Synthesis of Aromatic Analogs of 8(S)-HETE and Their Biological Evaluation as Activators of the PPAR Nuclear Receptors
A new family of 8‐HETE analogs has been synthesized as dual PPAR α and γ agonists. A versatile strategy has been developed to allow modulations not only around the aromatic core but also on the side chains of these analogs. The affinity of these compounds towards the PPARα and PPARγ receptors is rep...
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Veröffentlicht in: | European Journal of Organic Chemistry 2006-05, Vol.2006 (9), p.2181-2196 |
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Format: | Artikel |
Sprache: | eng |
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