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UC-514321

Catalog No.
BA2996
A selective TET1 inhibitor
Grouped product items
SizePriceStock Qty
1mL(10 mM in DMSO)
$198.00
Ship with 10-15 days
1mg
$76.00
Ship with 10-15 days
5mg
$180.00
Ship with 10-15 days
10mg
$306.00
Ship with 10-15 days
For scientific research use only and should not be used for diagnostic or medical purposes.

Tel: +1-832-696-8203

Email: [email protected]

Worldwide Distributors

Background

UC-514321 is a new type of small molecule compound, which is a structural analogue of NSC370284 but shows higher biological activity. Studies have shown that UC-514321 can effectively target the STAT3/5 signaling pathway and selectively inhibit the expression of the TET1 gene, thereby exerting a significant anti-tumor effect. In both the in vitro cell model and the in vivo animal model of acute myeloid leukemia (AML), UC-514321 demonstrated excellent anti-leukemia activity, effectively inhibiting the proliferation of AML cells and inducing cell apoptosis. Furthermore, UC-514321 demonstrated low toxicity and high safety in animal experiments, suggesting that it has good potential for clinical transformation. Therefore, UC-514321, as an efficient and low-toxicity STAT3/5 inhibitor and TET1 expression regulator, is expected to become a new candidate drug for the treatment of AML.

Chemical Properties

Physical AppearanceA solid
StorageStore at -20°C
M.Wt441.56
Cas No.299420-83-0
FormulaC26H35NO5
Chemical Name 6-((3,5-di-tert-butyl-4-hydroxyphenyl)(morpholino)methyl)benzo[d][1,3]dioxol-5-ol
SDFDownload SDF
Canonical SMILESOC(C=C(OCO1)C1=C2)=C2C(C3=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C3)N4CCOCC4
Shipping ConditionSmall Molecules with Blue Ice, Modified Nucleotides with Dry Ice.
General tips We do not recommend long-term storage for the solution, please use it up soon.

Quality Control

Quality Control & MSDS

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Chemical structure

UC-514321