References
- G. M. Blackburn, M. J. Gait, D. Loakes, D. M. Williams, Eds., in Nucleic Acids Chem. Biol. Royal Society Of Chemistry, Cambridge, 2007, pp. i–iv.
- Ferrero, M.; Gotor, V. Biocatalytic Selective Modifications of Conventional Nucleosides, Carbocyclic Nucleosides, and C-Nucleosides. Chem. Rev. 2000, 100, 4319–4347. DOI: 10.1021/cr000446y.
- Seley-Radtke, K. L.; Yates, M. K. The Evolution of Nucleoside Analogue Antivirals: A Review for Chemists and Non-Chemists. Part 1: Early Structural Modifications to the Nucleoside Scaffold. Antiviral Res. 2018, 154, 66–86. DOI: 10.1016/j.antiviral.2018.04.004.
- C. K. Chu, D. C. Baker, Eds., Nucleosides and Nucleotides as Antitumor and Antiviral Agents, Springer US, Boston, MA, 1993.
- Thirumaran, R.; Prendergast, G. C.; Gilman, P. B. in Cancer Immunother. Elsevier, 2007, pp. 101–116.
- Parker, W. B. Enzymology of Purine and Pyrimidine Antimetabolites Used in the Treatment of Cancer. Chem. Rev. 2009, 109, 2880–2893. DOI: 10.1021/cr900028p.
- Cohen, M. H.; Johnson, J. R.; Justice, R.; Pazdur, R. FDA Drug Approval Summary: nelarabine (Arranon) for the Treatment of T-Cell Lymphoblastic Leukemia/Lymphoma. Oncologist. 2008, 13, 709–714. DOI: 10.1634/theoncologist.2006-0017.
- McLaughlin, P.; Robertson, L. E.; Keating, M. J. Cancer Treat. Res. 1996, 3–14.
- Avendaño, C.; Menéndez, J. C. Medicinal Chemistry of Anticancer Drugs. Elsevier, 2008.
- Sampath, D.; Rao, V. A.; Plunkett, W. Mechanisms of Apoptosis Induction by Nucleoside Analogs. Oncogene 2003, 22, 9063–9074. DOI: 10.1038/sj.onc.1207229.
- Lamanna, N.; Weiss, M. Adv. Pharmacol. 2004, 107–125.
- Luo, Z.; Jiang, Z.; Jiang, W.; Lin, D. C-H Amination of Purine Derivatives via Radical Oxidative Coupling. J. Org. Chem. 2018, 83, 3710–3718. DOI: 10.1021/acs.joc.8b00066.
- 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. DOI: 10.1016/j.bmcl.2006.07.092.
- Senthilvelan, A.; Shanmugasundaram, M.; Kore, A. R. An Efficient Synthesis of 3'-O-Triazole Modified Guanosine-5'-O-Monophosphate Using Click Chemistry. Nucleosides Nucleotides Nucleic Acids 2019, 38, 418–427. DOI: 10.1080/15257770.2018.1554223.
- Tuncbilek, M.; Bilget Guven, E.; Onder, T.; Atalay, R. C. Synthesis of Novel 6-(4-Substituted Piperazine-1-yl)-9-(β-D-Ribofuranosyl)Purine Derivatives, Which Lead to Senescence-Induced Cell Death in Liver Cancer Cells. J. Med. Chem. 2012, 55, 3058–3065. DOI: 10.1021/jm3001532.
- Chen, X.; Kopecky, D. J.; Mihalic, J.; Jeffries, S.; Min, X.; Heath, J.; Deignan, J.; Lai, S.; Fu, Z.; Guimaraes, C.; et al. Structure-Guided Design, Synthesis, and Evaluation of Guanine-Derived Inhibitors of the eIF4E mRNA-Cap Interaction. J. Med. Chem. 2012, 55, 3837–3851., DOI: 10.1021/jm300037x.
- Gillerman, I.; Fischer, B. An Improved One-Pot Synthesis of Nucleoside 5'-Triphosphate Analogues. Nucleosides Nucleotides Nucleic Acids 2010, 29, 245–256. DOI: 10.1080/15257771003709569.
- Korboukh, I.; Hull-Ryde, E. A.; Rittiner, J. E.; Randhawa, A. S.; Coleman, J.; Fitzpatrick, B. J.; Setola, V.; Janzen, W. P.; Frye, S. V.; Zylka, M. J.; Jin, J. Orally Active Adenosine A(1) Receptor Agonists with Antinociceptive Effects in Mice. J. Med. Chem. 2012, 55, 6467–6477. DOI: 10.1021/jm3004834.
- Lee Bennett, L.; Smithers, D.; Rose, L. M.; Adamson, D. J.; Brockman, R. W. Mode of Action of 2-Amino-6-Chloro-1-Deazapurine. Biochem. Pharmacol. 1984, 33, 261–271. DOI: 10.1016/0006-2952(84)90484-2.
- Moreau, C.; Kirchberger, T.; Zhang, B.; Thomas, M. P.; Weber, K.; Guse, A. H.; Potter, B. V. L. Aberrant Cyclization Affords a C-6 Modified Cyclic Adenosine 5'-Diphosphoribose Analogue with Biological Activity in Jurkat T Cells. J. Med. Chem. 2012, 55, 1478–1489. DOI: 10.1021/jm201127y.
- Swarbrick, J. M.; Graeff, R.; Zhang, H.; Thomas, M. P.; Hao, Q.; Potter, B. V. L. Cyclic Adenosine 5'-Diphosphate Ribose Analogs without a "Southern" Ribose Inhibit ADP-Ribosyl Cyclase-Hydrolase CD38. J. Med. Chem. 2014, 57, 8517–8529. DOI: 10.1021/jm501037u.