Date published: 2026-5-6

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Sorafenib N-Oxide (CAS 583840-03-3)

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Alternate Names:
Sorafenib N-Oxide is also known as BAY 67-3472.
Application:
Sorafenib N-Oxide is an active metabolite of Sorafenib, a potent Raf kinase, FLT3, and acute myeloid leukemia cell inhibitor.
CAS Number:
583840-03-3
Molecular Weight:
480.82
Molecular Formula:
C21H16ClF3N4O4
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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Sorafenib N-Oxide is a metabolite of Sorafenib, a potent Raf kinase inhibitor. In addition to Raf-1, B-RAF, and receptor tyrosine kinases, Sorafenib N-Oxide also inhibits FLT3 that contains the internal tandem duplication mutation and inhibits proliferation of MV4-11 acute myeloid leukemia (AML) cells expressing FLT3-ITD. Sorafenib N-Oxide is selective for AML cell lines containing FLT3-ITD over lines containing wild FLT3. Sorafenib N-Oxide can function as a linear-mixed inhibitor of CYP3A4. Sorafenib N-oxide acts as a linear-mixed inhibitor of the cytochrome P450 (CYP) isoform CYP3A4 with a Ki value of 15 µM in human liver microsomes.


Sorafenib N-Oxide (CAS 583840-03-3) References

  1. Quantitation of sorafenib and its active metabolite sorafenib N-oxide in human plasma by liquid chromatography-tandem mass spectrometry.  |  Li, L., et al. 2010. J Chromatogr B Analyt Technol Biomed Life Sci. 878: 3033-8. PMID: 20870468
  2. A quantitative HPLC-UV method for determination of serum sorafenib and sorafenib N-oxide and its application in hepatocarcinoma patients.  |  Shimada, M., et al. 2014. Tohoku J Exp Med. 233: 103-12. PMID: 24872323
  3. The Influence of Paracetamol on the Penetration of Sorafenib and Sorafenib N-Oxide Through the Blood-Brain Barrier in Rats.  |  Karbownik, A., et al. 2020. Eur J Drug Metab Pharmacokinet. 45: 801-808. PMID: 32776310
  4. Baicalin Enhanced Oral Bioavailability of Sorafenib in Rats by Inducing Intestine Absorption.  |  Wei, J., et al. 2021. Front Pharmacol. 12: 761763. PMID: 34819863
  5. Pharmacokinetic Drug Interaction Study of Sorafenib and Morphine in Rats.  |  Karbownik, A., et al. 2021. Pharmaceutics. 13: PMID: 34959453
  6. The Role of Uptake and Efflux Transporters in the Disposition of Glucuronide and Sulfate Conjugates.  |  Järvinen, E., et al. 2021. Front Pharmacol. 12: 802539. PMID: 35095509
  7. Pharmacokinetic Exposures Associated With Oral Administration of Sorafenib in Dogs With Spontaneous Tumors.  |  Cawley, JR., et al. 2022. Front Vet Sci. 9: 888483. PMID: 35664857
  8. Hesperetin mitigates sorafenib-induced cardiotoxicity in mice through inhibition of the TLR4/NLRP3 signaling pathway.  |  Zaafar, D., et al. 2022. PLoS One. 17: e0271631. PMID: 35944026
  9. Pharmacokinetic Interactions between Canagliflozin and Sorafenib or Lenvatinib in Rats.  |  Cui, Y., et al. 2022. Molecules. 27: PMID: 36080187
  10. A high throughput method for Monitoring of Sorafenib, regorafenib, cabozantinib and their metabolites with UPLC-MS/MS in rat plasma.  |  Gu, EM., et al. 2022. Front Pharmacol. 13: 955263. PMID: 36160432
  11. Inhibitory effects of Thai herbal extracts on the cytochrome P450 3A-mediated the metabolism of gefitinib, lapatinib and sorafenib.  |  Rodseeda, C., et al. 2022. Toxicol Rep. 9: 1846-1852. PMID: 36518483
  12. Efficacy and safety of lenvatinib versus sorafenib in first-line treatment of advanced hepatocellular carcinoma: A meta-analysis.  |  Luo, J., et al. 2022. Front Oncol. 12: 1010726. PMID: 36620586
  13. The Role of Organic Cation Transporters in the Pharmacokinetics, Pharmacodynamics and Drug-Drug Interactions of Tyrosine Kinase Inhibitors.  |  Xiu, F., et al. 2023. Int J Mol Sci. 24: PMID: 36768423

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Sorafenib N-Oxide, 1 mg

sc-208399A
1 mg
$203.00

Sorafenib N-Oxide, 5 mg

sc-208399
5 mg
$490.00

Sorafenib N-Oxide, 25 mg

sc-208399B
25 mg
$1775.00

Sorafenib N-Oxide, 50 mg

sc-208399C
50 mg
$3060.00