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ZQ-16
- Soluble in DMSO and EtOH
- MF: C10H16N2O2S
- MW: 228.31
Description
ZQ-16 is a potent and selective agonist of G-protein coupled receptor 84 (GPR84). It activates GPR84 (EC50: 134–139 nM for cAMP; 0.213 µM for calcium mobilization) with high selectivity and has no cross-activity at 100 µM against related FFARs including GPR40, GPR41, GPR119, or GPR120. ZQ-16 induced phosphorylation of ERK1/2, and a dose-dependent reduction of forskolin-stimulated cAMP accumulation in HEK293 cells expressing GPR84.
GPR84 pharmacology is central to inflammatory signaling. ZQ-16 serves as a key tool supporting mechanistic studies of GPR84, free fatty acids (FFAs), and ERK1 pathways across biochemical, cellular, and disease-model assays.
Key Features
- Potent and selective GPR84 agonist
- Activates GPR84 (EC50: 134 nM for cAMP)
- Highly selective over related FFARs
- Potent and selective small-molecule GPR84 agonist (EC50 value 0.139 µM in a calcium mobilization assay)
Applications
- GPR84 pharmacology and target-validation studies
- GPR84 pathway and signaling assays
- Disease-model research related to inflammation
- Receptor signaling, ligand profiling and functional response assays
More Information
| Parent CAS No. | 376616-73-8 |
|---|---|
| Chemical Name | 2-(hexylthio)pyrimidine-4,6-diol |
| SMILES | C1(SCCCCCC)=NC(O)=CC(O)=N1 |
| MFCD | N.A. |
| InChi | InChI=1S/C10H16N2O2S/c1-2-3-4-5-6-15-10-11-8(13)7-9(14)12-10/h7H,2-6H2,1H3,(H2,11,12,13,14) |
| InChiKey | UYXOAKRMLQKLQX-UHFFFAOYSA-N |
| CID | 1912564 |
| Short Description | GPR84 agonist |
References
- Q Zhang et al. Discovery and Characterization of a Novel Small-Molecule Agonist for Medium-Chain Free Fatty Acid Receptor G Protein-Coupled Receptor 84. J Pharmacol Exp Ther. 2016 May;357(2):337-44.
- Y Liu et al. Design and Synthesis of 2-Alkylpyrimidine-4,6-diol and 6-Alkylpyridine-2,4-diol as Potent GPR84 Agonists. ACS Med Chem Lett. 2016 Mar 30;7(6):579-83.


