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Progress in Medicinal Chemistry - F.D. (SmithKIine Beecham Pharmaceuticals
New Frontiers Science Park (North)
Third Avenue) King - Bog

Bag om Progress in Medicinal Chemistry

This volume includes information on recent advances in five important areas: an account of inhibitors of the caspase family of proteolytic enzymes that represent a new class of anti-inflammatory and antiapoptotic agents of potential value in rheumatoid arthritis; and a survey of semi-synthetic and totally synthetic antibiotics and anti-HIV agents and their sites of interaction; the development of inhibitors of the intracellular enzyme acyl-CoA: cholesterol O-acyltransferase (ACAT) for the treatment of hypercholesterolemia; a description of recent progress in growth hormone secretagogues, with the focus on strategies to improve oral bioavailability and duration of action; and information on inhibition of the proteolytic enzyme, hepatitis C protease N-3(NS3), (required for vital replication) as one of the most attractive targets for HCV infections.

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  • Sprog:
  • Engelsk
  • ISBN:
  • 9780444511430
  • Indbinding:
  • Hardback
  • Sideantal:
  • 450
  • Udgivet:
  • 15. april 2004
  • Størrelse:
  • 152x229x23 mm.
  • Vægt:
  • 690 g.
  • 2-4 uger.
  • 12. december 2024

Normalpris

  • BLACK NOVEMBER

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Beskrivelse af Progress in Medicinal Chemistry

This volume includes information on recent advances in five important areas: an account of inhibitors of the caspase family of proteolytic enzymes that represent a new class of anti-inflammatory and antiapoptotic agents of potential value in rheumatoid arthritis; and a survey of semi-synthetic and totally synthetic antibiotics and anti-HIV agents and their sites of interaction; the development of inhibitors of the intracellular enzyme acyl-CoA: cholesterol O-acyltransferase (ACAT) for the treatment of hypercholesterolemia; a description of recent progress in growth hormone secretagogues, with the focus on strategies to improve oral bioavailability and duration of action; and information on inhibition of the proteolytic enzyme, hepatitis C protease N-3(NS3), (required for vital replication) as one of the most attractive targets for HCV infections.

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