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QP6126

Chemical Structure : QP6126

CAS No.: 3027434-53-0

QP6126 (QP-6126)

Catalog No.: PC-28153Not For Human Use, Lab Use Only.

QP6126 is a highly potent, orally bioavailable inhibitor of Glutaminyl-peptide cyclotransferase-like protein (QPCTL) with IC50 of 2.3 nM.

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Purity & Documentation Purity: >98% (HPLC)

Biological Activity

QP6126 is a highly potent, orally bioavailable inhibitor of Glutaminyl-peptide cyclotransferase-like protein (QPCTL) with IC50 of 2.3 nM.
QP6126 dose-dependently inhibits the formation of pGlu-CD47 in human HEK293T cells and melanoma A375 cells, also significantly and dose-dependently suppresses the binding of recombinant mouse SIRPα protein to CD47 in B16F10 cells.
QP6126 reduces pGlu-CD47, disrupts CD47-SIRPα interaction, and sensitizes melanoma cells to macrophage phagocytosis.
QP6126 exhibited orally active antitumor effects that synergized with anti-PD-1 therapy in B16F10 melanoma mouse model.

Physicochemical Properties

M.Wt 365.43
Formula C20H16D3FN6
Appearance Solid
CAS No.
Storage
Solide Powder
-20°C 12 Months; 4°C 6 Months
In Solvent
-80°C 6 Months; -20°C 6 Months
Shipping
Solubility

10 mM in DMSO

Chemical Name/SMILES

3-(6-fluoropyridin-3-yl)-2-(4-(4-(methyl-d3)-4H-1,2,4-triazol-3-yl)piperidin-1-yl)benzonitrile

References

1. Xie L, et al. Int Immunopharmacol. 2026 Sep 7;189:117345.

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