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ATI-450

Chemical Structure : ATI-450

CAS No.: 1640282-42-3

ATI-450 (CDD-450, Zunsemetinib, CDD450)

Catalog No.: PC-35136Not For Human Use, Lab Use Only.

Zunsemetinib (ATI-450, CDD-450) is an unique inhibitor that selectively blocks p38α activation of proinflammatory kinase MAPK-MK2 while sparing p38α activation of PRAK and ATF2.

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

    Biological Activity

    Zunsemetinib (ATI-450, CDD-450) is an unique inhibitor that selectively blocks p38α activation of proinflammatory kinase MAPK-MK2 while sparing p38α activation of PRAK and ATF2.
    Zunsemetinib (ATI-450) is an orally bioavailable small molecule inhibitor of mitogen-activated protein kinase-activated protein kinase 2 (MAPKAPK2, MK2) pathway.
    Zunsemetinib (ATI-450, CDD-450) shows no effect on NLRP3 expression, but decreases IL-1β expression by promoting IL-1β mRNA degradation.
    Zunsemetinib (ATI-450, CDD-450) accelerates TNF-α and IL-6 mRNA decay, inhibites inflammation in mice with cryopyrinopathy, and is as efficacious as global p38α inhibitors in attenuating arthritis in rats and cytokine expression by cells from patients with cryopyrinopathy and rheumatoid arthritis.

    Physicochemical Properties

    M.Wt 513.93
    Formula C25H22ClF2N5O3
    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

    (2'S)-3-Chloro-4-[(3,5-difluoro-2-pyridinyl)methoxy]-2'-[2-(1-hydroxy-1-methylethyl)-4-pyrimidinyl]-5',6-dimethyl[1(2H),4'-bipyridin]-2-one

    References

    1. Wang C, et al. J Exp Med. 2018 May 7;215(5):1315-1325.

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