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Medicinal Chemistry Approaches to Tuberculosis and Trypanosomiasis

Om Medicinal Chemistry Approaches to Tuberculosis and Trypanosomiasis

Some of the more recent efforts in tuberculosis (TB) and trypanosomiasis drug discovery from both Product Development Partnerships (PDPs) and academia are highlighted in this this volume. Drug discovery approaches include both target- and phenotypic whole cell screening- approaches. Regarding the latter, mechanism of action studies through target identification are also illustrated. Provides an overview of the status of some of the current novel compounds in development as well as new emerging treatment options targeting novel mechanisms of actionIdentification of hits from phenotypic whole cell screening, followed by target identificationStrategies aimed at improving the efficacy of existing clinically used anti-TB drugs by taking advantage inhibitors of mycobacterial transcriptional regulators to boost the anti-tubercular activity, and circumvent acquired-resistance

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  • Språk:
  • Engelsk
  • ISBN:
  • 9780128175569
  • Bindende:
  • Hardback
  • Sider:
  • 188
  • Utgitt:
  • 7 september 2019
  • Dimensjoner:
  • 152x229x0 mm.
  • Vekt:
  • 480 g.
  Gratis frakt
Leveringstid: 2-4 uker
Forventet levering: 11 oktober 2024

Beskrivelse av Medicinal Chemistry Approaches to Tuberculosis and Trypanosomiasis

Some of the more recent efforts in tuberculosis (TB) and trypanosomiasis drug discovery from both Product Development Partnerships (PDPs) and academia are highlighted in this this volume. Drug discovery approaches include both target- and phenotypic whole cell screening- approaches. Regarding the latter, mechanism of action studies through target identification are also illustrated.
Provides an overview of the status of some of the current novel compounds in development as well as new emerging treatment options targeting novel mechanisms of actionIdentification of hits from phenotypic whole cell screening, followed by target identificationStrategies aimed at improving the efficacy of existing clinically used anti-TB drugs by taking advantage inhibitors of mycobacterial transcriptional regulators to boost the anti-tubercular activity, and circumvent acquired-resistance

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