TUG-2208 (compound 42a) is a GPR84 agonist (pEC50=8.98) with low lipophilicity and good solubility, in vitro permeability and microsomal stability.
TUG-2208 (0.1; 1 mM 4; 96 h) shows excellent stability in mouse liver microsomes[1].
TUG-2208 (10 μM) exhibits over 1000-fold selectivity for GPR84 compared to other free fatty acid receptors (FFA1, FFA2, FFA3, FFA4)[1].
References:
[1]. Ieremias L, et al., Structure-Activity Relationship Studies and Optimization of 4-Hydroxypyridones as GPR84 Agonists. J Med Chem. 2024 Feb 21.
















