Abstract
A new class of 7-azaindole analogs of MK-7246 as potent and selective CRTH2 antagonists is reported. The SAR leading to the identification of the optimal azaindole regioisomer as well as the pharmacokinetics and off-target activities of the most potent antagonists are disclosed.
Copyright © 2010 Elsevier Ltd. All rights reserved.
MeSH terms
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Animals
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Carbolines / chemistry
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Humans
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Indoles / chemistry*
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Indoles / pharmacokinetics
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Indoles / pharmacology*
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Rats
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Rats, Sprague-Dawley
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Receptors, Immunologic / antagonists & inhibitors*
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Receptors, Immunologic / metabolism*
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Receptors, Prostaglandin / antagonists & inhibitors*
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Receptors, Prostaglandin / metabolism*
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Structure-Activity Relationship
Substances
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((7R)-7-(((4-fluorophenyl)sulfonyl)(methyl)amino)-6,7,8,9-tetrahydropyrido(1,2-a)indol-10-yl)acetic acid
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7-azaindole dimer
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Carbolines
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Indoles
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Receptors, Immunologic
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Receptors, Prostaglandin
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prostaglandin D2 receptor