Abstract
A suitable inhibitor of activated thrombin activatable fibrinolysis inhibitor (TAFIa) has the potential to be a novel treatment for thrombosis. The TAFIa inhibitor UK-396082 (1) was used as a starting point to seek more potent analogues. With knowledge of encouraging human pharmacokinetics and toleration for the clinical candidate (1), the programme continued to seek structure-activity relationships (SAR) that could positively impact on both potency and half-life, and therefore the projected dose of any future nominated clinical agent. A series of oxygenated analogues based on compound 1 were prepared to evaluate changes in pharmacology, selectivity and pharmacokinetics.
Copyright 2009 Elsevier Ltd. All rights reserved.
MeSH terms
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Administration, Oral
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Amino Acids / chemical synthesis
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Amino Acids / chemistry*
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Amino Acids / pharmacokinetics
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Animals
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Carboxypeptidase B2 / antagonists & inhibitors*
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Carboxypeptidase B2 / metabolism
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Fibrinolytic Agents / chemical synthesis
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Fibrinolytic Agents / chemistry*
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Fibrinolytic Agents / pharmacokinetics
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Half-Life
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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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Oxygen / chemistry*
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Protease Inhibitors / chemical synthesis
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Protease Inhibitors / chemistry*
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Protease Inhibitors / pharmacokinetics
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Rats
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Structure-Activity Relationship
Substances
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5-amino-2-((1-n-propyl-1H-imidazol-4-yl)methyl)pentanoic acid
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Amino Acids
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Fibrinolytic Agents
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Imidazoles
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Protease Inhibitors
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Carboxypeptidase B2
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Oxygen