Reveals a concise synthesis of hydroxylauric acids and demonstrates that hydroxy position dictates FFA1, FFA4, and GPR84 activation, highlighting lipid structure-activity relationships.
Saturated hydroxy fatty acids make up a class of underexplored lipids with potentially interesting biological activities. We report a succinct and general synthetic route to saturated hydroxy fatty acids hydroxylated at position 6 or higher, and exemplify this with the synthesis of hydroxylauric acids. All regioisomers of hydroxylauric acids were tested on free fatty acid receptors FFA1, FFA4 and GPR84. The results show that the introduction of a hydroxy group and its position have a high impact on receptor activity.
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Kaspersen et al. (2017) studied this question.
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