Abstract
Two dinucleoside polyphosphate NAD analogs, P1-(adenosine-5')-P3-(nicotinamide riboside-5')triphosphate (Np3A, 1) and P1-(adenosine-5')-P4-(nicotinamide riboside-5')tetraphosphate (Np4A, 2), were synthesized and tested as inhibitors of both microbial and human recombinant NMN adenylyltransferase. Compounds 1 and 2 proved to be selective inhibitors of microbial enzymes.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Enzyme Inhibitors / chemical synthesis*
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Enzyme Inhibitors / chemistry
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Enzyme Inhibitors / pharmacology
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Humans
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NAD / analogs & derivatives*
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NAD / chemical synthesis*
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NAD / chemistry
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NAD / pharmacology
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Nicotinamide-Nucleotide Adenylyltransferase / antagonists & inhibitors*
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Recombinant Proteins / antagonists & inhibitors
Substances
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Enzyme Inhibitors
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Recombinant Proteins
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NAD
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Nicotinamide-Nucleotide Adenylyltransferase