Chemical Structure : TS-002266
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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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.
| M.Wt | 639.53 | |
| Formula | C31H32Cl2N6O5 | |
| Appearance | Solid | |
| Storage |
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| Solubility |
10 mM in DMSO |
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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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