The present invention relates to novel free fatty acid receptor (FFAR) agonists of general formula (I), in particular agonists of FFAR1, and to the use of said FFAR agonists as medicaments, in particular for treatment and/or prevention of type 2 diabetes mellitus (T2DM), R1-S-CH2-OXA-R2 (l) wherein OXA is selected from the group consisting of 1,3-oxazolyl 1,2,4-oxadiazolyl or 1,3,4-oxadiazolyl, R1 is selected from 1,3,5- triazinyl and pyrimidinyl and R2 is phenyl.
本发明涉及一种新型自由
脂肪酸受体(FFAR)激动剂,其一般式为(I),特别是FFAR1的激动剂,并将所述FFAR激动剂用作药物,特别用于治疗和/或预防2型糖尿病(T2
DM),其中OXA选自1,3-
噁唑基1,2,4-噁二唑基或
1,3,4-噁二唑基的群,R1选自
1,3,5-三嗪基和
嘧啶基,R2为苯基。