-
1
-
-
33845449051
-
Peginterferon and ribavirin for chronic hepatitis C
-
Hoofnagle, J. H.; Seef, L. B. Peginterferon and ribavirin for chronic hepatitis C N. Engl. J. Med. 2006, 355, 2444-2451
-
(2006)
N. Engl. J. Med.
, vol.355
, pp. 2444-2451
-
-
Hoofnagle, J.H.1
Seef, L.B.2
-
2
-
-
41349099226
-
Emerging drugs for hepatitis C
-
Soriano, V.; Madejon, A.; Vispo, E.; Labarga, P.; Garcia-Samaniego, J.; Martin-Carbonero, L.; Sheldon, J.; Bottecchia, M.; Tuma, P.; Barreiro, P. Emerging drugs for hepatitis C Expert Opin. Emerging Drugs 2008, 13, 1-19
-
(2008)
Expert Opin. Emerging Drugs
, vol.13
, pp. 1-19
-
-
Soriano, V.1
Madejon, A.2
Vispo, E.3
Labarga, P.4
Garcia-Samaniego, J.5
Martin-Carbonero, L.6
Sheldon, J.7
Bottecchia, M.8
Tuma, P.9
Barreiro, P.10
-
3
-
-
67649625180
-
Progress towards improving antiviral therapy for hepatitis C with hepatitis C virus polymerase inhibitors. Part 1: Nucleoside analogues
-
Brown, N. A. Progress towards improving antiviral therapy for hepatitis C with hepatitis C virus polymerase inhibitors. Part 1: Nucleoside analogues Expert Opin. Invest. Drugs 2009, 18, 709-725
-
(2009)
Expert Opin. Invest. Drugs
, vol.18
, pp. 709-725
-
-
Brown, N.A.1
-
4
-
-
33645232568
-
The novel nucleoside analog R1479 (4′-azidocytidine) is a potent inhibitor of NS5B-dependent RNA synthesis and hepatitis C virus replication in cell culture
-
Klumpp, K.; Leveque, V.; Le Pogam, S.; Ma, H.; Jiang, W.-R.; Kang, H.; Granycome, C.; Singer, M.; Laxton, C.; Hang, J. Q.; Sarma, K.; Smith, D. B.; Heindl, D.; Hobbs, C. J.; Merrett, J. H.; Symons, J.; Cammack, N.; Martin, J. A.; Devos, R.; Najera, I. The novel nucleoside analog R1479 (4′- azidocytidine) is a potent inhibitor of NS5B-dependent RNA synthesis and hepatitis C virus replication in cell culture J. Biol. Chem. 2006, 281, 3793-3799
-
(2006)
J. Biol. Chem.
, vol.281
, pp. 3793-3799
-
-
Klumpp, K.1
Leveque, V.2
Le Pogam, S.3
Ma, H.4
Jiang, W.-R.5
Kang, H.6
Granycome, C.7
Singer, M.8
Laxton, C.9
Hang, J.Q.10
Sarma, K.11
Smith, D.B.12
Heindl, D.13
Hobbs, C.J.14
Merrett, J.H.15
Symons, J.16
Cammack, N.17
Martin, J.A.18
Devos, R.19
Najera, I.20
more..
-
5
-
-
4744364179
-
Structure - activity relationship of heterobase-modified 2′-C-methyl ribonucleosides as inhibitors of hepatitis C virus RNA replication
-
DOI 10.1021/jm040068f
-
Eldrup, A. B.; Prhavc, Ml.; Brooks, J.; Bhat, B.; Prakash, T. P.; Song, Q.; Bera, S.; Bhat, N.; Dande, P.; Cook, P. D.; Bennett, C. F.; Carroll, S. S.; Ball, R. G.; Bosserman, M.; Burlein, C.; Colwell, L. F.; Fay, J. F.; Flores, O. A.; Getty, K.; LaFemina, R. L.; Leone, J.; MacCoss, M.; McMasters, D. R.; Tomassini, J. E.; Langen, D. V.; Wolanski, B.; Olsen, D. B. Structure-Activity Relationship of heterobase modified 2′- C -methyl ribonucleosides as inhibitors of hepatitis C virus RNA replicaton J. Med. Chem. 2004, 47, 5284-5297 (Pubitemid 39314927)
-
(2004)
Journal of Medicinal Chemistry
, vol.47
, Issue.21
, pp. 5284-5297
-
-
Eldrup, A.B.1
Prhavc, M.2
Brooks, J.3
Bhat, B.4
Prakash, T.P.5
Song, Q.6
Bera, S.7
Bhat, N.8
Dande, P.9
Cook, P.D.10
Bennett, C.F.11
Carroll, S.S.12
Ball, R.G.13
Bosserman, M.14
Burlein, C.15
Colwell, L.F.16
Fay, J.F.17
Flores, O.A.18
Getty, K.19
LaFemina, R.L.20
Leone, J.21
MacCoss, M.22
McMasters, D.R.23
Tomassini, J.E.24
Von Langen, D.25
Wolanski, B.26
Olsen, D.B.27
more..
-
6
-
-
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
-
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
-
-
67649971795
-
The application of phosphoramidate ProTide technology to the potent anti-HCV aompound 4′-azidocytidine
-
McGuigan, C.; Kelleher, M. R.; Perrone, P.; Mulready, S.; Luoni, G.; Daverio, F.; Klumpp, K.; Smith, D. B. The application of phosphoramidate ProTide technology to the potent anti-HCV aompound 4′-azidocytidine Bioorg. Med. Chem. Lett. 2009, 19, 4250-4254
-
(2009)
Bioorg. Med. Chem. Lett.
, vol.19
, pp. 4250-4254
-
-
McGuigan, C.1
Kelleher, M.R.2
Perrone, P.3
Mulready, S.4
Luoni, G.5
Daverio, F.6
Klumpp, K.7
Smith, D.B.8
-
9
-
-
67649999890
-
The phosphoramidate ProTide approach greatly enhances the activity of beta-2′- C -methylpurines against Hepatitis C Virus
-
McGuigan, C.; Perrone, P.; Madela, K.; Neyts, J. The phosphoramidate ProTide approach greatly enhances the activity of beta-2′- C -methylpurines against Hepatitis C Virus Bioorg. Med. Chem. Lett. 2009, 19, 4316-4320
-
(2009)
Bioorg. Med. Chem. Lett.
, vol.19
, pp. 4316-4320
-
-
McGuigan, C.1
Perrone, P.2
Madela, K.3
Neyts, J.4
-
10
-
-
67649629173
-
PSI-7851: A novel liver-targeting nucleotide prodrug for the treatment of Hepatitis C
-
presented at 59th Annual Meeting of the American Association for the Study of Liver Diseases, Oct 31-Nov 4, 2008, San Francisco, CA, poster 1901
-
Furman, P. A.; Wang, P. Y.; Niu, C. R.; Bao, D. H.; Symonds, W.; Nagarathnam, D.; Steuer, H. M.; Rachakonda, S.; Ross, B. S.; Otto, M. J.; Sofia, M. PSI-7851: A novel liver-targeting nucleotide prodrug for the treatment of Hepatitis C. Hepatology 2009, 48 (Suppl), presented at 59th Annual Meeting of the American Association for the Study of Liver Diseases, Oct 31-Nov 4, 2008, San Francisco, CA, poster 1901.
-
(2009)
Hepatology
, vol.48
, Issue.SUPPL
-
-
Furman, P.A.1
Wang, P.Y.2
Niu, C.R.3
Bao, D.H.4
Symonds, W.5
Nagarathnam, D.6
Steuer, H.M.7
Rachakonda, S.8
Ross, B.S.9
Otto, M.J.10
Sofia, M.11
-
11
-
-
67649899409
-
Activation of GS-7340 and other Tenofovir phosphonoamidate prodrugs by human proteases
-
Birkus, G.; Kutty, N.; He, G.-X.; Mulato, A.; Lee, W.; McDermott, M; Cihlar, T. Activation of GS-7340 and other Tenofovir phosphonoamidate prodrugs by human proteases Antiviral Res. 2007, 74, A57
-
(2007)
Antiviral Res.
, vol.74
, pp. 57
-
-
Birkus, G.1
Kutty, N.2
He, G.-X.3
Mulato, A.4
Lee, W.5
McDermott, M.6
Cihlar, T.7
-
12
-
-
69549122650
-
An efficient and diastereoselective synthesis of PSI-6130: A clinically efficacious inhibitor of HCV NS5BpPolymerase
-
Notably, the agent has recently been resolved into its separate diastereoisomers. See: Chun, B. K.; Rachakonda, S.; Du, J. F.; Khan, N.; Shi, J. X.; Stee, W.; Cleary, D.; Ross, B. S.; Sofia, M. J. An efficient and diastereoselective synthesis of PSI-6130: a clinically efficacious inhibitor of HCV NS5BpPolymerase J. Org. Chem. 2009, 74, 6819-6824
-
(2009)
J. Org. Chem.
, vol.74
, pp. 6819-6824
-
-
Chun, B.K.1
Rachakonda, S.2
Du, J.F.3
Khan, N.4
Shi, J.X.5
Stee, W.6
Cleary, D.7
Ross, B.S.8
Sofia, M.J.9
-
13
-
-
0031764896
-
Synthesis, anti-human immunodeficiency virus activity and esterase lability of some novel carboxylic ester-modified phosphoramidate derivatives of stavudine (d4T)
-
McGuigan, C.; Sutton, P. W.; Cahard, D.; Turner, K.; OLeary, G.; Wang, Y.; Gumbleton, M.; De Clercq, E.; Balzarini, J. Synthesis, anti-human immunodeficiency virus activity and esterase lability of some novel carboxylic ester-modified phosphoramidate derivatives of stavudine (d4T) Antivir. Chem. Chemother. 1998, 9, 473-479
-
(1998)
Antivir. Chem. Chemother.
, vol.9
, pp. 473-479
-
-
McGuigan, C.1
Sutton, P.W.2
Cahard, D.3
Turner, K.4
Oleary, G.5
Wang, Y.6
Gumbleton, M.7
De Clercq, E.8
Balzarini, J.9
-
14
-
-
77954348139
-
-
Presented at EASL, 25th April 2009, poster no. 966
-
Zhou, X. J.; Pietropaolo, K.; Sullivan-Bólyai, J.; Kuca, B.; Liu, W.; Xu, L.; Belanger, B.; Khan, S.; Mayers, D. IDX184, A liver-targeted nucleotide HCV polymerase inhibitor: Results of a first-in-man safety and pharmacokinetic study. Presented at EASL, 25th April 2009, poster no. 966.
-
IDX184, A Liver-targeted Nucleotide HCV Polymerase Inhibitor: Results of A First-in-man Safety and Pharmacokinetic Study
-
-
Zhou, X.J.1
Pietropaolo, K.2
Sullivan-Bólyai, J.3
Kuca, B.4
Liu, W.5
Xu, L.6
Belanger, B.7
Khan, S.8
Mayers, D.9
-
15
-
-
69949098496
-
The application of phosphoramidate ProTide technology to Acyclovir confers anti-HIV inhibition
-
Derudas, M.; Carta, D.; Brancale, A.; Vanpouille, C.; Lisco, A.; Margolis, L.; Balzarini, J.; McGuigan, C. The application of phosphoramidate ProTide technology to Acyclovir confers anti-HIV inhibition J. Med. Chem. 2009, 52, 5520-5530
-
(2009)
J. Med. Chem.
, vol.52
, pp. 5520-5530
-
-
Derudas, M.1
Carta, D.2
Brancale, A.3
Vanpouille, C.4
Lisco, A.5
Margolis, L.6
Balzarini, J.7
McGuigan, C.8
-
16
-
-
77954334526
-
-
ClogP values were calculated using ChemOffice Ultra 11.0
-
ClogP values were calculated using ChemOffice Ultra 11.0.
-
-
-
-
17
-
-
0030872397
-
Phosphoramidate derivatives of d4T as inhibitiors of HIV: The effect of amino acid variation
-
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 inhibitiors of HIV: the effect of amino acid variation Antiviral Res. 1997, 35, 195-204
-
(1997)
Antiviral Res.
, vol.35
, 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
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