Abstract
Syntheses and nitric oxide synthase inhibitory activity of cyclic amidines containing 5,6- 6,6- and 7,6-fused systems are described. X-ray structure determination facilitated the assignment of the stereochemistry of the most active compounds perhydro-2-iminoisoquinoline (8a) and perhydro-2-iminopyrindine (10a). Both 8a and 10a are very potent inhibitors of iNOS, with excellent selectivity over eNOS and they are orally active in rats with long duration suitable for once or twice a day dosing.
MeSH terms
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Administration, Oral
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Amidines / administration & dosage
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Amidines / chemistry*
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Animals
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Bridged Bicyclo Compounds / administration & dosage
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Bridged Bicyclo Compounds / chemistry*
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Cell Line
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Enzyme Inhibitors / administration & dosage*
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Enzyme Inhibitors / pharmacology
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Nitric Oxide Synthase / antagonists & inhibitors*
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Nitric Oxide Synthase Type II
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Pyridines / administration & dosage
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Pyridines / chemistry*
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Quinolines / administration & dosage
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Quinolines / chemistry*
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Rats
Substances
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Amidines
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Bridged Bicyclo Compounds
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Enzyme Inhibitors
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Pyridines
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Quinolines
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Nitric Oxide Synthase
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Nitric Oxide Synthase Type II
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Nos2 protein, rat