Chemistry:AR420626

From HandWiki

AR420626 is an experimental drug which acts as a reasonably potent and highly selective agonist for the free fatty acid receptor FFAR3 (GPR41).[1][2] It has been used to research the role of FFAR3 in various disease processes such as diabetes,[3] asthma,[4] eczema[4] and some forms of cancer,[5] as well as regulation of gastrointestinal hormone release.[6]

Further reading

References

  1. "Complex pharmacology of novel allosteric free fatty acid 3 receptor ligands". Molecular Pharmacology 86 (2): 200–210. August 2014. doi:10.1124/mol.114.093294. PMID 24870406. 
  2. "Structure-Activity Relationship Studies of Tetrahydroquinolone Free Fatty Acid Receptor 3 Modulators". Journal of Medicinal Chemistry 63 (7): 3577–3595. April 2020. doi:10.1021/acs.jmedchem.9b02036. PMID 32141297. 
  3. "Gαi -coupled GPR41 activation increases Ca2+ influx in C2C12 cells and shows a therapeutic effect in diabetic animals". Obesity (Silver Spring, Md.) 31 (7): 1871–1883. July 2023. doi:10.1002/oby.23786. PMID 37309717. 
  4. 4.0 4.1 "Free fatty acid 3 receptor agonist AR420626 reduces allergic responses in asthma and eczema in mice". International Immunopharmacology 127. January 2024. doi:10.1016/j.intimp.2023.111428. PMID 38159551. 
  5. "AR420626, a selective agonist of GPR41/FFA3, suppresses growth of hepatocellular carcinoma cells by inducing apoptosis via HDAC inhibition". Therapeutic Advances in Medical Oncology 12. 2020. doi:10.1177/1758835920913432. PMID 33014144. 
  6. "Free fatty acid receptor 3 activation suppresses neurogenic motility in rat proximal colon". Neurogastroenterology and Motility 30 (1). January 2018. doi:10.1111/nmo.13157. PMID 28714277.