Biochemically based design of cyclooxygenase-2 (COX-2) inhibitors: Facile conversion of nonsteroidal antiinflammatory drugs to potent and highly selective COX-2 inhibitors

Samankaltaisia teoksia

• Selectivity of nonsteroidal antiinflammatory drugs as inhibitors of constitutive and inducible cyclooxygenase.
  Tekijä: Mitchell, J A, et al.
  Julkaistu: (1993)
• The 2′-Trifluoromethyl Analogue of Indomethacin Is a Potent and Selective COX-2 Inhibitor
  Tekijä: Blobaum, Anna L., et al.
  Julkaistu: (2013)
• Conjugates of Cisplatin and Cyclooxygenase Inhibitors as Potent Antitumor Agents Overcoming Cisplatin Resistance()
  Tekijä: Neumann, Wilma, et al.
  Julkaistu: (2014)
• ortho-Carbaborane Derivatives of Indomethacin as Cyclooxygenase (COX)-2 Selective Inhibitors
  Tekijä: Scholz, Matthias, et al.
  Julkaistu: (2012)
• nido-Dicarbaborate Induces Potent and Selective Inhibition of Cyclooxygenase-2()
  Tekijä: Neumann, Wilma, et al.
  Julkaistu: (2015)