Journal
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS
Volume 19, Issue 5, Pages 1431-1433Publisher
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.bmcl.2009.01.033
Keywords
Fluoroalkyl; Cyclobutenediones; CXCR2-CXCR1 dual antagonist
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A series of potent and orally bioavailable 3,4-diaminocyclobutenediones with various fluoroalkyl groups as a side chain were prepared and found to show significant improvements in the binding affinities towards both CXCR2 and CXCR1 receptors. (C) 2009 Elsevier Ltd. All rights reserved.
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