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Inhibition of bacterial cytokinesis by curcumin analogues

  • At: 2014 FIP Congress in PSWC, Melbourne (Australia)
  • Type: Presentation
  • By: GROUNDWATER, Paul William (UNIVERSITY OF SYDNEY, FACULTY OF PHARMACY, Sydney, Australia)
  • Co-author(s): Liao, Vivian (UNIVERSITY OF SYDNEY, Sydney, Australia)
    Narlawar, Rajeshwar (UNIVERSITY OF SYDNEY, Sydney, Australia)
    Hibbs, David (UNIVERSITY OF SYDNEY, Sydney, Australia)
    Panda, Dulal (Indian Institute of Technology Bombay, Department of Biosciences, Mumbai, India)
    Doddareddy, Munikumar (UNIVERSITY OF SYDNEY, Sydney, Australia)
    Bhattacharya, Anusri (Indian Institute of Technology Bombay, Department of Biosciences, Mumbai, India)
    Shalini (Indian Institute of Technology Bombay, Department of Biosciences, Mumbai, India)
    Perry, John (Freeman Hospital, Newcastle, United Kingdom)
    Marrs, Emma (Freeman Hospital, Newcastle, United Kingdom)
  • Abstract:

    Background: Curcumin is the major bioactive constituent of turmeric, the rhizome of Curcuma longa. It has activity against a number of cellular targets and has been used as a lead in many areas of drug discovery. No maximum tolerated dose has been determined for curcumin, but its potential for clinical application is limited due to its poor

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Last update 4 October 2019

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