Поисковый запрос: (<.>A=McGuigan, Christopher$<.>) |
Общее количество найденных документов : 20
Показаны документы с 1 по 20
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1.
| Certain phosphoramidate derivatives of dideoxy uridine (ddU) are active against HIV and successfully by-pass thymidine kinase // FEBS Lett., 1994. Vol. 351&(!&), N 1.-С.11-14
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2.
| Certain phosphoramidate derivatives of dideoxy uridine (ddU) are active against HIV and successfully by-pass thymidine kinase // FEBS Lett., 1994. Vol. 351&(!&), N 1.-С.11-14
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3.
| 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 // FEBS Lett., 1997. Vol. 410, N 2-3.-С.324-328
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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 // FEBS Lett., 1997. Vol. 410, N 2-3.-С.324-328
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5.
| Exploiting the anti-HIV-1 activity of acyclovir: Suppression of primary and drug-resistant HIV isolates and potentiation of the activity of ribavirin // Antimicrob. Agents and Chemother., 2012. Vol. 56, N 5.-С.2604-2611
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6.
| Intracellular delivery of bioactive AZT nucleotides by aryl phosphate derivatives of AZT // J. Med. Chem., 1993. Vol. 36, N 8.-С.1048-1052
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7.
| Intracellular delivery of bioactive AZT Nucleotides by Aryl Phosphate Derivatives of AZT // J. Med. Chem., 1993. Vol. 36, N 8.-С.1048-1052
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8.
| McGuigan Antiviral purine derivatives
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9.
| McGuigan Antiviral purine derivatives
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10.
| McGuigan Preparation of novel N-substituted phospholipids via phosphoramidite intermediates // J. Chem. Soc. Perkin Trans. 1, 1992, N 1.-С.51-55
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11.
| McGuigan Synthesis and biological evaluation of substituted phosphate triester alkyl lyso phospholipids (ALPs) as novel potential anti-neoplastic agents // FEBS Lett., 1995. Vol. 372, N 2-3.-С.259-263
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12.
| Mechanisms associated with HIV-1 resistance to acyclovir by the V751 mutation in reverse transcriptase // J. Biol. Chem., 2009. Vol. 284, N 32.-С.21496-21504
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13.
| Mechanisms associated with HIV-1 resistance to acyclovir by the V751 mutation in reverse transcriptase // J. Biol. Chem., 2009. Vol. 284, N 32.-С.21496-21504
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14.
| Novel aryl substituted bicyclic furo nucleosides as extremely potent and selective anti-VZV agents // Nucleosides , Nucleotides and Nucl. Acids, 2001. Vol. 20, N 4-7.-С.287-296
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15.
| Novel aryl substituted bicyclic furo nucleosides as extremely potent and selective anti-VZV agents // Nucleosides , Nucleotides and Nucl. Acids, 2001. Vol. 20, N 4-7.-С.287-296
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16.
| Phosphoramidate ProTides of 2'-C-methylguanosine as highly potent inhibitors of hepatitis C virus: Study of their in vitro and in vivo properties // J. Med. Chem., 2010. Vol. 53, N 13.-С.4949-4957
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17.
| Phosphoramidate ProTides of 2'-C-methylguanosine as highly potent inhibitors of hepatitis C virus: Study of their in vitro and in vivo properties // J. Med. Chem., 2010. Vol. 53, N 13.-С.4949-4957
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18.
| Stereoselective and concentration-dependent polarized epithelial permeability of a series of phosphoramidate triester prodrugs of d4T: An in vitro study in Caco-2 and Madin-Darb canine kidney cell monolayers // J. Pharmacol. and Exp. Ther., 2003. Vol. 307, N 3.-С.1112-1119
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19.
| The application of phosphoramidate protide technology to acyclovir confers anti-HIV inhibition // J. Med. Chem., 2009. Vol. 52, N 17.-С.5520-5530
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20.
| The application of phosphoramidate protide technology to acyclovir confers anti-HIV inhibition // J. Med. Chem., 2009. Vol. 52, N 17.-С.5520-5530
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