Abstract
A series of substituted 2-aminopyridines was prepared and evaluated as inhibitors of human nitric oxide synthases (NOS). 4,6-Disubstitution enhanced both potency and specificity for the inducible NOS with the most potent compound having an IC50 of 28 nM.
MeSH terms
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Aminopyridines / chemical synthesis*
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Aminopyridines / pharmacology
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Enzyme Inhibitors / chemical synthesis*
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Enzyme Inhibitors / pharmacology
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Humans
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Nitric Oxide Synthase / antagonists & inhibitors*
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Structure-Activity Relationship
Substances
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Aminopyridines
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Enzyme Inhibitors
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Nitric Oxide Synthase