Article ID Journal Published Year Pages File Type
1378765 Bioorganic & Medicinal Chemistry Letters 2005 5 Pages PDF
Abstract

Various 6-aryl-3-cyano/methoxycarbonyl-4-methylsulfanyl-2H-pyran-2-ones have been synthesized as a potential substitute of 2,4-thiazolidinedione head group to express potent PPAR-γ transactivation response. Some of the screened compounds have shown promising PPAR-γ agonistic activity.

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Related Topics
Physical Sciences and Engineering Chemistry Organic Chemistry
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