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UC-514321 

Cat. No. M29859
UC-514321  Structure
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Quality Control & Documentation
Biological Activity

UC-514321, a structural analog of NSC370284 with higher activity, directly targets STAT3/5 and represses TET1 expression, but not TET2 or TET3. UC-514321 has the potential to treat acute myeloid leukemia (AML) both in vitro and in vivo, with low toxicity.

Chemical Information
Molecular Weight 441.56
Formula C26H35NO5
CAS Number 299420-83-0
Form Solid
Solubility (25°C) Ethanol 50 mg/mL (ultrasonic)
DMSO 25 mg/mL (ultrasonic)
Storage Powder          -20°C   3 years ;  4°C   2 years
In solvent       -80°C   6 months ;  -20°C   1 month
Conversion of different model animals based on BSA (PMID: 27057123)
Species Mouse Rat Rabbit Guinea pig Hamster Dog
Weight (kg) 0.02 0.15 1.8 0.4 0.08 10
Body Surface Area (m2) 0.007 0.025 0.15 0.05 0.02 0.5
Km factor 3 6 12 8 5 20
Animal A (mg/kg) = Animal B (mg/kg) multiplied by  Animal B Km
Animal A Km

For example, to modify the dose of Compound A used for a mouse (20 mg/kg) to a dose based on the BSA for a rat, multiply 20 mg/kg by the Km factor for a mouse and then divide by the Km factor for a rat. This calculation results in a rat equivalent dose for Compound A of 10 mg/kg.

References

[1] Xi Jiang, et al. Nat Commun. Targeted inhibition of STAT/TET1 axis as a therapeutic strategy for acute myeloid leukemia

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  Catalog
Abmole Inhibitor Catalog




Keywords: UC-514321  supplier, STAT, inhibitors, activators


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