Abstract
Two novel cycloSal-d4T monophosphates (d4TMPs) with increased steric demand have been synthesized via a new synthetic route. While 3-cyclohexyl-cycloSal d4TMP did not show a significantly reduced inhibitory potency toward human butyrylcholinesterase, the opposite was the case for the second novel pronucleotide, bis-(cycloSal-d4TMP).
MeSH terms
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Antiviral Agents / pharmacology
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Binding Sites
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Butyrylcholinesterase / chemistry*
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Chemistry, Pharmaceutical / methods
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Cholinesterase Inhibitors / chemical synthesis*
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Cholinesterase Inhibitors / pharmacology*
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Drug Design
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Enzyme Inhibitors / chemical synthesis*
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Enzyme Inhibitors / pharmacology
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Humans
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Hydrogen-Ion Concentration
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Hydrolysis
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Models, Chemical
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Nucleotides / chemistry
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Nucleotides / pharmacology*
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Stereoisomerism
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Temperature
Substances
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Antiviral Agents
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Cholinesterase Inhibitors
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Enzyme Inhibitors
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Nucleotides
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Butyrylcholinesterase