Chemical Structure : UMR2-705
Catalog No.: PC-26134Not For Human Use, Lab Use Only.
UMR2-705 is a novel Tumor Necrosis Factor Receptor 2 (TNFR2) agonist peptide, promotes Tregs expansion without affecting CD8+ T cells or conventional effector T cells (Teffs), acting through TNFR2 signaling.
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UMR2-705 is a novel Tumor Necrosis Factor Receptor 2 (TNFR2) agonist peptide, promotes Tregs expansion without affecting CD8+ T cells or conventional effector T cells (Teffs), acting through TNFR2 signaling.
UMR2-705 induces dose-dependent expansion of Tregs in murine CD4+ T cells and human PBMCs. selectively promotes Treg expansion through TNFR2 signaling.
UMR2-705 (25 mg/kg/day x 3 days) increases the proportion of Tregs in the spleen and lymph nodes in Balb/c mice.
UMR2-705 mitigates LPS-induced systemic inflammation and cytokine production, promotes dendritic cell accumulation in vivo and enhances their capacity to expand regulatory T cells in vitro.
UMR2-705 activates inflammation-associated signaling pathways, increases expression of multiple members of the TNF receptor superfamily, including Tnfrsf10b (TRAILR2), Tnfrsf9 (4-1BB), Tnfrsf18 (GITR), Tnfrsf1b (TNFR2), and Tnfrsf4 (OX40), on CD4+ T cells.
| M.Wt | 836.00 | |
| Formula | C40H65N7O12 | |
| Appearance | Solid | |
| Storage |
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| Solubility |
10 mM in DMSO |
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1. Ping Liao, et al. Front Immunol. 2025 Nov 26:16:1696587.

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