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首页-小分子抑制剂&激动剂-Proteasome/Ubiquitin-Ubiquitin-conjugating Enzyme (E2)-UBE2D3 inhibitor QX-6
UBE2D3 inhibitor QX-6

Chemical Structure : UBE2D3 inhibitor QX-6

CAS No.: 2264085-55-2

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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纯度 & COA & 质检文件 纯度: >98% (HPLC)

生物&药学活性

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.

物理化学性质&存储条件

分子量 458.40
分子式 C24H28BrNO3
外观性状 Solid
CAS No.
储存条件
固体粉末
-20°C 12 个月; 4°C 6 个月
配置液
-80°C 6 个月; -20°C 6 个月
Shipping
Solubility

10 mM in DMSO

Chemical Name/SMILES

(3S,3aS,9bR)-8-((2-bromobenzyl)oxy)-3-((dimethylamino)methyl)-6,9-dimethyl-3a,4,5,9b-tetrahydronaphtho[1,2-b]furan-2(3H)-one

参考文献

1. Wang S, et al. Nat Commun. 2025 Nov 28;16(1):10733.

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