Active Ingredient History

NOW
  • Now
Dabrafenib is a selective, orally bioavailable inhibitor of Mutant BRAF protein kinase with potential antineoplastic activity. Dabrafenib inhibits BRAF kinases with in vitro IC50 values of 0.65, 0.5, and 1.84 nM for BRAF V600E, BRAF V600K, and BRAF V600D enzymes, respectively. Dabrafenib also inhibits wild-type BRAF and CRAF kinases with IC50 values of 3.2 and 5.0 nM. BRAF belongs to the the raf/mil family of serine/threonine protein kinases and plays a role in regulating the MAP kinase/ERKs signaling pathway, which may be constitutively activated due to BRAF gene mutations. Mutations in BRAF are associated with increased growth and proliferation of cancer cells. By inhibiting BRAF kinase dabrafenib negatively regulates the proliferation of tumor cells which contain a mutated BRAF gene. Dabrafenib (in combination with trametinib or alone) is indicated for the treatment of unresectable or metastatic melanoma with BRAF V600E mutation   NCATS

  • SMILES: CC(C)(C)c1nc(c2cccc(NS(=O)(=O)c3c(F)cccc3F)c2F)c(s1)c4ccnc(N)n4
  • InChIKey: BFSMGDJOXZAERB-UHFFFAOYSA-N
  • Mol. Mass: 519.57
  • ALogP: 5.36
  • ChEMBL Molecules:
More Chemistry
  • Mechanism of Action:
  • Multi-specific: Missing data
  • Black Box: No
  • Availability: Prescription Only
  • Delivery Methods: Oral
  • Pro Drug: No

Drug Pricing (per unit)

Australia

$32.0656 - $47.9235

United States

$49.7393 - $90.7523
More Pricing Detail

Note: This drug pricing data is preliminary, incomplete, and may contain errors.

daborafenib plus trametinib | dabrafenib | dabrafenib mesilate | dabrafenib mesylate | gsk2118436 | gsk 2118436 | gsk-2118436 | gsk2118436a | gsk2118436b | methane sulfonate salt | tafinlar

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