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| Product | Description | |
|---|---|---|
| Omidenepag | Omidenepag (UR-7276), a pharmacologically active form of Omidenepag Isopropyl, is a selective, non-prostanoid EP2 receptor agonist, with an EC 50 of 1.1 nM. Omidenepag shows binding affinities (IC 50 ) 10 nM for h-EP2 [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: UR-7276. CAS No. 1187451-41-7. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-17642. |  |
| Omidenepag | This active molecular is a prostaglandin receptor agonist and detailed information has not been published yet. Synonyms: Omidenepag; UR-7276; UR 7276; UR7276; (6-((N-(4-(1H-pyrazol-1-yl)benzyl)pyridine-3-sulfonamido)methyl)pyridin-2-yl)glycine. Grades: 98%. CAS No. 1187451-41-7. Molecular formula: C23H22N6O4S. Mole weight: 478.53. |  |
| Omidenepag isopropyl | Omidenepag isopropyl is a selective EP2 receptor agonist. Omidenepag isopropyl is converted to the active product Omidenepag during corneal penetration, and Omidenepag is a highly selective EP2 receptor agonist. Omidenepag isopropyl shows only weak affinity for EP1, EP2, and FP receptors. Omidenepag isopropyl is under development for the treatment of glaucoma as an intraocular pressure (IOP)-lowering agent. Uses: Scientific research. Group: Signaling pathways. Alternative Names: DE-117. CAS No. 1187451-19-9. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-111406. | |
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