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The nucleoside analog clitocine is a potent and efficacious readthrough agent
The nucleoside analog clitocine is a potent and efficacious readthrough agent
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The nucleoside analog clitocine is a potent and efficacious readthrough agent

Friesen, Westley J ; Trotta, Christopher R ; Tomizawa, Yuki ; Zhuo, Jin ; Johnson, Briana ; Sierra, Jairo ; Roy, Bijoyita ; Weetall, Marla ; Hedrick, Jean ; Sheedy, Josephine ; Takasugi, James ; Moon, Young-Choon ; Babu, Suresh ; Baiazitov, Ramil ; Leszyk, John D ; Davis, Thomas W ; Colacino, Joseph M ; Peltz, Stuart W ; Welch, Ellen M

RNA (Cambridge), 2017-04, Vol.23 (4), p.567-577 [Periódico revisado por pares]

United States: Cold Spring Harbor Laboratory Press

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2
Synthesis and evaluation of thymidine kinase 1-targeting carboranyl pyrimidine nucleoside analogs for boron neutron capture therapy of cancer
Synthesis and evaluation of thymidine kinase 1-targeting carboranyl pyrimidine nucleoside analogs for boron neutron capture therapy of cancer
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Synthesis and evaluation of thymidine kinase 1-targeting carboranyl pyrimidine nucleoside analogs for boron neutron capture therapy of cancer

Agarwal, Hitesh K. ; Khalil, Ahmed ; Ishita, Keisuke ; Yang, Weilian ; Nakkula, Robin J. ; Wu, Lai-Chu ; Ali, Tehane ; Tiwari, Rohit ; Byun, Youngjoo ; Barth, Rolf F. ; Tjarks, Werner

European journal of medicinal chemistry, 2015-07, Vol.100, p.197-209 [Periódico revisado por pares]

France: Elsevier Masson SAS

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3
Synthesis of 5-isoxazol-3-yl-pyrimidine nucleosides as potential antileishmanial agents
Synthesis of 5-isoxazol-3-yl-pyrimidine nucleosides as potential antileishmanial agents
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Synthesis of 5-isoxazol-3-yl-pyrimidine nucleosides as potential antileishmanial agents

Guo, Shenghai ; Wang, Jiliang ; Zhang, Xinying ; Cojean, Sandrine ; Loiseau, Philippe M. ; Fan, Xuesen

Bioorganic & medicinal chemistry letters, 2015-07, Vol.25 (13), p.2617-2620 [Periódico revisado por pares]

England: Elsevier Ltd

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4
Synthesis and characterization of 2′-C-Me branched C-nucleosides as HCV polymerase inhibitors
Synthesis and characterization of 2′-C-Me branched C-nucleosides as HCV polymerase inhibitors
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Synthesis and characterization of 2′-C-Me branched C-nucleosides as HCV polymerase inhibitors

Cho, Aesop ; Zhang, Lijun ; Xu, Jie ; Babusis, Darius ; Butler, Thomas ; Lee, Rick ; Saunders, Oliver L. ; Wang, Ting ; Parrish, Jay ; Perry, Jason ; Feng, Joy Y. ; Ray, Adrian S. ; Kim, Choung U.

Bioorganic & medicinal chemistry letters, 2012-06, Vol.22 (12), p.4127-4132 [Periódico revisado por pares]

Amsterdam: Elsevier Ltd

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5
Triazole pyrimidine nucleosides as inhibitors of Ribonuclease A. Synthesis, biochemical, and structural evaluation
Triazole pyrimidine nucleosides as inhibitors of Ribonuclease A. Synthesis, biochemical, and structural evaluation
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Triazole pyrimidine nucleosides as inhibitors of Ribonuclease A. Synthesis, biochemical, and structural evaluation

Parmenopoulou, Vanessa ; Chatzileontiadou, Demetra S.M. ; Manta, Stella ; Bougiatioti, Stamatina ; Maragozidis, Panagiotis ; Gkaragkouni, Dimitra-Niki ; Kaffesaki, Eleni ; Kantsadi, Anastassia L. ; Skamnaki, Vassiliki T. ; Zographos, Spyridon E. ; Zounpoulakis, Panagiotis ; Balatsos, Nikolaos A.A. ; Komiotis, Dimitris ; Leonidas, Demetres D.

Bioorganic & medicinal chemistry, 2012-12, Vol.20 (24), p.7184-7193 [Periódico revisado por pares]

Amsterdam: Elsevier Ltd

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6
Synthesis and Pharmacokinetics of Valopicitabine (NM283), an Efficient Prodrug of the Potent Anti-HCV Agent 2‘-C-Methylcytidine
Synthesis and Pharmacokinetics of Valopicitabine (NM283), an Efficient Prodrug of the Potent Anti-HCV Agent 2‘-C-Methylcytidine
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Synthesis and Pharmacokinetics of Valopicitabine (NM283), an Efficient Prodrug of the Potent Anti-HCV Agent 2‘-C-Methylcytidine

Pierra, Claire ; Amador, Agnès ; Benzaria, Samira ; Cretton-Scott, Erika ; D'Amours, Marc ; Mao, John ; Mathieu, Steven ; Moussa, Adel ; Bridges, Edward G ; Standring, David N ; Sommadossi, Jean-Pierre ; Storer, Richard ; Gosselin, Gilles

Journal of medicinal chemistry, 2006-11, Vol.49 (22), p.6614-6620 [Periódico revisado por pares]

Washington, DC: American Chemical Society

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7
Synthesis, cytostatic and anti-HIV evaluations of the new unsaturated acyclic C-5 pyrimidine nucleoside analogues
Synthesis, cytostatic and anti-HIV evaluations of the new unsaturated acyclic C-5 pyrimidine nucleoside analogues
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Synthesis, cytostatic and anti-HIV evaluations of the new unsaturated acyclic C-5 pyrimidine nucleoside analogues

Gazivoda, Tatjana ; Raić-Malić, Silvana ; Krištafor, Vedran ; Makuc, Damjan ; Plavec, Janez ; Bratulić, Siniša ; Kraljević-Pavelić, Sandra ; Pavelić, Krešimir ; Naesens, Lieve ; Andrei, Graciela ; Snoeck, Robert ; Balzarini, Jan ; Mintas, Mladen

Bioorganic & medicinal chemistry, 2008-05, Vol.16 (10), p.5624-5634 [Periódico revisado por pares]

Oxford: Elsevier Ltd

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8
The binding of C5-alkynyl and alkylfurano[2,3-d]pyrimidine glucopyranonucleosides to glycogen phosphorylase b: Synthesis, biochemical and biological assessment
The binding of C5-alkynyl and alkylfurano[2,3-d]pyrimidine glucopyranonucleosides to glycogen phosphorylase b: Synthesis, biochemical and biological assessment
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The binding of C5-alkynyl and alkylfurano[2,3-d]pyrimidine glucopyranonucleosides to glycogen phosphorylase b: Synthesis, biochemical and biological assessment

Kantsadi, A.L. ; Manta, S. ; Psarra, A.-M.G. ; Dimopoulou, A. ; Kiritsis, C. ; Parmenopoulou, V. ; Skamnaki, V.T. ; Zoumpoulakis, P. ; Zographos, S.E. ; Leonidas, D.D. ; Komiotis, D.

European journal of medicinal chemistry, 2012-08, Vol.54, p.740-749 [Periódico revisado por pares]

France: Elsevier Masson SAS

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9
Inhibition of Herpesvirus Replication by 5-Substituted 4′-Thiopyrimidine Nucleosides
Inhibition of Herpesvirus Replication by 5-Substituted 4′-Thiopyrimidine Nucleosides
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Inhibition of Herpesvirus Replication by 5-Substituted 4′-Thiopyrimidine Nucleosides

PRICHARD, Mark N ; QUENELLE, Debra C ; SECRIST, John A ; KERN, Earl R ; HARTLINE, Caroll B ; HARDEN, Emma A ; JEFFERSON, Geraldine ; FREDERICK, Samuel L ; DAILY, Shannon L ; WHITLEY, Richard J ; TIWARI, Kamal N ; MADDRY, Joseph A

Antimicrobial Agents and Chemotherapy, 2009-12, Vol.53 (12), p.5251-5258 [Periódico revisado por pares]

Washington, DC: American Society for Microbiology

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10
Adenosine Kinase Inhibitors. 6. Synthesis, Water Solubility, and Antinociceptive Activity of 5-Phenyl-7-(5-deoxy-β-d-ribofuranosyl)pyrrolo[2,3-d]pyrimidines Substituted at C4 with Glycinamides and Related Compounds
Adenosine Kinase Inhibitors. 6. Synthesis, Water Solubility, and Antinociceptive Activity of 5-Phenyl-7-(5-deoxy-β-d-ribofuranosyl)pyrrolo[2,3-d]pyrimidines Substituted at C4 with Glycinamides and Related Compounds
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Adenosine Kinase Inhibitors. 6. Synthesis, Water Solubility, and Antinociceptive Activity of 5-Phenyl-7-(5-deoxy-β-d-ribofuranosyl)pyrrolo[2,3-d]pyrimidines Substituted at C4 with Glycinamides and Related Compounds

Bookser, Brett C ; Ugarkar, Bheemarao G ; Matelich, Michael C ; Lemus, Robert H ; Allan, Matthew ; Tsuchiya, Megumi ; Nakane, Masami ; Nagahisa, Atsushi ; Wiesner, James B ; Erion, Mark D

Journal of medicinal chemistry, 2005-12, Vol.48 (24), p.7808-7820 [Periódico revisado por pares]

Washington, DC: American Chemical Society

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