Result Number | Material Type | Add to My Shelf Action | Record Details and Options |
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1 |
Material Type: Artigo
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Selective prebiotic formation of RNA pyrimidine and DNA purine nucleosidesXu, Jianfeng ; Chmela, Václav ; Green, Nicholas J ; Russell, David A ; Janicki, Mikołaj J ; Góra, Robert W ; Szabla, Rafał ; Bond, Andrew D ; Sutherland, John DNature (London), 2020-06, Vol.582 (7810), p.60-66 [Periódico revisado por pares]England: Nature Publishing GroupTexto completo disponível |
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2 |
Material Type: Artigo
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Synthesis of Pyrazolo[4′,3′:5,6]pyrano[2,3-d]pyrimidine Derivatives for Antiviral EvaluationShamroukh, Ahmed H. ; Zaki, Magdi E. A. ; Morsy, Eman M. H. ; Abdel-Motti, Faiza M. ; Abdel-Megeid, Farouk M. E.Archiv der Pharmazie (Weinheim), 2007-05, Vol.340 (5), p.236-243 [Periódico revisado por pares]Weinheim: WILEY-VCH VerlagTexto completo disponível |
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3 |
Material Type: Artigo
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Synthesis of Purine and 7-Deazapurine Nucleoside Analogues of 6-N-(4-Nitrobenzyl)adenosine; Inhibition of Nucleoside Transport and Proliferation of Cancer CellsRayala, Ramanjaneyulu ; Theard, Patricia ; Ortiz, Heysell ; Yao, Sylvia ; Young, James D. ; Balzarini, Jan ; Robins, Morris J. ; Wnuk, Stanislaw F.ChemMedChem, 2014-09, Vol.9 (9), p.2186-2192 [Periódico revisado por pares]Weinheim: WILEY-VCH VerlagTexto completo disponível |
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4 |
Material Type: Artigo
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An efficient and facile methodology for bromination of pyrimidine and purine nucleosides with sodium monobromoisocyanurate (SMBI)Maity, Jyotirmoy ; Stromberg, RogerMolecules (Basel, Switzerland), 2013-10, Vol.18 (10), p.12740-12750 [Periódico revisado por pares]Switzerland: MDPI AGTexto completo disponível |
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5 |
Material Type: Artigo
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Carboxymethylsulfonylated Ribopyrimidines: Rational Design of Ribonuclease A Inhibitors Employing Chemical LogicDatta, Dhrubajyoti ; Dasgupta, Swagata ; Pathak, TanmayaChemMedChem, 2016-03, Vol.11 (6), p.620-628 [Periódico revisado por pares]Germany: Blackwell Publishing LtdTexto completo disponível |
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6 |
Material Type: Artigo
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Synthesis of 1′-C-Cyano Pyrimidine Nucleosides and Characterization as HCV Polymerase InhibitorsKirschberg, Thorsten A. ; Mish, Michael ; Squires, Neil H. ; Zonte, Sebastian ; Aktoudianakis, Evangelos ; Metobo, Sammy ; Butler, Thomas ; Ju, Xie ; Cho, Aesop ; Ray, Adrian S. ; Kim, Choung U.Nucleosides, nucleotides & nucleic acids, 2015-11, Vol.34 (11), p.763-785 [Periódico revisado por pares]United States: Taylor & FrancisTexto completo disponível |
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7 |
Material Type: Artigo
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Synthesis and Anti-HCV Activity of 4-Methoxy-7H-Pyrrolo[2,3-d] Pyrimidine Carbocyclic NucleosidesThiyagarajan, Anandarajan ; Toyama, Masaaki ; Baba, Masanori ; Sharon, Ashoke ; Bal, ChandralataNucleosides, nucleotides & nucleic acids, 2016-06, Vol.35 (6), p.305-314 [Periódico revisado por pares]United States: Taylor & FrancisTexto completo disponível |
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8 |
Material Type: Artigo
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Disaccharide Pyrimidine Nucleosides and Their Derivatives: A Novel Group of Cell-Penetrating Inhibitors of Poly(ADP-Ribose) Polymerase 1Efremova, Anna S. ; Zakharenko, Alexandra L. ; Shram, Stanislav I. ; Kulikova, Irina V. ; Drenichev, Mikhail S. ; Sukhanova, Maria V. ; Khodyreva, Svetlana N. ; Myasoedov, Nikolay F. ; Lavrik, Olga I. ; Mikhailov, Sergey N.Nucleosides, nucleotides & nucleic acids, 2013-09, Vol.32 (9), p.510-528 [Periódico revisado por pares]United States: Taylor & Francis GroupTexto completo disponível |
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9 |
Material Type: Artigo
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Regioselective Synthesis of Pyrazolo[3,4-D]Pyrimidine Based Carbocyclic Nucleosides as Possible Antiviral AgentKasula, Mohan ; Samunuri, Ramakrishnamraju ; Chakravarty, Harapriya ; Bal, Chandralata ; Baba, Masanori ; Jha, Ashok Kumar ; Sharon, AshokeNucleosides, nucleotides & nucleic acids, 2016-01, Vol.35 (1), p.43-52 [Periódico revisado por pares]United States: Taylor & FrancisTexto completo disponível |
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10 |
Material Type: Artigo
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Synthesis and Antiviral Screening of Some Thieno[2,3-d]Pyrimidine NucleosidesRashad, A. E. ; Ali, M. A.Nucleosides, nucleotides & nucleic acids, 2006-01, Vol.25 (1), p.17-28 [Periódico revisado por pares]United States: Taylor & Francis GroupTexto completo disponível |