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Radotinib(IY-5511) (Synonyms: IY-5511)

Catalog No.GC11140

Bcr-Abl tyrosine kinase inhibitor

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Radotinib(IY-5511) Chemical Structure

Cas No.: 926037-48-1

Tamaño Precio Disponibilidad Cantidad
10mM (in 1mL DMSO)
90,00 $
Disponible
5mg
52,00 $
Disponible
10mg
81,00 $
Disponible
25mg
156,00 $
Disponible
50mg
245,00 $
Disponible
100mg
392,00 $
Disponible
500mg
1.176,00 $
Disponible
1g
1.882,00 $
Disponible

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Sample solution is provided at 25 µL, 10mM.

Description Protocol Chemical Properties Product Documents Related Products

Radotinib(IY-5511) is a novel and selective Bcl-Abl tyrosine kinase inhibitor. [1]

Bcl-Abl is a constitutively activated chimeric tyrosine kinase which is the genetic abnormality expressed in patient with CML (chronic myeloid leukemia).

In vitro, radotinib couples to Bcr-Abl and reduce the phosphorylation of Bcr-Abl target protein CrkL. The pre-clinical studies shows superiority of radotinib to imatinib in both wild-type and mutant BCR-ABL1 positive CML cell lines. [1]

In a phase I clinical trial, dose up to 1000 mg/day of radotinib exhibits no dose-limiting toxicities. Phase II study proves radotinib to be an effective and well tolerated in chronic phase-chronic myeloid leukemia patients with resistance and/or intolerance to Bcr-Abl1 tyrosine kinase inhibitors. [1]

Reference:
1.  Kim SH, Menon H, Jootar S et al. Efficacy and safety of radotinib in chronic phase chronic myeloid leukemia patients with resistance or intolerance to BCR-ABL1 tyrosine kinase inhibitors. Haematologica. 2014 Jul;99(7):1191-6.

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