, K.; Remington, S. J. 2.8 Å Structure of yeast serine carboxypeptidase. Biochemistry 1994, 33, 11106-11120.
-
(1994)
Biochemistry
, vol.33
, pp. 11106-11120
-
-
Endrizzi, J.A.1
Breddam, K.2
Remington, S.J.3
-
18
-
-
0032868230
-
Carboxypeptidase, Y structural basis for protein sorting and catalytic triad
-
Jung, G.; Ueno, H.; Hayashi, R.; Carboxypeptidase, Y structural basis for protein sorting and catalytic triad. J. Biochem. 1999, 126, 1-6.
-
(1999)
J. Biochem.
, vol.126
, pp. 1-6
-
-
Jung, G.1
Ueno, H.2
Hayashi, R.3
-
19
-
-
0037162392
-
Hint, Fhit, and GaIT: Function, structure, evolution, and mechanism of three branches of the histidine triad superfamily of nucleotide hydrolases and transferase
-
Brenner, C. Hint, Fhit, and GaIT: function, structure, evolution, and mechanism of three branches of the histidine triad superfamily of nucleotide hydrolases and transferase. Biochemistry 2002, 41, 9003-9014.
-
(2002)
Biochemistry
, vol.41
, pp. 9003-9014
-
-
Brenner, C.1
|