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94 related items for PubMed ID: 18066914
1. 5-diacetoxymethyl-cycloSal-d4TMP - A prototype of enzymatically activated cycloSal-pronucleotides. Gisch N, Balzarini J, Meier C. Nucleosides Nucleotides Nucleic Acids; 2007; 26(6-7):861-4. PubMed ID: 18066914 [Abstract] [Full Text] [Related]
2. Enzymatically activated cycloSal-d4T-monophosphates: The third generation of cycloSal-pronucleotides. Gisch N, Balzarini J, Meier C. J Med Chem; 2007 Apr 05; 50(7):1658-67. PubMed ID: 17335187 [Abstract] [Full Text] [Related]
3. cycloSal-d4TMP pronucleotides structural variations, mechanistic insights and antiviral activity. Meiera C, Renzea J, Ducho C, Balzarini J. Curr Top Med Chem; 2002 Oct 05; 2(10):1111-21. PubMed ID: 12173970 [Abstract] [Full Text] [Related]
9. cycloSal-2',3'-dideoxy-2',3'-didehydrothymidine monophosphate (cycloSal-d4TMP): synthesis and antiviral evaluation of a new d4TMP delivery system. Meier C, Lorey M, De Clercq E, Balzarini J. J Med Chem; 1998 Apr 23; 41(9):1417-27. PubMed ID: 9554875 [Abstract] [Full Text] [Related]
10. 5-(1-Acetoxyvinyl)-cycloSaligenyl-2',3'-dideoxy-2',3'- didehydrothymidine monophosphates, a second type of new, enzymatically activated cycloSaligenyl pronucleotides. Gisch N, Pertenbreiter F, Balzarini J, Meier C. J Med Chem; 2008 Dec 25; 51(24):8115-23. PubMed ID: 19053827 [Abstract] [Full Text] [Related]
11. Cyclosal-pronucleotides--development of first and second generation chemical trojan horses for antiviral chemotherapy. Meier C, Meerbach A, Balzarini J. Front Biosci; 2004 Jan 01; 9():873-90. PubMed ID: 14766416 [Abstract] [Full Text] [Related]
12. Stereoselective synthesis and antiviral activity of methyl-substituted cycloSal-pronucleotides. Rios Morales EH, Balzarini J, Meier C. J Med Chem; 2012 Aug 23; 55(16):7245-52. PubMed ID: 22827702 [Abstract] [Full Text] [Related]
14. Doubly loaded cycloSaligenyl-pronucleotides - 5,5'-Bis-(cycloSaligenyl-2',3'-dideoxy-2',3'-didehydrothymidine monophosphates). Gisch N, Balzarini J, Meier C. J Med Chem; 2009 Jun 11; 52(11):3464-73. PubMed ID: 19438207 [Abstract] [Full Text] [Related]
15. "Lock-in" modified cyclosal nucleotides--the second generation of cyclosal prodrugs. Vukadinović D, Böge NP, Balzarini J, Meier C. Nucleosides Nucleotides Nucleic Acids; 2005 Jun 11; 24(5-7):939-42. PubMed ID: 16248067 [Abstract] [Full Text] [Related]
16. Comparative study of bis(benzyl)phosphate triesters of 2',3'-dideoxy-2',3'-didehydrothymidine (d4T) and cyclosal-d4TMP--hydrolysis, mechanistic insights and anti-HIV activity. Meier C, Muus U, Renze J, Naesens L, De Clercq E, Balzarini J. Antivir Chem Chemother; 2002 Mar 11; 13(2):101-14. PubMed ID: 12238528 [Abstract] [Full Text] [Related]
18. Application of the cycloSal-prodrug approach for improving the biological potential of phosphorylated biomolecules. Meier C, Balzarini J. Antiviral Res; 2006 Sep 11; 71(2-3):282-92. PubMed ID: 16735066 [Abstract] [Full Text] [Related]
19. Characterization of the activation pathway of phosphoramidate triester prodrugs of stavudine and zidovudine. Saboulard D, Naesens L, Cahard D, Salgado A, Pathirana R, Velazquez S, McGuigan C, De Clercq E, Balzarini J. Mol Pharmacol; 1999 Oct 11; 56(4):693-704. PubMed ID: 10496951 [Abstract] [Full Text] [Related]
20. Benzyl-functionalized cycloSal-d4T monophosphates. Renze J, Plath M, Ducho C, Balzarini J, De Clercq E, Meier C. Nucleosides Nucleotides Nucleic Acids; 2001 Oct 11; 20(4-7):931-4. PubMed ID: 11563147 [Abstract] [Full Text] [Related] Page: [Next] [New Search]