Abstract
A novel series of 1H-2-phenyl-substituted-pyrazolo[2,3-d][1,2,4]triazine-3,7-diones (3a-g) as potential inhibitors of Human Leukocyte Elastase (HLE) are reported, the acyl-pyrazole being probably involved in the inhibition mechanism of the serino-protease enzymes. The most potent inhibitor both in vivo and in vitro was 2-o-methoxyphenyl-5-methyl-6-nitro-pyrazolo[2,3-d][1,2,4]triazine-3,7-di one (3e), which significantly suppressed the HLE-induced pulmonary injury in rats when administered orally (100 mg/kg, 3 h prior to HLE administration.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Animals
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Chemical Phenomena
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Chemistry, Physical
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Enzyme Inhibitors / chemical synthesis*
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Enzyme Inhibitors / pharmacology*
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Hemorrhage / chemically induced
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Hemorrhage / pathology
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Humans
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Leukocyte Elastase / antagonists & inhibitors*
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Lung Diseases / chemically induced
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Lung Diseases / pathology
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Male
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Pyrazoles / chemical synthesis*
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Pyrazoles / pharmacology
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Rats
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Rats, Sprague-Dawley
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Thiazines / chemical synthesis*
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Thiazines / pharmacology
Substances
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Enzyme Inhibitors
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Pyrazoles
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Thiazines
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Leukocyte Elastase