Article ID Journal Published Year Pages File Type
10593194 Bioorganic & Medicinal Chemistry Letters 2012 6 Pages PDF
Abstract
We previously reported CXCR3 clinical candidate compound, AMG 487. This Letter reported the efforts to discover the second generation of CXCR3 antagonist. From these efforts, compounds 25 is a much potent analog than AMG 487 with excellent bioavailability in multiple preclinical species and demonstrated efficacy in a mouse model of bleomycin-induced leukocytes trafficking into the lung.
Related Topics
Physical Sciences and Engineering Chemistry Organic Chemistry
Authors
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