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TS-002266

Chemical Structure : TS-002266

CAS No.: 2702325-64-0

TS-002266 (TS002266)

Catalog No.: PC-27674Not For Human Use, Lab Use Only.

TS-002266 is a potent and selective RNA terminal uridylyl transferase enzymes 4 and 7 (TUT4/7) inhibitor, blocks miRNA uridylation in vitro with biochemical IC50 of 69 and 16 nM for TUT4 and TUT7, respectively.

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    Biological Activity

    TS-002266 is a potent and selective RNA terminal uridylyl transferase enzymes 4 and 7 (TUT4/7) inhibitor, blocks miRNA uridylation in vitro with biochemical IC50 of 69 and 16 nM for TUT4 and TUT7, respectively.
    TS-002266 substantially reduces uridylation and demonstrate in vitro and in vivo antiproliferative activity specifically in FOCAD-deleted cancer.
    TS-002266 significantly decreases the proliferation and colony formation of human NOMO-1 cells.
    TS-002266 sensitizes AML cells to venetoclax in a variety of blood cancers.
    TS-002266 reduces their proliferation and induces apoptosis in murine Meis1/Hoxa9 transformed cells.
    TS-002266 exhibits reduced colony formation capacity in primary AML patient samples.

    Physicochemical Properties

    M.Wt 639.53
    Formula C31H32Cl2N6O5
    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

    (R)-6-Chloro-7-(2-(((3-chloro-4-methoxypyridin-2-yl)oxy)methyl)pyrrolidin-1-yl)-1-(6-(3-(dimethylamino)azetidin-1-yl)pyridin-3-yl)-4-oxo-1,4-dihydroquinoline-3-carboxylic acid

    References

    1. Triboulet R, et al. Mol Cancer Ther. 2024 Dec 3;23(12):1779-1788.

    2. Mapperley C, et al. Sci Adv. 2026 Aug 14;12(33):eaec3399.

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