Abstract
The synthesis, SAR, and in vivo activity of inhibitors of delta-5 desaturase are described. Ring-constraint of the initial series provided access to a variety of in vitro active chemotypes, from which the indazole was selected. Examples from the indazole series displayed in vivo activity in reducing the enzymatic activity of liver delta-5 desaturase.
Keywords:
Delta-5 desaturase; In vivo efficacy; Indazole; Metabolic syndrome; Ring constraint.
Copyright © 2015 Elsevier Ltd. All rights reserved.
MeSH terms
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Amides / chemical synthesis
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Amides / chemistry
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Amides / pharmacology*
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Animals
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Delta-5 Fatty Acid Desaturase
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Dose-Response Relationship, Drug
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Drug Design*
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Enzyme Inhibitors / chemical synthesis
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Enzyme Inhibitors / chemistry
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Enzyme Inhibitors / pharmacology*
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Fatty Acid Desaturases / antagonists & inhibitors*
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Fatty Acid Desaturases / metabolism
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Humans
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Liver / enzymology
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Metabolic Syndrome / drug therapy*
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Metabolic Syndrome / enzymology
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Metabolic Syndrome / metabolism
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Mice
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Molecular Structure
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Structure-Activity Relationship
Substances
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Amides
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Delta-5 Fatty Acid Desaturase
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Enzyme Inhibitors
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Fatty Acid Desaturases