-
1
-
-
0026077714
-
Synthesis of 2-amino-9-(3′-azido-2′,3′-dideoxy-beta-D- erythro-pentofuranosyl)-6-methoxy-9H-purine (AzddMAP) and Azdd- Guo
-
Almond, M. R., J. L. Collins, B. E. Reitter, J. L. Rideout, G. A. Freeman, and M. H. St. Clair. 1991. Synthesis of 2-amino-9-(3′-azido- 2′,3′-dideoxy-beta-D-erythro-pentofuranosyl)-6-methoxy-9H-purine (AzddMAP) and Azdd- Guo. Tetrahedron Lett. 32:5745-5748.
-
(1991)
Tetrahedron Lett.
, vol.32
, pp. 5745-5748
-
-
Almond, M.R.1
Collins, J.L.2
Reitter, B.E.3
Rideout, J.L.4
Freeman, G.A.5
St Clair, M.H.6
-
2
-
-
0023181651
-
Selective inhibition of human immunodeficiency virus (HIV) by 3′-azido-2′, 3′-dideoxyguanosine in vitro
-
Baba, M., R. Pauwels, J. Balzarini, P. Herdewijn, and E. De Clercq. 1987. Selective inhibition of human immunodeficiency virus (HIV) by 3′-azido-2′, 3′-dideoxyguanosine in vitro. Biochem. Biophys. Res. Commun. 145:1080-1086.
-
(1987)
Biochem. Biophys. Res. Commun.
, vol.145
, pp. 1080-1086
-
-
Baba, M.1
Pauwels, R.2
Balzarini, J.3
Herdewijn, P.4
De Clercq, E.5
-
3
-
-
34547105526
-
Selection of mutations in the connection and RNase H domains of human immunodeficiency virus type 1 reverse transcriptase that increase resistance to 3′-azido-3′-dideoxythymidine
-
DOI 10.1128/JVI.02203-06
-
Brehm, J. H., D. Koontz, J. D. Meteer, V. Pathak, N. Sluis-Cremer, and J. W. Mellors. 2007. Selection of mutations in the connection and RNase H domains of human immunodeficiency virus type 1 reverse transcriptase that increase resistance to 3′-azido-3′-dideoxythymidine. J. Virol. 81:7852-7859. (Pubitemid 47101471)
-
(2007)
Journal of Virology
, vol.81
, Issue.15
, pp. 7852-7859
-
-
Brehm, J.H.1
Koontz, D.2
Meteer, J.D.3
Pathak, V.4
Sluis-Cremer, N.5
Mellors, J.W.6
-
4
-
-
0021118703
-
Quantitative analysis of dose-effect relationships: The combined effects of multiple drugs or enzyme inhibitors
-
Chou, T. C., and P. Talalay. 1984. Quantitative analysis of dose-effect relationships: the combined effects of multiple drugs or enzyme inhibitors. Adv. Enzyme Regul. 22:27-55.
-
(1984)
Adv. Enzyme Regul.
, vol.22
, pp. 27-55
-
-
Chou, T.C.1
Talalay, P.2
-
5
-
-
38649089790
-
Design and profiling of GS-9148, a novel nucleotide analog active against nucleoside-resistant variants of human immunodeficiency virus type 1, and its orally bioavailable phosphonoamidate prodrug, GS-9131
-
Cihlar, T., A. S. Ray, C. G. Boojamra, L. Zhang, H. Hui, G. Laflamme, J. E. Vela, D. Grant, J. Chen, F. Myrick, K. L. White, Y. Gao, K. Y. Lin, J. L. Douglas, N. T. Parkin, A. Carey, R. Pakdaman, and R. L. Mackman. 2008. Design and profiling of GS-9148, a novel nucleotide analog active against nucleoside-resistant variants of human immunodeficiency virus type 1, and its orally bioavailable phosphonoamidate prodrug, GS-9131. Antimicrob. Agents Chemother. 52:655-665.
-
(2008)
Antimicrob. Agents Chemother.
, vol.52
, pp. 655-665
-
-
Cihlar, T.1
Ray, A.S.2
Boojamra, C.G.3
Zhang, L.4
Hui, H.5
Laflamme, G.6
Vela, J.E.7
Grant, D.8
Chen, J.9
Myrick, F.10
White, K.L.11
Gao, Y.12
Lin, K.Y.13
Douglas, J.L.14
Parkin, N.T.15
Carey, A.16
Pakdaman, R.17
Mackman, R.L.18
-
6
-
-
0029069647
-
2-Amino-9-(3-azido-2,3-dideoxy-beta-D-erythro-pentofuranosyl) -6-substituted-9H-purines: Synthesis and anti-HIV activity
-
Freeman, G. A., S. R. Shaver, J. L. Rideout, and S. A. Short. 1995. 2-Amino-9-(3-azido-2,3-dideoxy-beta-D-erythro-pentofuranosyl) -6-substituted-9H-purines: synthesis and anti-HIV activity. Bioorg. Med. Chem. 3:447-458.
-
(1995)
Bioorg. Med. Chem.
, vol.3
, pp. 447-458
-
-
Freeman, G.A.1
Shaver, S.R.2
Rideout, J.L.3
Short, S.A.4
-
7
-
-
0027287973
-
Differential phosphorylation of azidothymidine, dideoxycytidine, and dideoxyinosine in resting and activated peripheral blood mononuclear cells
-
Gao, W. Y., T. Shirasaka, D. G. Johns, S. Broder, and H. Mitsuya. 1993. Differential phosphorylation of azidothymidine, dideoxycytidine, and dideoxyinosine in resting and activated peripheral blood mononuclear cells. J. Clin. Investig. 91:2326-2333.
-
(1993)
J. Clin. Investig.
, vol.91
, pp. 2326-2333
-
-
Gao, W.Y.1
Shirasaka, T.2
Johns, D.G.3
Broder, S.4
Mitsuya, H.5
-
8
-
-
0025912292
-
Factors contributing to the inhibition of HIV reverse transcriptase by chain-terminating nucleotides in vitro and in vivo
-
Goody, R. S., B. Muller, and T. Restle. 1991. Factors contributing to the inhibition of HIV reverse transcriptase by chain-terminating nucleotides in vitro and in vivo. FEBS Lett. 291:1-5.
-
(1991)
FEBS Lett.
, vol.291
, pp. 1-5
-
-
Goody, R.S.1
Muller, B.2
Restle, T.3
-
9
-
-
0023642850
-
Inhibition of HIV-induced cytopathogenicity in vitro by 3′-azido-2′,3′-dideoxyguanosine
-
Hartmann, H., G. Hunsmann, and F. Eckstein. 1987. Inhibition of HIV-induced cytopathogenicity in vitro by 3′-azido-2′,3′- dideoxyguanosine. Lancet i:40-41.
-
(1987)
Lancet
, vol.1
, pp. 40-41
-
-
Hartmann, H.1
Hunsmann, G.2
Eckstein, F.3
-
10
-
-
0023713363
-
Synthesis and anti-HIV activity of different sugar-modified pyrimidine and purine nucleosides
-
Herdewijn, P., J. Balzarini, M. Baba, R. Pauwels, A. Van Aerschot, G. Janssen, and E. De Clercq. 1988. Synthesis and anti-HIV activity of different sugar-modified pyrimidine and purine nucleosides. J. Med. Chem. 31:2040-2048.
-
(1988)
J. Med. Chem.
, vol.31
, pp. 2040-2048
-
-
Herdewijn, P.1
Balzarini, J.2
Baba, M.3
Pauwels, R.4
Van Aerschot, A.5
Janssen, G.6
De Clercq, E.7
-
11
-
-
0001238747
-
Synthesis of 3′-azido-2′,3′-dideoxyribofuranosylpurines
-
Imazawa, M., and F. Eckstein. 1978. Synthesis of 3′-azido-2′, 3′-dideoxyribofuranosylpurines. J. Org. Chem. 43:3044-3048.
-
(1978)
J. Org. Chem.
, vol.43
, pp. 3044-3048
-
-
Imazawa, M.1
Eckstein, F.2
-
12
-
-
0028916224
-
Rapid quench kinetic analysis of polymerases, adenosine triphosphatases, and enzyme intermediates
-
Johnson, K. A. 1995. Rapid quench kinetic analysis of polymerases, adenosine triphosphatases, and enzyme intermediates. Methods Enzymol. 249:38-61.
-
(1995)
Methods Enzymol.
, vol.249
, pp. 38-61
-
-
Johnson, K.A.1
-
13
-
-
0034651781
-
Quantitation of dihydropyrimidine dehydrogenase expression by real-time reverse transcription polymerase chain reaction
-
Johnson, M. R., K. Wang, J. B. Smith, M. J. Heslin, and R. B. Diasio. 2000. Quantitation of dihydropyrimidine dehydrogenase expression by real-time reverse transcription polymerase chain reaction. Anal. Biochem. 278:175-184.
-
(2000)
Anal. Biochem.
, vol.278
, pp. 175-184
-
-
Johnson, M.R.1
Wang, K.2
Smith, J.B.3
Heslin, M.J.4
Diasio, R.B.5
-
14
-
-
0028789990
-
Purification and characterization of human immunodeficiency virus type 1 reverse transcriptase
-
Le Grice, S. F., C. E. Cameron, and S. J. Benkovic. 1995. Purification and characterization of human immunodeficiency virus type 1 reverse transcriptase. Methods Enzymol. 262:130-144.
-
(1995)
Methods Enzymol.
, vol.262
, pp. 130-144
-
-
Le Grice, S.F.1
Cameron, C.E.2
Benkovic, S.J.3
-
15
-
-
0025191211
-
Rapid purification of homodimer and heterodimer HIV-1 reverse transcriptase by metal chelate affinity chromatography
-
Le Grice, S. F., and F. Gruninger-Leitch. 1990. Rapid purification of homodimer and heterodimer HIV-1 reverse transcriptase by metal chelate affinity chromatography. Eur. J. Biochem. 187:307-314.
-
(1990)
Eur. J. Biochem.
, vol.187
, pp. 307-314
-
-
Le Grice, S.F.1
Gruninger-Leitch, F.2
-
16
-
-
58149509960
-
Novel resistance profile of the potent nucleoside analogue reverse transcriptase inhibitor 3′-azido-2′,3′-dideoxyguanosine
-
Meteer, J., D. Koontz, K. L. Rapp, M. Detorio, M. Ruckstuhl, R. F. Schinazi, and J. W. Mellors. 2008. Novel resistance profile of the potent nucleoside analogue reverse transcriptase inhibitor 3′-azido-2′, 3′-dideoxyguanosine. Antivir. Ther. 13:A5.
-
(2008)
Antivir. Ther.
, vol.13
-
-
Meteer, J.1
Koontz, D.2
Rapp, K.L.3
Detorio, M.4
Ruckstuhl, M.5
Schinazi, R.F.6
Mellors, J.W.7
-
17
-
-
14744267571
-
In vitro activity of structurally diverse nucleoside analogs against human immunodeficiency virus type 1 with the K65R mutation in reverse transcriptase
-
Parikh, U. M., D. L. Koontz, C. K. Chu, R. F. Schinazi, and J. W. Mellors. 2005. In vitro activity of structurally diverse nucleoside analogs against human immunodeficiency virus type 1 with the K65R mutation in reverse transcriptase. Antimicrob. Agents Chemother. 49:1139-1144.
-
(2005)
Antimicrob. Agents Chemother.
, vol.49
, pp. 1139-1144
-
-
Parikh, U.M.1
Koontz, D.L.2
Chu, C.K.3
Schinazi, R.F.4
Mellors, J.W.5
-
18
-
-
33745158157
-
A simple method of estimating fifty per cent endpoints
-
Reed, L. J., and H. Muench. 1938. A simple method of estimating fifty per cent endpoints. Am. J. Hyg. 27:493-497.
-
(1938)
Am. J. Hyg.
, vol.27
, pp. 493-497
-
-
Reed, L.J.1
Muench, H.2
-
19
-
-
0023757114
-
Combinations of isoprinosine and 3′-azido-3′-deoxythymidine in lymphocytes infected with human immunodeficiency virus type 1
-
Schinazi, R. F., D. L. Cannon, B. H. Arnold, and D. Martino-Saltzman. 1988. Combinations of isoprinosine and 3′-azido-3′-deoxythymidine in lymphocytes infected with human immunodeficiency virus type 1. Antimicrob. Agents Chemother. 32:1784-1787.
-
(1988)
Antimicrob. Agents Chemother.
, vol.32
, pp. 1784-1787
-
-
Schinazi, R.F.1
Cannon, D.L.2
Arnold, B.H.3
Martino-Saltzman, D.4
-
20
-
-
33747100570
-
Pharmacology of current and promising nucleosides for the treatment of human immunodeficiency viruses
-
Schinazi, R. F., B. I. Hernandez-Santiago, and S. J. Hurwitz. 2006. Pharmacology of current and promising nucleosides for the treatment of human immunodeficiency viruses. Antivir. Res. 71:322-334.
-
(2006)
Antivir. Res.
, vol.71
, pp. 322-334
-
-
Schinazi, R.F.1
Hernandez-Santiago, B.I.2
Hurwitz, S.J.3
-
21
-
-
0025362229
-
Activities of 3′-azido-3′- Deoxythymidine nucleotide dimers in primary lymphocytes infected with human immunodeficiency virus type 1
-
Schinazi, R. F., J. P. Sommadossi, V. Saalmann, D. L. Cannon, M. Y. Xie, G. C. Hart, G. A. Smith, and E. F. Hahn. 1990. Activities of 3′-azido-3′- deoxythymidine nucleotide dimers in primary lymphocytes infected with human immunodeficiency virus type 1. Antimicrob. Agents Chemother. 34:1061-1067.
-
(1990)
Antimicrob. Agents Chemother.
, vol.34
, pp. 1061-1067
-
-
Schinazi, R.F.1
Sommadossi, J.P.2
Saalmann, V.3
Cannon, D.L.4
Xie, M.Y.5
Hart, G.C.6
Smith, G.A.7
Hahn, E.F.8
-
22
-
-
3042762534
-
Nucleoside inhibitors of human immunodeficiency virus type 1 reverse transcriptase
-
Sharma, P. L., V. Nurpeisov, B. Hernandez-Santiago, T. Beltran, and R. F. Schinazi. 2004. Nucleoside inhibitors of human immunodeficiency virus type 1 reverse transcriptase. Curr. Top. Med. Chem. 4:895-919.
-
(2004)
Curr. Top. Med. Chem.
, vol.4
, pp. 895-919
-
-
Sharma, P.L.1
Nurpeisov, V.2
Hernandez-Santiago, B.3
Beltran, T.4
Schinazi, R.F.5
-
23
-
-
23844479950
-
The 3′-azido group is not the primary determinant of 3′-azido-3′-deoxythymidine (AZT) responsible for the excision phenotype of AZT-resistant HIV-1
-
Sluis-Cremer, N., D. Arion, U. Parikh, D. Koontz, R. F. Schinazi, J. W. Mellors, and M. A. Parniak. 2005. The 3′-azido group is not the primary determinant of 3′-azido-3′-deoxythymidine (AZT) responsible for the excision phenotype of AZT-resistant HIV-1. J. Biol. Chem. 280:29047-29052.
-
(2005)
J. Biol. Chem.
, vol.280
, pp. 29047-29052
-
-
Sluis-Cremer, N.1
Arion, D.2
Parikh, U.3
Koontz, D.4
Schinazi, R.F.5
Mellors, J.W.6
Parniak, M.A.7
-
24
-
-
0035174783
-
Phosphorylation of nucleoside analog antiretrovirals: A review for clinicians
-
Stein, D. S., and K. H. Moore. 2001. Phosphorylation of nucleoside analog antiretrovirals: a review for clinicians. Pharmacotherapy 21:11-34.
-
(2001)
Pharmacotherapy
, vol.21
, pp. 11-34
-
-
Stein, D.S.1
Moore, K.H.2
-
25
-
-
0036894245
-
Antiviral activities and cellular toxicities of modified 2′,3′-dideoxy-2′,3′-didehydrocytidine analogues
-
Stuyver, L. J., S. Lostia, M. Adams, J. S. Mathew, B. S. Pai, J. Grier, P. M. Tharnish, Y. Choi, Y. Chong, H. Choo, C. K. Chu, M. J. Otto, and R. F. Schinazi. 2002. Antiviral activities and cellular toxicities of modified 2′,3′-dideoxy-2′,3′-didehydrocytidine analogues. Antimicrob. Agents Chemother. 46:3854-3860.
-
(2002)
Antimicrob. Agents Chemother.
, vol.46
, pp. 3854-3860
-
-
Stuyver, L.J.1
Lostia, S.2
Adams, M.3
Mathew, J.S.4
Pai, B.S.5
Grier, J.6
Tharnish, P.M.7
Choi, Y.8
Chong, Y.9
Choo, H.10
Chu, C.K.11
Otto, M.J.12
Schinazi, R.F.13
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