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Journal Abstract Search
144 related items for PubMed ID: 18066777
1. New developments of the "lock-in" modified cycloSal-d4TMPs. Vukadinović-Tenter D, Balzarini J, Meier C. Nucleosides Nucleotides Nucleic Acids; 2007; 26(10-12):1325-8. PubMed ID: 18066777 [Abstract] [Full Text] [Related]
2. Bis-cycloSal-d4T-monophosphates: drugs that deliver two molecules of bioactive nucleotides. Ducho C, Görbig U, Jessel S, Gisch N, Balzarini J, Meier C. J Med Chem; 2007 Mar 22; 50(6):1335-46. PubMed ID: 17328534 [Abstract] [Full Text] [Related]
3. 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]
4. "Lock-in" modified cyclosal nucleotides--the second generation of cyclosal prodrugs. Vukadinović D, Böge NP, Balzarini J, Meier C. Nucleosides Nucleotides Nucleic Acids; 2005 Aug 23; 24(5-7):939-42. PubMed ID: 16248067 [Abstract] [Full Text] [Related]
5. 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]
6. 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]
7. 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]
8. 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]
9. Application of the cycloSal-prodrug approach for improving the biological potential of phosphorylated biomolecules. Meier C, Balzarini J. Antiviral Res; 2006 Sep 25; 71(2-3):282-92. PubMed ID: 16735066 [Abstract] [Full Text] [Related]
10. Diastereoselective synthesis of aryloxy phosphoramidate prodrugs of 3'-deoxy-2',3'-didehydrothymidine monophosphate. Roman CA, Balzarini J, Meier C. J Med Chem; 2010 Nov 11; 53(21):7675-81. PubMed ID: 20945915 [Abstract] [Full Text] [Related]
11. cycloSal-Pronucleotides of 2',3'-dideoxyadenosine and 2', 3'-dideoxy-2',3'-didehydroadenosine: synthesis and antiviral evaluation of a highly efficient nucleotide delivery system. Meier C, Knispel T, De Clercq E, Balzarini J. J Med Chem; 1999 May 06; 42(9):1604-14. PubMed ID: 10229629 [Abstract] [Full Text] [Related]
12. 5-diacetoxymethyl-cycloSal-d4TMP - A prototype of enzymatically activated cycloSal-pronucleotides. Gisch N, Balzarini J, Meier C. Nucleosides Nucleotides Nucleic Acids; 2007 May 06; 26(6-7):861-4. PubMed ID: 18066914 [Abstract] [Full Text] [Related]
13. d4TMP delivery from 7-substituted cycloSal-d4TMPs. Meier C, Renze JT, Balzarini J, De Clercq E. Nucleosides Nucleotides Nucleic Acids; 2003 May 06; 22(5-8):825-7. PubMed ID: 14565288 [Abstract] [Full Text] [Related]
14. 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 06; 13(2):101-14. PubMed ID: 12238528 [Abstract] [Full Text] [Related]
15. Synthesis, stability, and biological evaluation of 1,3-dihydrobenzo[c]furan analogue of d4T and its SATE pronucleotide. Len C, Selouane A, Postel D, Villa P, Aubertin AM, Egron D, Gosselin G, Périgaud C. Nucleosides Nucleotides Nucleic Acids; 2003 Mar 06; 22(5-8):943-5. PubMed ID: 14565317 [Abstract] [Full Text] [Related]
16. Deoxyribonucleoside 2'- or 3'-mixed disulfides: prodrugs to target ribonucleotide reductase and/or to inhibit HIV reverse transcription. Roy B, Chambert S, Lepoivre M, Aubertin AM, Balzarini J, Décout JL. J Med Chem; 2003 Jun 19; 46(13):2565-8. PubMed ID: 12801219 [Abstract] [Full Text] [Related]
17. Design and synthesis of lipophilic phosphoramidate d4T-MP prodrugs expressing high potency against HIV in cell culture: structural determinants for in vitro activity and QSAR. Siddiqui AQ, McGuigan C, Ballatore C, Zuccotto F, Gilbert IH, De Clercq E, Balzarini J. J Med Chem; 1999 Oct 07; 42(20):4122-8. PubMed ID: 10514282 [Abstract] [Full Text] [Related]