-
1
-
-
0034452004
-
Purine nucleoside phosphorylases: Properties, functions, and clinical aspects
-
Bzowska, A.; Kulikowska, E.; Shugar, D. Purine nucleoside phosphorylases: properties, functions, and clinical aspects. Pharmacol. Ther. 2000, 88, 349-425.
-
(2000)
Pharmacol. Ther.
, vol.88
, pp. 349-425
-
-
Bzowska, A.1
Kulikowska, E.2
Shugar, D.3
-
2
-
-
0025218997
-
Acid-stable 2′-fluoro purine dideoxynucleosides as active agents against HIV
-
Marquez, V.E.; Tseng, C.K.-H.; Mitsura, H.; Aoik, S.; Kelley, J.A.; Ford, H., Jr.; Roth, J.S.; Broder, S.; Johns, D.G.; Driscoll, J.S. Acid-stable 2′-fluoro purine dideoxynucleosides as active agents against HIV. J. Med. Chem. 1990, 33 (3), 978-985.
-
(1990)
J. Med. Chem.
, vol.33
, Issue.3
, pp. 978-985
-
-
Marquez, V.E.1
Tseng, C.K.-H.2
Mitsura, H.3
Aoik, S.4
Kelley, J.A.5
Ford Jr., H.6
Roth, J.S.7
Broder, S.8
Johns, D.G.9
Driscoll, J.S.10
-
3
-
-
0002053132
-
Purine nucleoside phosphorylase and 5-methylthioadenosine phosphorylase: Targets of chemotherapy
-
Sartorelli, A.C., Lazo, J.S., Bertino, J.R., Eds.; Academic: New York
-
Parks, R.E., Jr.; Stoeckler, J.D.; Cambor, C.; Savarese, T.M.; Crabtree, G.W.; Chu, S.-H. Purine nucleoside phosphorylase and 5-methylthioadenosine phosphorylase: targets of chemotherapy. In Molecular Actions and Targets for Cancer Chemotherapeutic Agents; Sartorelli, A.C., Lazo, J.S., Bertino, J.R., Eds.; Academic: New York, 1981; 229-252.
-
(1981)
Molecular Actions and Targets for Cancer Chemotherapeutic Agents
, pp. 229-252
-
-
Parks Jr., R.E.1
Stoeckler, J.D.2
Cambor, C.3
Savarese, T.M.4
Crabtree, G.W.5
Chu, S.-H.6
-
4
-
-
0021259707
-
9-Deazaadenosine - A new potent antitumor agent
-
Chu, M.Y.; Zuckerman, L.B.; Sato, S.; Crabtree, G.W.; Bogden, A.E.; Lim, M.-I.; Klein, R.S. 9-Deazaadenosine - a new potent antitumor agent. Biochem. Pharmacol. 1984, 33 (8), 1229-1234.
-
(1984)
Biochem. Pharmacol.
, vol.33
, Issue.8
, pp. 1229-1234
-
-
Chu, M.Y.1
Zuckerman, L.B.2
Sato, S.3
Crabtree, G.W.4
Bogden, A.E.5
Lim, M.-I.6
Klein, R.S.7
-
5
-
-
0020520051
-
9-Deazaadenosine. Cytocidal activity and effects on nucleic acids and protein synthesis in human colon carcinoma cells in culture
-
Glazer, R.I.; Hartman, K.D.; Knode, M.C. 9-Deazaadenosine. Cytocidal activity and effects on nucleic acids and protein synthesis in human colon carcinoma cells in culture. Mol. Pharmacol. 1983, 24, 309-315.
-
(1983)
Mol. Pharmacol.
, vol.24
, pp. 309-315
-
-
Glazer, R.I.1
Hartman, K.D.2
Knode, M.C.3
-
6
-
-
0021367736
-
Biological action of inosine analogs in Leishmania and Trypanosoma spp
-
Marr, J.J.; Berens, R.L.; Cohn, N.K.; Nelson, D.J.; Klein, R.S. Biological action of inosine analogs in Leishmania and Trypanosoma spp. Antimicrob. Agents Chemother. 1984, 25 (2), 292-295.
-
(1984)
Antimicrob. Agents Chemother.
, vol.25
, Issue.2
, pp. 292-295
-
-
Marr, J.J.1
Berens, R.L.2
Cohn, N.K.3
Nelson, D.J.4
Klein, R.S.5
-
7
-
-
0021929879
-
Inosine analogs as chemotherapeutic agents for African trypanosomes: Metabolism in trypanosomes and efficacy in tissue culture
-
Fish, W.R.; Marr, J.J.; Berens, R.L.; Looker, D.L.; Nelson, D.J.; LaFon, S.W.; Balber, A.E. Inosine analogs as chemotherapeutic agents for African trypanosomes: metabolism in trypanosomes and efficacy in tissue culture. Antimicrob. Agents Chemother. 1985, 27 (1), 33-36.
-
(1985)
Antimicrob. Agents Chemother.
, vol.27
, Issue.1
, pp. 33-36
-
-
Fish, W.R.1
Marr, J.J.2
Berens, R.L.3
Looker, D.L.4
Nelson, D.J.5
LaFon, S.W.6
Balber, A.E.7
-
8
-
-
0023791782
-
Potent and selective activity of a new carbocyclic nucleoside analog (Carbovir: NSC 614846) against human immunodeficiency virus in vitro
-
Vince, R.; Hua, M.; Brownell, J.; Daluge, S.; Lee, F.; Shannon, W.M.; Lavelle, G.C.; Quails, J.; Weislow, O.S.; Kiser, R.; Canonico, P.G.; Schultz, R.H.; Narayanan, V.L.; Mayo, J.G.; Shoemaker, R.H.; Boyd, M.R. Potent and selective activity of a new carbocyclic nucleoside analog (Carbovir: NSC 614846) against human immunodeficiency virus in vitro. Biochem. Biophys. Res. Commun. 1988, 156 (2), 1046-1053.
-
(1988)
Biochem. Biophys. Res. Commun.
, vol.156
, Issue.2
, pp. 1046-1053
-
-
Vince, R.1
Hua, M.2
Brownell, J.3
Daluge, S.4
Lee, F.5
Shannon, W.M.6
Lavelle, G.C.7
Quails, J.8
Weislow, O.S.9
Kiser, R.10
Canonico, P.G.11
Schultz, R.H.12
Narayanan, V.L.13
Mayo, J.G.14
Shoemaker, R.H.15
Boyd, M.R.16
-
9
-
-
0030982931
-
1592U89, 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. 1592U89, A novel carbocyclic nucleoside analog with potent, selective anti-human immunodeficiency virus activity. Antimicrob. Agents Chemother. 1997, 41 (5), 1082-1093.
-
(1997)
Antimicrob. Agents Chemother.
, vol.41
, Issue.5
, 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
-
10
-
-
0030903443
-
Unique intracellular activation of the potent anti-human immunodeficiency virus agent 1592U89
-
Faletto, M.B.; Miller, W.H.; Garvey, E.P.; St. Clair, M.H.; Daluge, S.M.; Good, S.S. Unique intracellular activation of the potent anti-human immunodeficiency virus agent 1592U89. Antimicrob. Agents Chemother. 1997, 41 (5), 1099-1107.
-
(1997)
Antimicrob. Agents Chemother.
, vol.41
, Issue.5
, pp. 1099-1107
-
-
Faletto, M.B.1
Miller, W.H.2
Garvey, E.P.3
St. Clair, M.H.4
Daluge, S.M.5
Good, S.S.6
-
11
-
-
0024554252
-
General syntheses of 2′,3′-dideoxynucleosides and 2′,3′-didehydro-2′,3′-dideoxynucleosides
-
Chu, C.K.; Bhadti, V.S.; Doboszewski, B.; Gu, Z.P.; Kosugi, Y.; Pullaiah, K.C.; Van Roey, P. General syntheses of 2′,3′-dideoxynucleosides and 2′,3′-didehydro-2′,3′-dideoxynucleosides. J. Org. Chem. 1989, 54 (9), 2217-2225.
-
(1989)
J. Org. Chem.
, vol.54
, Issue.9
, pp. 2217-2225
-
-
Chu, C.K.1
Bhadti, V.S.2
Doboszewski, B.3
Gu, Z.P.4
Kosugi, Y.5
Pullaiah, K.C.6
Van Roey, P.7
-
12
-
-
0024418643
-
Preparation of 1-(2,3-dideoxy-β-D-glycero-pent-2-enofuranosyl) thymine (d4T) and 2′,3′-dideoxyadenosine (ddA): General methods for the synthesis of 2′,3′-olefinic and 2′,3′-dideoxy nucleoside analogues active against HIV
-
Mansuri, M.M.; Starrett, J.E., Jr.; Wos, J.A.; Tortolani, D.R.; Brodfuehrer, P.R.; Howell, H.G.; Martin, J.C. Preparation of 1-(2,3-dideoxy-β-D-glycero-pent-2-enofuranosyl)thymine (d4T) and 2′,3′-dideoxyadenosine (ddA): general methods for the synthesis of 2′,3′-olefinic and 2′,3′-dideoxy nucleoside analogues active against HIV. J. Org. Chem. 1989, 54 (20), 4780-4785.
-
(1989)
J. Org. Chem.
, vol.54
, Issue.20
, pp. 4780-4785
-
-
Mansuri, M.M.1
Starrett Jr., J.E.2
Wos, J.A.3
Tortolani, D.R.4
Brodfuehrer, P.R.5
Howell, H.G.6
Martin, J.C.7
-
13
-
-
0029943676
-
Nucleosides synthesis of 2′,3′-dideoxy- and 2′,3′-didehydro-2′,3′-dideoxyisoguanosine as potential antiretroviral agents
-
Chen, C.-S.; Chem, J.-W. Nucleosides VIII: synthesis of 2′,3′-dideoxy- and 2′,3′-didehydro-2′,3′- dideoxyisoguanosine as potential antiretroviral agents. Nucleosides Nucleotides 1996, 15 (7&8), 1253-1261.
-
(1996)
Nucleosides Nucleotides
, vol.15
, Issue.7-8
, pp. 1253-1261
-
-
Chen, C.-S.1
Chem VIII, J.-W.2
-
14
-
-
0002851963
-
Reactions of 2-acyloxyisobutyryl halides with nucleosides. IV. A facile synthesis of 2′,3′-unsaturated nucleosides using chromous acetate
-
Jain, T.C.; Jenkins, I.D.; Russell, A.F.; Verheyden, J.P.H.; Moffatt, J.G. Reactions of 2-acyloxyisobutyryl halides with nucleosides. IV. A facile synthesis of 2′,3′-unsaturated nucleosides using chromous acetate. J. Org. Chem. 1974, 39 (1), 30-38.
-
(1974)
J. Org. Chem.
, vol.39
, Issue.1
, pp. 30-38
-
-
Jain, T.C.1
Jenkins, I.D.2
Russell, A.F.3
Verheyden, J.P.H.4
Moffatt, J.G.5
-
15
-
-
0026507714
-
A new synthesis of 2′,3′-dideoxyinosine
-
Bhat, V.; Stocker, E.; Ugarkar, B.G. A new synthesis of 2′,3′-dideoxyinosine. Synth. Commun. 1992, 22 (10), 1481-1486.
-
(1992)
Synth. Commun.
, vol.22
, Issue.10
, pp. 1481-1486
-
-
Bhat, V.1
Stocker, E.2
Ugarkar, B.G.3
-
16
-
-
13144285694
-
Synthesis and biological evaluation of 2- and 7-substituted 9-deazaadenosine analogues
-
Liu, M.-C.; Luo, M.-Z.; Mozdziesz, D.E.; Sartorelli, A.C. Synthesis and biological evaluation of 2- and 7-substituted 9-deazaadenosine analogues. Nucleosides Nucleotides Nucleic Acids 2005, 24 (1), 45-62.
-
(2005)
Nucleosides Nucleotides Nucleic Acids
, vol.24
, Issue.1
, pp. 45-62
-
-
Liu, M.-C.1
Luo, M.-Z.2
Mozdziesz, D.E.3
Sartorelli, A.C.4
-
17
-
-
0026561408
-
Aryl phosphate derivatives of AZT retain activity against HIV1 in cell lines which are resistant to the action of AZT
-
McGuigan, C.; Pathirana, R.N.; Mahmood, N.; Devine, K.G.; Hay, A.J. Aryl phosphate derivatives of AZT retain activity against HIV1 in cell lines which are resistant to the action of AZT. Antiviral Res. 1992, 17, 311-321.
-
(1992)
Antiviral Res.
, vol.17
, pp. 311-321
-
-
McGuigan, C.1
Pathirana, R.N.2
Mahmood, N.3
Devine, K.G.4
Hay, A.J.5
-
18
-
-
0037144688
-
Nucleic acid related compounds. 116. Nonaqueous diazotization of aminopurine nucleosides. Mechanistic considerations and efficient procedures with tert-butyl nitrite or sodium nitrite
-
Francom, P.; Janeba, Z.; Shibuya, S.; Robins, M.J. Nucleic acid related compounds. 116. Nonaqueous diazotization of aminopurine nucleosides. Mechanistic considerations and efficient procedures with tert-butyl nitrite or sodium nitrite. J. Org. Chem. 2002, 67 (19), 6788-6796.
-
(2002)
J. Org. Chem.
, vol.67
, Issue.19
, pp. 6788-6796
-
-
Francom, P.1
Janeba, Z.2
Shibuya, S.3
Robins, M.J.4
-
19
-
-
0033532945
-
Theoretical studies of DNA base deamination. 2. Ab initio study of DNA base diazonium ions and of their linear, unimolecular dediazonation paths
-
Glaser, R.; Rayat, S.; Lewis, M.; Son, M.-S.; Meyer, S. Theoretical studies of DNA base deamination. 2. Ab initio study of DNA base diazonium ions and of their linear, unimolecular dediazonation paths. J. Am. Chem. Soc. 1999, 121 (26), 6108-6119.
-
(1999)
J. Am. Chem. Soc.
, vol.121
, Issue.26
, pp. 6108-6119
-
-
Glaser, R.1
Rayat, S.2
Lewis, M.3
Son, M.-S.4
Meyer, S.5
-
20
-
-
0028212546
-
Synthesis and biological evaluation of 2′,3′-dideoxy-L- pyrimicline nucleosides as potential antiviral agents against human immunodeficiency virus (HIV) and hepatitis B virus
-
Lin, T.-S.; Luo, M.-Z.; Liu, M.-C.; Pai, S.B.; Dutschman, G.E.; Cheng, Y.-C. Synthesis and biological evaluation of 2′,3′-dideoxy-L- pyrimicline nucleosides as potential antiviral agents against human immunodeficiency virus (HIV) and hepatitis B virus. J. Med. Chem. 1994, 37 (6), 798-803.
-
(1994)
J. Med. Chem.
, vol.37
, Issue.6
, pp. 798-803
-
-
Lin, T.-S.1
Luo, M.-Z.2
Liu, M.-C.3
Pai, S.B.4
Dutschman, G.E.5
Cheng, Y.-C.6
-
21
-
-
0028943957
-
Incorporation of 2′-deoxy-9-deazaguanosine and 2′-deoxy-7- deaza-6-thioguanosine into G-rich oligodeoxyribonucleotides
-
Rao, T.S.; Lewis, A.F.; Hill, T.S.; Revankar, G.R. Incorporation of 2′-deoxy-9-deazaguanosine and 2′-deoxy-7-deaza-6-thioguanosine into G-rich oligodeoxyribonucleotides. Nucleosides Nucleotides 1995, 14 (1&2), 1-12.
-
(1995)
Nucleosides Nucleotides
, vol.14
, Issue.1-2
, pp. 1-12
-
-
Rao, T.S.1
Lewis, A.F.2
Hill, T.S.3
Revankar, G.R.4
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