-
1
-
-
0036835590
-
Hepatitis C therapeutics: Current status and emerging strategies
-
Tan, S.L.; Pause, A.; Shi, Y.; Sonenberg, N. Hepatitis C therapeutics: current status and emerging strategies. Nat. Rev. Drug Discovery 2002, 1, 867-881.
-
(2002)
Nat. Rev. Drug Discovery
, vol.1
, pp. 867-881
-
-
Tan, S.L.1
Pause, A.2
Shi, Y.3
Sonenberg, N.4
-
2
-
-
0034619980
-
Peginterferon alfa-2a in patients with chronic hepatitis C and cirrhosis
-
Heathcote, E.; Shiffman, M.; Cooksley, W.; Dusheiko, G.M.; Lee, S.S.; Balart, L.; Reindollar, R.; Reddy, R.K.; Wright, T.L.; Lin, A.; Hoffman, J.; De Pamphilis, J. Peginterferon alfa-2a in patients with chronic hepatitis C and cirrhosis. N. Engl. J. Med. 2000, 343, 1673-1680.
-
(2000)
N. Engl. J. Med.
, vol.343
, pp. 1673-1680
-
-
Heathcote, E.1
Shiffman, M.2
Cooksley, W.3
Dusheiko, G.M.4
Lee, S.S.5
Balart, L.6
Reindollar, R.7
Reddy, R.K.8
Wright, T.L.9
Lin, A.10
Hoffman, J.11
De Pamphilis, J.12
-
3
-
-
0344495985
-
Synthesis and evaluation of optically pure dioxolanes as inhibitors of hepatitis C virus RNA replication
-
a) Bera, S.; Malik, L.; Bhat, B.; Carroll, S.S.; MacCoss, M.; Olsen, D.B.; Tomassini, J.E.; Eldrup, A.B. Synthesis and evaluation of optically pure dioxolanes as inhibitors of hepatitis C virus RNA replication. Bioorg. Med. Chem. Lett. 2003, 13, 4455-4458;
-
(2003)
Bioorg. Med. Chem. Lett.
, vol.13
, pp. 4455-4458
-
-
Bera, S.1
Malik, L.2
Bhat, B.3
Carroll, S.S.4
MacCoss, M.5
Olsen, D.B.6
Tomassini, J.E.7
Eldrup, A.B.8
-
4
-
-
4744364179
-
Structure - activity relationship of heterobase-modified 2′-C-methyl ribonucleosides as inhibitors of hepatitis C virus RNA replication
-
DOI 10.1021/jm040068f
-
b) Eldrup, A.B.; Prhavc, M.; 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.; Von Langen, D.; Wolanski, B.; Olsen, D.B. Structure-activity relationship of heterobase-modified 2′ -C-methyl ribonucleosides as inhibitors of hepatitis C virus RNA replication. 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..
-
5
-
-
23944469297
-
Design, synthesis, and antiviral activity of 2′-deoxy-2′- fluoro-2′-C-methylcytidine, a potent inhibitor of hepatitis C virus replication
-
c) Clark, J.L.; Hollecker, L.; Mason, J.C.; Stuyver, L.J.; Tharnish, P.M.; Lostia, S.; McBrayer, T.R.; Schinazi, R.F.; Watanabe, K.A.; Otto, M.J.; Furman, P.A.; Stec, W.J.; Patterson, S.E.; Pankiewicz, K.W. Design, synthesis, and antiviral activity of 2′-deoxy-2′-fluoro-2′-C- methylcytidine, a potent inhibitor of hepatitis C virus replication. J. Med. Chem. 2005, 48, 5504-5508.
-
(2005)
J. Med. Chem.
, vol.48
, pp. 5504-5508
-
-
Clark, J.L.1
Hollecker, L.2
Mason, J.C.3
Stuyver, L.J.4
Tharnish, P.M.5
Lostia, S.6
McBrayer, T.R.7
Schinazi, R.F.8
Watanabe, K.A.9
Otto, M.J.10
Furman, P.A.11
Stec, W.J.12
Patterson, S.E.13
Pankiewicz, K.W.14
-
6
-
-
59449085771
-
The design, synthesis, and antiviral activity of 4′-azidocytidine analogues against hepatitis C virus replication: The discovery of 4′-azidoarabinocytidine
-
d) Smith, D.B.; Kalayanov, G.; Sund, C.; Winqvist, A.; Pinho, P.; Maltseva, T.; Morisson, V.; Leveque, V.; Rajyaguru, S.; Le Pogam, S.; Najera, I.; Benkestock, K.; Zhou, X.X.; Maag, H.; Cammack, N.; Martin, J.A.; Swallow, S.; Johansson, N.G.; Klumpp, K.; Smith, M. The design, synthesis, and antiviral activity of 4′-azidocytidine analogues against hepatitis C virus replication: the discovery of 4′-azidoarabinocytidine. J. Med. Chem. 2009, 52, 219-223.
-
(2009)
J. Med. Chem.
, vol.52
, pp. 219-223
-
-
Smith, D.B.1
Kalayanov, G.2
Sund, C.3
Winqvist, A.4
Pinho, P.5
Maltseva, T.6
Morisson, V.7
Leveque, V.8
Rajyaguru, S.9
Le Pogam, S.10
Najera, I.11
Benkestock, K.12
Zhou, X.X.13
Maag, H.14
Cammack, N.15
Martin, J.A.16
Swallow, S.17
Johansson, N.G.18
Klumpp, K.19
Smith, M.20
more..
-
7
-
-
0036231063
-
Trends in the design of nucleoside analogues as anti-HIV drugs
-
El Kouni, M.H. Trends in the design of nucleoside analogues as anti-HIV drugs. Curr. Pharm. Des. 2002, 8, 581-593.
-
(2002)
Curr. Pharm. Des.
, vol.8
, pp. 581-593
-
-
El Kouni, M.H.1
-
8
-
-
0037809239
-
Inhibition of hepatitis C virus RNA replication by 2′-modified nucleoside analogs
-
DOI 10.1074/jbc.M210914200
-
Carrol, S.S.; Tomassini, J.E.; Bosserman, M.; Getty, K.; Stahlhut, M.W.; Eldrup, A.B.; Bhat, B.; Hall, D.; Simcoe, A.L.; LaFemina, R.; Rutkowski, C.A.;Wolanski, B.; Yang, Z.; Migliaccio, G.; De Francesco, R.; Kuo, L.C.; MacCoss, M.; Olsen, D.B. Inhibition of hepatitis C virus RNA replication by 2′-modified nucleoside analogs. J. Biol. Chem. 2003, 278, 11979-11984. (Pubitemid 36800172)
-
(2003)
Journal of Biological Chemistry
, vol.278
, Issue.14
, pp. 11979-11984
-
-
Carroll, S.S.1
Tomassini, J.E.2
Bosserman, M.3
Getty, K.4
Stahlhut, M.W.5
Eldrup, A.B.6
Bhat, B.7
Hall, D.8
Simcoe, A.L.9
LaFemina, R.10
Rutkowski, C.A.11
Wolanski, B.12
Yang, Z.13
Migliaccio, G.14
De Francesco, R.15
Kuo, L.C.16
MacCoss, M.17
Olsen, D.B.18
-
9
-
-
11144355286
-
Structure-activity relationship of purine ribonucleosides for inhibition of hepatitis C virus RNA-dependent RNA polymerase
-
Eldrup, A.B.; Allerson, C.R.; Bennett, C.F.; Bera, S.; Bhat, B.; Bhat, N.; Bosserman, M.R.; Brooks, J.; Burlein, C.; Carrol, S.S.; Cook, P.D.; Getty, K.L.; MacCoss, M.; McMasters, D.R.; Olsen, D.B.; Prakash, T.P.; Prhavc, M.; Song, Q.L.; Tomassini, J.E.; Xia, J. Structure-activity relationship of purine ribonucleosides for inhibition of hepatitis C virus RNA-dependent RNA polymerase. J. Med. Chem. 2004, 47, 2283-2295.
-
(2004)
J. Med. Chem.
, vol.47
, pp. 2283-2295
-
-
Eldrup, A.B.1
Allerson, C.R.2
Bennett, C.F.3
Bera, S.4
Bhat, B.5
Bhat, N.6
Bosserman, M.R.7
Brooks, J.8
Burlein, C.9
Carrol, S.S.10
Cook, P.D.11
Getty, K.L.12
MacCoss, M.13
McMasters, D.R.14
Olsen, D.B.15
Prakash, T.P.16
Prhavc, M.17
Song, Q.L.18
Tomassini, J.E.19
Xia, J.20
more..
-
10
-
-
51649093129
-
Efficient synthesis of 4′-cyclopropylated carbovir analogues with use of ring-closing metathesis from glycolate
-
Liu, L.J.; Yoo, J.C.; Hong, J.H. Efficient synthesis of 4′-cyclopropylated carbovir analogues with use of ring-closing metathesis from glycolate. Nucleosides Nucleotides Nucleic Acids 2008, 27, 1186-1196.
-
(2008)
Nucleosides Nucleotides Nucleic Acids
, vol.27
, pp. 1186-1196
-
-
Liu, L.J.1
Yoo, J.C.2
Hong, J.H.3
-
11
-
-
0037597933
-
Convenient monoketalization of 1,4-cyclohexanedione. Synthesis of new quinone methides
-
Hyatt, J.A. Convenient monoketalization of 1,4-cyclohexanedione. Synthesis of new quinone methides. J. Org. Chem. 1983, 48, 129-131.
-
(1983)
J. Org. Chem.
, vol.48
, pp. 129-131
-
-
Hyatt, J.A.1
-
12
-
-
0001685085
-
Simple stereoselective version of the Claisen rearrangement leading to trans-trisubstituted olefinic bonds. Synthesis of squalene
-
a) Johnson, W.S.; Werthmann, L.; Bartlett, W.R.; Brocksom, T.J.; Li, T.T.; Faulkner, D.J.; Petersen, M.R. Simple stereoselective version of the Claisen rearrangement leading to trans-trisubstituted olefinic bonds. Synthesis of squalene. J. Am. Chem. Soc. 1970, 92, 741-743;
-
(1970)
J. Am. Chem. Soc.
, vol.92
, pp. 741-743
-
-
Johnson, W.S.1
Werthmann, L.2
Bartlett, W.R.3
Brocksom, T.J.4
Li, T.T.5
Faulkner, D.J.6
Petersen, M.R.7
-
13
-
-
4344610661
-
Claisen rearrangement over the past nine decades
-
b) Castro, A.M.M. Claisen rearrangement over the past nine decades. Chem. Rev. 2004, 104, 2939-3002;
-
(2004)
Chem. Rev.
, vol.104
, pp. 2939-3002
-
-
Castro, A.M.M.1
-
14
-
-
33845279007
-
The thermal, aliphatic Claisen rearrangement
-
c) Ziegler, F.E. The thermal, aliphatic Claisen rearrangement. Chem. Rev. 1988, 88, 1423-1452;
-
(1988)
Chem. Rev.
, vol.88
, pp. 1423-1452
-
-
Ziegler, F.E.1
-
15
-
-
33845471185
-
Catalysis of the Cope and Claisen rearrangements
-
d) Lutz, R. Catalysis of the Cope and Claisen rearrangements. Chem. Rev. 1984, 84, 205-297.
-
(1984)
Chem. Rev.
, vol.84
, pp. 205-297
-
-
Lutz, R.1
-
16
-
-
0344006321
-
Olefin metathesis and beyond
-
a) Furstner, A. Olefin metathesis and beyond. Ange. Chem. Int. Ed. Engl. 2000, 39, 3012-3043;
-
(2000)
Ange. Chem. Int. Ed. Engl.
, vol.39
, pp. 3012-3043
-
-
Furstner, A.1
-
17
-
-
22744448499
-
Metathesis reactions in total synthesis
-
b) Nicolaou, K.C.; Bulger, P.G.; Sarlah, D. Metathesis reactions in total synthesis. Ange. Chem. Int. Ed. Engl. 2005, 44, 4490-4527;
-
(2005)
Ange. Chem. Int. Ed. Engl.
, vol.44
, pp. 4490-4527
-
-
Nicolaou, K.C.1
Bulger, P.G.2
Sarlah, D.3
-
18
-
-
33748368508
-
Search for solutions to the reactivity and selectivity problems in enyne metathesis
-
c) Hansen, E.C.; Lee, D. Search for solutions to the reactivity and selectivity problems in enyne metathesis. Acc. Chem. Res. 2006, 39, 509-519.
-
(2006)
Acc. Chem. Res.
, vol.39
, pp. 509-519
-
-
Hansen, E.C.1
Lee, D.2
-
19
-
-
0037144693
-
An efficient synthesis of novel carbocyclic nucleosides with use of ring-closing metathesis from D-lactose
-
Hong, J.H.; Shim, M.J.; Ro, B.O.; Ko, O.H. An efficient synthesis of novel carbocyclic nucleosides with use of ring-closing metathesis from D-lactose. J. Org. Chem. 2002, 67, 6837-6840.
-
(2002)
J. Org. Chem.
, vol.67
, pp. 6837-6840
-
-
Hong, J.H.1
Shim, M.J.2
Ro, B.O.3
Ko, O.H.4
-
20
-
-
0031552104
-
An expeditious route to carbocyclic nucleosides: (-)-Aristeromycin and (-)-carbodine
-
Burlina, F.; Favre, A.; Fourrey, J.-L.; Thomas, M. An expeditious route to carbocyclic nucleosides: (?)-aristeromycin and (?)-carbodine. Bioorg. Med. Chem. Lett. 1997, 7, 247-250.
-
(1997)
Bioorg. Med. Chem. Lett.
, vol.7
, pp. 247-250
-
-
Burlina, F.1
Favre, A.2
Fourrey, J.-L.3
Thomas, M.4
-
21
-
-
0141632671
-
Dynamics of subgenomic hepatitis C virus replicon RNA levels in Huh-7 cells after exposure to nucleoside antimetabolite
-
Stuyver, L.J.; McBrayer, T.R.; Tharnish, P.M.; Hassan, A.E.A.; Chu, C.K.; Pankiewicz, K.W.; Watanabe, K.A.; Schinazi, R.F.; Otto, M.J. Dynamics of subgenomic hepatitis C virus replicon RNA levels in Huh-7 cells after exposure to nucleoside antimetabolite. J. Virol. 2003, 77, 10689-10694.
-
(2003)
J. Virol.
, vol.77
, pp. 10689-10694
-
-
Stuyver, L.J.1
McBrayer, T.R.2
Tharnish, P.M.3
Hassan, A.E.A.4
Chu, C.K.5
Pankiewicz, K.W.6
Watanabe, K.A.7
Schinazi, R.F.8
Otto, M.J.9
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