-
1
-
-
0022996630
-
Phosphorylation of 3′-azido-3′-deoxythymidine and selective interaction of the 5′-triphosphate with human immunodeficiency virus reverse transcriptase
-
Furman, P.A.; Fyfe, J.A.; St. Clair, M.H.; Weinhold, K.; Rideout, J.L.; Freeman, G.A.; Nusinoff-Lehrman, S.; Bolognesi, D.P.; Broder, S.; Mitsuya, H.; Barry, D.W. Phosphorylation of 3′-azido-3′-deoxythymidine and selective interaction of the 5′-triphosphate with human immunodeficiency virus reverse transcriptase. Proc. Natl. Acad. Sci. U. S. A. 1986, 83, 8333-8337.
-
(1986)
Proc. Natl. Acad. Sci. U. S. A.
, vol.83
, pp. 8333-8337
-
-
Furman, P.A.1
Fyfe, J.A.2
St. Clair, M.H.3
Weinhold, K.4
Rideout, J.L.5
Freeman, G.A.6
Nusinoff-Lehrman, S.7
Bolognesi, D.P.8
Broder, S.9
Mitsuya, H.10
Barry, D.W.11
-
2
-
-
0023837875
-
The phase I studies of 2′,3′-dideoxycytidine in human immunodeficiency virus infection as single agent and alternating with zidovudine (AZT)
-
Yarchoan, R.; Thomas, R.V.; Allain, J.-P.; McAtee, N.; Dubinsky, R.; Mitsuya, H.; Lawley, T.J.; Safai, B.; Myers, C.E.; Perno, C.F.; Klecker, R.W.; Wills, R.J.; Fischl, M.A.; McNeely, M.C.; Pluda, J.M.; Leuther, M.; Collins, J.M.; Broder, S. The phase I studies of 2′,3′-dideoxycytidine in human immunodeficiency virus infection as single agent and alternating with zidovudine (AZT). Lancet 1988, 1, 76-81.
-
(1988)
Lancet
, vol.1
, pp. 76-81
-
-
Yarchoan, R.1
Thomas, R.V.2
Allain, J.-P.3
McAtee, N.4
Dubinsky, R.5
Mitsuya, H.6
Lawley, T.J.7
Safai, B.8
Myers, C.E.9
Perno, C.F.10
Klecker, R.W.11
Wills, R.J.12
Fischl, M.A.13
McNeely, M.C.14
Pluda, J.M.15
Leuther, M.16
Collins, J.M.17
Broder, S.18
-
3
-
-
0024349612
-
In vivo activity against HIV and favorable toxicity profile of 2′,3′-dideoxyinosine
-
Yarchoan, R.; Mitsuya, H.; Thomas, R.V.; Pluda, J.M.; Hartman, N.R.; Perno, C.F.; Marczyk, K.S.; Allain, J.-P.; Johns, D.G.; Broder, S. In vivo activity against HIV and favorable toxicity profile of 2′,3′- dideoxyinosine. Science 1989, 245, 412-415.
-
(1989)
Science
, vol.245
, pp. 412-415
-
-
Yarchoan, R.1
Mitsuya, H.2
Thomas, R.V.3
Pluda, J.M.4
Hartman, N.R.5
Perno, C.F.6
Marczyk, K.S.7
Allain, J.-P.8
Johns, D.G.9
Broder, S.10
-
4
-
-
0023196616
-
Potent and selective in vitro activity of 3′-deoxy thymidine-2′-ene (3′-deoxy-2′,3′dideoxydehydrothymidine) against human immunodeficiency virus
-
Lin, T.-S.; Schinazi, R.F.; Prusoff, W.H. Potent and selective in vitro activity of 3′-deoxy thymidine-2′-ene (3′-deoxy-2′, 3′dideoxydehydrothymidine) against human immunodeficiency virus. Biochem. Pharmacol. 1987, 36, 2713-2718.
-
(1987)
Biochem. Pharmacol.
, vol.36
, pp. 2713-2718
-
-
Lin, T.-S.1
Schinazi, R.F.2
Prusoff, W.H.3
-
5
-
-
7344264636
-
Activities of the four optical isomers of 2′,3′-dideoxy- 3′-thiacytidine (BCH-189) against human immunodeficiency virus type I in human lymphocytes
-
Schinazi, R.F.; Chu, C.K.; Peck, A.; McMillan, A.; Mathis, R.; Cannon, D.; Jeong, L.S.; Beach, J.W.; Choi, W.B.; Yeola, S.; Liotta, D.C. Activities of the four optical isomers of 2′,3′-dideoxy-3′-thiacytidine (BCH-189) against human immunodeficiency virus type I in human lymphocytes. Antimicrob. Agents Chemother. 1992, 36, 672-676.
-
(1992)
Antimicrob. Agents Chemother.
, vol.36
, pp. 672-676
-
-
Schinazi, R.F.1
Chu, C.K.2
Peck, A.3
McMillan, A.4
Mathis, R.5
Cannon, D.6
Jeong, L.S.7
Beach, J.W.8
Choi, W.B.9
Yeola, S.10
Liotta, D.C.11
-
6
-
-
0030782524
-
Synthesis, in vitro biological evaluation and oral bioavailability of 9-[2-[(phosphonomethoxy)propyl] adenine (PMPA) prodrugs
-
Arimilli, M.N.; Kim, C.U.; Dougherty, J.; Mulato, A.; Oliyai, R.; Shaw, J.P.; Cundy, K.C.; Bischofberger, N. Synthesis, in vitro biological evaluation and oral bioavailability of 9-[2-[(phosphonomethoxy)propyl] adenine (PMPA) prodrugs. Antivir. Chem. Chemother. 1997, 8, 557-564.
-
(1997)
Antivir. Chem. Chemother.
, vol.8
, pp. 557-564
-
-
Arimilli, M.N.1
Kim, C.U.2
Dougherty, J.3
Mulato, A.4
Oliyai, R.5
Shaw, J.P.6
Cundy, K.C.7
Bischofberger, N.8
-
7
-
-
0030982931
-
A novel carbocyclic nucleoside analog with potent, selective anti-human immunodeficiency virus activity
-
Daluge, S.M.; Good, S.S.; Faletto, M.B.; Miller, W.H.; St Clair, M.H.; Boone, L.R.; Tisdale, M.; Parry, N.R.; Reardon, J.E.; Dornsife, R.E.; Averett, D.R.; Krenitsky, T.A. A novel carbocyclic nucleoside analog with potent, selective anti-human immunodeficiency virus activity. Antimicrob. Agents Chemother. 1997, 41, 1082-1093.
-
(1997)
Antimicrob. Agents Chemother.
, vol.41
, pp. 1082-1093
-
-
Daluge, S.M.1
Good, S.S.2
Faletto, M.B.3
Miller, W.H.4
St. Clair, M.H.5
Boone, L.R.6
Tisdale, M.7
Parry, N.R.8
Reardon, J.E.9
Dornsife, R.E.10
Averett, D.R.11
Krenitsky, T.A.12
-
8
-
-
0028148674
-
Effects of antiviral nucleoside analogs on human DNA polymerase and mitochondrial DNA synthesis
-
Martin, J.L.; Brown, C.E.; Mattews-Davis, N.; Reardon, J.E. Effects of antiviral nucleoside analogs on human DNA polymerase and mitochondrial DNA synthesis. Antimicrob. Agents Chemother. 1994, 38, 2743-2749.
-
(1994)
Antimicrob. Agents Chemother.
, vol.38
, pp. 2743-2749
-
-
Martin, J.L.1
Brown, C.E.2
Mattews-Davis, N.3
Reardon, J.E.4
-
9
-
-
0000226527
-
Mitochondrial toxicity of antiviral nucleoside analogues
-
Parker, W.B.; Cheng, Y.C. Mitochondrial toxicity of antiviral nucleoside analogues. J. NIH Res. 1994, 6, 57-61.
-
(1994)
J. NIH Res.
, vol.6
, pp. 57-61
-
-
Parker, W.B.1
Cheng, Y.C.2
-
11
-
-
0028940084
-
Emergence of human-immunodeficiency-virus type-1 variants with resistance to multiple dideoxynucleosides in patients receiving therapy with dideoxynucleosides
-
Shirasaka, T.; Kavlick, M.F.; Ueno, T.; Gao, W.Y.; Kojima, E.; Alcaide, M.L.; Chokekijchai, S.; Roy, B.M.; Arnol, E.; Yarchoan, R.; Mitsuya, H. Emergence of human-immunodeficiency-virus type-1 variants with resistance to multiple dideoxynucleosides in patients receiving therapy with dideoxynucleosides. Proc. Natl. Acad. Sci. U.S.A. 1995, 92, 2398-2402.
-
(1995)
Proc. Natl. Acad. Sci. U.S.A.
, vol.92
, pp. 2398-2402
-
-
Shirasaka, T.1
Kavlick, M.F.2
Ueno, T.3
Gao, W.Y.4
Kojima, E.5
Alcaide, M.L.6
Chokekijchai, S.7
Roy, B.M.8
Arnol, E.9
Yarchoan, R.10
Mitsuya, H.11
-
12
-
-
0021939927
-
Synthesis and antiviral activity of the carbocyclic analogues of (E)-5-(2-halovinyl)-2′-deoxyuridines and (E)-5-(2-halovinyl)-2′- deoxycytidines
-
Herdewijn, P.; De Clercq, E.; Balzarini, J.; Vanderhaeghe, H. Synthesis and antiviral activity of the carbocyclic analogues of (E)-5-(2-halovinyl)- 2′-deoxyuridines and (E)-5-(2-halovinyl)-2′-deoxycytidines. J. Med. Chem. 1985, 28, 550-555.
-
(1985)
J. Med. Chem.
, vol.28
, pp. 550-555
-
-
Herdewijn, P.1
De Clercq, E.2
Balzarini, J.3
Vanderhaeghe, H.4
-
13
-
-
0026567167
-
Synthesis of chiral carbocyclic nucleosides
-
Borthwick, A.D.; Biggadike, K. Synthesis of chiral carbocyclic nucleosides. Tetrahedron 1992, 48, 571-623.
-
(1992)
Tetrahedron
, vol.48
, pp. 571-623
-
-
Borthwick, A.D.1
Biggadike, K.2
-
14
-
-
0027931662
-
Synthesis of carbocyclic nucleosides
-
Agrofoglio, L.; Suhas, E.; Farese, A.; Condom, R.; Challand, S.; Earl, R.A.; Guedj, R. Synthesis of carbocyclic nucleosides. Tetrahedron 1994, 50, 10611-10670.
-
(1994)
Tetrahedron
, vol.50
, pp. 10611-10670
-
-
Agrofoglio, L.1
Suhas, E.2
Farese, A.3
Condom, R.4
Challand, S.5
Earl, R.A.6
Guedj, R.7
-
15
-
-
0035991863
-
Efficacies of entecavir against lamivudine-resistance hepatitis B virus replication and recombinant polymerase in vitro
-
Levine, S.; Hernandez, D.; Yamanaka, G.; Zhang, S.; Rose, R.; Weinheimer, S.; Colonno, R.J. Efficacies of entecavir against lamivudine-resistance hepatitis B virus replication and recombinant polymerase in vitro. Antimicrob. Agents Chemother. 2002, 46, 2525-2532.
-
(2002)
Antimicrob. Agents Chemother.
, vol.46
, pp. 2525-2532
-
-
Levine, S.1
Hernandez, D.2
Yamanaka, G.3
Zhang, S.4
Rose, R.5
Weinheimer, S.6
Colonno, R.J.7
-
16
-
-
0018800321
-
The mechanism of action of S-adenosylhomocysteinase
-
Palmer, J.L.; Abeles, R.H. The mechanism of action of S-adenosylhomocysteinase. J. Biol. Chem. 1979, 254, 1217-1226.
-
(1979)
J. Biol. Chem.
, vol.254
, pp. 1217-1226
-
-
Palmer, J.L.1
Abeles, R.H.2
-
17
-
-
0020284631
-
Pharmacological and biochemical aspects of S-adenosylhomocysteine and S-adenosylhomocysteine hydrolase
-
Ueland, P.M. Pharmacological and biochemical aspects of S-adenosylhomocysteine and S-adenosylhomocysteine hydrolase. Pharmacol. Rev. 1982, 34, 223-253.
-
(1982)
Pharmacol. Rev.
, vol.34
, pp. 223-253
-
-
Ueland, P.M.1
-
18
-
-
0346333446
-
Synthesis of 4′α-C phenyl-branched carbocyclic nucleoside using ring-closing metathesis
-
Hong, J.H.; Ko, O.H. Synthesis of 4′α-C phenyl-branched carbocyclic nucleoside using ring-closing metathesis. Bull. Korean Chem. Soc. 2003, 24, 1289-1292.
-
(2003)
Bull. Korean Chem. Soc.
, vol.24
, pp. 1289-1292
-
-
Hong, J.H.1
Ko, O.H.2
-
19
-
-
0034670585
-
An efficient, general asymmetric synthesis of carbocyclic nucleosides: Application of an asymmetric aldol/ring-closing metathesis strategy
-
Crimmins, M.T.; King, B.W.; Zuercher, W.J.; Choy, A.L. An efficient, general asymmetric synthesis of carbocyclic nucleosides: application of an asymmetric aldol/ring-closing metathesis strategy. J. Org. Chem. 2000, 65, 8499-8509.
-
(2000)
J. Org. Chem.
, vol.65
, pp. 8499-8509
-
-
Crimmins, M.T.1
King, B.W.2
Zuercher, W.J.3
Choy, A.L.4
|