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The design and synthesis of novel, potent and orally bioavailable N-aryl piperazine-1-carboxamide CCR2 antagonists with very high hERG selectivity

✍ Scribed by John G. Cumming; Justin F. Bower; David Waterson; Alan Faull; Philip J. Poyser; Paul Turner; Benjamin McDermott; Andrew D. Campbell; Julian Hudson; Michael James; Jon Winter; Christine Wood

Book ID: 113496916
Publisher: Elsevier Science
Year: 2012
Tongue: English
Weight: 503 KB
Volume: 22
Category: Article
ISSN: 0960-894X
DOI: 10.1016/j.bmcl.2012.04.118

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