-
9
-
-
24744436849
-
-
Hocek M., Nauš P., Pohl R., Votruba I., Furman P.A., Tharnish P.M., and Otto M.J.. J. Med. Chem. 48 (2005) 5869
-
(2005)
J. Med. Chem.
, vol.48
, pp. 5869
-
-
Hocek, M.1
Nauš, P.2
Pohl, R.3
Votruba, I.4
Furman, P.A.5
Tharnish, P.M.6
Otto, M.J..7
-
11
-
-
12444326148
-
-
Ding Y., Girardet J.-L., Hong Z., Lai V.C.H., An H., Koh Y.-h., Shaw S.Z., and Zhong W. Bioorg. Med. Chem. Lett. 15 (2005) 709
-
(2005)
Bioorg. Med. Chem. Lett.
, vol.15
, pp. 709
-
-
Ding, Y.1
Girardet, J.-L.2
Hong, Z.3
Lai, V.C.H.4
An, H.5
Koh, Y.-h.6
Shaw, S.Z.7
Zhong, W.8
-
12
-
-
0036284117
-
-
Fernandez F., Garcia-Mera X., Morales M., Rodriguez-Borges J., and De Clercq E. Synthesis (2002) 1084
-
(2002)
Synthesis
, pp. 1084
-
-
Fernandez, F.1
Garcia-Mera, X.2
Morales, M.3
Rodriguez-Borges, J.4
De Clercq, E.5
-
19
-
-
0345145203
-
-
Gumina G., Chong Y., Choo H., Song G.-Y., and Chu C.K. Curr. Top. Med. Chem. 2 (2002) 1065
-
(2002)
Curr. Top. Med. Chem.
, vol.2
, pp. 1065
-
-
Gumina, G.1
Chong, Y.2
Choo, H.3
Song, G.-Y.4
Chu, C.K.5
-
20
-
-
0035172399
-
-
Bryant M.L., Bridges E.G., Placidi L., Faraj A., Loi A.G., Pierra C., Dukhan D., Gosselin G., Imbach J.L., Hernandez B., Juodawlkis A., Tennant B., Korba B., Cote P., Marion P., Cretton-Scott E., Schinazi R.F., and Sommadossi J.P. Antimicrob. Agents Chemother. 45 (2001) 229
-
(2001)
Antimicrob. Agents Chemother.
, vol.45
, pp. 229
-
-
Bryant, M.L.1
Bridges, E.G.2
Placidi, L.3
Faraj, A.4
Loi, A.G.5
Pierra, C.6
Dukhan, D.7
Gosselin, G.8
Imbach, J.L.9
Hernandez, B.10
Juodawlkis, A.11
Tennant, B.12
Korba, B.13
Cote, P.14
Marion, P.15
Cretton-Scott, E.16
Schinazi, R.F.17
Sommadossi, J.P.18
-
21
-
-
0037293520
-
-
Recent examples:
-
Recent examples:. Mugnaini C., Botta M., Coletta M., Corelli F., Focher F., Marini S., Renzulli M.L., and Verri A. Bioorg. Med. Chem. 11 (2003) 357
-
(2003)
Bioorg. Med. Chem.
, vol.11
, pp. 357
-
-
Mugnaini, C.1
Botta, M.2
Coletta, M.3
Corelli, F.4
Focher, F.5
Marini, S.6
Renzulli, M.L.7
Verri, A.8
-
22
-
-
1642388408
-
-
Zhu W., Chong Y.H., Choo H., Mathews J., Schinazi R.F., and Chu C.K. J. Med. Chem. 47 (2004) 1631
-
(2004)
J. Med. Chem.
, vol.47
, pp. 1631
-
-
Zhu, W.1
Chong, Y.H.2
Choo, H.3
Mathews, J.4
Schinazi, R.F.5
Chu, C.K.6
-
23
-
-
26644435308
-
-
Seela F., Lin W., Kazimierczuk Z., Rosemeyer H., Glacon V., Peng X., He Y., Ming X., Andrzejewska M., Gorska A., Zhang X., and La Colla P. Nucleosides Nucleotides Nucleic Acids 24 (2005) 859
-
(2005)
Nucleosides Nucleotides Nucleic Acids
, vol.24
, pp. 859
-
-
Seela, F.1
Lin, W.2
Kazimierczuk, Z.3
Rosemeyer, H.4
Glacon, V.5
Peng, X.6
He, Y.7
Ming, X.8
Andrzejewska, M.9
Gorska, A.10
Zhang, X.11
La Colla, P.12
-
24
-
-
33644884485
-
-
Clinch K., Evans G.B., Fleet G.W.J., Furneaux R.H., Johnson S.W., Lenz D.H., Mee S.P.H., Rands P.R., Schramm V.L., Taylor Ringia E.A., and Tyler P.C. Org. Biomol. Chem. 4 (2006) 1131
-
(2006)
Org. Biomol. Chem.
, vol.4
, pp. 1131
-
-
Clinch, K.1
Evans, G.B.2
Fleet, G.W.J.3
Furneaux, R.H.4
Johnson, S.W.5
Lenz, D.H.6
Mee, S.P.H.7
Rands, P.R.8
Schramm, V.L.9
Taylor Ringia, E.A.10
Tyler, P.C.11
-
28
-
-
37049090684
-
-
note
-
3). Spectral data were in accord with those of d-enantiomer: Buck, I.M.; Reese, C.B. J. Chem. Soc., Perkin Trans. 1 1990, 2937-2942.
-
-
-
-
31
-
-
33746027041
-
-
Šilhár P., Pohl R., Votruba I., Klepetářová B., and Hocek M. Collect. Czech. Chem. Commun. 71 (2006) 788
-
(2006)
Collect. Czech. Chem. Commun.
, vol.71
, pp. 788
-
-
Šilhár, P.1
Pohl, R.2
Votruba, I.3
Klepetářová, B.4
Hocek, M.5
-
32
-
-
33748300224
-
-
note
-
2O)].
-
-
-
-
33
-
-
0345188811
-
-
Lohmann V., Korner F., Koch J., Herian U., Theilmann L., and Bartenschlager R. Science 285 (1999) 110
-
(1999)
Science
, vol.285
, pp. 110
-
-
Lohmann, V.1
Korner, F.2
Koch, J.3
Herian, U.4
Theilmann, L.5
Bartenschlager, R.6
-
34
-
-
33748315496
-
-
Triphosphates were prepared from the corresponding nucleosides by Chemcyte Inc., San Diego, USA.
-
-
-
-
35
-
-
33748318804
-
-
note
-
50 was calculated by nonlinear regression analysis using GraphPad software package.
-
-
-
-
37
-
-
33748310144
-
-
note
-
33P-labeled-GpC primer, 20 μM oligonucleotide, 1 mM nucleotide triphosphate, and 2 μM of NS5B-delta55 enzyme, at 34 °C for 60 min. The reaction mixture was resolved on 20% denaturing acrylamide gel and quantified by PhosphorImager (Amersham).
-
-
-
|