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Ifidancitinib

Chemical Structure : Ifidancitinib

CAS No.: 1236667-40-5

Ifidancitinib (ATI-502, ATI-50002, R507)

Catalog No.: PC-49397Not For Human Use, Lab Use Only.

Ifidancitinib (ATI-502, ATI-50002, R507) is a potent and selective next-generation JAK1/3 inhibitor, potently inhibits γc cytokine signaling.

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

Biological Activity

Ifidancitinib (ATI-502, ATI-50002, R507) is a potent and selective next-generation JAK1/3 inhibitor, potently inhibits γc cytokine signaling.
Ifidancitinib strongly inhibited IL-2-stimulated STAT5 phosphorylation in mouse T cells.
Ifidancitinib also exhibited potent inhibitory effects on JAK1/2-mediated IFN-γ signaling.
Ifidancitinib treatment significantly reduced the population of NKG2D+CD8+ T cells in a dose-dependent manner.
Ifidancitinib impaired murine T cell proliferation and human T cell function in vitro and in vivo.
Ifidancitinib prevented the onset of alopecia in alopecia areata (AA) skin grafted C3H/HeJ mice.
Ifidancitinib induced multiple co-inhibitory receptors in CD44+CD62L- CD8+ T cells.
Ifidancitinib exhibited potent anti-inflammatory effects both in vitro and in C3H/HeJ mice in vivo, suppressed IFN-γ signaling with the reduced expression of IFN-γ-dependent genes such as MHC class I, CXCL10, and CXCL11.

Physicochemical Properties

M.Wt 395.394
Formula C20H18FN5O3
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

5-[[2-(4-fluoro-3-methoxy-5-methylanilino)-5-methylpyrimidin-4-yl]amino]-3H-1,3-benzoxazol-2-one

References

1. Zhenpeng Dai, et al. Front Immunol. 2022 Sep 20;13:955038.

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