Intracellular Trapping of CycloSal-Pronucleotides by Enzymatic Cleavage

By Jessen H. J.   Tonn V.   Meier C.  

Nucleosides, Nucleotides & Nucleic Acids, Vol. 26, Iss. 6-7, 2007-06 ,pp. : 827-830

Taylor & Francis Ltd

Access to resources Recommend Favorite

New Developments of the "Lock-in" Modified cycloSal-d4TMPs

By Vukadinovic-Tenter Dalibor   Balzarini Jan   Meier Chris  

Nucleosides, Nucleotides & Nucleic Acids, Vol. 26, Iss. 10-12, 2007-10 ,pp. : 1325-1328

Taylor & Francis Ltd

Access to resources Recommend Favorite

“Lock-in” Modified Cyclo Sal Nucleotides—The Second Generation of Cyclo Sal Prodrugs

By Vukadinović D.   Böge N.   Balzarini J.   Meier C.  

Nucleosides, Nucleotides & Nucleic Acids, Vol. 24, Iss. 5-7, 2005-04 ,pp. : 939-942

Taylor & Francis Ltd

Access to resources Recommend Favorite

Novel Cyclo sal Nucleotides with Reduced Inhibitory Potency Toward Human Butyrylcholinesterase

By Ducho C.   Jessel S.   Gisch N.   Balzarini J.   Meier C.  

Nucleosides, Nucleotides & Nucleic Acids, Vol. 24, Iss. 5-7, 2005-04 ,pp. : 519-522

Taylor & Francis Ltd

Access to resources Recommend Favorite

Synthesis of N 3 ,5′-Cyclo-4-(β-d-Ribofuranosyl)- vic -Triazolo[4,5- b ]Pyridin-5-One and Its 3′-Deoxysugar Analogue as Potential Anti-Hepatitis C Virus Agents

By Wang Peiyuan   Hollecker Laurent   Pankiewicz Krzysztof   Patterson Steven   Whitaker Tony   McBrayer Tamara   Tharnish Phillip   Stuyver Lieven   Schinazi Raymond   Otto Michael   Watanabe Kyoichi  

Nucleosides, Nucleotides & Nucleic Acids, Vol. 24, Iss. 5-7, 2005-04 ,pp. : 957-960

Taylor & Francis Ltd

Access to resources Recommend Favorite