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TEXTBOOK

Top Drugs
Top Synthetic Routes

John Saunders

Price: £10.99 (paper)
ISBN-13: 978-0-19-850100-8
Publication date: 18 May 2000
96 pages, 90 line illus, 246x189 mm
Series: Oxford Chemistry Primers number 90
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Description
  • Shows how the organic chemistry taught at undergraduate level is applied by medicinal chemists in industry
  • Enables students to see the importance of stereospecific syntheses and see how advances from academia have revolutionised the pharmaceutical industry
  • Explains how an understanding of modern organic chemistry is pivotal to the overall drug discovery process
  • Encourages students to search other more detailed texts
Today's top selling drugs have been uncovered from two major sources: natural products and laboratory synthesis. Those synthesised directly by medicinal chemists usually have been the result of a protracted discovery programme using a natural product (e.g. a hormone or an enzyme substrate) or a screening lead as a starting point. Many of the major categories of human disease cardiovascular, gastrointestinal, central nervous system, inflammatory and infectious diseases are included. After a short introduction to the discovery and mechanism of action of each drug, the syntheses of the best selling drugs are reviewed. Where the information exists in the literature, the original research method to each drug is compared with more recent approaches which aim either at improving the route or at validating newer methodologies or reagents in the context of drug synthesis. Since, for many drugs, the marketed product was originally prepared as a racemic mixture, perhaps the most important comparison is between that route and alternatives which involve some element of asymmetric synthesis.

Readership: Mainly organic chemistry students studying pharmacology but also medicinal chemistry students, pharmacology undergraduates and biological chemistry undergraduates.

Contents
1. Inhibitors of angiotensin converting enzyme as effective antihypertensive agents
2. Blockade of angiotensin-II receptors
3. Calcium channel blockers in the treatment of angina and hypertension
4. Antagonists of histamine receptors (Hnull) as anti-ulcer remedies
5. Proton pump inhibitors as gastric acid secretion inhibitors
6. Modulation of central serotonin in the treatment of depression
7. Hypnotic, anxiolytic, anticonvulsant and muscle relaxant agents: ligands for benzodiazepine receptors
8. Another histamine receptor: blockers of the Hnull receptor for the treatment of seasonal allergic rhinitis
9. Nucleoside analogues which inhibit HIV reverse transcriptase
10. Quinolones as anti-bacterial DNA gyrase inhibitors
Abbreviations
Index

Authors, editors, and contributors


John Saunders


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Chemistry

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