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Seletalisib

Chemical Structure : Seletalisib

CAS No.: 1362850-20-1

Seletalisib (UCB-5857, UCB5857)

Catalog No.: PC-45071Not For Human Use, Lab Use Only.

Seletalisib (UCB-5857) is a potent, ATP-competitive, and selective PI3Kδ inhibitor with IC50 of 12 nM.

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Purity & Documentation Purity: >98% (HPLC) Select Batch:

Biological Activity

Seletalisib (UCB-5857) is a potent, ATP-competitive, and selective PI3Kδ inhibitor with IC50 of 12 nM.
Seletalisib (UCB-5857) shows significant selectivity to PI3Kδ with respect to the other class I PI3K isoforms (204-303 fold).
Seletalisib (UCB-5857) blocks AKT phosphorylation following activation of the B-cell receptor in a B-cell line.
Seletalisib (UCB-5857) blocks human T-cell production of several cytokines from activated T-cells, and inhibits B-cell proliferation and cytokine release.
Seletalisib (UCB-5857) dose-dependently inhibits anti-CD3-antibody-induced interleukin 2 release in mice.

Physicochemical Properties

M.Wt 482.8451
Formula C23H14ClF3N6O
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

DMSO: ≥83.3 mg/mL

Chemical Name/SMILES

Pyrido[3,2-d]pyrimidin-4-amine, N-[(1R)-1-[8-chloro-2-(1-oxido-3-pyridinyl)-3-quinolinyl]-2,2,2-trifluoroethyl]-

References

1. Allen RA, et al. J Pharmacol Exp Ther. 2017 Jun;361(3):429-440.

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