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PUBMED FOR HANDHELDS

Journal Abstract Search


137 related items for PubMed ID: 32421343

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  • 28. Synthesis, anti-human immunodeficiency virus activity and esterase lability of some novel carboxylic ester-modified phosphoramidate derivatives of stavudine (d4T).
    McGuigan C, Sutton PW, Cahard D, Turner K, O'Leary G, Wang Y, Gumbleton M, De Clercq E, Balzarini J.
    Antivir Chem Chemother; 1998 Nov; 9(6):473-9. PubMed ID: 9865385
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  • 30. The ProTides Boom.
    Mehellou Y.
    ChemMedChem; 2016 Jun 06; 11(11):1114-6. PubMed ID: 27159529
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  • 31. The presence of substituents on the aryl moiety of the aryl phosphoramidate derivative of d4T enhances anti-HIV efficacy in cell culture: A structure-activity relationship.
    Siddiqui AQ, Ballatore C, McGuigan C, De Clercq E, Balzarini J.
    J Med Chem; 1999 Feb 11; 42(3):393-9. PubMed ID: 9986709
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  • 32. Second generation of cycloSal-pronucleotides with esterase-cleavable sites: the "lock-in"-concept.
    Meier C, Ruppel MF, Vukadinović D, Balzarini J.
    Nucleosides Nucleotides Nucleic Acids; 2004 Feb 11; 23(1-2):89-115. PubMed ID: 15043139
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  • 34. Enhancing the aqueous solubility of d4T-based phosphoramidate prodrugs.
    Siddiqui A, McGuigan C, Ballatore C, Srinivasan S, De Clercq E, Balzarini J.
    Bioorg Med Chem Lett; 2000 Feb 21; 10(4):381-4. PubMed ID: 10714505
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  • 35. Intracellular delivery of bioactive AZT nucleotides by aryl phosphate derivatives of AZT.
    McGuigan C, Pathirana RN, Balzarini J, De Clercq E.
    J Med Chem; 1993 Apr 16; 36(8):1048-52. PubMed ID: 8478904
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  • 38. Anti-HIV pronucleotides: decomposition pathways and correlation with biological activities.
    Egron D, Lefebvre I, Périgaud C, Beltran T, Pompon A, Gosselin G, Aubertin AM, Imbach JL.
    Bioorg Med Chem Lett; 1998 May 05; 8(9):1045-50. PubMed ID: 9871705
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