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  • The Chemistry and Biology of Isoquinoline Alkaloids

    The Chemistry and Biology of Isoquinoline Alkaloids by Phillipson, J.D.; Roberts, M.F.; Zenk, M.H.;

    Series: Proceedings in Life Sciences;

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      • Publisher's listprice EUR 160.49
      • The price is estimated because at the time of ordering we do not know what conversion rates will apply to HUF / product currency when the book arrives. In case HUF is weaker, the price increases slightly, in case HUF is stronger, the price goes lower slightly.

        66 563 Ft (63 393 Ft + 5% VAT)
      • Discount 20% (cc. 13 313 Ft off)
      • Discounted price 53 250 Ft (50 714 Ft + 5% VAT)

    66 563 Ft

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    Product details:

    • Edition number Softcover reprint of the original 1st ed. 1985
    • Publisher Springer Berlin Heidelberg
    • Date of Publication 20 November 2011
    • Number of Volumes 1 pieces, Book

    • ISBN 9783642701306
    • Binding Paperback
    • No. of pages304 pages
    • Size 244x170 mm
    • Weight 555 g
    • Language English
    • Illustrations IX, 304 p.
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    Long description:

    Isoquinolines form one of the largest groups of plant alkaloids and they in­ clude a number of valuable clinical agents such as codeine, morphine, eme­ tine and tubocurarine. Research into different aspects of isoquinolines con­ tinues in profusion, attracting the talents of botanists, chemists, bioche­ mists, analysts, pharmacists and pharmacologists. Many of these aspects are of an interdisciplinary nature, and in April 1984, The Phytochemical Society of Europe arranged a 3-day symposium on The Chemistry and Bi­ ology of Isoquinoline Alkaloids in order to provide a forum for scientists of differing disciplines who are united by a common interest in this one class of natural product. Each chapter in this volume is based on a lecture given at this symposium. Attempts have been made to make the aims and objectives, experimental findings and conclusions reached, intelligible to scientists of differing backgrounds. The introductory chapter, which is mainly based on a historical discus­ sion, stresses that plants containing isoquinolines have proved to be both a boon and a curse to mankind. The Opium Poppy, Papaver somniferum, produces the medicinally used alkaloids morphine, codeine, noscapine and papaverine whilst it also continues to provide drugs of abuse, particularly morphine and its readily prepared O,O-diacetyl derivative, heroin. Numer­ ous other alkaloids have been isolated from other members of the Papaver­ acea, and a knowledge of their presence and distribution within the various species has proved a useful adjunct to systematic botanical studies.

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    Table of Contents:

    Plants as a Source of Isoquinoline Alkaloids.- Chemotaxonomy of the Papaveraceae Alkaloids.- Structure Activities and Pharmacological Properties of the Opium Alkaloids.- The Occurrence of Simple Isoquinolines in Plants.- Erythrina Alkaloids.- Annonaceae Alkaloids.- The Chemistry and Pharmacology of Cularine Alkaloids.- Bisbenzylisoquinoline Alkaloids.- Natural Degradative Routes for the Aporphines.- Synthesis and Structure-Activity Relationships of Aporphines as Dopamine Receptor Agonists and Antagonists.- The Chemistry and Pharmacology of Morphinan Alkaloids.- The Development of a Practical Total Synthesis of Natural and Unnatural Codeine, Morphine and Thebaine.- Biomimetic and Total Synthesis of Monoterpenoid Isoquinoline Alkaloids.- The Biosynthesis of Isoquinoline Alkaloids.- Biosynthesis of Morphinan Alkaloids.- Enzymology of Benzylisoquinoline Alkaloid Formation.- Morphinan Alkaloids from Plant Cell Cultures.- The Production of Isoquinoline Alkaloids by Plant Cell Cultures.- Cytodifferentiation and Papaver Alkaloid Accumulation.

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