RAF-709

• Description :

  A novel potent, selective, and orally bioavailable RAF inhibitor with biochemical IC50 of 0.4 nM and 0.5 nM for BRAF and CRAF, respectively.

• Stability :

  ≥ 2 years

• Purity :

  >98% (HPLC)

• Weight :

  542.5495

• Molecular Formula :

  C28H29F3N4O4

• Notes :

  Research use only, not for human use.

• Receptor :

  B-Raf|C-Raf

• CAS Number :

  1628838-42-5