Setogepram
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Other names | PBI-4050, Fezagepras |
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Formula | C13H18O2 |
Molar mass | 206.285 g·mol−1 |
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Setogepram (PBI-4050, Fezagepras) is an experimental drug which acts as a mixed agonist-antagonist for certain free fatty acid receptors, being an agonist at FFAR1 (GPR40) but an antagonist at GPR84. It has antiinflammatory and anti-fibrotic effects and has reached Phase II human clinical trials for treatment of idiopathic pulmonary fibrosis.[1][2][3][4][5]
References
[edit]- ^ Li Y, Chung S, Li Z, Overstreet JM, Gagnon L, Grouix B, et al. (May 2018). "Fatty acid receptor modulator PBI-4050 inhibits kidney fibrosis and improves glycemic control". JCI Insight. 3 (10). doi:10.1172/jci.insight.120365. PMC 6012516. PMID 29769449.
- ^ Khalil N, Manganas H, Ryerson CJ, Shapera S, Cantin AM, Hernandez P, et al. (March 2019). "Phase 2 clinical trial of PBI-4050 in patients with idiopathic pulmonary fibrosis". The European Respiratory Journal. 53 (3). doi:10.1183/13993003.00663-2018. PMC 6422836. PMID 30578394.
- ^ Nguyen QT, Nsaibia MJ, Sirois MG, Calderone A, Tardif JC, Fen Shi Y, et al. (January 2020). "PBI-4050 reduces pulmonary hypertension, lung fibrosis, and right ventricular dysfunction in heart failure". Cardiovascular Research. 116 (1): 171–182. doi:10.1093/cvr/cvz034. PMID 30753422.
- ^ Chen LH, Zhang Q, Xie X, Nan FJ (December 2020). "Modulation of the G-Protein-Coupled Receptor 84 (GPR84) by Agonists and Antagonists". Journal of Medicinal Chemistry. 63 (24): 15399–15409. doi:10.1021/acs.jmedchem.0c01378. PMID 33267584.
- ^ Gagnon L, Leduc M, Thibodeau JF, Zhang MZ, Grouix B, Sarra-Bournet F, et al. (May 2018). "A Newly Discovered Antifibrotic Pathway Regulated by Two Fatty Acid Receptors: GPR40 and GPR84". The American Journal of Pathology. 188 (5): 1132–1148. doi:10.1016/j.ajpath.2018.01.009. PMID 29454750.