-
1
-
-
84869272942
-
-
Geneva, Switzerland, Revised October 2000. WHO Web site
-
(a) Hepatitis C. Fact Sheet No. 164; World Health Organization (WHO): Geneva, Switzerland, Revised October 2000. WHO Web site: http://www.who.int/ mediacentre/factsheets/fs164/en/
-
Fact Sheet
, Issue.164
-
-
Hepatitis, C.1
-
2
-
-
0033916804
-
Epidemiology of hepatitis C: Geographic differences and temporal trends
-
(b) Wasley, A.; Alter, M. J. Epidemiology of hepatitis C: geographic differences and temporal trends. Semin.Liver Dis. 2000, 20, 1-16.
-
(2000)
Semin.Liver Dis
, vol.20
, pp. 1-16
-
-
Wasley, A.1
Alter, M.J.2
-
3
-
-
0242456086
-
-
Brown, R. S. Jr; Gaglio, P. J. Scope of worldwide hepatitis C problem. Liver Transplant. 2003, 9, S10-S13.
-
(c) Brown, R. S. Jr; Gaglio, P. J. Scope of worldwide hepatitis C problem. Liver Transplant. 2003, 9, S10-S13.
-
-
-
-
4
-
-
0035811625
-
Hepatitis C virus infection
-
Lauer, G. M.; Walker, B. D. Hepatitis C virus infection. N. Engl. J. Med. 2001, 345, 41-52.
-
(2001)
N. Engl. J. Med
, vol.345
, pp. 41-52
-
-
Lauer, G.M.1
Walker, B.D.2
-
5
-
-
0032547938
-
Interferon alfa-2b alone or in combination with ribavirin as initial treatment for chronic hepatitis C
-
(a) McHutchison, J. G.; Gordon, S. C.; Schiff, E. R.; Shiffman, M. L.; Lee, W. M.; Rustgi, V. K.; Goodman, Z. D.; Ling, M-H.; Cort, S.; Albrecht, J. K. Interferon alfa-2b alone or in combination with ribavirin as initial treatment for chronic hepatitis C. N. Engl. J. Med. 1998, 339, 1485-1492.
-
(1998)
N. Engl. J. Med
, vol.339
, pp. 1485-1492
-
-
McHutchison, J.G.1
Gordon, S.C.2
Schiff, E.R.3
Shiffman, M.L.4
Lee, W.M.5
Rustgi, V.K.6
Goodman, Z.D.7
Ling, M.-H.8
Cort, S.9
Albrecht, J.K.10
-
6
-
-
0037179698
-
Peginterferon alfa-2a plus ribavirin for chronic hepatitis C virus infection
-
(b) Fried, M. W.; Shiffman, M. L.; Reddy, K. R.; Smith, C.; Marinos, G.; Goncales, F. L., Jr.; Haussinger, D.; Diago, M.; Carosi, G.; Dhumeaux, D.; Craxi, A.; Lin, A.; Hoffman, J.; Yu, J. Peginterferon alfa-2a plus ribavirin for chronic hepatitis C virus infection. N. Engl. J. Med. 2002, 347, 975-982.
-
(2002)
N. Engl. J. Med
, vol.347
, pp. 975-982
-
-
Fried, M.W.1
Shiffman, M.L.2
Reddy, K.R.3
Smith, C.4
Marinos, G.5
Goncales Jr., F.L.6
Haussinger, D.7
Diago, M.8
Carosi, G.9
Dhumeaux, D.10
Craxi, A.11
Lin, A.12
Hoffman, J.13
Yu, J.14
-
7
-
-
0032585237
-
Randomised trial of interferon α2b plus ribavirin for 48 weeks or for 24 weeks versus interferon α2b plus placebo for 48 weeks for treatment of chronic infection with hepatitis C virus
-
Poynard, T.; Marcellin, P.; Lee, S. S.; Niederau, C.; Minuk, G. S.; Ideo, G.; Bain, V.; Heathcote, J.; Zeuzem, S.; Trepo, C.; Albrecht, J. Randomised trial of interferon α2b plus ribavirin for 48 weeks or for 24 weeks versus interferon α2b plus placebo for 48 weeks for treatment of chronic infection with hepatitis C virus. Lancet 1998, 352, 1426-1432.
-
(1998)
Lancet
, vol.352
, pp. 1426-1432
-
-
Poynard, T.1
Marcellin, P.2
Lee, S.S.3
Niederau, C.4
Minuk, G.S.5
Ideo, G.6
Bain, V.7
Heathcote, J.8
Zeuzem, S.9
Trepo, C.10
Albrecht, J.11
-
8
-
-
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. G.; 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.G.3
Overby, L.R.4
Bradley, D.W.5
Houghton, M.6
-
9
-
-
23944476834
-
Unraveling hepatitis C virus replication from genome to function
-
Lindenbach, B. D.; Rice, C. M. Unraveling hepatitis C virus replication from genome to function. Nature 2005, 436, 933-938.
-
(2005)
Nature
, vol.436
, pp. 933-938
-
-
Lindenbach, B.D.1
Rice, C.M.2
-
10
-
-
0027287798
-
Nonstructural protein 3 of the hepatitis C virus encodes a serine-type proteinase required for cleavage at the NS3/4 and NS4/5 junctions
-
Bartenschlager, R.; Ahlborn-Laake, L.; Mous, J.; Jacobsen, H. Nonstructural protein 3 of the hepatitis C virus encodes a serine-type proteinase required for cleavage at the NS3/4 and NS4/5 junctions. J. Virol. 1993, 67, 3835-3844.
-
(1993)
J. Virol
, vol.67
, pp. 3835-3844
-
-
Bartenschlager, R.1
Ahlborn-Laake, L.2
Mous, J.3
Jacobsen, H.4
-
11
-
-
24344442462
-
The therapeutic potential of NS3 protease inhibitors in HCV infection
-
(a) Goudreau, N.; Llinàs-Brunet, M. The therapeutic potential of NS3 protease inhibitors in HCV infection. Expert Opin. Invest. Drugs 2005, 14, 1129-1144.
-
(2005)
Expert Opin. Invest. Drugs
, vol.14
, pp. 1129-1144
-
-
Goudreau, N.1
Llinàs-Brunet, M.2
-
12
-
-
36749001029
-
The way forward in HCV treatment-finding the right path
-
(b) Manns, M. P.; Foster, G. R.; Rockstroh, J. K.; Zeuzem, S.; Zoulim, F.; Houghton, M. The way forward in HCV treatment-finding the right path. Nat. Rev. Drug Discovery 2007, 6, 991-1000.
-
(2007)
Nat. Rev. Drug Discovery
, vol.6
, pp. 991-1000
-
-
Manns, M.P.1
Foster, G.R.2
Rockstroh, J.K.3
Zeuzem, S.4
Zoulim, F.5
Houghton, M.6
-
13
-
-
34548271074
-
Novel protease and polymerase inhibitors for the treatment of hepatitis C virus infection
-
(c) Sheldon, J.; Barreiro, P.; Soriano, V. Novel protease and polymerase inhibitors for the treatment of hepatitis C virus infection. Expert Opin. Invest. Drugs 2007, 16, 1171-1181.
-
(2007)
Expert Opin. Invest. Drugs
, vol.16
, pp. 1171-1181
-
-
Sheldon, J.1
Barreiro, P.2
Soriano, V.3
-
14
-
-
33749241866
-
-
Venkatraman, S, Bogen, S. L, Arasappan, A, Bennett, F, Chen, K, Jao, E, Liu, Y-T, Lovey, R, Hendrata, S, Huang, Y, Pan, W, Parekh, T, Pinto, P, Popov, V, Pike, R, Ruan, S, Santhanam, B, Vibulbhan, B, Wu, W, Yang, W, Kong, J, Liang, X, Wong, J, Liu, R, Butkiewicz, N, Chase, R, Hart, A, Agrawal, S, Ingravallo, P, Pichardo, J, Kong, R, Baroudy, B, Malcolm, B, Guo, Z, Prongay, A, Madision, Broske, L, Cui, X, Cheng, K-C, Hsieh, T. Y, Brisson, J-M, Prelusky, D, Korfmacher, W, White, R, Bogonowich, Knipp, S, Pavlovsky, A, Prudence, B, Saksena, A. K, Ganguly, A, Piwinski, J, Girijavallabhan, V, Njoroge, F. G. Discovery of (1R,5S)-N-[3-amino-1, cyclobutylmethyl)-2-3-dioxopropyl]-3-[2(S, 1,1-dimethylethyl)-amino] carbonyl]amio]-3,3-dimethyl-1-oxobutyl, 6,6-dimethyl-3-azabicyclo[3.1.0]hexan- 2(S)-carboxamide SCH 503034, a selective, potent, orally bioavailable, hepatitis C virus NS3 protease inhibitor: a potential therapeutic agent for
-
Venkatraman, S.; Bogen, S. L.; Arasappan, A.; Bennett, F.; Chen, K.; Jao, E.; Liu, Y-T.; Lovey, R.; Hendrata, S.; Huang, Y.; Pan, W.; Parekh, T.; Pinto, P.; Popov, V.; Pike, R.; Ruan, S.; Santhanam, B.; Vibulbhan, B.; Wu, W.; Yang, W.; Kong, J.; Liang, X.; Wong, J.; Liu, R.; Butkiewicz, N.; Chase, R.; Hart, A.; Agrawal, S.; Ingravallo, P.; Pichardo, J.; Kong, R.; Baroudy, B.; Malcolm, B.; Guo, Z.; Prongay, A.; Madision, Broske, L.; Cui, X.; Cheng, K-C.; Hsieh, T. Y.; Brisson, J-M.; Prelusky, D.; Korfmacher, W.; White, R.; Bogonowich - Knipp, S.; Pavlovsky, A.; Prudence, B.; Saksena, A. K.; Ganguly, A.; Piwinski, J.; Girijavallabhan, V.; Njoroge, F. G. Discovery of (1R,5S)-N-[3-amino-1- (cyclobutylmethyl)-2-3-dioxopropyl]-3-[2(S) - [[[(1,1-dimethylethyl)-amino] carbonyl]amio]-3,3-dimethyl-1-oxobutyl] - 6,6-dimethyl-3-azabicyclo[3.1.0]hexan- 2(S)-carboxamide (SCH 503034), a selective, potent, orally bioavailable, hepatitis C virus NS3 protease inhibitor: a potential therapeutic agent for the treatment of hepatitis C infection. J. Med. Chem. 2006, 49, 6074-6086.
-
-
-
-
15
-
-
84869265006
-
Release Aug 4th, 2008: Top-Line Results of Boceprevir Phase II Study Showed High Rate of Sustained Response (SVR) in Genotype 1 Treatment-Naive Hepatitis C Patients; Schering-Plough: Kenilworth, NJ
-
Schering-Plough Press Release Aug 4th, 2008: Top-Line Results of Boceprevir Phase II Study Showed High Rate of Sustained Response (SVR) in Genotype 1 Treatment-Naive Hepatitis C Patients; Schering-Plough: Kenilworth, NJ, 2008. Schering-Plough Web site: http://www.schering-plough.com/news/news- article.aspx?reqid=1182855.
-
(2008)
Schering-Plough Web site
-
-
-
16
-
-
4444266055
-
P4 and P1′ optimization of bicycloproline P2 bearing tetrapeptidyl α-keto - amides as HCV protease inhibitors
-
(a) Yip, Y.; Victor, F.; Lamar, J.; Johnson, R.; Wang, Q. M.; Glass, J. I.; Yumibe, N.; Wakulchik, M.; Munroe, J.; Chen, S.-H. P4 and P1′ optimization of bicycloproline P2 bearing tetrapeptidyl α-keto - amides as HCV protease inhibitors. Bioorg. Med. Chem. Lett. 2004, 14, 5007-5011.
-
(2004)
Bioorg. Med. Chem. Lett
, vol.14
, pp. 5007-5011
-
-
Yip, Y.1
Victor, F.2
Lamar, J.3
Johnson, R.4
Wang, Q.M.5
Glass, J.I.6
Yumibe, N.7
Wakulchik, M.8
Munroe, J.9
Chen, S.-H.10
-
17
-
-
20144370536
-
P1 and P1′ optimization of [3,4] - bicycloproline P2 incorporated tetrapeptidyl α-ketoamide based HCV protease inhibitors
-
(b) Chen, S.-H.; Lamar, J.; Yip, Y.; Victor, F.; Johnson, R. B.; Wang, Q. M.; Glass, J. I.; Heinz, B.; Colacino, J.; Guo, D.; Tebbe, M.; Munroe, J. E. P1 and P1′ optimization of [3,4] - bicycloproline P2 incorporated tetrapeptidyl α-ketoamide based HCV protease inhibitors. Lett. Drug Des. Discovery 2005, 2, 118-123.
-
(2005)
Lett. Drug Des. Discovery
, vol.2
, pp. 118-123
-
-
Chen, S.-H.1
Lamar, J.2
Yip, Y.3
Victor, F.4
Johnson, R.B.5
Wang, Q.M.6
Glass, J.I.7
Heinz, B.8
Colacino, J.9
Guo, D.10
Tebbe, M.11
Munroe, J.E.12
-
18
-
-
33644636312
-
-
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.
-
(c) 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.
-
-
-
-
19
-
-
0344201903
-
-
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.; George, T. S.; 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.
-
(a) 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.; George, T. S.; 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.
-
-
-
-
20
-
-
12144290054
-
Structure - activity study on a novel series of macrocyclic inhibitors of the hepatitis C virus NS3 protease leading to the discovery ofBILN 2061
-
(b) 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 ofBILN 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
-
21
-
-
42949098441
-
Design and microwave-assisted synthesis of novel macrocyclic peptides active at melanocortin receptors: Discovery of potent and selective hMC5R receptor antagonists
-
For recent examples, see the following: a
-
For recent examples, see the following: (a) Grieco, P.; Cai, M.; Liu, L.; Mayorov, A.; Chandler, K.; Trivedi, D.; Lin, G.; Campiglia, P.; Novellino, E.; Hruby, V. J. Design and microwave-assisted synthesis of novel macrocyclic peptides active at melanocortin receptors: discovery of potent and selective hMC5R receptor antagonists. J. Med. Chem. 2008, 51, 2701-2707.
-
(2008)
J. Med. Chem
, vol.51
, pp. 2701-2707
-
-
Grieco, P.1
Cai, M.2
Liu, L.3
Mayorov, A.4
Chandler, K.5
Trivedi, D.6
Lin, G.7
Campiglia, P.8
Novellino, E.9
Hruby, V.J.10
-
22
-
-
33845361616
-
Discovery of a new class of macrocyclic antagonists to the human motilin receptor
-
(b) Marsault, E.; Hoveyda, H. R.; Peterson, M. L.; Saint-Louis, C.; Landry, A.; Vézina, M.; Ouellet, L.; Wang, Z.; Ramaseshan, M.; Beaubien, S.; Benakli, K.; Beauchemin, S.; Déziel, R.; Peeters, T.; Fraser, G. L. Discovery of a new class of macrocyclic antagonists to the human motilin receptor. J. Med. Chem. 2006, 49, 7190-7197.
-
(2006)
J. Med. Chem
, vol.49
, pp. 7190-7197
-
-
Marsault, E.1
Hoveyda, H.R.2
Peterson, M.L.3
Saint-Louis, C.4
Landry, A.5
Vézina, M.6
Ouellet, L.7
Wang, Z.8
Ramaseshan, M.9
Beaubien, S.10
Benakli, K.11
Beauchemin, S.12
Déziel, R.13
Peeters, T.14
Fraser, G.L.15
-
23
-
-
0036514662
-
Cyclization strategies in peptide derived drug design
-
For reviews, see the following: c
-
For reviews, see the following: (c) Li, P.; Roller, P. P. Cyclization strategies in peptide derived drug design. Curr. Top. Med. Chem. 2002, 2, 325-341.
-
(2002)
Curr. Top. Med. Chem
, vol.2
, pp. 325-341
-
-
Li, P.1
Roller, P.P.2
-
24
-
-
0036254144
-
Current synthetic approaches to peptide and peptidomimetic cyclization
-
(d) Li, P.; Roller, P. P.; Xu, J. Current synthetic approaches to peptide and peptidomimetic cyclization. Curr. Org. Chem. 2002, 6, 411-440.
-
(2002)
Curr. Org. Chem
, vol.6
, pp. 411-440
-
-
Li, P.1
Roller, P.P.2
Xu, J.3
-
25
-
-
23444441022
-
Design and synthesis of depeptidized macrocyclic inhibitors of hepatitis C NS3-4A protease using structure-based drug design
-
(a) Venkatraman, S.; Njoroge, F. G.; Girijavallabhan, V. M.; Madison, V.; Yao, N. H.; Prongay, A. J.; Butkiewicz, N.; Pichardo, J. Design and synthesis of depeptidized macrocyclic inhibitors of hepatitis C NS3-4A protease using structure-based drug design. J. Med. Chem. 2005, 48, 5088-5091.
-
(2005)
J. Med. Chem
, vol.48
, pp. 5088-5091
-
-
Venkatraman, S.1
Njoroge, F.G.2
Girijavallabhan, V.M.3
Madison, V.4
Yao, N.H.5
Prongay, A.J.6
Butkiewicz, N.7
Pichardo, J.8
-
26
-
-
27744486088
-
Proline-based macrocyclic inhibitors of the hepatitis C virus: Stereo - selective synthesis and biological activity
-
(b) Chen, K. X.; Njoroge, F. G.; Vibulbhan, B.; Prongay, A.; Pichardo, J.; Madison, V.; Buevich, A.; Chan, T.-M. Proline-based macrocyclic inhibitors of the hepatitis C virus: stereo - selective synthesis and biological activity. Angew. Chem., Int. Ed. 2005, 44, 7024-7028.
-
(2005)
Angew. Chem., Int. Ed
, vol.44
, pp. 7024-7028
-
-
Chen, K.X.1
Njoroge, F.G.2
Vibulbhan, B.3
Prongay, A.4
Pichardo, J.5
Madison, V.6
Buevich, A.7
Chan, T.-M.8
-
27
-
-
32344431531
-
Novel potent hepatitis C virus NS3 serine protease inhibitors derived from proline-based macrocycles
-
(c) Chen, K. X.; Njoroge, F. G.; Arasappan, A.; Venkatraman, S.; Vibulbhan, B.; Yang, W.; Parekh, T. N.; Pichardo, J.; Prongay, A.; Cheng, K.-C.; Butkiewicz, N.; Yao, N.; Madison, V.; Girijavallabhan, V. Novel potent hepatitis C virus NS3 serine protease inhibitors derived from proline-based macrocycles. J. Med. Chem. 2006,49, 995-1005.
-
(2006)
J. Med. Chem
, vol.49
, pp. 995-1005
-
-
Chen, K.X.1
Njoroge, F.G.2
Arasappan, A.3
Venkatraman, S.4
Vibulbhan, B.5
Yang, W.6
Parekh, T.N.7
Pichardo, J.8
Prongay, A.9
Cheng, K.-C.10
Butkiewicz, N.11
Yao, N.12
Madison, V.13
Girijavallabhan, V.14
-
28
-
-
33746934147
-
P2-P4 macrocyclic inhibitors of hepatitis C virus NS3-4A serine protease
-
(d) Arasappan, A.; Njoroge, F. G.; Chen, K. X.; Venkatraman, S.; Parekh, T. N.; Gu, H.; Pichardo, J.; Butkiewicz, N.; Prongay, A.; Madison, V.; Girijavallabhan, V. P2-P4 macrocyclic inhibitors of hepatitis C virus NS3-4A serine protease. Bioorg. Med. Chem. Lett. 2006, 16, 3960-3965.
-
(2006)
Bioorg. Med. Chem. Lett
, vol.16
, pp. 3960-3965
-
-
Arasappan, A.1
Njoroge, F.G.2
Chen, K.X.3
Venkatraman, S.4
Parekh, T.N.5
Gu, H.6
Pichardo, J.7
Butkiewicz, N.8
Prongay, A.9
Madison, V.10
Girijavallabhan, V.11
-
29
-
-
33646449468
-
-
Bogen, S. L.; Arasappan, A.; Bennett, F.; Chen, K.; Jao, E.; Liu, Y. - T.; Lovey, R. G.; Venkatraman, S.; Pan, W.; Parekh, T.; Pike, R. E.; Ruan, S.; Liu, R.; Baroudy, B.; Agrawal, S.; Chase, R.; Ingravallo, P.; Pichardo, J.; Prongay, A.; Brisson, J.-M.; Hsieh, T. Y.; Cheng, K.-C.; Kemp, S. J.; Levy, O. E.; Lim-Wilby, M.; Tamura, S. Y.; Saksena, A. K.; Girijavallabhan, V.; Njoroge, F. G. Discovery of SCH 446211 (SCH 6): a new ketoamide inhibitor of the HCV NS3 serine protease and HCV subgenomic RNA replication. J. Med. Chem. 2006, 49, 2750-2757.
-
Bogen, S. L.; Arasappan, A.; Bennett, F.; Chen, K.; Jao, E.; Liu, Y. - T.; Lovey, R. G.; Venkatraman, S.; Pan, W.; Parekh, T.; Pike, R. E.; Ruan, S.; Liu, R.; Baroudy, B.; Agrawal, S.; Chase, R.; Ingravallo, P.; Pichardo, J.; Prongay, A.; Brisson, J.-M.; Hsieh, T. Y.; Cheng, K.-C.; Kemp, S. J.; Levy, O. E.; Lim-Wilby, M.; Tamura, S. Y.; Saksena, A. K.; Girijavallabhan, V.; Njoroge, F. G. Discovery of SCH 446211 (SCH 6): a new ketoamide inhibitor of the HCV NS3 serine protease and HCV subgenomic RNA replication. J. Med. Chem. 2006, 49, 2750-2757.
-
-
-
-
30
-
-
57849169322
-
Potent inhibitors of HCV-NS3 protease derived from boronic acids
-
doi: 10.1016/j.bmcl. 2008.10.124
-
(a) Venkatraman, S.; Wu, W.; Prongay, A.; Girijavallabhan, V.; Njoroge, F. G. Potent inhibitors of HCV-NS3 protease derived from boronic acids. Bioorg. Med. Chem. Lett. 2008, doi: 10.1016/j.bmcl. 2008.10.124.
-
Bioorg. Med. Chem. Lett
, vol.2008
-
-
Venkatraman, S.1
Wu, W.2
Prongay, A.3
Girijavallabhan, V.4
Njoroge, F.G.5
-
31
-
-
0035847669
-
The identification of α-ketoamides as potent inhibitors ofhepatitis C virus NS3-4A proteinase
-
(b) Bennett, J. M.; Campbell, A. D.; Campbell, A. J.; Carr, M. G.; Dunsdon, R. M.; Greening, J. R.; Hurst, D. N.; Jennings, N. S.; Jones, P. S.; Jordan, S.; Kay, P. B.; O'Brien, M. A.; King - Underwood, J.; Raynham, T. M.; Wilkinson, C. S.; Wilkinson, T. C. I.; Wilson, F. X. The identification of α-ketoamides as potent inhibitors ofhepatitis C virus NS3-4A proteinase. Bioorg. Med. Chem. Lett. 2001, 11, 355-357.
-
(2001)
Bioorg. Med. Chem. Lett
, vol.11
, pp. 355-357
-
-
Bennett, J.M.1
Campbell, A.D.2
Campbell, A.J.3
Carr, M.G.4
Dunsdon, R.M.5
Greening, J.R.6
Hurst, D.N.7
Jennings, N.S.8
Jones, P.S.9
Jordan, S.10
Kay, P.B.11
O'Brien, M.A.12
King - Underwood, J.13
Raynham, T.M.14
Wilkinson, C.S.15
Wilkinson, T.C.I.16
Wilson, F.X.17
-
32
-
-
0034678789
-
-
Han, W.; Hu, Z.; Jiang, X.; Decicco, C. P. α-Ketoamides, α-ketoesters and a-diketones as HCV NS3 protease inhibitors. Bioorg. Med. Chem. Lett. 2000, 10, 711-713.
-
(c) Han, W.; Hu, Z.; Jiang, X.; Decicco, C. P. α-Ketoamides, α-ketoesters and a-diketones as HCV NS3 protease inhibitors. Bioorg. Med. Chem. Lett. 2000, 10, 711-713.
-
-
-
-
33
-
-
0033151691
-
-
Zhang, R.; Beyer, B. M.; Durkin, J.; Ingram, R.; Njoroge, F. G.; Windsor, W. T.; Malcolm, B. A. A continuous spectrophotometric assay for the hepatitis C virus serine protease. Anal. Biochem. 1999, 270, 268-275.
-
Zhang, R.; Beyer, B. M.; Durkin, J.; Ingram, R.; Njoroge, F. G.; Windsor, W. T.; Malcolm, B. A. A continuous spectrophotometric assay for the hepatitis C virus serine protease. Anal. Biochem. 1999, 270, 268-275.
-
-
-
-
34
-
-
0345188811
-
Replication of subgenomic hepatitis C virus RNAs in a hepatoma cell line
-
Lohmann, V.; Korner, F.; Koch, J.-O.; Herian, U.; Theilmann, L.; Bartenschlager, R. Replication of subgenomic hepatitis C virus RNAs in a hepatoma cell line. Science 1999, 285, 110-113.
-
(1999)
Science
, vol.285
, pp. 110-113
-
-
Lohmann, V.1
Korner, F.2
Koch, J.-O.3
Herian, U.4
Theilmann, L.5
Bartenschlager, R.6
-
35
-
-
34547948019
-
Application of ring-closing metathesis for the synthesis of macrocyclic peptido - mimetics as inhibitors of HCV NS3 protease
-
Velazquez, F.; Venkatraman, S.; Wu, W.; Blackman, M.; Prongay, A.; Girijavallabhan, V.; Shih, N.-Y.; Njoroge, F. G. Application of ring-closing metathesis for the synthesis of macrocyclic peptido - mimetics as inhibitors of HCV NS3 protease. Org. Lett. 2007, 9, 3061-3064.
-
(2007)
Org. Lett
, vol.9
, pp. 3061-3064
-
-
Velazquez, F.1
Venkatraman, S.2
Wu, W.3
Blackman, M.4
Prongay, A.5
Girijavallabhan, V.6
Shih, N.-Y.7
Njoroge, F.G.8
-
36
-
-
34547652788
-
Practical and efficient method for amino acid derivatives containing β-quaternary center: Application toward synthesis of hepatitis C virus NS3 serine protease inhibitors
-
Arasappan, A.; Venkatraman, S.; Padilla, A. I.; Wu, W.; Meng, T.; Jin, Y.; Wong, J.; Prongay, A.; Girijavallabhan, V.; Njoroge, F. G. Practical and efficient method for amino acid derivatives containing β-quaternary center: application toward synthesis of hepatitis C virus NS3 serine protease inhibitors. Tetrahedron Lett. 2007, 48, 6343-6347.
-
(2007)
Tetrahedron Lett
, vol.48
, pp. 6343-6347
-
-
Arasappan, A.1
Venkatraman, S.2
Padilla, A.I.3
Wu, W.4
Meng, T.5
Jin, Y.6
Wong, J.7
Prongay, A.8
Girijavallabhan, V.9
Njoroge, F.G.10
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