Chemical Structure : UBE2D3 inhibitor QX-6
货号: PC-25849Not For Human Use, Lab Use Only.
UBE2D3 inhibitor QX-6 is a potent UBE2D3 (UbcH5c) inhibitor, binds to the catalytic active domain of UBE2D3 with MST KD of 12.68 nM, enhances IFN-γ-induced antigen peptide presentation in cancer cells.
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UBE2D3 inhibitor QX-6 is a potent UBE2D3 (UbcH5c) inhibitor, binds to the catalytic active domain of UBE2D3 with MST KD of 12.68 nM, enhances IFN-γ-induced antigen peptide presentation in cancer cells.
QX-6 inhibited the E2-ubiquitin thioester conjugate activity of UBE2D3 in cell-free assays and inhibited TAP2 K63 linkage polyubiquitination in vitro.
QX-6 treatment enhanced and prolonged antigen presentation in IFN-γ-activated cancer cells, a response attenuated by UBE2D3.
QX-6 at doses of 10–100 mg/kg significantly inhibited tumor growth in immunocompetent subcutaneous KPC model, increased the population of tumor-infiltrating T lymphocytes in C57BL/6 mice.
QX-6 synergistically enhanced TCR-T-cell immunotherapy against PDAC, promoted the cytotoxicity of tumor-infiltrating CD8+ T cells in both CD45.2 donors and CD45.1 recipients.
| 分子量 | 458.40 | |
| 分子式 | C24H28BrNO3 | |
| 外观性状 | Solid | |
| 储存条件 |
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| Solubility |
10 mM in DMSO |
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1. Wang S, et al. Nat Commun. 2025 Nov 28;16(1):10733.
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