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  • Wiley-Blackwell  (3)
  • 1985-1989  (1)
  • 1970-1974  (2)
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Year
  • 1
    Electronic Resource
    Electronic Resource
    Mass spectrometry of underivatized 15-hydroxyeicosatetraenoic acid and 15-hydroxyeicosapentaenoic acid (1988)
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 17 (1988), S. 459-461 
    Details
    ISSN: 1052-9306
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A direct mass spectrometric method for 15-hydroxy metabolites of arachidonic acid and of eicosapentaenoic acid is described. 15-Hydroxyeicosanoids have the capacity to inhibit the formation of leukotrienes, potent mediators of inflammation formed by the 5-lipoxygenase pathway of arachidonic acid metabolism and may therefore have anti-inflammatory properties. 15-Hydroxyeicosatetraenoic acid (15-HETE) and 15-hydroxyeicosapentaenoic acid (15-HEPE) were synthesized using soybean lipoxygenase and arachidonic acid and eicosapentaenoic acid as substrates. These hydroxy fatty acids were then purified by reversed-phase high-performance liquid chromatography. This modified procedure provides rapid synthesis of multimilligram quantities of 15-hydroxyeicosanoids for in vitro and in vivo studies. Electron impact mass spectra of 15-HETE and 15-HEPE could be obtained directly without derivatizations.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/bms.1200170608
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  • 2
    Electronic Resource
    Electronic Resource
    Mass spectrometric studies of some 4-acyl substituted 1-phenyl-3-methyl-5-pyrazolones (1973)
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 7 (1973), S. 89-96 
    Details
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The electron-impact-induced fragmentation of 1-phenyl-3-methyl-5-pyrazolone and six 4-acyl substituted derivatives, have been studied with the aid of deuterium labelling, high resolution mass measurements and the metastable defocusing technique. The mass spectra of the pure keto and the pure enol forms do not show any significant differences. The predominant decomposition of the 4-acyl substituted pyrazolones is the α-cleavage with respect to the carbonyl group leading to intense peaks at m/e 201 by loss of the alkyl group. In the case of benzoyl and ethoxycarbonyl derivatives the α-cleavage is associated with a specific hydrogen rearrangement causing the loss of a benzene and an ethyl alcohol molecule, respectively.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/oms.1210070114
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  • 3
    Electronic Resource
    Electronic Resource
    Mass spectrometry of some pyrrolizidine alkaloids (1970)
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 4 (1970), S. 249-256 
    Details
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The mass spectra of nine pyrrolizidine alkaloids retronecine, heliotridine, 7-angeloylretronecine, 7-angeloylheliotridine, echimidine, heliosupine, lasiocarpine, heliotrine and echinatine -  were studied. Particularly the structures of the ions m/e 214, 197 and 156 in the spectrum of heliotrine are discussed. The ionization and appearance potentials for selected ions were measured for the first six alkaloids, which are pairs of epimers.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/oms.1210040129
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    Paper (German National Licenses)
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