Article ID Journal Published Year Pages File Type
10592456 Bioorganic & Medicinal Chemistry Letters 2012 6 Pages PDF
Abstract
A series of 1,3-thiazole derivatives were synthesized as potent, orally bioavailable S1P3-sparing S1P1 agonists. One of them, 24c, exhibited favorable efficacy in rat on host versus graft reaction (HvGR). The pharmacokinetic data for other compounds are shown as well.
Related Topics
Physical Sciences and Engineering Chemistry Organic Chemistry
Authors
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