Abstract
The inhibition of aldosterone synthase (CYP11B2) may be an effective treatment of hypertension and heart failure, among other ailments. Previously reported benzimidazole CYP11B2 inhibitors led the way for bioisosteric imidazopyridines that are both potent and selective over CYP11B1.
Keywords:
Aldosterone; CYP11B2; Heart failure; Hypertension; Imidazopyridine.
Copyright © 2016 Elsevier Ltd. All rights reserved.
MeSH terms
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Animals
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Cricetulus
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Cytochrome P-450 CYP11B2 / antagonists & inhibitors*
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Humans
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Imidazoles / chemical synthesis
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Imidazoles / chemistry
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Imidazoles / pharmacokinetics
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Imidazoles / pharmacology*
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Macaca mulatta
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Male
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Microsomes, Liver / metabolism
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Pyridines / chemical synthesis
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Pyridines / chemistry
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Pyridines / pharmacokinetics
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Pyridines / pharmacology*
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Rats, Wistar
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Steroid 11-beta-Hydroxylase / antagonists & inhibitors
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Structure-Activity Relationship
Substances
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Imidazoles
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Pyridines
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Cytochrome P-450 CYP11B2
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Steroid 11-beta-Hydroxylase