Abstract
Phosphonated carbocyclic 2'-oxa-3'-aza-nucleosides have been synthesized in good yields by 1,3-dipolar cycloaddition methodology. The cytotoxicity and the reverse transcriptase inhibitory activity of the obtained compounds have been investigated. Phosphonated carbocyclic 2'-oxa-3'-aza-nucleosides, while showing low levels of cytotoxicity, exert a specific inhibitor activity on two different reverse transcriptases, which is comparable with that of AZT, opening new perspectives on their possible use as therapeutic agents, in anti-retroviral and anti-HBV chemotherapy.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Antiviral Agents / chemical synthesis*
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Antiviral Agents / pharmacology
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Antiviral Agents / toxicity
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Aza Compounds / chemical synthesis*
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Aza Compounds / pharmacology
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Aza Compounds / toxicity
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Humans
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In Vitro Techniques
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Leukocytes, Mononuclear / drug effects
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Leukocytes, Mononuclear / enzymology
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Nitrogen Oxides / chemistry
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Nucleosides / chemical synthesis*
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Nucleosides / pharmacology
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Nucleosides / toxicity
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Organophosphonates / chemical synthesis*
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Organophosphonates / pharmacology
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Organophosphonates / toxicity
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Reverse Transcriptase Inhibitors / chemical synthesis*
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Reverse Transcriptase Inhibitors / pharmacology
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Reverse Transcriptase Inhibitors / toxicity
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Stereoisomerism
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Structure-Activity Relationship
Substances
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Antiviral Agents
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Aza Compounds
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Nitrogen Oxides
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Nucleosides
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Organophosphonates
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Reverse Transcriptase Inhibitors
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nitrones