Design and Synthesis of Indomethacin Analogues That Inhibit P-Glycoprotein and/or Multidrug Resistant Protein without Cox Inhibitory Activity

Design and Synthesis of Indomethacin Analogues That Inhibit P-Glycoprotein and/or Multidrug Resistant Protein without Cox Inhibitory Activity Indomethacin Analogues that Enhance Doxorubicin Cytotoxicity in Multidrug Resistant Cells without Cox Inhibitory Activity Modulation of MRP-1-Mediated Multidrug Resistance by Indomethacin Analogues Design, synthesis, and evaluation of novel indomethacin–antioxidant codrugs as gastrosparing NSAIDs Ester and Amide Derivatives of the Nonsteroidal Antiinflammatory Drug, Indomethacin, as Selective Cyclooxygenase-2 Inhibitors Synthesis and biological evaluation of indomethacin analogs possessing a N-difluoromethyl-1,2-dihydropyrid-2-one ring system: A search for novel cyclooxygenase and lipoxygenase inhibitors Structural modification of indomethacin toward selective inhibition of COX-2 with a significant increase in van der Waals contributions Synthesis of 2-Methyl-3-indolylacetic Derivatives as Anti-Inflammatory Agents That Inhibit Preferentially Cyclooxygenase 1 without Gastric Damage Synthesis and evaluation of carbaborane derivatives of indomethacin as cyclooxygenase inhibitors Design, synthesis and bioactivities of Celecoxib analogues or derivatives