-
1
-
-
59149085501
-
The global burden of hepatitis C
-
Lavanchy, D. The global burden of hepatitis C Liver Int. 2009, 29 (Suppl. 1) 74-81
-
(2009)
Liver Int.
, vol.29
, Issue.SUPPL. 1
, pp. 74-81
-
-
Lavanchy, D.1
-
2
-
-
23944480609
-
Hepatitis C and liver transplantation
-
Brown, R. S. Hepatitis C and liver transplantation Nature 2005, 436, 973-978
-
(2005)
Nature
, vol.436
, pp. 973-978
-
-
Brown, R.S.1
-
3
-
-
0024509701
-
Isolation of a cDNA clone derived from a blood-borne non-A, non-B viral hepatitis genome
-
Choo, Q. L.; Kuo, G.; Weiner, A. J.; Overby, L. R.; Bradley, D. W.; Houghton, M. Isolation of a cDNA clone derived from a blood-borne non-A, non-B viral hepatitis genome Science 1989, 244, 359-362
-
(1989)
Science
, vol.244
, pp. 359-362
-
-
Choo, Q.L.1
Kuo, G.2
Weiner, A.J.3
Overby, L.R.4
Bradley, D.W.5
Houghton, M.6
-
4
-
-
65449136656
-
Diagnosis, management, and treatment of hepatitis C: An update
-
Ghany, M. G.; Strader, D. B.; Thomas, D. L.; Seeff, L. B. Diagnosis, management, and treatment of hepatitis C: an update Hepatology 2009, 49, 1335-1374
-
(2009)
Hepatology
, vol.49
, pp. 1335-1374
-
-
Ghany, M.G.1
Strader, D.B.2
Thomas, D.L.3
Seeff, L.B.4
-
5
-
-
34249024924
-
Replication of hepatitis C virus
-
Moradpour, D.; Penin, F.; Rice, C. M. Replication of hepatitis C virus Nat. Rev. Microbiol. 2007, 5, 453-463
-
(2007)
Nat. Rev. Microbiol.
, vol.5
, pp. 453-463
-
-
Moradpour, D.1
Penin, F.2
Rice, C.M.3
-
6
-
-
0033920304
-
Hepatitis C virus-encoded enzymatic activities and conserved RNA elements in the 3′ nontranslated region are essential for virus replication in vivo
-
Kolykhalov, A. A.; Mihalik, K.; Feinstone, S. M.; Rice, C. M. Hepatitis C virus-encoded enzymatic activities and conserved RNA elements in the 3′ nontranslated region are essential for virus replication in vivo J. Virol. 2000, 74, 2046-2051
-
(2000)
J. Virol.
, vol.74
, pp. 2046-2051
-
-
Kolykhalov, A.A.1
Mihalik, K.2
Feinstone, S.M.3
Rice, C.M.4
-
8
-
-
0344201903
-
An NS3 protease inhibitor with antiviral effects in humans infected with hepatitis C virus
-
Lamarre, D.; Anderson, P. C.; Bailey, M.; Beaulieu, P.; Bolger, G.; Bonneau, P.; Bos, M.; Cameron, D. R.; Cartier, M.; Cordingley, M. G.; Faucher, A. M.; Goudreau, N.; Kawai, S. H.; Kukolj, G.; Lagace, L.; LaPlante, S. R.; Narjes, H.; Poupart, M. A.; Rancourt, J.; Sentjens, R. E., St; George, R.; Simoneau, B.; Steinmann, G.; Thibeault, D.; Tsantrizos, Y. S.; Weldon, S. M.; Yong, C. L.; Llinas-Brunet, M. An NS3 protease inhibitor with antiviral effects in humans infected with hepatitis C virus Nature 2003, 426, 186-189
-
(2003)
Nature
, vol.426
, pp. 186-189
-
-
Lamarre, D.1
Anderson, P.C.2
Bailey, M.3
Beaulieu, P.4
Bolger, G.5
Bonneau, P.6
Bos, M.7
Cameron, D.R.8
Cartier, M.9
Cordingley, M.G.10
Faucher, A.M.11
Goudreau, N.12
Kawai, S.H.13
Kukolj, G.14
Lagace, L.15
Laplante, S.R.16
Narjes, H.17
Poupart, M.A.18
Rancourt, J.19
Sentjens, R.E.St.20
George, R.21
Simoneau, B.22
Steinmann, G.23
Thibeault, D.24
Tsantrizos, Y.S.25
Weldon, S.M.26
Yong, C.L.27
Llinas-Brunet, M.28
more..
-
9
-
-
7644232426
-
Short-term antiviral efficacy of BILN 2061, a hepatitis C virus serine protease inhibitor, in hepatitis C genotype 1 patients
-
Hinrichsen, H.; Benhamou, Y.; Wedemeyer, H.; Reiser, M.; Sentjens, R. E.; Calleja, J. L.; Forns, X.; Erhardt, A.; Cronlein, J.; Chaves, R. L.; Yong, C. L.; Nehmiz, G.; Steinmann, G. G. Short-term antiviral efficacy of BILN 2061, a hepatitis C virus serine protease inhibitor, in hepatitis C genotype 1 patients Gastroenterology 2004, 127, 1347-1355
-
(2004)
Gastroenterology
, vol.127
, pp. 1347-1355
-
-
Hinrichsen, H.1
Benhamou, Y.2
Wedemeyer, H.3
Reiser, M.4
Sentjens, R.E.5
Calleja, J.L.6
Forns, X.7
Erhardt, A.8
Cronlein, J.9
Chaves, R.L.10
Yong, C.L.11
Nehmiz, G.12
Steinmann, G.G.13
-
10
-
-
33644636312
-
Preclinical profile of VX-950, a potent, selective, and orally bioavailable inhibitor of hepatitis C virus NS3-4A serine protease
-
Perni, R. B.; Almquist, S. J.; Byrn, R. A.; Chandorkar, G.; Chaturvedi, P. R.; Courtney, L. F.; Decker, C. J.; Dinehart, K.; Gates, C. A.; Harbeson, S. L.; Heiser, A.; Kalkeri, G.; Kolaczkowski, E.; Lin, K.; Luong, Y. P.; Rao, B. G.; Taylor, W. P.; Thomson, J. A.; Tung, R. D.; Wei, Y.; Kwong, A. D.; Lin, C. Preclinical profile of VX-950, a potent, selective, and orally bioavailable inhibitor of hepatitis C virus NS3-4A serine protease Antimicrob. Agents Chemother. 2006, 50, 899-909
-
(2006)
Antimicrob. Agents Chemother.
, vol.50
, pp. 899-909
-
-
Perni, R.B.1
Almquist, S.J.2
Byrn, R.A.3
Chandorkar, G.4
Chaturvedi, P.R.5
Courtney, L.F.6
Decker, C.J.7
Dinehart, K.8
Gates, C.A.9
Harbeson, S.L.10
Heiser, A.11
Kalkeri, G.12
Kolaczkowski, E.13
Lin, K.14
Luong, Y.P.15
Rao, B.G.16
Taylor, W.P.17
Thomson, J.A.18
Tung, R.D.19
Wei, Y.20
Kwong, A.D.21
Lin, C.22
more..
-
11
-
-
33644639990
-
SCH 503034, a mechanism-based inhibitor of hepatitis C virus NS3 protease, suppresses polyprotein maturation and enhances the antiviral activity of alpha interferon in replicon cells
-
Malcolm, B. A.; Liu, R.; Lahser, F.; Agrawal, S.; Belanger, B.; Butkiewicz, N.; Chase, R.; Gheyas, F.; Hart, A.; Hesk, D.; Ingravallo, P.; Jiang, C.; Kong, R.; Lu, J.; Pichardo, J.; Prongay, A.; Skelton, A.; Tong, X.; Venkatraman, S.; Xia, E.; Girijavallabhan, V.; Njoroge, F. G. SCH 503034, a mechanism-based inhibitor of hepatitis C virus NS3 protease, suppresses polyprotein maturation and enhances the antiviral activity of alpha interferon in replicon cells Antimicrobial Agents Chemother. 2006, 50, 1013-1020
-
(2006)
Antimicrobial Agents Chemother.
, vol.50
, pp. 1013-1020
-
-
Malcolm, B.A.1
Liu, R.2
Lahser, F.3
Agrawal, S.4
Belanger, B.5
Butkiewicz, N.6
Chase, R.7
Gheyas, F.8
Hart, A.9
Hesk, D.10
Ingravallo, P.11
Jiang, C.12
Kong, R.13
Lu, J.14
Pichardo, J.15
Prongay, A.16
Skelton, A.17
Tong, X.18
Venkatraman, S.19
Xia, E.20
Girijavallabhan, V.21
Njoroge, F.G.22
more..
-
12
-
-
24944472318
-
Discovery of small-molecule inhibitors of HCV NS3-4A protease as potential therapeutic agents against HCV infection
-
Chen, S. H.; Tan, S. L. Discovery of small-molecule inhibitors of HCV NS3-4A protease as potential therapeutic agents against HCV infection Curr. Med. Chem. 2005, 12, 2317-2342
-
(2005)
Curr. Med. Chem.
, vol.12
, pp. 2317-2342
-
-
Chen, S.H.1
Tan, S.L.2
-
13
-
-
34249081116
-
Discovery of the HCV NS3/4A protease inhibitor (1 R,5 S)- N -[3-amino-1-(cyclobutylmethyl)-2,3-dioxopropyl]-3-[2(S)-[[[(1,1-dimethylethyl) amino]carbonyl]amino]-3,3-dimethyl-1-oxobutyl]-6,6-dimethyl-3-azabicyclo[3.1.0] hexan-2(S)-carboxamide (Sch 503034) II. Key steps in structure-based optimization
-
Prongay, A. J.; Guo, Z.; Yao, N.; Pichardo, J.; Fischmann, T.; Strickland, C.; Myers, J., Jr.; Weber, P. C.; Beyer, B. M.; Ingram, R.; Hong, Z.; Prosise, W. W.; Ramanathan, L.; Taremi, S. S.; Yarosh-Tomaine, T.; Zhang, R.; Senior, M.; Yang, R. S.; Malcolm, B.; Arasappan, A.; Bennett, F.; Bogen, S. L.; Chen, K.; Jao, E.; Liu, Y. T.; Lovey, R. G.; Saksena, A. K.; Venkatraman, S.; Girijavallabhan, V.; Njoroge, F. G.; Madison, V. Discovery of the HCV NS3/4A protease inhibitor (1 R,5 S)- N -[3-amino-1-(cyclobutylmethyl)-2,3-dioxopropyl] -3-[2(S)-[[[(1,1-dimethylethyl)amino]carbonyl]amino]-3,3-dimethyl-1-oxobutyl]-6, 6-dimethyl-3-azabicyclo[3.1.0]hexan-2(S)-carboxamide (Sch 503034) II. Key steps in structure-based optimization J. Med. Chem. 2007, 50, 2310-2318
-
(2007)
J. Med. Chem.
, vol.50
, pp. 2310-2318
-
-
Prongay, A.J.1
Guo, Z.2
Yao, N.3
Pichardo, J.4
Fischmann, T.5
Strickland, C.6
Myers Jr., J.7
Weber, P.C.8
Beyer, B.M.9
Ingram, R.10
Hong, Z.11
Prosise, W.W.12
Ramanathan, L.13
Taremi, S.S.14
Yarosh-Tomaine, T.15
Zhang, R.16
Senior, M.17
Yang, R.S.18
Malcolm, B.19
Arasappan, A.20
Bennett, F.21
Bogen, S.L.22
Chen, K.23
Jao, E.24
Liu, Y.T.25
Lovey, R.G.26
Saksena, A.K.27
Venkatraman, S.28
Girijavallabhan, V.29
Njoroge, F.G.30
Madison, V.31
more..
-
14
-
-
0032493405
-
Peptide-based inhibitors of the hepatitis C virus serine protease
-
Llinas-Brunet, M.; Bailey, M.; Fazal, G.; Goulet, S.; Halmos, T.; Laplante, S.; Maurice, R.; Poirier, M.; Poupart, M. A.; Thibeault, D.; Wernic, D.; Lamarre, D. Peptide-based inhibitors of the hepatitis C virus serine protease Bioorg. Med. Chem. Lett. 1998, 8, 1713-1718
-
(1998)
Bioorg. Med. Chem. Lett.
, vol.8
, pp. 1713-1718
-
-
Llinas-Brunet, M.1
Bailey, M.2
Fazal, G.3
Goulet, S.4
Halmos, T.5
Laplante, S.6
Maurice, R.7
Poirier, M.8
Poupart, M.A.9
Thibeault, D.10
Wernic, D.11
Lamarre, D.12
-
15
-
-
0038343796
-
Product inhibition of the hepatitis C virus NS3 protease
-
Steinkuhler, C.; Biasiol, G.; Brunetti, M.; Urbani, A.; Koch, U.; Cortese, R.; Pessi, A.; De Francesco, R. Product inhibition of the hepatitis C virus NS3 protease Biochemistry 1998, 37, 8899-8905
-
(1998)
Biochemistry
, vol.37
, pp. 8899-8905
-
-
Steinkuhler, C.1
Biasiol, G.2
Brunetti, M.3
Urbani, A.4
Koch, U.5
Cortese, R.6
Pessi, A.7
De Francesco, R.8
-
16
-
-
0038682329
-
Studies on the C-terminal of hexapeptide inhibitors of the hepatitis C virus serine protease
-
Llinas-Brunet, M.; Bailey, M.; Deziel, R.; Fazal, G.; Gorys, V.; Goulet, S.; Halmos, T.; Maurice, R.; Poirier, M.; Poupart, M. A.; Rancourt, J.; Thibeault, D.; Wernic, D.; Lamarre, D. Studies on the C-terminal of hexapeptide inhibitors of the hepatitis C virus serine protease Bioorg. Med. Chem. Lett. 1998, 8, 2719-2724
-
(1998)
Bioorg. Med. Chem. Lett.
, vol.8
, pp. 2719-2724
-
-
Llinas-Brunet, M.1
Bailey, M.2
Deziel, R.3
Fazal, G.4
Gorys, V.5
Goulet, S.6
Halmos, T.7
Maurice, R.8
Poirier, M.9
Poupart, M.A.10
Rancourt, J.11
Thibeault, D.12
Wernic, D.13
Lamarre, D.14
-
17
-
-
0037471233
-
Macrocyclic inhibitors of the NS3 protease as potential therapeutic agents of hepatitis C virus infection
-
Tsantrizos, Y. S.; Bolger, G.; Bonneau, P.; Cameron, D. R.; Goudreau, N.; Kukolj, G.; LaPlante, S. R.; Llinas-Brunet, M.; Nar, H.; Lamarre, D. Macrocyclic inhibitors of the NS3 protease as potential therapeutic agents of hepatitis C virus infection Angew. Chem., Int. Ed. 2003, 42, 1356-1360
-
(2003)
Angew. Chem., Int. Ed.
, vol.42
, pp. 1356-1360
-
-
Tsantrizos, Y.S.1
Bolger, G.2
Bonneau, P.3
Cameron, D.R.4
Goudreau, N.5
Kukolj, G.6
Laplante, S.R.7
Llinas-Brunet, M.8
Nar, H.9
Lamarre, D.10
-
18
-
-
12144290054
-
Structure-activity study on a novel series of macrocyclic inhibitors of the hepatitis C virus NS3 protease leading to the discovery of BILN 2061
-
Llinas-Brunet, M.; Bailey, M. D.; Bolger, G.; Brochu, C.; Faucher, A. M.; Ferland, J. M.; Garneau, M.; Ghiro, E.; Gorys, V.; Grand-Maitre, C.; Halmos, T.; Lapeyre-Paquette, N.; Liard, F.; Poirier, M.; Rheaume, M.; Tsantrizos, Y. S.; Lamarre, D. Structure-activity study on a novel series of macrocyclic inhibitors of the hepatitis C virus NS3 protease leading to the discovery of BILN 2061 J. Med. Chem. 2004, 47, 1605-1608
-
(2004)
J. Med. Chem.
, vol.47
, pp. 1605-1608
-
-
Llinas-Brunet, M.1
Bailey, M.D.2
Bolger, G.3
Brochu, C.4
Faucher, A.M.5
Ferland, J.M.6
Garneau, M.7
Ghiro, E.8
Gorys, V.9
Grand-Maitre, C.10
Halmos, T.11
Lapeyre-Paquette, N.12
Liard, F.13
Poirier, M.14
Rheaume, M.15
Tsantrizos, Y.S.16
Lamarre, D.17
-
19
-
-
2342501873
-
Peptide-based inhibitors of the hepatitis C virus NS3 protease: Structure-activity relationship at the C-terminal position
-
Rancourt, J.; Cameron, D. R.; Gorys, V.; Lamarre, D.; Poirier, M.; Thibeault, D.; Llinas-Brunet, M. Peptide-based inhibitors of the hepatitis C virus NS3 protease: Structure-activity relationship at the C-terminal position J. Med. Chem. 2004, 47, 2511-2522
-
(2004)
J. Med. Chem.
, vol.47
, pp. 2511-2522
-
-
Rancourt, J.1
Cameron, D.R.2
Gorys, V.3
Lamarre, D.4
Poirier, M.5
Thibeault, D.6
Llinas-Brunet, M.7
-
20
-
-
0014211618
-
On the size of the active site in proteases. I. Papain
-
Schechter, I.; Berger, A. On the size of the active site in proteases. I. Papain Biochem. Biophys. Res. Commun. 1967, 27, 157-162
-
(1967)
Biochem. Biophys. Res. Commun.
, vol.27
, pp. 157-162
-
-
Schechter, I.1
Berger, A.2
-
21
-
-
79955557748
-
A 28-day mechanistic time course study in the rhesus monkey with hepatitis C virus protease inhibitor BILN 2061
-
submitted 2010
-
Stoltz, J. H.; Stern, J. O.; Huang, Q.; Seidler, R. W.; Pack, F. D.; Knight, B. L. A 28-day mechanistic time course study in the rhesus monkey with hepatitis C virus protease inhibitor BILN 2061. Toxicol. Pathol., submitted 2010.
-
Toxicol. Pathol.
-
-
Stoltz, J.H.1
Stern, J.O.2
Huang, Q.3
Seidler, R.W.4
Pack, F.D.5
Knight, B.L.6
-
23
-
-
57049176125
-
Preclinical characteristics of the hepatitis C virus NS3/4A protease inhibitor ITMN-191 (R7227)
-
Seiwert, S. D.; Andrews, S. W.; Jiang, Y.; Serebryany, V.; Tan, H.; Kossen, K.; Rajagopalan, P. T.; Misialek, S.; Stevens, S. K.; Stoycheva, A.; Hong, J.; Lim, S. R.; Qin, X.; Rieger, R.; Condroski, K. R.; Zhang, H.; Do, M. G.; Lemieux, C.; Hingorani, G. P.; Hartley, D. P.; Josey, J. A.; Pan, L.; Beigelman, L.; Blatt, L. M. Preclinical characteristics of the hepatitis C virus NS3/4A protease inhibitor ITMN-191 (R7227) Antimicrob. Agents Chemother. 2008, 52, 4432-4441
-
(2008)
Antimicrob. Agents Chemother.
, vol.52
, pp. 4432-4441
-
-
Seiwert, S.D.1
Andrews, S.W.2
Jiang, Y.3
Serebryany, V.4
Tan, H.5
Kossen, K.6
Rajagopalan, P.T.7
Misialek, S.8
Stevens, S.K.9
Stoycheva, A.10
Hong, J.11
Lim, S.R.12
Qin, X.13
Rieger, R.14
Condroski, K.R.15
Zhang, H.16
Do, M.G.17
Lemieux, C.18
Hingorani, G.P.19
Hartley, D.P.20
Josey, J.A.21
Pan, L.22
Beigelman, L.23
Blatt, L.M.24
more..
-
24
-
-
65749112245
-
In vitro activity and preclinical profile of TMC435350, a potent hepatitis C virus protease inhibitor
-
Lin, T. I.; Lenz, O.; Fanning, G.; Verbinnen, T.; Delouvroy, F.; Scholliers, A.; Vermeiren, K.; Rosenquist, A.; Edlund, M.; Samuelsson, B.; Vrang, L.; de Kock, H.; Wigerinck, P.; Raboisson, P.; Simmen, K. In vitro activity and preclinical profile of TMC435350, a potent hepatitis C virus protease inhibitor Antimicrob. Agents Chemother. 2009, 53, 1377-1385
-
(2009)
Antimicrob. Agents Chemother.
, vol.53
, pp. 1377-1385
-
-
Lin, T.I.1
Lenz, O.2
Fanning, G.3
Verbinnen, T.4
Delouvroy, F.5
Scholliers, A.6
Vermeiren, K.7
Rosenquist, A.8
Edlund, M.9
Samuelsson, B.10
Vrang, L.11
De Kock, H.12
Wigerinck, P.13
Raboisson, P.14
Simmen, K.15
-
25
-
-
73849106636
-
MK-7009, a potent and selective inhibitor of hepatitis C virus NS3/4A protease
-
Liverton, N. J.; Carroll, S. S.; DiMuzio, J.; Fandozzi, C.; Graham, D. J.; Hazuda, D.; Holloway, M. K.; Ludmerer, S. W.; McCauley, J. A.; McIntyre, C. J.; Olsen, D. B.; Rudd, M. T.; Stahlhut, M.; Vacca, J. P. MK-7009, a potent and selective inhibitor of hepatitis C virus NS3/4A protease Antimicrob. Agents Chemother. 2010, 54, 305-311
-
(2010)
Antimicrob. Agents Chemother.
, vol.54
, pp. 305-311
-
-
Liverton, N.J.1
Carroll, S.S.2
Dimuzio, J.3
Fandozzi, C.4
Graham, D.J.5
Hazuda, D.6
Holloway, M.K.7
Ludmerer, S.W.8
McCauley, J.A.9
McIntyre, C.J.10
Olsen, D.B.11
Rudd, M.T.12
Stahlhut, M.13
Vacca, J.P.14
-
26
-
-
10644231764
-
A systematic approach to the optimization of substrate-based inhibitors of the hepatitis C virus NS3 protease: Discovery of potent and specific tripeptide inhibitors
-
Llinas-Brunet, M.; Bailey, M. D.; Ghiro, E.; Gorys, V.; Halmos, T.; Poirier, M.; Rancourt, J.; Goudreau, N. A systematic approach to the optimization of substrate-based inhibitors of the hepatitis C virus NS3 protease: discovery of potent and specific tripeptide inhibitors J. Med. Chem. 2004, 47, 6584-6594
-
(2004)
J. Med. Chem.
, vol.47
, pp. 6584-6594
-
-
Llinas-Brunet, M.1
Bailey, M.D.2
Ghiro, E.3
Gorys, V.4
Halmos, T.5
Poirier, M.6
Rancourt, J.7
Goudreau, N.8
-
27
-
-
4444345444
-
Synthesis of BILN 2061, an HCV NS3 protease inhibitor with proven antiviral effect in humans
-
Faucher, A. M.; Bailey, M. D.; Beaulieu, P. L.; Brochu, C.; Duceppe, J. S.; Ferland, J. M.; Ghiro, E.; Gorys, V.; Halmos, T.; Kawai, S. H.; Poirier, M.; Simoneau, B.; Tsantrizos, Y. S.; Llinas-Brunet, M. Synthesis of BILN 2061, an HCV NS3 protease inhibitor with proven antiviral effect in humans Org. Lett. 2004, 6, 2901-2904
-
(2004)
Org. Lett.
, vol.6
, pp. 2901-2904
-
-
Faucher, A.M.1
Bailey, M.D.2
Beaulieu, P.L.3
Brochu, C.4
Duceppe, J.S.5
Ferland, J.M.6
Ghiro, E.7
Gorys, V.8
Halmos, T.9
Kawai, S.H.10
Poirier, M.11
Simoneau, B.12
Tsantrizos, Y.S.13
Llinas-Brunet, M.14
-
28
-
-
22244469722
-
Synthesis of (1 R,2 S)-1-amino-2-vinylcyclopropanecarboxylic acid vinyl-ACCA) derivatives: Key intermediates for the preparation of inhibitors of the hepatitis C virus NS3 protease
-
Beaulieu, P. L.; Gillard, J.; Bailey, M. D.; Boucher, C.; Duceppe, J. S.; Simoneau, B.; Wang, X. J.; Zhang, L.; Grozinger, K.; Houpis, I.; Farina, V.; Heimroth, H.; Krueger, T.; Schnaubelt, J. Synthesis of (1 R,2 S)-1-amino-2-vinylcyclopropanecarboxylic acid vinyl-ACCA) derivatives: key intermediates for the preparation of inhibitors of the hepatitis C virus NS3 protease J. Org. Chem. 2005, 70, 5869-5879
-
(2005)
J. Org. Chem.
, vol.70
, pp. 5869-5879
-
-
Beaulieu, P.L.1
Gillard, J.2
Bailey, M.D.3
Boucher, C.4
Duceppe, J.S.5
Simoneau, B.6
Wang, X.J.7
Zhang, L.8
Grozinger, K.9
Houpis, I.10
Farina, V.11
Heimroth, H.12
Krueger, T.13
Schnaubelt, J.14
-
29
-
-
0026664898
-
Synthesis and transformations of 2,6-bis(1,1-dimethylethyl)-4-[2- (thiazolyl)ethenyl]phenols
-
Unangst, P. C.; Connor, D. T. Synthesis and transformations of 2,6-bis(1,1-dimethylethyl)-4-[2-(thiazolyl)ethenyl]phenols J. Heterocycl. Chem. 1992, 29, 1097-1100
-
(1992)
J. Heterocycl. Chem.
, vol.29
, pp. 1097-1100
-
-
Unangst, P.C.1
Connor, D.T.2
-
30
-
-
79953224799
-
Potency, safety and pharmacokinetics of the NS3/4A protease inhibitor BI201335 in patients with chronic HCV genotype-1 infection
-
submitted 2010
-
Manns, M. P.; Bourliare, M.; Benhamou, Y.; Pol, S.; Bonacini, M.; Trepo, C.; Wright, D.; Berg, T.; Calleja, J. L.; White, P. W.; Stern, J. O.; Steinmann, G.; Yong, C. L.; Kukolj, G.; Scherer, J.; Boecher, W. O. Potency, safety and pharmacokinetics of the NS3/4A protease inhibitor BI201335 in patients with chronic HCV genotype-1 infection. J. Hepatol., submitted 2010.
-
J. Hepatol.
-
-
Manns, M.P.1
Bourliare, M.2
Benhamou, Y.3
Pol, S.4
Bonacini, M.5
Trepo, C.6
Wright, D.7
Berg, T.8
Calleja, J.L.9
White, P.W.10
Stern, J.O.11
Steinmann, G.12
Yong, C.L.13
Kukolj, G.14
Scherer, J.15
Boecher, W.O.16
-
31
-
-
72949094879
-
Protease and helicase activities of hepatitis C virus genotype 4, 5, and 6 NS3-NS4A proteins
-
Massariol, M. J.; Zhao, S.; Marquis, M.; Thibeault, D.; White, P. W. Protease and helicase activities of hepatitis C virus genotype 4, 5, and 6 NS3-NS4A proteins Biochem. Biophys. Res. Commun. 2010, 391, 692-697
-
(2010)
Biochem. Biophys. Res. Commun.
, vol.391
, pp. 692-697
-
-
Massariol, M.J.1
Zhao, S.2
Marquis, M.3
Thibeault, D.4
White, P.W.5
-
32
-
-
3142700044
-
Sensitivity of NS3 serine proteases from hepatitis C virus genotypes 2 and 3 to the inhibitor BILN 2061
-
Thibeault, D.; Bousquet, C.; Gingras, R.; Lagace, L.; Maurice, R.; White, P. W.; Lamarre, D. Sensitivity of NS3 serine proteases from hepatitis C virus genotypes 2 and 3 to the inhibitor BILN 2061 J. Virol. 2004, 78, 7352-7359
-
(2004)
J. Virol.
, vol.78
, pp. 7352-7359
-
-
Thibeault, D.1
Bousquet, C.2
Gingras, R.3
Lagace, L.4
Maurice, R.5
White, P.W.6
Lamarre, D.7
-
33
-
-
63549101398
-
Identification of a lipid kinase as a host factor involved in hepatitis C virus RNA replication
-
Vaillancourt, F. H.; Pilote, L.; Cartier, M.; Lippens, J.; Liuzzi, M.; Bethell, R. C.; Cordingley, M. G.; Kukolj, G. Identification of a lipid kinase as a host factor involved in hepatitis C virus RNA replication Virology 2009, 387, 5-10
-
(2009)
Virology
, vol.387
, pp. 5-10
-
-
Vaillancourt, F.H.1
Pilote, L.2
Cartier, M.3
Lippens, J.4
Liuzzi, M.5
Bethell, R.C.6
Cordingley, M.G.7
Kukolj, G.8
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