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• W2892295719 abstract "Free fatty acid receptor 2 (FFA2/GPR43) is a receptor for short-chain fatty acids reported to be involved in regulation of metabolism, appetite, fat accumulation, and inflammatory responses and is a potential target for treatment of various inflammatory and metabolic diseases. By bioisosteric replacement of the central pyrrolidine core of a previously disclosed FFA2 agonist with a synthetically more tractable thiazolidine, we were able to rapidly synthesize and screen analogues modified at both the 2- and 3-positions on the thiazolidine core. Herein, we report SAR exploration of thiazolidine FFA2 agonists and the identification of 31 (TUG-1375), a compound with significantly increased potency (7-fold in a cAMP assay) and reduced lipophilicity (50-fold reduced clogP) relative to the pyrrolidine lead structure. The compound has high solubility, high chemical, microsomal, and hepatocyte stability, and favorable pharmacokinetic properties and was confirmed to induce human neutrophil mobilization and to inhibit lipolysis in murine adipocytes." @default.
• W2892295719 created "2018-09-27" @default.
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• W2892295719 date "2018-09-24" @default.
• W2892295719 modified "2023-10-03" @default.
• W2892295719 title "Discovery of a Potent Thiazolidine Free Fatty Acid Receptor 2 Agonist with Favorable Pharmacokinetic Properties" @default.
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• W2892295719 doi "https://doi.org/10.1021/acs.jmedchem.8b00855" @default.
• W2892295719 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/30247908" @default.
• W2892295719 hasPublicationYear "2018" @default.
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