-
1
-
-
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.
-
(1989)
Science
, vol.244
, pp. 359
-
-
Choo, Q.-L.1
Kuo, G.2
Weiner, A.J.3
Overby, L.R.4
Bradley, D.W.5
Houghton, M.6
-
3
-
-
0030588528
-
World Health Organization: Hepatitis C. Seroprevalence of hepatitis C virus (HCV) in a population sample
-
World Health Organization: Hepatitis C. Seroprevalence of hepatitis C virus (HCV) in a population sample. Wkly Epidemiol. Rec. 1996, 71, 346-349.
-
(1996)
Wkly. Epidemiol. Rec.
, vol.71
, pp. 346-349
-
-
-
4
-
-
0036483611
-
Treatment of chronic hepatitis C with PEGylated interferon and rivavarin
-
Cornberg, M.; Wedemeyer, H.; Manns, M. P. Treatment of chronic hepatitis C with PEGylated interferon and rivavarin. Curr. Gastroenterol. Rep. 2002, 4, 23-30.
-
(2002)
Curr. Gastroenterol. Rep.
, vol.4
, pp. 23-30
-
-
Cornberg, M.1
Wedemeyer, H.2
Manns, M.P.3
-
5
-
-
0033992516
-
Overview of hepatitis C virus genome structure, polyprotein processing, and protein properties
-
Reed, K. E.; Rice, C. M. Overview of hepatitis C virus genome structure, polyprotein processing, and protein properties. Curr. Top. Microbiol. Immunol. 2000, 242, 55-84.
-
(2000)
Curr. Top. Microbiol. Immunol.
, vol.242
, pp. 55-84
-
-
Reed, K.E.1
Rice, C.M.2
-
6
-
-
0003072207
-
Therapies for Hepatitis C Infection: Targeting the Non-Structural Proteins of HCV
-
Beaulieu, P. L.; Llinàs-Brunet, M. Therapies for Hepatitis C Infection: Targeting the Non-Structural Proteins of HCV. Curr. Med. Chem.: Anti-Infect. Agents 2002, 1, 163-176.
-
(2002)
Curr. Med. Chem.: Anti-Infect. Agents
, vol.1
, pp. 163-176
-
-
Beaulieu, P.L.1
Llinàs-Brunet, M.2
-
7
-
-
0029962944
-
Conservation and variability in the structure of serine proteinases of the chymotrypsin family
-
Lesk, A. M.; Fordham, W. D. Conservation and variability in the structure of serine proteinases of the chymotrypsin family. J. Mol. Biol. 1996, 258, 501-537.
-
(1996)
J. Mol. Biol.
, vol.258
, pp. 501-537
-
-
Lesk, A.M.1
Fordham, W.D.2
-
8
-
-
0034940307
-
Hepatitis C Virus Serine Protease Inhibitors: Current Progress and Future Challenges
-
Steinkuhler, C.; Koch, U.; Narjes, F.; Matassa, V. G. Hepatitis C Virus Serine Protease Inhibitors: Current Progress and Future Challenges. Curr. Med. Chem. 2001, 8, 919-932.
-
(2001)
Curr. Med. Chem.
, vol.8
, pp. 919-932
-
-
Steinkuhler, C.1
Koch, U.2
Narjes, F.3
Matassa, V.G.4
-
9
-
-
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.
-
(2000)
J. Virol.
, vol.74
, pp. 2046
-
-
Kolykhalov, A.A.1
Mihalik, K.2
Feinstone, S.M.3
Rice, C.M.4
-
10
-
-
0032493405
-
Peptide-based inhibitors of the hepatitis C virus serine protease
-
Llinàs-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
-
-
Llinàs-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
-
11
-
-
0038343796
-
Product inhibition of the hepatitis C virus NS3 protease
-
Steinkühler, C.; Biasiol, G.; Brunette, 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
-
-
Steinkühler, C.1
Biasiol, G.2
Brunette, M.3
Urbani, A.4
Koch, U.5
Cortese, R.6
Pessi, A.7
De Francesco, R.8
-
12
-
-
0034675706
-
Highly potent and selective peptide-based inhibitors of the hepatitis C virus serine protease: Towards smaller inhibitors
-
Llinàs-Brunet, M.; Bailey, M.; Fazal, G.; Ghiro, E.; Gorys, V.; Goulet, S.; Halmos, T.; Maurice, R.; Poirier, M.; Poupart, M.-A.; Rancourt, J.; Thibeault, D.; Wernic, D.; Lamarre, D. Highly potent and selective peptide-based inhibitors of the hepatitis C virus serine protease: towards smaller inhibitors. Bioorg. Med. Chem. Lett. 2000, 10, 2267-2270.
-
(2000)
Bioorg. Med. Chem. Lett.
, vol.10
, pp. 2267-2270
-
-
Llinàs-Brunet, M.1
Bailey, M.2
Fazal, G.3
Ghiro, E.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
-
13
-
-
0038165472
-
An NS3 serine protease inhibitor abrogates replication of subgenomic hepatitis C virus RNA
-
Pause, A.; Kukolj, G.; Bailey, M.; Brault, M.; Dô, F.; Halmos, T.; Lagacé, L.; Maurice, R.; Marquis, M.; McKercher, G.; Pellerin, C.; Pilote, L.; Thibeault, D.; Lamarre, D. An NS3 serine protease inhibitor abrogates replication of subgenomic hepatitis C virus RNA. J. Biol. Chem. 2003, 278, 20374-20380.
-
(2003)
J. Biol. Chem.
, vol.278
, pp. 20374-20380
-
-
Pause, A.1
Kukolj, G.2
Bailey, M.3
Brault, M.4
Dô, F.5
Halmos, T.6
Lagacé, L.7
Maurice, R.8
Marquis, M.9
McKercher, G.10
Pellerin, C.11
Pilote, L.12
Thibeault, D.13
Lamarre, D.14
-
14
-
-
0347991962
-
NMR Structural Characterization of Peptide Inhibitors Bound to the HCV NS3 Protease: Design of a New P2 Substituent
-
Goudreau, N.; Cameron, D. R.; Bonneau, P.; Gorys, V.; Plouffe, C.; Poirier, M.; Lamarre, D.; Llinàs-Brunet, M. NMR Structural Characterization of Peptide Inhibitors Bound to the HCV NS3 Protease: Design of a New P2 Substituent. J. Med. Chem. 2004, 47, 123-132.
-
(2004)
J. Med. Chem.
, vol.47
, pp. 123-132
-
-
Goudreau, N.1
Cameron, D.R.2
Bonneau, P.3
Gorys, V.4
Plouffe, C.5
Poirier, M.6
Lamarre, D.7
Llinàs-Brunet, M.8
-
15
-
-
2342501873
-
Peptide-Based Inhibitors of the Hepatitis C Virus NS3 Protease: Structure-Activity Relationship at the C-Terminal Position
-
in press
-
Rancourt, J.; Cameron, D.; Gorys, V.; Lamarre, D.; Poirier, M.; Thibeault, D.; Llinàs-Brunet, M. Peptide-Based Inhibitors of the Hepatitis C Virus NS3 Protease: Structure-Activity Relationship at the C-Terminal Position. J. Med. Chem., in press.
-
J. Med. Chem.
-
-
Rancourt, J.1
Cameron, D.2
Gorys, V.3
Lamarre, D.4
Poirier, M.5
Thibeault, D.6
Llinàs-Brunet, M.7
-
16
-
-
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.; Llinàs-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
Llinàs-Brunet, M.8
Nar, H.9
Lamarre, D.10
-
17
-
-
0344201903
-
Discovery of BILN 2061-An NS3 preotease inhibitors with first antiviral proof-of-concept in humans infected with hepatitis C virus
-
Lamarre, D.; Anderson, P.; Bailey, M.; Beaulieu, P.; Bolger, G.; Bonneau, P.; Bös, M.; Cameron, D.; Cartier, M.; Cordingley, M.; Faucher, A.-M.; Goudreau, N.; Kawai, S.; Kukolj, G.; Lagacé, L.; LaPlante, S.; Narjes, H.; Poupart, M.-A.; Rancourt, J.; St-George, R.; Sentjens, R. E.; Simoneau, B.; Steinmann, G.; Thibeault, D.; Tsantrizos, Y.; Weldon, A. M.; Yong, C.-L.; Llinàs-Brunet, M. Discovery of BILN 2061-An NS3 preotease inhibitors with first antiviral proof-of-concept in humans infected with hepatitis C virus. Nature 2003, 426, 186-189.
-
(2003)
Nature
, vol.426
, pp. 186-189
-
-
Lamarre, D.1
Anderson, P.2
Bailey, M.3
Beaulieu, P.4
Bolger, G.5
Bonneau, P.6
Bös, M.7
Cameron, D.8
Cartier, M.9
Cordingley, M.10
Faucher, A.-M.11
Goudreau, N.12
Kawai, S.13
Kukolj, G.14
Lagacé, L.15
LaPlante, S.16
Narjes, H.17
Poupart, M.-A.18
Rancourt, J.19
St-George, R.20
Sentjens, R.E.21
Simoneau, B.22
Steinmann, G.23
Thibeault, D.24
Tsantrizos, Y.25
Weldon, A.M.26
Yong, C.-L.27
Llinàs-Brunet, M.28
more..
-
18
-
-
1642285777
-
-
Manuscript in preparation
-
Tsantrizos, Y. S.; et al. Manuscript in preparation.
-
-
-
Tsantrizos, Y.S.1
-
19
-
-
0038682329
-
Studies on the C-terminal of hexapeptide inhibitors of the hepatitis C virus serine protease
-
Llinàs-Brunet, M.; Bailey, M.; Déziel, R.; Fazal, G.; Gorys, V.; Goulet, S.; Halmos, T.; Maurice, R.; Poirier, M.; Poupart, M.-A.; Rancourt, J.; Thibeault, D.; Wernic, D.; Lamarre, D. I. 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
-
-
Llinàs-Brunet, M.1
Bailey, M.2
Déziel, 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.I.14
-
20
-
-
0035854304
-
Solid-phase synthesis of peptidomimetic inhibitors for the hepatitis C virus NS3 protease
-
Poupart, M.-A.; Cameron, D. R.; Chabot, C.; Ghiro, E.; Goudreau, N.; Goulet, S.; Poirier, M.; Tsantrizos, Y. Solid-phase synthesis of peptidomimetic inhibitors for the hepatitis C virus NS3 protease. J. Org. Chem. 2001, 66, 4743-4751.
-
(2001)
J. Org. Chem.
, vol.66
, pp. 4743-4751
-
-
Poupart, M.-A.1
Cameron, D.R.2
Chabot, C.3
Ghiro, E.4
Goudreau, N.5
Goulet, S.6
Poirier, M.7
Tsantrizos, Y.8
-
21
-
-
0033603427
-
Solution structure of substrate-based ligands when bound to hepatitis C virus NS3 protease domain
-
LaPlante, S. R.; Cameron, D. C.; Aubry, N.; Lefebvre, S.; Kukolj, G.; Maurice, R.; Thibeault, D.; Lamarre, D.; Llinàs-Brunet, M. Solution structure of substrate-based ligands when bound to hepatitis C virus NS3 protease domain. J. Biol. Chem. 1999, 274, 18618-18624.
-
(1999)
J. Biol. Chem.
, vol.274
, pp. 18618-18624
-
-
LaPlante, S.R.1
Cameron, D.C.2
Aubry, N.3
Lefebvre, S.4
Kukolj, G.5
Maurice, R.6
Thibeault, D.7
Lamarre, D.8
Llinàs-Brunet, M.9
-
22
-
-
0034675819
-
NMR line-broadening and transferred NOESY as a medicinal chemistry tool for studying inhibitors of the hepatitis C virus NS3 protease domain
-
LaPlante, S. R.; Aubry, N.; Bonneau, P. R.; Kukolj, G.; Lamarre, D.; Lefebvre, S.; Li, H.; Llinàs-Brunet, M.; Plouffe, C.; Cameron, D. R. NMR line-broadening and transferred NOESY as a medicinal chemistry tool for studying inhibitors of the hepatitis C virus NS3 protease domain. Bioorg. Med. Chem. Lett. 2000, 10, 2271-2274.
-
(2000)
Bioorg. Med. Chem. Lett.
, vol.10
, pp. 2271-2274
-
-
LaPlante, S.R.1
Aubry, N.2
Bonneau, P.R.3
Kukolj, G.4
Lamarre, D.5
Lefebvre, S.6
Li, H.7
Llinàs-Brunet, M.8
Plouffe, C.9
Cameron, D.R.10
-
23
-
-
1642295510
-
-
note
-
50) were determined using the assays described in ref 13. The values reported are an average of at least four determinations.
-
-
-
-
24
-
-
0003463148
-
-
John Wiley & Sons: New York
-
Greene, T. W., Wuts, P. G. M., Eds. Protective Groups in Organic Synthesis, 3rd ed.; John Wiley & Sons: New York, 1999; p 518.
-
(1999)
Protective Groups in Organic Synthesis, 3rd Ed.
, pp. 518
-
-
Greene, T.W.1
Wuts, P.G.M.2
-
25
-
-
0031024171
-
Experimental and computational approaches to estimate solubility and permeability in drug discovery and development settings
-
Lipinski, C. A.; Lombardo, F.; Dominy, B. W.; Feeney, P. J. Experimental and computational approaches to estimate solubility and permeability in drug discovery and development settings. Adv. Drug Delivery Rev. 1997, 1-3, 3-25.
-
(1997)
Adv. Drug Delivery Rev.
, vol.1-3
, pp. 3-25
-
-
Lipinski, C.A.1
Lombardo, F.2
Dominy, B.W.3
Feeney, P.J.4
-
26
-
-
1642320083
-
-
note
-
Rats were administered compounds as either an oral gavage or intravenous bolus dose in a vehicle consisting of PEG400/water (70:30). Protocols for the experiments are described in the supporting information of ref 16.
-
-
-
-
27
-
-
1642334582
-
Metabolism and disposition of the HIV-1 protease inhibitors Ritonavir (ABT-538) in rats, dogs and humans
-
Denissen, J. F.; Grabowski, B. A.; Johnson, M. K.; Buko, A. M.; Kempf, D. J.; Thomas, S. B.; Surber, B. W. Metabolism and disposition of the HIV-1 protease inhibitors Ritonavir (ABT-538) in rats, dogs and humans. Drug Metab. Dispos. 1995, 23, 185-189.
-
(1995)
Drug Metab. Dispos.
, vol.23
, pp. 185-189
-
-
Denissen, J.F.1
Grabowski, B.A.2
Johnson, M.K.3
Buko, A.M.4
Kempf, D.J.5
Thomas, S.B.6
Surber, B.W.7
-
28
-
-
1642324914
-
-
Macrocyclic peptides active against the Hepatitis C virus. U.S. Patent 6,608,027 B1, 2003
-
Tsantrizos, Y. S.; Cameron, D.; Faucher, A.-M.; Ghiro, E.; Goudreau, N.; Halmos, T.; Llinàs-Brunet, M.; Boehringer Ingelheim (Canada) Ltd. Macrocyclic peptides active against the Hepatitis C virus. U.S. Patent 6,608, 027 B1, 2003.
-
-
-
Tsantrizos, Y.S.1
Cameron, D.2
Faucher, A.-M.3
Ghiro, E.4
Goudreau, N.5
Halmos, T.6
Llinàs-Brunet, M.7
-
29
-
-
0037243532
-
Removable Phosphine Reagents for the Mitsunobu Reaction
-
Yoakim, C.; Guse, I.; O'Meara, J. A.; Thavonekham, B. Removable Phosphine Reagents for the Mitsunobu Reaction. Synlett 2003, 473-476.
-
(2003)
Synlett
, pp. 473-476
-
-
Yoakim, C.1
Guse, I.2
O'Meara, J.A.3
Thavonekham, B.4
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