Abstract
Utilizing X-ray crystal structure analysis, (3S,5R)-5-[4-(2-chlorophenyl)-2,2-dimethyl-5-oxopiperazin-1-yl]piperidine-3-carboxamides were designed and identified as renin inhibitors. The most potent compound 15 demonstrated favorable pharmacokinetic and pharmacodynamic profiles in rat.
Copyright © 2012 Elsevier Ltd. All rights reserved.
MeSH terms
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Angiotensin-Converting Enzyme Inhibitors / chemical synthesis
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Angiotensin-Converting Enzyme Inhibitors / chemistry
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Angiotensin-Converting Enzyme Inhibitors / pharmacology*
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Animals
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Crystallography, X-Ray
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Dose-Response Relationship, Drug
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Drug Discovery*
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Haplorhini
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Humans
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Models, Molecular
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Molecular Conformation
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Piperazines / chemical synthesis
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Piperazines / chemistry
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Piperazines / pharmacology*
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Piperidines / chemical synthesis
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Piperidines / chemistry
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Piperidines / pharmacology*
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Renin / antagonists & inhibitors*
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Renin / blood
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Renin / metabolism
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Structure-Activity Relationship
Substances
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(3S,5R)-5-(4-(2-chlorophenyl)-2,2-dimethyl-5-oxopiperazin-1-yl)piperidine-3-carboxamide
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Angiotensin-Converting Enzyme Inhibitors
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Piperazines
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Piperidines
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Renin