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  • 1
    ISSN: 1432-1440
    Keywords: Sialyltransferase activity ; Malignant diseases ; Immobilized acceptor ; Sialyltransferase-Aktivität ; Maligne Erkrankungen ; Trägergebundener Akzeptor
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Description / Table of Contents: Zusammenfassung Sialyltransferase-Aktivität von Patienten mit malignen Erkrankungen wurde den Werten von Personen gegenübergestellt, die keine klinischen Symptome und Beschwerden aufwiesen. Dabei zeigte sich, daß in 80% der untersuchten pathologischen Fälle eine deutliche Erhöhung der Serum-Sialyltransferase im Vergleich zum Normalkollektiv festgestellt werden konnte. Ferner konnten wir durch kovalente Bindung von Asialo-Fetuin als Akzeptor an Sepharose 4B eine Vereinfachung der Bestimmungsmethode erreichen.
    Notes: Summary Sialyltransferase activity was estimated in serum samples of patients with cancer and controls using immobilized asialo-fetuin as the acceptor and cytidine-5′-monophospho [14C] sialic acid as the donor. The data suggest that increased enzyme activity can be found in more than 80% of the samples from patients with malignant diseases.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The unsubstituted and p-substituted benzoates 2b-2e of 3-dimethylamino-2,2bis(p-nitrophenyl)-propanol (2a) undergo quantitative fragmentation in 80% ethanol yielding 1,1-bis(p-nitrophenyl)-ethylene (5) besides formaldehyde and dimethylamine, the hydrolysis products of the imonium ion 3. The corresponding alcohol 2a, however, yields 2,2-bis(p-nitrophenyl)-ethanol (9) in addition to fragmentation products. Conversely, no fragmentation is observed with the benzoates 6b-6e of 3-dimethylamino-2,2-diphenylpropanol (6a) which lack electronwithdrawing substituents in the β-phenyl groups.These results are in agreement with a two-step carbanion mechanism (Scheme 2) involving the ionization of the aminoalkohol 2a and its esters 2b-2e to the imonium ion 3 and the carbanions 4a-4e. The latter undergo competitive cleavage, recombination and protonation to 5, 2 and 9, respectively, depending on the nucleofugal activity of -X.These conclusions are supported by the first-order rate constants for the benzoates 2b-2e which differ merely by a factor of three. Since the p-substituents in the benzoate groups have only a minor effect on the reaction rate the bonds to the nucleofugal groups are not appreciably broken in the rate determining step.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Biomedical Materials Research 25 (1991), S. 1169-1181 
    ISSN: 0021-9304
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine , Technology
    Notes: A new type of biocompatible copolymer comprising small fragments of heparin, (octa- to dodecasaccharides) copolymerized with a synthetic monomeric component, viz. acrylamide, has been prepared. The heparin fragments are produced by enzymatic or chemical means and are copolymerized, directly or after suitable derivatization, with acrylamide as the major polymerizable component. The polymeric material incorporates the heparin segments as pendant moieties such that their essential functional groups and structural features for specific binding with the selective serine protease coagulation factor inhibitor antithrombin III are preserved. An important feature of this copolymer is its biocompatibility which relates specifically to its antithrombotic and antithrombogenic activity derived from those of heparin fragments. The biological activity of heparin fragments and copolymers thereof are determined in terms of APTT and anti-Xa activity, their antithrombotic potential being expressed as a ratio of anti-Xa activity to APTT. The copolymers reported have biological activities similar to equivalent amounts of respective heparin fragments, and show higher antithrombotic activity compared to intact heparin or commercially available low-molecular-weight heparin (4,000-6,000 Da).
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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