149 related articles for article (PubMed ID: 20924954)
1. Design and synthesis of dually branched 5'-norcarbocyclic adenosine phosphonodiester analogue as a new anti-HIV prodrug.
Oh CH; Liu LJ; Hong JH
Nucleosides Nucleotides Nucleic Acids; 2010 Oct; 29(10):721-33. PubMed ID: 20924954
[TBL] [Abstract][Full Text] [Related]
2. Synthesis of novel 6'-spirocyclopropyl-5'-norcarbocyclic adenosine phosphonic Acid analogues as potent anti-hiv agents.
Liu LJ; Kim E; Hong JH
Nucleosides Nucleotides Nucleic Acids; 2011 Oct; 30(10):784-97. PubMed ID: 21967289
[TBL] [Abstract][Full Text] [Related]
3. Synthesis of novel 4'-cyclopropyl-5'-norcarbocyclic adenosine phosphonic acid analogues.
Shen GH; Hong JH
Nucleosides Nucleotides Nucleic Acids; 2010 Nov; 29(11):905-19. PubMed ID: 21128176
[TBL] [Abstract][Full Text] [Related]
4. Synthesis and anti-HIV evaluation of new acyclic phosphonate nucleotide analogues and their bis(SATE) derivatives.
Li H; Hong JH
Nucleosides Nucleotides Nucleic Acids; 2010 Aug; 29(8):581-90. PubMed ID: 20661812
[TBL] [Abstract][Full Text] [Related]
5. Design and synthesis of carbocyclic versions of furanoid nucleoside phosphonic Acid analogues as potential anti-hiv agents.
Kim E; Shen GH; Hong JH
Nucleosides Nucleotides Nucleic Acids; 2011 Oct; 30(10):798-813. PubMed ID: 21967290
[TBL] [Abstract][Full Text] [Related]
6. Design, synthesis, and anti-HIV activity of 4'-modified carbocyclic nucleoside phosphonate reverse transcriptase inhibitors.
Boojamra CG; Parrish JP; Sperandio D; Gao Y; Petrakovsky OV; Lee SK; Markevitch DY; Vela JE; Laflamme G; Chen JM; Ray AS; Barron AC; Sparacino ML; Desai MC; Kim CU; Cihlar T; Mackman RL
Bioorg Med Chem; 2009 Feb; 17(4):1739-46. PubMed ID: 19179082
[TBL] [Abstract][Full Text] [Related]
7. Design and synthesis of novel SATE derivatives of acyclic isocytosine and 9-deazaadenine C-nucleosides.
Liu LJ; Hong JH
Nucleosides Nucleotides Nucleic Acids; 2010 Mar; 29(3):257-66. PubMed ID: 20408056
[TBL] [Abstract][Full Text] [Related]
8. A novel and efficient one-pot synthesis of symmetrical diamide (bis-amidate) prodrugs of acyclic nucleoside phosphonates and evaluation of their biological activities.
Jansa P; Baszczyňski O; Dračínský M; Votruba I; Zídek Z; Bahador G; Stepan G; Cihlar T; Mackman R; Holý A; Janeba Z
Eur J Med Chem; 2011 Sep; 46(9):3748-54. PubMed ID: 21664011
[TBL] [Abstract][Full Text] [Related]
9. Design and synthesis of novel threosyl-5'- deoxyphosphonic acid purine analogues as potent anti-HIV agents.
Liu LJ; Kim E; Hong JH
Nucleosides Nucleotides Nucleic Acids; 2012 May; 31(5):411-22. PubMed ID: 22497256
[TBL] [Abstract][Full Text] [Related]
10. Self-assembled drug delivery systems. Part 4. In vitro/in vivo studies of the self-assemblies of cholesteryl-phosphonyl zidovudine.
Jin Y; Xing L; Tian Y; Li M; Gao C; Du L; Dong J; Chen H
Int J Pharm; 2009 Oct; 381(1):40-8. PubMed ID: 19646518
[TBL] [Abstract][Full Text] [Related]
11. Investigations of nucleoside H-phosphonamidate in the design of nucleotide prodrug.
Egron D; Imbach JL; Gosselin G; Aubertin AM; Périgaud C
Nucleosides Nucleotides Nucleic Acids; 2003; 22(5-8):895-7. PubMed ID: 14565305
[TBL] [Abstract][Full Text] [Related]
12. Synthesis, anti-HIV activity, and resistance profiles of ribose modified nucleoside phosphonates.
Mackman RL; Boojamra CG; Prasad V; Zhang L; Lin KY; Petrakovsky O; Babusis D; Chen J; Douglas J; Grant D; Hui HC; Kim CU; Markevitch DY; Vela J; Ray A; Cihlar T
Bioorg Med Chem Lett; 2007 Dec; 17(24):6785-9. PubMed ID: 18029175
[TBL] [Abstract][Full Text] [Related]
13. Prodrugs of HIV protease inhibitors-saquinavir, indinavir and nelfinavir-derived from diglycerides or amino acids: synthesis, stability and anti-HIV activity.
Gaucher B; Rouquayrol M; Roche D; Greiner J; Aubertin AM; Vierling P
Org Biomol Chem; 2004 Feb; 2(3):345-57. PubMed ID: 14747863
[TBL] [Abstract][Full Text] [Related]
14. Synthesis and anti-HIV activity of cyclic pyrimidine phosphonomethoxy nucleosides and their prodrugs: a comparison of phosphonates and corresponding nucleosides.
Mackman RL; Zhang L; Prasad V; Boojamra CG; Chen J; Douglas J; Grant D; Laflamme G; Hui H; Kim CU; Parrish J; Stoycheva AD; Swaminathan S; Wang K; Cihlar T
Nucleosides Nucleotides Nucleic Acids; 2007; 26(6-7):573-7. PubMed ID: 18066858
[TBL] [Abstract][Full Text] [Related]
15. Design of new mononucleotide prodrugs: aryl (SATE) phosphotriester derivatives.
Peyrottes S; Schlienger N; Beltran T; Lefebvre I; Pompon A; Gosselin G; Aubertin AM; Imbach JL; Périgaud C
Nucleosides Nucleotides Nucleic Acids; 2001; 20(4-7):315-21. PubMed ID: 11563043
[TBL] [Abstract][Full Text] [Related]
16. [Design, synthesis and anti-HBV activity of L-amino acid ester prodrugs of acyclic nucleoside phosphonates].
Fu XZ; Jiang SH; Yang YS; Ji RY
Yao Xue Xue Bao; 2008 May; 43(5):495-503. PubMed ID: 18717337
[TBL] [Abstract][Full Text] [Related]
17. 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; 22(5-8):943-5. PubMed ID: 14565317
[TBL] [Abstract][Full Text] [Related]
18. Short synthesis and antiviral activity of acyclic phosphonic acid nucleoside analogues.
Liu LJ; Yoo JC; Hong JH
Nucleosides Nucleotides Nucleic Acids; 2009 Feb; 28(2):150-64. PubMed ID: 19219742
[TBL] [Abstract][Full Text] [Related]
19. Dipeptide derivatives of AZT: synthesis, chemical stability, activation in human plasma, hPEPT1 affinity, and antiviral activity.
Santos C; Morais J; Gouveia L; de Clercq E; Pannecouque C; Nielsen CU; Steffansen B; Moreira R; Gomes P
ChemMedChem; 2008 Jun; 3(6):970-8. PubMed ID: 18389514
[TBL] [Abstract][Full Text] [Related]
20. A step further in the SATE mononucleotide prodrug approach.
Peyrottes S; Villard AL; Coussot G; Augustijns P; Lefebvre I; Aubertin AM; Gosselin G; Périgaud C
Nucleic Acids Symp Ser (Oxf); 2008; (52):539-40. PubMed ID: 18776492
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
