Flezurafenib

Flezurafenib
Clinical data
Other namesJZP-815
Identifiers
  • 5-[[(3S)-3-[5-(4-fluorophenyl)-1H-imidazol-2-yl]-3,4-dihydro-2H-chromen-6-yl]oxy]-3,4-dihydro-1H-1,8-naphthyridin-2-one
CAS Number
PubChem CID
IUPHAR/BPS
UNII
KEGG
Chemical and physical data
FormulaC26H21FN4O3
Molar mass456.477 g·mol−1
3D model (JSmol)
  • C1CC(=O)NC2=NC=CC(=C21)OC3=CC4=C(C=C3)OC[C@@H](C4)C5=NC=C(N5)C6=CC=C(C=C6)F
  • InChI=InChI=1S/C26H21FN4O3/c27-18-3-1-15(2-4-18)21-13-29-25(30-21)17-11-16-12-19(5-7-22(16)33-14-17)34-23-9-10-28-26-20(23)6-8-24(32)31-26/h1-5,7,9-10,12-13,17H,6,8,11,14H2,(H,29,30)(H,28,31,32)/t17-/m1/s1
  • Key:TWJSMWXWCWQPRO-QGZVFWFLSA-N

Flezurafenib is an investigational new drug designed as a rapidly accelerated fibrosarcoma (RAF) kinase inhibitor which is being evaluated for the treatment of cancer. Developed by Jazz Pharmaceuticals, this novel therapeutic agent is currently being explored for its efficacy against solid tumors and hematological malignancies harboring oncogenic mutations that activate the RAS-RAF-MAPK signaling pathway.[1][2] As of January 2025, flezurafenib has reached Phase 1 clinical trials, where it is being evaluated for the treatment of advanced cancers and advanced malignant solid neoplasms.[1]

References

  1. ^ a b "JZP-815". PatSnap.
  2. ^ Riaud M, Maxwell J, Soria-Bretones I, Dankner M, Li M, Rose AA (February 2024). "The role of CRAF in cancer progression: from molecular mechanisms to precision therapies". Nature Reviews. Cancer. 24 (2): 105–122. doi:10.1038/s41568-023-00650-x. PMID 38195917.


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