Abstract
A novel series of guanidinebenzoate enteropeptidase and trypsin dual inhibitors has been discovered and SAR studies were conducted. Optimization was focused on improving properties for gut restriction, including increased aqueous solubility, lower cellular permeability, and reduced oral bioavailability. Lead compounds were identified with efficacy in a mouse fecal protein excretion study.
Keywords:
Enteropeptidase inhibitor; Guanidinebenzoate; Gut-restriction; Trypsin inhibitor.
Copyright © 2021 Elsevier Ltd. All rights reserved.
MeSH terms
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Animals
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Benzoates / chemical synthesis
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Benzoates / pharmacokinetics
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Benzoates / pharmacology*
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CHO Cells
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Cattle
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Cricetulus
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Diet, High-Fat
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Enteropeptidase / antagonists & inhibitors*
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Feces / chemistry
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Guanidines / chemical synthesis
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Guanidines / pharmacokinetics
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Guanidines / pharmacology*
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Humans
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Metabolic Syndrome / drug therapy
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Metabolic Syndrome / enzymology
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Mice
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Mice, Inbred C57BL
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Molecular Structure
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Obesity / drug therapy
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Obesity / enzymology
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Proteins / metabolism
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Structure-Activity Relationship
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Trypsin Inhibitors / chemical synthesis
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Trypsin Inhibitors / pharmacokinetics
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Trypsin Inhibitors / pharmacology*
Substances
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Benzoates
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Guanidines
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Proteins
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Trypsin Inhibitors
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Enteropeptidase