Design, synthesis, and biological evaluation of novel pan agonists of FFA1, PPARγ and PPARδ
The free fatty acid receptor 1 (FFA1) and peroxisome proliferator-activated receptors (PPARs) have attracted interest as potent targets for the treatment of metabolic syndrome such as type 2 diabetes. Based on the hypothesis that the dual agonists of PPARs and FFA1 would act as insulin sensitizers a...
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Veröffentlicht in: | European journal of medicinal chemistry 2018-11, Vol.159, p.267-276 |
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Sprache: | eng |
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