BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

133 related articles for article (PubMed ID: 1495007)

  • 1. Potential prodrug derivatives of 2',3'-didehydro-2',3'-dideoxynucleosides. Preparations and antiviral activities.
    Mullah KB; Rao TS; Balzarini J; De Clercq E; Bentrude WG
    J Med Chem; 1992 Jul; 35(15):2728-35. PubMed ID: 1495007
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Marked inhibitory activity of masked aryloxy aminoacyl phosphoramidate derivatives of dideoxynucleoside analogues against visna virus infection.
    Balzarini J; Cahard D; Wedgwood O; Salgado A; Velázquez S; Yarnold CJ; De Clercq E; McGuigan C; Thormar H
    J Acquir Immune Defic Syndr Hum Retrovirol; 1998 Apr; 17(4):296-302. PubMed ID: 9525429
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Anti-human immunodeficiency virus type 1 activities of dideoxynucleoside phosphotriester derivatives in primary monocytes/macrophages.
    Thumann-Schweitzer C; Gosselin G; Périgaud C; Benzaria S; Girardet JL; Lefebvre I; Imbach JL; Kirn A; Aubertin AM
    Res Virol; 1996; 147(2-3):155-63. PubMed ID: 8901435
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Conversion of 2',3'-dideoxyadenosine (ddA) and 2',3'-didehydro-2',3'-dideoxyadenosine (d4A) to their corresponding aryloxyphosphoramidate derivatives markedly potentiates their activity against human immunodeficiency virus and hepatitis B virus.
    Balzarini J; Kruining J; Wedgwood O; Pannecouque C; Aquaro S; Perno CF; Naesens L; Witvrouw M; Heijtink R; De Clercq E; McGuigan C
    FEBS Lett; 1997 Jun; 410(2-3):324-8. PubMed ID: 9237655
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Synthesis and anti-HIV evaluation of D4T and D4T 5'-monophosphate prodrugs.
    Sergheraert C; Pierlot C; Tartar A; Henin Y; Lemaitre M
    J Med Chem; 1993 Apr; 36(7):826-30. PubMed ID: 8385224
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Inhibition of HIV reproduction in cell culture by 5'-phosphonates of 3'-azido-2',3'-dideoxynucleosides].
    Tarusova NB; Khorlin AA; Kraevskiĭ AA; Korneeva MN; Nosik DN; Kruglov IV; Galegov GA; Bibilashvili RSh
    Mol Biol (Mosk); 1989; 23(6):1716-24. PubMed ID: 2633042
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Synthesis of the 2-chloro analogues of 3'-deoxyadenosine, 2',3'-dideoxyadenosine, and 2',3'-didehydro-2',3'-dideoxyadenosine as potential antiviral agents.
    Rosowsky A; Solan VC; Sodroski JG; Ruprecht RM
    J Med Chem; 1989 May; 32(5):1135-40. PubMed ID: 2785212
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Synthesis and antiviral (HIV-1, HBV) activities of 5-halo-6-methoxy(or azido)-5,6-dihydro-3'-fluoro-3'-deoxythymidine diastereomers. Potential prodrugs to 3'-fluoro-3'-deoxythymidine.
    Kumar R; Wang L; Wiebe LI; Knaus EE
    J Med Chem; 1994 Oct; 37(21):3554-60. PubMed ID: 7932583
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Synthesis and anti-HIV activity of carbocyclic 2',3'-didehydro-2',3'-dideoxy 2,6-disubstituted purine nucleosides.
    Vince R; Hua M
    J Med Chem; 1990 Jan; 33(1):17-21. PubMed ID: 2296018
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Hydroxy fatty acids for the delivery of dideoxynucleosides as anti-HIV agents.
    Gangadhara KL; Lescrinier E; Pannecouque C; Herdewijn P
    Bioorg Med Chem Lett; 2014 Feb; 24(3):817-20. PubMed ID: 24411122
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Antiviral activity of cyclosaligenyl prodrugs of acyclovir, carbovir and abacavir.
    Balzarini J; Haller-Meier F; De Clercq E; Meier C
    Antivir Chem Chemother; 2001 Sep; 12(5):301-6. PubMed ID: 11900349
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Synthesis, antiviral activity, and mechanism of drug resistance of D- and L-2',3'-didehydro-2',3'-dideoxy-2'-fluorocarbocyclic nucleosides.
    Wang J; Jin Y; Rapp KL; Bennett M; Schinazi RF; Chu CK
    J Med Chem; 2005 Jun; 48(11):3736-48. PubMed ID: 15916425
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Synthesis and antiviral activity of prodrugs of the nucleoside 1-[2',3'-dideoxy-3'-C-(hydroxymethyl)-beta-D-erythropentofuranosyl] cytosine.
    Mauldin SC; Paget CJ; Jones CD; Colacino JM; Baxter AJ; Staschke KA; Johansson NG; Vrang L
    Bioorg Med Chem; 1998 May; 6(5):577-85. PubMed ID: 9629471
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Potent and selective activity of 3'-azido-2,6-diaminopurine-2',3'-dideoxyriboside, 3'-fluoro-2,6-diaminopurine-2',3'-dideoxyriboside, and 3'-fluoro-2',3'-dideoxyguanosine against human immunodeficiency virus.
    Balzarini J; Baba M; Pauwels R; Herdewijn P; Wood SG; Robins MJ; de Clercq E
    Mol Pharmacol; 1988 Mar; 33(3):243-9. PubMed ID: 3258404
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 3'-Fluoro-2',3'-dideoxy-5-chlorouridine: most selective anti-HIV-1 agent among a series of new 2'- and 3'-fluorinated 2',3'-dideoxynucleoside analogues.
    Van Aerschot A; Herdewijn P; Balzarini J; Pauwels R; De Clercq E
    J Med Chem; 1989 Aug; 32(8):1743-9. PubMed ID: 2754700
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Antiviral activity and intracellular metabolism of bis(tButylSATE) phosphotriester of beta-L-2',3'dideoxyadenosine, a potent inhibitor of HIV and HBV replication.
    Placidi L; Faraj A; Loi AG; Pierra C; Egron D; Cretton-Scott E; Gosseli G; Périgaud C; Martin LT; Schinazi RF; Imbach JL; el Kouni MH; Bryant ML; Sommadossi JP
    Antivir Chem Chemother; 2001 Mar; 12(2):99-108. PubMed ID: 11527047
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Amidate Prodrugs of Deoxythreosyl Nucleoside Phosphonates as Dual Inhibitors of HIV and HBV Replication.
    Liu C; Dumbre SG; Pannecouque C; Huang C; Ptak RG; Murray MG; De Jonghe S; Herdewijn P
    J Med Chem; 2016 Oct; 59(20):9513-9531. PubMed ID: 27748590
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Potential anti-AIDS drugs. Lipophilic, adenosine deaminase-activated prodrugs.
    Barchi JJ; Marquez VE; Driscoll JS; Ford H; Mitsuya H; Shirasaka T; Aoki S; Kelley JA
    J Med Chem; 1991 May; 34(5):1647-55. PubMed ID: 2033591
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Synthesis and structure-activity relationships of 6-substituted 2',3'-dideoxypurine nucleosides as potential anti-human immunodeficiency virus agents.
    Chu CK; Ullas GV; Jeong LS; Ahn SK; Doboszewski B; Lin ZX; Beach JW; Schinazi RF
    J Med Chem; 1990 Jun; 33(6):1553-61. PubMed ID: 2342052
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Synthesis and Antiviral Evaluation of TriPPPro-AbacavirTP, TriPPPro-CarbovirTP, and Their 1',2'-cis-Disubstituted Analogues.
    Weising S; Sterrenberg V; Schols D; Meier C
    ChemMedChem; 2018 Sep; 13(17):1771-1778. PubMed ID: 29943432
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.