Abstract
1-2 Annulated adamantane piperidines 4, 6, 16, 17, 19, 23 and 25 were synthesized and evaluated for anti-influenza A virus activity. The stereoelectronic requirements for optimal antiviral potency were investigated. Piperidine 23 proved to be the most active of the compounds tested against influenza A virus, being 3.5-fold more active than amantadine, equipotent to rimantadine and 15-fold more potent than ribavirin. It is noteworthy that piperidine 23 displayed one of the highest selectivity indexes (SI>732) among aminoadamantanes or other cage structure amines tested till now.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Adamantane / chemical synthesis*
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Adamantane / chemistry
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Adamantane / pharmacology*
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Animals
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Antiviral Agents / chemical synthesis
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Antiviral Agents / chemistry
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Antiviral Agents / pharmacology
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Dogs
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Humans
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Influenza A Virus, H3N2 Subtype / drug effects*
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Magnetic Resonance Spectroscopy
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Molecular Structure
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Piperidines / chemical synthesis
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Piperidines / chemistry*
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Piperidines / pharmacology*
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Rimantadine / chemical synthesis
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Rimantadine / pharmacology
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Structure-Activity Relationship
Substances
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Antiviral Agents
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Piperidines
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Rimantadine
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Adamantane