Chemical Structure : UniPR1449
Catalog No.: PC-25847Not For Human Use, Lab Use Only.
UniPR1449 is a selective EphA receptor inhibitor with IC50 of 8.1 uM in EphA2-ephrin-A1 displacement assay, inhibits the interaction of ephrin-A1 with all EphA receptor subtypes (IC50=5.5-11 uM).
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UniPR1449 is a selective EphA receptor inhibitor with IC50 of 8.1 uM in EphA2-ephrin-A1 displacement assay, inhibits the interaction of ephrin-A1 with all EphA receptor subtypes (IC50=5.5-11 uM).
UniPR1449 does not affect the binding of ephrin-B1 with EphB receptor subtypes.
UniPR1449 blocks ephrin-A1-induced EphA2 phosphorylation, internalization, and degradation in GBM cell lines.
significantly reduces proliferation and S-phase entry in patient-derived GSCs.
UniPR1449 impairs VEGF-induced angiogenesis in the chick chorioallantoic membrane (CAM) assay.
| M.Wt | 700.94 | |
| Formula | C41H52N2O6S | |
| Appearance | Solid | |
| Storage |
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| Solubility |
10 mM in DMSO |
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1. Guidetti L, et al. Eur J Med Chem. 2024 Oct 5;276:116681.
2. Zappia A, et al. Biochem Pharmacol. 2025 Dec;242(Pt 4):117398.

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