Shopping Cart
Remove All
Your shopping cart is currently empty
Synonyms: IY-5511 dihydrochloride
Radotinib dihydrochloride
| Pack Size | Price | USA Stock | Global Stock | Quantity |
|---|---|---|---|---|
| 10 mg | Inquiry | 10-14 weeks | 10-14 weeks | |
| 50 mg | Inquiry | 10-14 weeks | 10-14 weeks |
| Description | Radotinib (IY-5511) dihydrochloride is an orally bioavailable and brain-penetrant selective tyrosine kinase Bcr-Abl1 inhibitor with an IC50 of 34 nM. It exhibits antiprion and antitumor activities by inhibiting tumor cell proliferation, inducing cell cycle arrest, and triggering apoptosis. Radotinib dihydrochloride is applicable in research on chronic myeloid leukemia, multiple myeloma, other tumors, and prion-related neurodegenerative diseases. |
| In vitro | Radotinib dihydrochloride (0-100 μM; 72 h) significantly inhibits the proliferation of various multiple myeloma cell lines, induces apoptosis, and causes cell cycle arrest by targeting the STAT3 and JAK2 signaling pathways. Additionally, Radotinib dihydrochloride (0-40 μM; 24 h) reduces PrPSc levels in ZW13-2 neuronal cells infected with pruritus strains 22L or 139A. |
| In vivo | Radotinib (100 mg/kg; administered via intraperitoneal injection; once daily, excluding weekends; for 21 days) dihydrochloride demonstrates antitumor activity in a nude mouse model implanted with IM-9 cells. Additionally, Radotinib (100 mg/kg; administered via oral gavage; for 4-8 weeks) dihydrochloride extends the survival time and reduces PrPSc deposition in hamsters infected with the 263K pruritus strain. |
| Synonyms | IY-5511 dihydrochloride |
| Molecular Weight | 603.43 |
| Formula | C27H23Cl2F3N8O |
| Cas No. | 926037-85-6 |
| Smiles | O=C(C1=CC=C(C)C(NC2=NC(C3=NC=CN=C3)=CC=N2)=C1)NC4=CC(C(F)(F)F)=CC(N5C=NC(C)=C5)=C4.Cl.Cl |
| Storage | Powder: -20°C for 3 years | In solvent: -80°C for 1 year Shipping with blue ice/Shipping at ambient temperature. |
Dissolve 2 mg of the compound in 100 μL DMSO
to obtain a stock solution at a concentration of 20 mg/mL . If the required concentration exceeds the compound's known solubility, please contact us for technical support before proceeding.
1) Add 100 μL of the DMSO
stock solution to 400 µL PEG300
and mix thoroughly until the solution becomes clear.
2) Add 50 µL Tween 80 and mix well until fully clarified.
3) Add 450 µL Saline,PBS or ddH2O
and mix thoroughly until a homogeneous solution is obtained.
| Size | Quantity | Unit Price | Amount | Operation |
|---|

Copyright © 2015-2026 TargetMol Chemicals Inc. All Rights Reserved.