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A small molecule focal adhesion kinase (FAK) inhibitor, targeting Y397 site: 1-(2-hydroxyethyl) -3, 5, 7-triaza-1-azoniatricyclo [3.3.1.13,7]decane; bromide effectively inhibits FAK autophosphorylation activity and decreases cancer cell viability, clonogenicity and tumor growth in vivo

  • Vita M. Golubovskaya
  • , Sheila Figel
  • , Baotran T. Ho
  • , Christopher P. Johnson
  • , Michael Yemma
  • , Grace Huang
  • , Min Zheng
  • , Carl Nyberg
  • , Andrew Magis
  • , David A. Ostrov
  • , Irwin H. Gelman
  • , William G. Cance

Research output: Contribution to journal › Article › peer-review

84 Scopus citations

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Pharmacology, Toxicology and Pharmaceutical Science