Defactinib

Pharmaceutical From Wikipedia, the free encyclopedia

Defactinib (INN, codenamed VS-6063) is an inhibitor of PTK2, also known as focal adhesion kinase (FAK), Pyk2, and MELK which was developed by Pfizer and licensed to Verastem Oncology as a potential treatment for solid tumors.

Other namesPF-04554878, VS-6063
CAS Number
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Defactinib
Clinical data
Other namesPF-04554878, VS-6063
Identifiers
  • N-methyl-4-[[4-[[3-[methyl(methylsulfonyl)amino]pyrazin-2-yl]methylamino]-5-(trifluoromethyl)pyrimidin-2-yl]amino]benzamide
CAS Number
PubChem CID
DrugBank
ChemSpider
UNII
KEGG
ChEMBL
PDB ligand
CompTox Dashboard (EPA)
Chemical and physical data
FormulaC20H21F3N8O3S
Molar mass510.50 g·mol−1
3D model (JSmol)
  • CNC(=O)C1=CC=C(C=C1)NC2=NC=C(C(=N2)NCC3=NC=CN=C3N(C)S(=O)(=O)C)C(F)(F)F
  • InChI=1S/C20H21F3N8O3S/c1-24-18(32)12-4-6-13(7-5-12)29-19-28-10-14(20(21,22)23)16(30-19)27-11-15-17(26-9-8-25-15)31(2)35(3,33)34/h4-10H,11H2,1-3H3,(H,24,32)(H2,27,28,29,30)
  • Key:FWLMVFUGMHIOAA-UHFFFAOYSA-N
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Development for mesothelioma was discontinued in 2015 due to lack of efficacy in a placebo-controlled phase II trial.[1][2] Subsequent research in patients with specific NF2 mutations also found limited activity.[3]

The co-packaged medication avutometinib/defactinib was approved for medical use in the United States in May 2025.[4][5]

References

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