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| Product | Description | |
|---|---|---|
| Fezagepras | Fezagepras (Setogepram) acts as an orally active agonist for GPR40 and as an antagonist or inverse agonist for GPR84 [1]. Fezagepras decreases renal, liver and pancreatic fibrosis [1] [2]. Fezagepras exerts anti-fibrotic, anti-inflammatory and anti-proliferative actions [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Setogepram; PBI-4050. CAS No. 1002101-19-0. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-100775A. |  |
| Fezagepras sodium | Fezagepras (Setogepram) sodium acts as an orally active agonist for GPR40 and as an antagonist or inverse agonist for GPR84 [1]. Fezagepras sodium decreases renal, liver and pancreatic fibrosis [1] [2]. Fezagepras sodium exerts anti-fibrotic, anti-inflammatory and anti-proliferative actions [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Setogepram sodium; PBI-4050 sodium. CAS No. 1254472-97-3. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-100775. | |
| Fezagepras sodium | Fezagepras sodium is an orally active GPR40 agonist, as well as an antagonist or inverse agonist of GPR84, with anti-fibrotic, anti-inflammatory and anti-proliferative effects. It reduces fibrosis in the renal, liver and pancreas. Synonyms: Setogepram sodium; PBI-4050 sodium; 3-Pentylbenzenacetic acid sodium salt; Benzeneacetic acid, 3-pentyl-, sodium salt (1:1). Grade: ≥95%. CAS No. 1254472-97-3. Molecular formula: C13H17NaO2. Mole weight: 228.26. |  |
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