Synthesis and antiviral activity of phosphoralaninate derivatives of methylenecyclopropane analogues of nucleosides (Q28372606)

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R G Ptak

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J M Breitenbach

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J S Lin

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Y C Cheng

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J C Drach

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E R Kern

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J Zemlicka

Mechanism of anti-HIV action of masked alaninyl d4T-MP derivatives

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language of work or name

English

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publication date

August 1999

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published in

Antiviral Research

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volume

43

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issue

1

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page(s)

37-53

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Synthesis and evaluation of the anti-HIV activity of aza and deaza analogues of isoddA and their phosphates as prodrugs.

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Intracellular delivery of bioactive AZT nucleotides by aryl phosphate derivatives of AZT.

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Aryl phosphate derivatives of AZT retain activity against HIV1 in cell lines which are resistant to the action of AZT

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Phosphoramidate derivatives of 2′,3′-didehydro-2′,3′-dideoxyadenosine [d4A] have markedly improved anti-HIV potency and selectivity

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(Z)- and (E)-2-((Hydroxymethyl)cyclopropylidene)methyladenine and -guanine. New Nucleoside Analogues with a Broad-Spectrum Antiviral Activity

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The Stereochemical Basis of Template Function

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Effective treatment of murine cytomegalovirus infections with methylenecyclopropane analogues of nucleosides

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Purine Nucleoside Phosphorylase. 3. Reversal of Purine Base Specificity by Site-Directed Mutagenesis

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In vitro anti-human immunodeficiency virus activities of Z- and E-methylenecyclopropane nucleoside analogues and their phosphoro-L-alaninate diesters

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Phosphodiester amidates of allenic nucleoside analogues: anti-HIV activity and possible mechanism of action

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Phosphodiester Amidates of Unsaturated Nucleoside Analogues: Synthesis and Anti-HIV Activity

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