Radotinib

Radotinib Structure
CAS No.
926037-48-1
Chemical Name:
Radotinib
Synonyms
Supect;Radotinib HCl;IY5511;CS-1712;Radotinib;IY5511 HCl.;Radotinib(IY-5511);RADOTINIB; IY5511 HCL.;Testosterone Impurity 43;4-methyl-N-[3-(4-methylimidazol-1-yl)-5-(trifluoromethyl)phe...
CBNumber:
CB32667981
Molecular Formula:
C27H21F3N8O
Molecular Weight:
530.5
MOL File:
926037-48-1.mol
Modify Date:
2024/7/2 8:55:06

Radotinib Properties

Density 1.40±0.1 g/cm3(Predicted)
storage temp. Store at -20°C
solubility ≥26.55 mg/mL in DMSO; insoluble in EtOH; insoluble in H2O
form solid
pka 12.94±0.70(Predicted)
color Light yellow to yellow

Radotinib Chemical Properties,Uses,Production

Description

Radotinib, an inhibitor of Bcr–Abl tyrosine kinase,was approved in January 2012 in Korea as a second-line treatment for chronic myeloid leukemia (CML). Radotinib is a TKI with a similar structure to the second-generation TKI, nilotinib, in which a pyridyl group has been replaced with a pyrazinemoiety. The in vitro activity of radotinib against a variety of tumor cell lines is disclosed in an issued patent. Radotinib was significantly more potent than imatinib in all of the cell lines tested. The synthesis of radotinib via amide coupling is described in the patent literature.

Uses

Radotinib is tyrosine kinase inhibitor. In a biological study, it can induce cytotoxicity in c-KIT-positive malignancies including acute myeloid leukemia and small cell lung cancer in human making it potential target agent for treatment of such malignancies. It is a COVID19-related research product.

Indications

Radotinib (Supect(R), Il-Yang Pharmaceutical) is a Bcr–Abl inhibitor that was approved in South Korea in 2012 for the treatment of imatinib-resistant CML. Radotinib, which has a terminal 4-(pyridine-2-yl) pyrimidine moiety, was developed based on the previously approved Bcr–Abl inhibitors nilotinib. Radotinib has equivalent efficacy with that of other second-generation Bcr–Abl inhibitors and is well tolerated in chronic-phase CML patients. The lower cost of radotinib compared with other FDA-approved Bcr–Abl inhibitors makes it an attractive alternative for the treatment of CML in developing nations.

Radotinib Preparation Products And Raw materials

Raw materials

Preparation Products

Global( 105)Suppliers
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CLEARSYNTH LABS LTD. +91-22-45045900 Hyderabad, India 6351 58 Inquiry
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Zhejiang J&C Biological Technology Co.,Limited +1-2135480471 +1-2135480471 China 10522 58 Inquiry
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Hefei TNJ Chemical Industry Co.,Ltd. 0551-65418684 +8618949823763 China 25363 58 Inquiry

Radotinib Spectrum

926037-48-1(Radotinib)Related Search:

IY5511 Radotinib Radotinib(IY-5511) 4-Methyl-N-[3-(4-methylimidazol-1-yl)-5-trifluoromethylphenyl]-3-(4-(pyrazin-2-yl)pyrimidin-2-ylamino)benzamide 4-methyl-N-[3-(4-methylimidazol-1-yl)-5-(trifluoromethyl)phe... Benzamide, 4-methyl-N-[3-(4-methyl-1H-imidazol-1-yl)-5-(trifluoromethyl)phenyl]-3-[[4-(2-pyrazinyl)-2-pyrimidinyl]amino]- RADOTINIB; IY5511 HCL. IY5511 HCl. CS-1712 Radotinib HCl Supect Testosterone Impurity 43 926037-48-1 C27H21F3N8O Inhibitors