Abstract
The discovery of a highly potent and selective EP(4) antagonist MF-766 is discussed. This N-benzyl indole derivative exhibits good pharmacokinetic profile and unprecedented in vivo potency in the rat AIA model.
Copyright 2010 Elsevier Ltd. All rights reserved.
MeSH terms
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Animals
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Arthritis / drug therapy
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Benzoates / chemistry
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Benzoates / pharmacology*
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Benzoates / therapeutic use
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Cells, Cultured
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Dogs
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Drug Discovery
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Drug Stability
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Hepatocytes
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Humans
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Indoles / chemistry
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Indoles / pharmacology*
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Indoles / therapeutic use
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Inflammation / drug therapy
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Pain / drug therapy*
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Pharmacokinetics
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Rats
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Receptors, Prostaglandin E / antagonists & inhibitors*
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Receptors, Prostaglandin E, EP4 Subtype
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Structure-Activity Relationship
Substances
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Benzoates
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Indoles
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PTGER4 protein, human
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Ptger4 protein, rat
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Receptors, Prostaglandin E
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Receptors, Prostaglandin E, EP4 Subtype