Article ID Journal Published Year Pages File Type
10593814 Bioorganic & Medicinal Chemistry Letters 2012 4 Pages PDF
Abstract
The synthesis and SAR of a novel series of 4-azabenzoxazole histamine H3 antagonists is described. Introduction of substituted phenyl, pyridyl and fused heterocyclic groups to the 6-position of the 4-azabenzoxazole core gave a series of compounds with good H3 antagonist activity in both ex vivo and in vivo assays.
Related Topics
Physical Sciences and Engineering Chemistry Organic Chemistry
Authors
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