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  • HMG-CoA reductase  (1)
  • derivative spectrophotometry  (1)
  • Springer  (2)
  • American Chemical Society (ACS)
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  • Springer  (2)
  • American Chemical Society (ACS)
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  • 1
    ISSN: 1436-5073
    Keywords: solid-phase spectrophotometry ; derivative spectrophotometry ; pyrocatechol violet ; tungsten determination ; natural and industrial waters
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Derivative spectrophotometry was applied to solid-phase spectrophotometry in order to enhance its sensitivity and remove the large background caused by the absorbance of the resin layer. Determination of micro-amounts of tungsten with pyrocatechol violet to form a 2∶1 green complex in acid medium which is fixed on a dextran-type anion-exchange resin (Sephadex QAEA-25) is described as an example for the application of this technique. The absorbance of the resin packed in a 1-mm spectrophotometric cell, was measured directly. The characteristic peak amplitude of the signal at 674 nm in the first-derivative spectrum is useful for quantitative determination of tungsten (3–16 μg 1−1; RSD 5.8%) in natural and industrial water samples.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Molecular and cellular biochemistry 105 (1991), S. 21-25 
    ISSN: 1573-4919
    Keywords: cholesterogenesis ; phenylketonuria ; HMG-CoA reductase ; MVAPP decarboxylase ; phenylalanine-derivatives
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: Abstract Phenylalanine, phenylpyruvate and phenylacetate produced a considerable inhibition of chick liver mevalonate 5-pyrophosphate decarboxylase while mevalonate kinase and mevalonate 5-phosphate kinase were not significantly affected. Phenolic derivatives of phenylalanine produced a similar inhibition of decarboxylase activity than that found in the presence of phenyl metabolites. The degree of inhibition was progressive with increasing concentrations of inhibitors (1.25–5.00 mM). Simultaneous supplementation of different metabolites in conditions similar to those in experimental phenylketonuria (0.25 mM each) produced a clear inhibition of liver decarboxylase and 3-hydroxy-3-methylglutaryl-CoA reductase. To our knowledge, this is the first report on the in vitro inhibition of both liver regulatory enzymes of cholesterogenesis in phenylketonuria-like conditions. Our results show a lower inhibition of decarboxylase than that of reductase but suggest an important regulatory role of decarboxylase in cholesterol synthesis.
    Type of Medium: Electronic Resource
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