L14-8
L14-8 is a potent ferroptosis inducer. L14-8 promotes PLK1 degradation via ubiquitination, increasing TP53 phosphorylation to enhance SAT1 transcription, thereby triggering ferroptosis and cancer cell death. L14-8 can be used for the study of advanced prostate cancer.
For research use only. We do not sell to patients.
- Formula: C30H25F2NO5
- Molecular Weight:517.52
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Storage:
Please store the product under the recommended conditions in the Certificate of Analysis.
To place orders, for customer services and technical support, please contact: MedChemExpress USA
Tel: 609-228-6898 E-mail: [email protected] [email protected]
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Biological Activity
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Chemical Information
- Purity & Documentation
- References
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Help & FAQs
Biological Activity
L14-8 (5-25 μM, 48 h) results in over 80% cell death in both C4-2B and 22Rv1 cells at 25 μM and does not significantly affect normal prostate cell growth[1].
L14-8 (10 μM, 24-48 h) induces ferroptosis by transcriptionally activating SAT1 expression and increase MDA level in C4-2B and 22Rv1 cells[1].
L14-8 (0-10 μM, 0-24 h) binds to PLK1 and enhances PLK1-mediated TP53 phosphorylation and expression, which is required for SAT1 transcription activation in C4-2B and 22Rv1 cells[1].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
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Cell Line:C4-2B and 22Rv1 cells
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Concentration:5 and 7.5 μM
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Incubation Time:72 h
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Result:Significantly rescued the inhibitory effect of L14-8 on the viability of C4-2B and 22Rv1 cells.
Significantly reduced the sensitivity of the cells after knocking out TP53.
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Cell Line:C4-2B and 22Rv1 cells
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Concentration:10 μM
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Incubation Time:48 h
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Result:Dramatically increased the the expression of ferroptosis-related genes SAT1.
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Cell Line:C4-2B and 22Rv1 cells
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Concentration:0, 1, 2, 4, 8, 12 and 24 h
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Incubation Time:72 h
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Result:Significantly increased the thermal stability of endogenous PLK1.
Led to an increase in the protein levels of TP53 and phosphorylated TP53 (p-TP53) .
Significantly shortened the half-life of PLK1.
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
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Animal Model:C4-2B cells xenografted model established in male 4-week-old BALB/c nude mice[1]
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Dosage:10 and 20 mg/kg
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Administration:Intraperitoneal injection (i.p.), once daily for 25 days
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Result:Significantly suppressed tumor growth in a dose-dependent manner.
Decreased cancer proliferation.
Had no changes in major organs such as the heart, kidney, liver, lung, and spleen with high doses.
Had similar liver and kidney function indices between vehicle treatment in lower doses.
Chemical Information
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Molecular Weight 517.52
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Formula C30H25F2NO5
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SMILES
FC1=CC=C([C@@H](OC(C=C)=O)CC[C@@H]2[C@@H](C3=CC=C(OC(C=C)=O)C=C3)N(C4=CC=C(F)C=C4)C2=O)C=C1
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Shipping
Room temperature in continental US; may vary elsewhere.
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Storage
Please store the product under the recommended conditions in the Certificate of Analysis.
Purity & Documentation
References
Calculators
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)
L14-8 Related Classifications
HY-175000 Related Classifications
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