-
1
-
-
0034492511
-
Therapeutic potential of purine analogue combinations in the treatment of lymphoid malignancies
-
Johnson, S. A.; Thomas, W. Therapeutic potential of purine analogue combinations in the treatment of lymphoid malignancies. Hematol. Oncol. 2000, 18, 141-153.
-
(2000)
Hematol. Oncol
, vol.18
, pp. 141-153
-
-
Johnson, S.A.1
Thomas, W.2
-
2
-
-
0034872409
-
Nucleoside analogues in the treatment of haematological malignancies
-
(b) Johnson, S. A. Nucleoside analogues in the treatment of haematological malignancies. Expert Opin. Pharmacother. 2001, 2, 929-943.
-
(2001)
Expert Opin. Pharmacother
, vol.2
, pp. 929-943
-
-
Johnson, S.A.1
-
3
-
-
4043137442
-
Purine nucleoside antimetabolites in development for the treatment of cancer
-
(c) Parker, W. B.; Secrist, J. A., III; Waud, W. R. Purine nucleoside antimetabolites in development for the treatment of cancer. Curr. Opin. Investig. Drugs 2004, 5, 592-596.
-
(2004)
Curr. Opin. Investig. Drugs
, vol.5
, pp. 592-596
-
-
Parker, W.B.1
Secrist III, J.A.2
Waud, W.R.3
-
4
-
-
0036636579
-
Nucleoside analogues and nucleobases in cancer treatment
-
(a) Galmarini, C. M.; Mackey, J. R.; Dumontet, C. Nucleoside analogues and nucleobases in cancer treatment. Lancet Oncol. 2002, 3, 415-242.
-
(2002)
Lancet Oncol
, vol.3
, pp. 415-242
-
-
Galmarini, C.M.1
Mackey, J.R.2
Dumontet, C.3
-
5
-
-
48949117194
-
Cytotoxic nucleoside analogues: Diffreent strategies to improve their clinical afficacy
-
(b) Galmarini, C. M.; Popowycz, F.; Joseph, B. Cytotoxic nucleoside analogues: diffreent strategies to improve their clinical afficacy. Curr. Med. Chem. 2008, 15, 1072-1082.
-
(2008)
Curr. Med. Chem
, vol.15
, pp. 1072-1082
-
-
Galmarini, C.M.1
Popowycz, F.2
Joseph, B.3
-
6
-
-
0021846445
-
Purine analogs and related nucleosides and nucleotides as antitumor agents
-
(a) Robins, R. K.; Revankar, G. R. Purine analogs and related nucleosides and nucleotides as antitumor agents. Med. Res. Rev. 1985, 5, 273-296.
-
(1985)
Med. Res. Rev
, vol.5
, pp. 273-296
-
-
Robins, R.K.1
Revankar, G.R.2
-
7
-
-
0025890427
-
Metabolism and action of purine nucleoside analogs
-
(b) Plunkett, W.; Saunders, P. P. Metabolism and action of purine nucleoside analogs. Pharmacol. Ther. 1991, 49, 239-268.
-
(1991)
Pharmacol. Ther
, vol.49
, pp. 239-268
-
-
Plunkett, W.1
Saunders, P.P.2
-
8
-
-
23844481419
-
Purine nucleoside analogues for the treatment of hematological malignancies: Pharmacology and clinical applications
-
(c) Robak, T.; Korycka, A.; Kasznicki, M.; Wrzesien-Kus, A.; Smolewski, P. Purine nucleoside analogues for the treatment of hematological malignancies: pharmacology and clinical applications. Curr. Cancer Drug Targets 2005, 5, 421-444.
-
(2005)
Curr. Cancer Drug Targets
, vol.5
, pp. 421-444
-
-
Robak, T.1
Korycka, A.2
Kasznicki, M.3
Wrzesien-Kus, A.4
Smolewski, P.5
-
9
-
-
0038268659
-
Drug resistance to cytotoxic nucleoside analogues
-
(d) Jordheim, L.; Galmarini, C. M.; Dumontet, C. Drug resistance to cytotoxic nucleoside analogues. Curr. Drug Targets 2003, 4, 443-460.
-
(2003)
Curr. Drug Targets
, vol.4
, pp. 443-460
-
-
Jordheim, L.1
Galmarini, C.M.2
Dumontet, C.3
-
10
-
-
33845515962
-
Recent developments to improve the efficacy of cytotoxic nucleoside analogues
-
(e) Jordheim, L. P.; Galmarini, C. M.; Dumontet, C. Recent developments to improve the efficacy of cytotoxic nucleoside analogues. Recent Pat. Anti-Cancer Drug Discovery 2006, 1, 163-170.
-
(2006)
Recent Pat. Anti-Cancer Drug Discovery
, vol.1
, pp. 163-170
-
-
Jordheim, L.P.1
Galmarini, C.M.2
Dumontet, C.3
-
11
-
-
67650685040
-
Enzymology of Purine and Pyrimidine Antimetabolites Used in the Treatment of Cancer
-
(f) Parker, W. B. Enzymology of Purine and Pyrimidine Antimetabolites Used in the Treatment of Cancer. Chem. Rev. 2009, 109, 2880-2893.
-
(2009)
Chem. Rev
, vol.109
, pp. 2880-2893
-
-
Parker, W.B.1
-
12
-
-
34548285424
-
Recent progress in the development of inhibitors of the hepatitis C virus RNA-dependent RNA polymerase
-
(a) Koch, U.; Narjes, F. Recent progress in the development of inhibitors of the hepatitis C virus RNA-dependent RNA polymerase. Curr. Top. Med. Chem. 2007, 7, 1302-1329.
-
(2007)
Curr. Top. Med. Chem
, vol.7
, pp. 1302-1329
-
-
Koch, U.1
Narjes, F.2
-
13
-
-
35748940578
-
Recent Progress on Novel HCV Inhibitors
-
(b) Zapf, C. W.; Bloom, J. D.; Levin, J. I. Chapter 18 Recent Progress on Novel HCV Inhibitors. Annu. Rep. Med. Chem. 2007, 42, 281-300.
-
(2007)
Annu. Rep. Med. Chem
, vol.42
, pp. 281-300
-
-
Zapf, C.W.1
Bloom, J.D.2
Levin, J.I.3
-
14
-
-
0034069172
-
Synthesis and Cytostatic Activity of Substituted 6-Phenylpurine Bases and Nucleosides: Application of the Suzuki-Miyaura Cross-Coupling Reactions of 6-Chloropurine Derivatives with Phenylboronic Acids
-
(a) Hocek, M.; Holý, A.; Votruba, I.; Dvořá ková, H. Synthesis and Cytostatic Activity of Substituted 6-Phenylpurine Bases and Nucleosides: Application of the Suzuki-Miyaura Cross-Coupling Reactions of 6-Chloropurine Derivatives with Phenylboronic Acids. J. Med. Chem. 2000, 43, 1817-1825.
-
(2000)
J. Med. Chem
, vol.43
, pp. 1817-1825
-
-
Hocek, M.1
Holý, A.2
Votruba, I.3
Dvořá ková, H.4
-
15
-
-
0035537024
-
Cytostatic 6-arylpurine nucleosides III. Synthesis and structure-activity relationship study in cytostatic activity of 6-aryl-, 6-hetaryl- and 6-benzylpurine ribonucleosides
-
(b) Hocek, M.; Holý, A.; Votruba, I.; Dvořá ková, H. Cytostatic 6-arylpurine nucleosides III. Synthesis and structure-activity relationship study in cytostatic activity of 6-aryl-, 6-hetaryl- and 6-benzylpurine ribonucleosides. Collect. Czech. Chem. Commun. 2001, 66, 483-499.
-
(2001)
Collect. Czech. Chem. Commun
, vol.66
, pp. 483-499
-
-
Hocek, M.1
Holý, A.2
Votruba, I.3
Dvořá ková, H.4
-
16
-
-
24744436849
-
Cytostatic 6-Arylpurine Nucleosides 6. SAR in Anti-HCV and Cytostatic Activity of Extended Series of 6-Hetarylpurine Ribonucleosides
-
Hocek, M.; Nauš, P.; Pohl, R.; Votruba, I.; Furman, P. A.; Tharnish, P. M.; Otto, M. J. Cytostatic 6-Arylpurine Nucleosides 6. SAR in Anti-HCV and Cytostatic Activity of Extended Series of 6-Hetarylpurine Ribonucleosides. J. Med. Chem. 2005, 48, 5869-5873.
-
(2005)
J. Med. Chem
, vol.48
, pp. 5869-5873
-
-
Hocek, M.1
Nauš, P.2
Pohl, R.3
Votruba, I.4
Furman, P.A.5
Tharnish, P.M.6
Otto, M.J.7
-
17
-
-
23044526799
-
Cytostatic 6-arylpurine nucleosides II. Synthesis of sugar-modified derivatives: 9-(2-deoxy-β-D-erythro-pentofuranosyl)-, 9-(5-deoxy-β-D- ribofuranosyl)-and 9-(2,3-dihydroxypropyl)-6-phenylpurines
-
Hocek, M.; Holý, A.; Votruba, I.; Dvořáková, H. Cytostatic 6-arylpurine nucleosides II. Synthesis of sugar-modified derivatives: 9-(2-deoxy-β-D-erythro-pentofuranosyl)-, 9-(5-deoxy-β-D- ribofuranosyl)-and 9-(2,3-dihydroxypropyl)-6-phenylpurines. Collect. Czech. Chem. Commun. 2000, 65, 1683-1697.
-
(2000)
Collect. Czech. Chem. Commun
, vol.65
, pp. 1683-1697
-
-
Hocek, M.1
Holý, A.2
Votruba, I.3
Dvořáková, H.4
-
18
-
-
33845587039
-
Cytostatic and Antiviral 6-Arylpurine Ribonucleosides, Part 8: Synthesis and Evaluation of 6-Substituted Purine 3′-Deoxyribonucleosides
-
Hocek, M.; Silhár, P.; Pohl, R. Cytostatic and Antiviral 6-Arylpurine Ribonucleosides, Part 8: Synthesis and Evaluation of 6-Substituted Purine 3′-Deoxyribonucleosides. Collect. Czech. Chem. Commun. 2006, 71, 1484-1496.
-
(2006)
Collect. Czech. Chem. Commun
, vol.71
, pp. 1484-1496
-
-
Hocek, M.1
Silhár, P.2
Pohl, R.3
-
19
-
-
12444326148
-
Synthesis of 9-(2-β-C-methyl-β-D-ribofuranosyl) -6-substituted purine derivatives as inhibitors of HCVRNA replication
-
Ding, Y.; Girardet, J.-L.; Hong, Z.; Lai, V. C. H.; An, H.; Koh, Y.-h.; Shaw, S. Z.; Zhong, W. Synthesis of 9-(2-β-C-methyl-β-D-ribofuranosyl) -6-substituted purine derivatives as inhibitors of HCVRNA replication. Bioorg. Med. Chem. Lett. 2005, 15, 709-713.
-
(2005)
Bioorg. Med. Chem. Lett
, vol.15
, pp. 709-713
-
-
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
-
20
-
-
0036284117
-
Synthesis and cytostatic activities of new 6-substituted purinylcarbonucleosides derived from indan
-
Fernandez, F.; Garcia-Mera, X.; Morales, M.; Rodriguez-Borges, J.; De Clercq, E. Synthesis and cytostatic activities of new 6-substituted purinylcarbonucleosides derived from indan. Synthesis 2002, 1084-1090.
-
(2002)
Synthesis
, pp. 1084-1090
-
-
Fernandez, F.1
Garcia-Mera, X.2
Morales, M.3
Rodriguez-Borges, J.4
De Clercq, E.5
-
21
-
-
33748316499
-
Cytostatic and Antiviral 6-Arylpurine Ribonucleosides, Part 7: Synthesis and Evaluation of 6-Substituted Purine L-Ribonucleosides
-
Hocek, M.; Šilhár, P.; Shih, I.; Mabery, E.; Mackman, R. Cytostatic and Antiviral 6-Arylpurine Ribonucleosides, Part 7: Synthesis and Evaluation of 6-Substituted Purine L-Ribonucleosides. Bioorg. Med. Chem. Lett. 2006, 16, 5290-5293.
-
(2006)
Bioorg. Med. Chem. Lett
, vol.16
, pp. 5290-5293
-
-
Hocek, M.1
Šilhár, P.2
Shih, I.3
Mabery, E.4
Mackman, R.5
-
22
-
-
0036011971
-
Cytostatic 6-arylpurine nucleosides IV. Synthesis of 2-substituted 6-phenylpurine ribonucleosides
-
Hocek, M.; Holý, A.; Dvořáková, H. Cytostatic 6-arylpurine nucleosides IV. Synthesis of 2-substituted 6-phenylpurine ribonucleosides. Collect. Czech. Chem. Commun. 2002, 67, 325-335.
-
(2002)
Collect. Czech. Chem. Commun
, vol.67
, pp. 325-335
-
-
Hocek, M.1
Holý, A.2
Dvořáková, H.3
-
23
-
-
0038044647
-
Cytostatic 6-arylpurine nucleosides V. Synthesis of 8-substituted 6-phenylpurine ribonucleosides
-
Hocek, M.; Hocková, D.; Štambaský, J. Cytostatic 6-arylpurine nucleosides V. Synthesis of 8-substituted 6-phenylpurine ribonucleosides. Collect. Czech. Chem. Commun. 2003, 68, 837-848.
-
(2003)
Collect. Czech. Chem. Commun
, vol.68
, pp. 837-848
-
-
Hocek, M.1
Hocková, D.2
Štambaský, J.3
-
24
-
-
53749094172
-
Synthesis of 6-(4,5-dihydrofuran-2-yl)- and 6-(tetrahydrofuran-2-yl)purine bases and nucleosides
-
Bambuch, V.; Pohl, R.; Hocek, M. Synthesis of 6-(4,5-dihydrofuran-2-yl)- and 6-(tetrahydrofuran-2-yl)purine bases and nucleosides. Eur. J. Org. Chem. 2008, 2783-2788.
-
(2008)
Eur. J. Org. Chem
, pp. 2783-2788
-
-
Bambuch, V.1
Pohl, R.2
Hocek, M.3
-
25
-
-
34548581964
-
Cytostatic evaluations of nucleoside analogs related to unnatural base pairs for a genetic expansion system
-
Kimoto, M.; Moriyama, K.; Yokoyama, S.; Hirao, I. Cytostatic evaluations of nucleoside analogs related to unnatural base pairs for a genetic expansion system. Bioorg. Med. Chem. Lett. 2007, 17, 5582-5585.
-
(2007)
Bioorg. Med. Chem. Lett
, vol.17
, pp. 5582-5585
-
-
Kimoto, M.1
Moriyama, K.2
Yokoyama, S.3
Hirao, I.4
-
26
-
-
52049118093
-
Cytostatic and Antiviral 6-Arylpurine Ribonucleosides IX: Synthesis and Evaluation of 6-Substituted 3-Deazapurine Ribonucleosides
-
Nauš, P.; Kuchař, M.; Hocek, M. Cytostatic and Antiviral 6-Arylpurine Ribonucleosides IX: Synthesis and Evaluation of 6-Substituted 3-Deazapurine Ribonucleosides. Collect. Czech. Chem. Commun. 2008, 73, 665-678.
-
(2008)
Collect. Czech. Chem. Commun
, vol.73
, pp. 665-678
-
-
Nauš, P.1
Kuchař, M.2
Hocek, M.3
-
27
-
-
0014237212
-
Analogs of 6-methyl-9β-D- ribofuranosylpurine
-
Montgomery, J. A.; Hewson, K. Analogs of 6-methyl-9β-D- ribofuranosylpurine. J. Med. Chem. 1968, 11, 48-52.
-
(1968)
J. Med. Chem
, vol.11
, pp. 48-52
-
-
Montgomery, J.A.1
Hewson, K.2
-
28
-
-
4644304167
-
Facile and Efficient Synthesis of 6-(Hydroxymethyl)purines
-
(a) Šilhár, P.; Pohl, R.; Votruba, I.; Hocek, M. Facile and Efficient Synthesis of 6-(Hydroxymethyl)purines. Org. Lett. 2004, 6, 3225-3228.
-
(2004)
Org. Lett
, vol.6
, pp. 3225-3228
-
-
Šilhár, P.1
Pohl, R.2
Votruba, I.3
Hocek, M.4
-
29
-
-
30344471252
-
Synthesis of 2-Substituted 6-(Hydroxymethyl)purine Bases and Nucleosides
-
(b) Šilhár, P.; Pohl, R.; Votruba, I.; Hocek, M. Synthesis of 2-Substituted 6-(Hydroxymethyl)purine Bases and Nucleosides. Collect. Czech. Chem. Commun. 2005, 70, 1669-1695.
-
(2005)
Collect. Czech. Chem. Commun
, vol.70
, pp. 1669-1695
-
-
Šilhár, P.1
Pohl, R.2
Votruba, I.3
Hocek, M.4
-
30
-
-
33744478243
-
Heterocyclic Analogs of Purine Nucleosides and Nucleotides
-
Townsend, L. B, Ed, Plenum Press: New York/ London
-
(a) Revankar G. R., Robins R. K. Heterocyclic Analogs of Purine Nucleosides and Nucleotides. In Chemistry of Nucleosides and Nucleotides; Townsend, L. B., Ed.; Plenum Press: New York/ London, 1988; Vol. 2, pp 200-246.
-
(1988)
Chemistry of Nucleosides and Nucleotides
, vol.2
, pp. 200-246
-
-
Revankar, G.R.1
Robins, R.K.2
-
31
-
-
33845303924
-
Antiviral Properties of Deazaadenine Nucleoside Derivatives
-
(b) Vittori, S.; Dal Ben, D.; Lambertucci, C.; Marucci, G.; Volpini, R.; Cristalli, G. Antiviral Properties of Deazaadenine Nucleoside Derivatives. Curr.Med. Chem. 2006, 13, 3529-3552.
-
(2006)
Curr.Med. Chem
, vol.13
, pp. 3529-3552
-
-
Vittori, S.1
Dal Ben, D.2
Lambertucci, C.3
Marucci, G.4
Volpini, R.5
Cristalli, G.6
-
32
-
-
78651053511
-
A New Antibiotic, Tubercidin
-
(a) Anzai, K.; Nakamura, G.; Suzuki, S. A New Antibiotic, Tubercidin. J. Antibiot. 1957, 10, 201-204.
-
(1957)
J. Antibiot
, vol.10
, pp. 201-204
-
-
Anzai, K.1
Nakamura, G.2
Suzuki, S.3
-
33
-
-
84855209589
-
Biological + Biochemical Properties of Analogue Antibiotic Tubercidin
-
(b) Acs, G.; Mori, M.; Reich, E. Biological + Biochemical Properties of Analogue Antibiotic Tubercidin. Proc. Nat. Acad. Sci. U.S.A. 1964, 52, 493-501.
-
(1964)
Proc. Nat. Acad. Sci. U.S.A
, vol.52
, pp. 493-501
-
-
Acs, G.1
Mori, M.2
Reich, E.3
-
34
-
-
0034721186
-
Adenosine Kinase Inhibitors. 1. Synthesis, Enzyme Inhibition, and Antiseizure Activity of 5-Iodotubercidin Analogues
-
(a) Ugarkar, B. G.; DaRe, J. M.; Kopcho, J. J.; Browne, C. E., III; Schanzer, J. M.; Wiesner, J. B.; Erion, M. D. Adenosine Kinase Inhibitors. 1. Synthesis, Enzyme Inhibition, and Antiseizure Activity of 5-Iodotubercidin Analogues. J. Med. Chem. 2000, 43, 2883-2893.
-
(2000)
J. Med. Chem
, vol.43
, pp. 2883-2893
-
-
Ugarkar, B.G.1
DaRe, J.M.2
Kopcho, J.J.3
Browne III, C.E.4
Schanzer, J.M.5
Wiesner, J.B.6
Erion, M.D.7
-
35
-
-
0034721142
-
Adenosine Kinase Iinhibitors. 2. Synthesis, Enzyme Inhibition, and Antiseizure Activity of Diaryltubercidin analogues
-
(b) Ugarkar, B. G.; Castellino, A. J.; DaRe, J. M.; Kopcho, J. J.; Wiesner, J. B.; Schanzer, J. M.; Erion, M. D. Adenosine Kinase Iinhibitors. 2. Synthesis, Enzyme Inhibition, and Antiseizure Activity of Diaryltubercidin analogues. J. Med. Chem. 2000, 43, 2894-2905.
-
(2000)
J. Med. Chem
, vol.43
, pp. 2894-2905
-
-
Ugarkar, B.G.1
Castellino, A.J.2
DaRe, J.M.3
Kopcho, J.J.4
Wiesner, J.B.5
Schanzer, J.M.6
Erion, M.D.7
-
36
-
-
46849115627
-
Structure-Activity Relationships of 7-Deaza-6-benzylthioinosine Analogues as Ligands of Toxoplasma gondii Adenosine Kinase
-
Kim, Y. A.; Sharon, A.; Chu, C. K.; Rais, R. H.; Al Safarjalani, O. N.; Naguib, F. N. M.; el Kouni, M. H. Structure-Activity Relationships of 7-Deaza-6-benzylthioinosine Analogues as Ligands of Toxoplasma gondii Adenosine Kinase. J. Med. Chem. 2008, 51, 3934-3945.
-
(2008)
J. Med. Chem
, vol.51
, pp. 3934-3945
-
-
Kim, Y.A.1
Sharon, A.2
Chu, C.K.3
Rais, R.H.4
Al Safarjalani, O.N.5
Naguib, F.N.M.6
el Kouni, M.H.7
-
37
-
-
4744364179
-
-
Eldrup, A. B.; Prhavc, M.; Brooks, J.; Bhat, B.; Prakash, T. P.; Song, Q. L.; 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.
-
(a) Eldrup, A. B.; Prhavc, M.; Brooks, J.; Bhat, B.; Prakash, T. P.; Song, Q. L.; 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.
-
-
-
-
38
-
-
11144355286
-
Structure - activity relationship of purine ribonucleosides for inhibition of hepatitis C virus RNA-dependent RNA polymerase
-
(b) Eldrup, A. B.; Allerson, C. R.; Bennett, C. F.; Bera, S.; Bhat, B.; Bhat, N.; Bosserman, M. R.; Brooks, J.; Burlein, C.; Carroll, 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
Carroll, 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..
-
39
-
-
4644257970
-
-
Olsen, D. B.; Eldrup, A. B.; Bartholomew, L.; Bhat, B.; Bosserman, M. R.; Ceccacci, A.; Colwell, L. F.; Fay, J. F.; Flores, O. A.; Getty, K. L.; Grobler, J. A.; LaFemina, R. L.; Markel, E. J.; Migliaccio, G.; Prhavc, M.; Stahlhut, M. W.; Tomassini, J. E.; MacCoss, M.; Hazuda, D. J.; Carroll, S. S. A 7-deazaadenosine analog is a potent and selective inhibitor of hepatitis C virus replication with excellent pharmacokinetic properties. Antimicrob. Agents Chemother. 2004, 48, 3944-3953.
-
(c) Olsen, D. B.; Eldrup, A. B.; Bartholomew, L.; Bhat, B.; Bosserman, M. R.; Ceccacci, A.; Colwell, L. F.; Fay, J. F.; Flores, O. A.; Getty, K. L.; Grobler, J. A.; LaFemina, R. L.; Markel, E. J.; Migliaccio, G.; Prhavc, M.; Stahlhut, M. W.; Tomassini, J. E.; MacCoss, M.; Hazuda, D. J.; Carroll, S. S. A 7-deazaadenosine analog is a potent and selective inhibitor of hepatitis C virus replication with excellent pharmacokinetic properties. Antimicrob. Agents Chemother. 2004, 48, 3944-3953.
-
-
-
-
40
-
-
0023584307
-
A Facile Synthesis of Tubercidin and Related 7-Deazapurine Nucleosides via the Stereospecific Sodium-Salt Glycosylation Procedure
-
Ramasamy, K.; Imamura, N.; Robins, R. K.; Revankar, G. R. A Facile Synthesis of Tubercidin and Related 7-Deazapurine Nucleosides via the Stereospecific Sodium-Salt Glycosylation Procedure. Tetrahedron Lett. 1987, 28, 5107-5110.
-
(1987)
Tetrahedron Lett
, vol.28
, pp. 5107-5110
-
-
Ramasamy, K.1
Imamura, N.2
Robins, R.K.3
Revankar, G.R.4
-
42
-
-
0001072616
-
Stereoselective Preparations of Ribofuranosyl Chlorides and Ribofuranosyl Acetates. Solvent Effects and Stereoselectivity in the Reaction of Ribofuranosyl Acetates with Trimethylallylsilane
-
Wilcox, C. S.; Otoski, R. M. Stereoselective Preparations of Ribofuranosyl Chlorides and Ribofuranosyl Acetates. Solvent Effects and Stereoselectivity in the Reaction of Ribofuranosyl Acetates with Trimethylallylsilane. Tetrahedron Lett. 1986, 27, 1011-1014.
-
(1986)
Tetrahedron Lett
, vol.27
, pp. 1011-1014
-
-
Wilcox, C.S.1
Otoski, R.M.2
-
43
-
-
0037242885
-
Syntheses of purines bearing carbon substituents in positions 2, 6 or 8 by metal- or organometal-mediated C-C bond-forming reactions
-
Reviews on cross-coupling reactions of purines: a
-
Reviews on cross-coupling reactions of purines: (a) Hocek, M. Syntheses of purines bearing carbon substituents in positions 2, 6 or 8 by metal- or organometal-mediated C-C bond-forming reactions. Eur. J. Org. Chem. 2003, 245-254.
-
(2003)
Eur. J. Org. Chem
, pp. 245-254
-
-
Hocek, M.1
-
44
-
-
0037944068
-
Palladium-assisted routes to nucleosides
-
(b) Agrofoglio, L. A.; Gillaizeau, I.; Saito, Y. Palladium-assisted routes to nucleosides. Chem. Rev. 2003, 103, 1875-1916.
-
(2003)
Chem. Rev
, vol.103
, pp. 1875-1916
-
-
Agrofoglio, L.A.1
Gillaizeau, I.2
Saito, Y.3
-
45
-
-
0041824571
-
Synthesis of Acyclic Nucleotide Analogues Derived from 6-Hetarylpurines via Cross-Coupling Reactions of 9-[2-(Diethoxyphosphonylmethoxy)ethyl]-6-iodopurine with Hetaryl Organometallic Reagents
-
(a) Hocek, M.; Masojídková, M.; Holý, A. Synthesis of Acyclic Nucleotide Analogues Derived from 6-Hetarylpurines via Cross-Coupling Reactions of 9-[2-(Diethoxyphosphonylmethoxy)ethyl]-6-iodopurine with Hetaryl Organometallic Reagents. Collect. Czech. Chem. Commun. 1997, 62, 136-146.
-
(1997)
Collect. Czech. Chem. Commun
, vol.62
, pp. 136-146
-
-
Hocek, M.1
Masojídková, M.2
Holý, A.3
-
46
-
-
0034340396
-
Synthesis of acyclic nucleotide analogues derived from 2-amino-6-C-substituted purines via cross-coupling reactions of 2-amino-9-{2-[(diisopropoxyphosphoryl)methoxy]ethyl} -6-halopurines with diverse organometallic reagents
-
(b) Česnek, M.; Hocek, M.; Holý, A. Synthesis of acyclic nucleotide analogues derived from 2-amino-6-C-substituted purines via cross-coupling reactions of 2-amino-9-{2-[(diisopropoxyphosphoryl)methoxy]ethyl} -6-halopurines with diverse organometallic reagents. Collect. Czech. Chem. Commun. 2000, 65, 1357-1373.
-
(2000)
Collect. Czech. Chem. Commun
, vol.65
, pp. 1357-1373
-
-
Česnek, M.1
Hocek, M.2
Holý, A.3
-
47
-
-
0042009118
-
Efficient One-Step Suzuki Arylation of Unprotected Halonucleosides, Using Water-Soluble palladium catalysts
-
(a) Western, E. C.; Daft, J. R.; Johnson, E. M.; Gannett, P. M.; Shaughnessy, K. H. Efficient One-Step Suzuki Arylation of Unprotected Halonucleosides, Using Water-Soluble palladium catalysts. J. Org. Chem. 2003, 68, 6767-6774.
-
(2003)
J. Org. Chem
, vol.68
, pp. 6767-6774
-
-
Western, E.C.1
Daft, J.R.2
Johnson, E.M.3
Gannett, P.M.4
Shaughnessy, K.H.5
-
48
-
-
33744821955
-
Cross-coupling Reactions of Unprotected Halopurine Bases, Nucleosides, Nucleotides and Nucleoside Triphosphates with 4-Boronophenylalanine in Water. Synthesis of (Purin-8-yl)- and (Purin-6-yl)-phenylalanines
-
(b) Čapek, P.; Pohl, R.; Hocek, M. Cross-coupling Reactions of Unprotected Halopurine Bases, Nucleosides, Nucleotides and Nucleoside Triphosphates with 4-Boronophenylalanine in Water. Synthesis of (Purin-8-yl)- and (Purin-6-yl)-phenylalanines. Org. Biomol. Chem. 2006, 4, 2278-2284.
-
(2006)
Org. Biomol. Chem
, vol.4
, pp. 2278-2284
-
-
Čapek, P.1
Pohl, R.2
Hocek, M.3
-
49
-
-
67149107342
-
Suzuki-Miyaura and Sonogashira coupling of 6-chloropurines and -nucleosides in water
-
(c) Pschierer, J.; Plenio, H. Suzuki-Miyaura and Sonogashira coupling of 6-chloropurines and -nucleosides in water. Org. Lett. 2009, 11, 2551-2554.
-
(2009)
Org. Lett
, vol.11
, pp. 2551-2554
-
-
Pschierer, J.1
Plenio, H.2
-
50
-
-
1542679244
-
Synthesis and Biological Activity of 5-Fluorotubercidin
-
Wang, X. J.; Seth, P. P.; Ranken, R.; Swayze, E. E.; Migawa, M. T. Synthesis and Biological Activity of 5-Fluorotubercidin. Nucleosides, Nucleotides Nucleic Acids 2004, 23, 161-170.
-
(2004)
Nucleosides, Nucleotides Nucleic Acids
, vol.23
, pp. 161-170
-
-
Wang, X.J.1
Seth, P.P.2
Ranken, R.3
Swayze, E.E.4
Migawa, M.T.5
-
51
-
-
34547730194
-
-
Seela, F.; Ming, X. 7-Functionalized 7-deazapurine β-D and β-L-ribonucleosides related to tubercidin and 7-deazainosine: glycosylation of pyrrolo[2,3-d]pyrimidines with 1-O-acetyl-2,3,5- tri-O-benzoyl-β-D or β-L-ribofuranose. Tetrahedron 2007, 63, 9850-9861.
-
Seela, F.; Ming, X. 7-Functionalized 7-deazapurine β-D and β-L-ribonucleosides related to tubercidin and 7-deazainosine: glycosylation of pyrrolo[2,3-d]pyrimidines with 1-O-acetyl-2,3,5- tri-O-benzoyl-β-D or β-L-ribofuranose. Tetrahedron 2007, 63, 9850-9861.
-
-
-
-
52
-
-
34347230544
-
Sulforhodamine B colorimetric assay for cytotoxicity screening
-
Vichai, V.; Kirtikara, K. Sulforhodamine B colorimetric assay for cytotoxicity screening. Nature Protoc. 2006, 1, 1112-1116.
-
(2006)
Nature Protoc
, vol.1
, pp. 1112-1116
-
-
Vichai, V.1
Kirtikara, K.2
-
53
-
-
0023792919
-
Evaluation of a Soluble Tetrazolium/Formazan Assay for Cell Growth and Drug Sensitivity in Culture Using Human and Other Tumor Cell Lines
-
Scudiero, D. A.; Shoemaker, R. H.; Paull, K. D.; Monks, A.; Tierney, S.; Nofziger, T. H.; Currens, M. J.; Seniff, D.; Boyd, M. R. Evaluation of a Soluble Tetrazolium/Formazan Assay for Cell Growth and Drug Sensitivity in Culture Using Human and Other Tumor Cell Lines. Cancer Res. 1988, 48, 4827-4833.
-
(1988)
Cancer Res
, vol.48
, pp. 4827-4833
-
-
Scudiero, D.A.1
Shoemaker, R.H.2
Paull, K.D.3
Monks, A.4
Tierney, S.5
Nofziger, T.H.6
Currens, M.J.7
Seniff, D.8
Boyd, M.R.9
-
54
-
-
33947430923
-
Simultaneous quantitation of the nucleotide analog adefovir, its phosphorylated anabolites and 2′-deoxyadenosine triphosphate by ion-pairing LC/MS/MS
-
Vela, J. E.; Olson, L. Y.; Huang, A.; Fridland, A.; Ray, A. S. Simultaneous quantitation of the nucleotide analog adefovir, its phosphorylated anabolites and 2′-deoxyadenosine triphosphate by ion-pairing LC/MS/MS. J. Chromatogr., B Anal. Technol. Biomed. Life Sci. 2007, 848, 335-343.
-
(2007)
J. Chromatogr., B Anal. Technol. Biomed. Life Sci
, vol.848
, pp. 335-343
-
-
Vela, J.E.1
Olson, L.Y.2
Huang, A.3
Fridland, A.4
Ray, A.S.5
-
55
-
-
35649007378
-
Synthesis and cytotoxic activity of various 5-[alkoxy-(4-nitro-phenyl]- methyl]-uracils in their racemic form
-
Spacilova, L.; Dzubak, P.; Hajduch, M.; Krupkova, S.; Hradil, P.; Hlavac, J. Synthesis and cytotoxic activity of various 5-[alkoxy-(4-nitro-phenyl]- methyl]-uracils in their racemic form. Biorg. Med. Chem. Lett. 2007, 17, 6647-6650.
-
(2007)
Biorg. Med. Chem. Lett
, vol.17
, pp. 6647-6650
-
-
Spacilova, L.1
Dzubak, P.2
Hajduch, M.3
Krupkova, S.4
Hradil, P.5
Hlavac, J.6
-
56
-
-
33750434863
-
4-Arylazo-3,5-diamino-1H-pyrazole CDK Inhibitors: SAR Study, Crystal Structure in Complex with CDK2, Selectivity, and Cellular Effects
-
Krystof, V.; Cankar, P.; Frysova, I.; Slouka, J.; Kontopidis, G.; Dzubak, P.; Hajduch, M.; Srovnal, J.; De Azavedo, W. F.; Orsag, M.; Paprskarova, M.; Rolcik, J.; Latr, A.; Fischer, P.; Strnad, M. 4-Arylazo-3,5-diamino-1H-pyrazole CDK Inhibitors: SAR Study, Crystal Structure in Complex with CDK2, Selectivity, and Cellular Effects. J. Med. Chem. 2006, 49, 6500-6509.
-
(2006)
J. Med. Chem
, vol.49
, pp. 6500-6509
-
-
Krystof, V.1
Cankar, P.2
Frysova, I.3
Slouka, J.4
Kontopidis, G.5
Dzubak, P.6
Hajduch, M.7
Srovnal, J.8
De Azavedo, W.F.9
Orsag, M.10
Paprskarova, M.11
Rolcik, J.12
Latr, A.13
Fischer, P.14
Strnad, M.15
|