Abstract
We describe the systematic optimization, focused on the improvement of CV-TI, of a series of CCR2 antagonists. This work resulted in the identification of 10 (((1S,3R)-1-isopropyl-3-((3S,4S)-3-methoxy-tetrahydro-2H-pyran-4-ylamino)cyclopentyl)(4-(5-(trifluoromethyl)pyridazin-3-yl)piperazin-1-yl)methanone) which possessed a low projected human dose 35-45mg BID and a CV-TI=3800-fold.
Copyright © 2011 Elsevier Ltd. All rights reserved.
MeSH terms
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Anti-Inflammatory Agents / chemistry
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Anti-Inflammatory Agents / pharmacokinetics
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Anti-Inflammatory Agents / pharmacology*
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Biological Assay
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Humans
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Inhibitory Concentration 50
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Microsomes / drug effects
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Microsomes / metabolism
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Models, Molecular*
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Molecular Structure
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Piperazines / chemistry*
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Piperazines / pharmacokinetics
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Piperazines / pharmacology*
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Protein Binding / drug effects
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Pyridazines / chemistry*
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Pyridazines / pharmacokinetics
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Pyridazines / pharmacology*
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Receptors, CCR2 / agonists*
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Receptors, CCR2 / blood
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Structure-Activity Relationship
Substances
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((1-isopropyl-3-(3-methoxy-tetrahydro-2H-pyran-4-ylamino)cyclopentyl)(4-(5-(trifluoromethyl)pyridazin-3-yl)piperazin-1-yl)methanone)
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Anti-Inflammatory Agents
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Piperazines
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Pyridazines
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Receptors, CCR2