Radotinib

Chemical compound
  • None
Identifiers
  • 4-Methyl-N-[3-(4-methylimidazol-1-yl)-5-(trifluoromethyl)phenyl]-3-[(4-pyrazin-2-ylpyrimidin-2-yl)amino]benzamide
CAS Number
  • 926037-48-1
PubChem CID
  • 16063245
ChemSpider
  • 17222861
UNII
  • I284LJY110
CompTox Dashboard (EPA)
  • DTXSID90239069 Edit this at Wikidata
Chemical and physical dataFormulaC27H21F3N8OMolar mass530.515 g·mol−13D model (JSmol)
  • Interactive image
  • Cc1cn(-c2cc(NC(=O)c3ccc(C)c(Nc4nccc(-c5cnccn5)n4)c3)cc(C(F)(F)F)c2)cn1
InChI
  • InChI=1S/C27H21F3N8O/c1-16-3-4-18(9-23(16)37-26-33-6-5-22(36-26)24-13-31-7-8-32-24)25(39)35-20-10-19(27(28,29)30)11-21(12-20)38-14-17(2)34-15-38/h3-15H,1-2H3,(H,35,39)(H,33,36,37)
  • Key:DUPWHXBITIZIKZ-UHFFFAOYSA-N

Radotinib (INN; trade name Supect), and sometimes referred to by its investigational name IY5511, is a drug for the treatment of different types of cancer, most notably Philadelphia chromosome-positive (Ph+) chronic myeloid leukemia (CML)[1] with resistance or intolerance of other Bcr-Abl tyrosine-kinase inhibitors, such as patients resistant or intolerant to imatinib.

Radotinib is being developed by Ilyang Pharmaceutical Co., Ltd of South Korea[2] and is co-marketed by Daewoong Pharmaceutical Co. Ltd, in South Korea.[3] Radotinib completed a multi-national Phase II clinical trial study in 2012[4] and in August 2011, Ilyang initiated a Phase III, multinational, multi-center, open-label, randomized study for first-line indication.[5] Its mechanism of action involves inhibition of the Bcr-Abl tyrosine kinase and of platelet-derived growth factor receptor (PDGFR).[6]

References

  1. ^ Bronson J, Black A, Dhar TG, Ellsworth BA, Merritt JR (2013). "To Market, To Market - 2012: Radotinib (Anticancer)". Annual Reports in Medicinal Chemistry. 48: 523–524. doi:10.1016/b978-0-12-417150-3.00028-4. ISBN 9780124171503.
  2. ^ "Il-Yang Pharmaceutical".
  3. ^ Yoon EK (23 October 2012). "Daewoong will market Ilyang's new leukemia drug". Daily Pharm News. Archived from the original on 2016-03-03.
  4. ^ Kim SH, Menon H, Jootar S, Saikia T, Kwak JY, Sohn SK, et al. (July 2014). "Efficacy and safety of radotinib in chronic phase chronic myeloid leukemia patients with resistance or intolerance to BCR-ABL1 tyrosine kinase inhibitors". Haematologica. 99 (7): 1191–1196. doi:10.3324/haematol.2013.096776. PMC 4077080. PMID 24705186.
  5. ^ Clinical trial number NCT01511289 for "A Phase 3 Multinational, Multi-center, Open-Label, Randomized Study of the Efficacy of Radotinib Versus Imatinib in Newly Diagnosed Ph+ CML Patients in Early Chronic Phase" at ClinicalTrials.gov
  6. ^ "Radotinib hydrochloride". NCI Drug Dictionary. National Cancer Institute. 2011-02-02.
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