Abstract
Design and synthesis of pyrazolodihydropyrimidines as KV1.5 blockers led to the discovery of 7d as a potent and selective antagonist. This compound showed atrial selective prolongation of effective refractory period in rabbits and was selected for clinical development.
Copyright 2010 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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Dogs
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Dose-Response Relationship, Drug
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Inhibitory Concentration 50
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Kv1.5 Potassium Channel / antagonists & inhibitors*
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Molecular Structure
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Potassium Channel Blockers / chemical synthesis*
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Potassium Channel Blockers / chemistry
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Potassium Channel Blockers / pharmacology
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Pyrazoles / pharmacology*
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Pyrrolidines / chemical synthesis
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Pyrrolidines / chemistry*
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Pyrrolidines / pharmacology
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Rabbits
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Rats
Substances
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Amides
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Kv1.5 Potassium Channel
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Potassium Channel Blockers
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Pyrazoles
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Pyrrolidines
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pyrrolidine