Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1366405 | Bioorganic & Medicinal Chemistry Letters | 2007 | 6 Pages |
Abstract
A series of low molecular weight antagonists of both the human and murine CC chemokine receptor 2, containing a 1-alkyl-3-(3-methyl-4-spiroindenylpiperidine)-substituted cyclopentanecarboxamide, is described. A SAR study of the C1 substituent revealed that short, branched alkyl groups such as isopropyl, isobutyl, or cyclopropyl are optimal for both human and murine CCR2 binding activity.
Graphical abstractA series of low molecular weight antagonists of both the human and murine CC chemokine receptor 2, containing a 1-alkyl-3-(3-methyl-4-spiroindenylpiperidine)-substituted cyclopentanecarboxamide, is described.Figure optionsDownload full-size imageDownload as PowerPoint slide
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Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Gabor Butora, Richard Jiao, William H. Parsons, Pasquale P. Vicario, Hong Jin, Julia M. Ayala, Margaret A. Cascieri, Lihu Yang,