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  • 1
    Publication Date: 1964-06-01
    Print ISSN: 0028-0836
    Electronic ISSN: 1476-4687
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Published by Springer Nature
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  • 2
    Electronic Resource
    Electronic Resource
    [s.l.] : Nature Publishing Group
    Nature 202 (1964), S. 1126-1126 
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] Of the secondary amines in tobacco, nornicotine is probably the most abundant. The smoke from a single cigarette contains about 5 mg nicotine and 100 jxg of secondary amine alkaloids, including anabasine, myos-mine and nornicotine7. Nitrosonornicotine was prepared by treating nornicotine (Fluka, ...
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Cellular and molecular neurobiology 19 (1999), S. 491-510 
    ISSN: 1573-6830
    Keywords: antipsychotic drugs ; cytochrome P450 ; polymorphism ; enzyme inhibition ; enzyme induction ; drug–drug interaction ; active metabolite
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract 1. Antipsychotic drugs are extensively metabolised by cytochrome P450 (CYP) enzymes. 2. Dispositions of a number of antipsychotic drugs have been shown to cosegregate with polymorphism of CYP2D6. 3. Metabolic drug–drug interactions have frequently been observed when antipsychotics are coadministered with other drugs. 4. Many antipsychotic drugs are converted to active metabolites which can contribute to the therapeutic or side effects of the parent drug. 5. Information concerning the individual CYP isoenzymes involved in the metabolism of antipsychotic drugs is important for the safe clinical use of this group of drugs.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 21 (1992), S. 165-175 
    ISSN: 1052-9306
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A combination of constant neutral loss (CNL) and daughter ion scanning tandem mass spectrometry was used to identify nine metabolites of the antimuscarinic drug cimetropium bromide. CNL mass spectrometry (-54 Da, corresponding to loss of -CH2-cyclopropyl with a concomitant gain of H) was used to rapidly screen an extract from a rat liver microsomal incubate. This sample had been subjected to only minimal purification involving zinc sulphate precipitation of the microsomal proteins followed by solid-phase extraction using a Sep-Pak C-18 reversed-phase cartridge. The ions detected in CNL mass spectrometry were subjected to collisionally activated dissociation and the resulting daughter ion spectra were compared with those acquired for synthetic standards. Four ions observed in CNL mass spectrometry were shown to be artifacts, produced either by the fast atom bombardment (FAB) ionization process or the incubation and/or extraction conditions. Their structures were determined from the daughter ion spectra acquired. It was also demonstrated that in the presence of high concentrations of the unmetabolized drug substrate, ions were formed during FAB ionization that possessed identical daughter ion spectra to previously identified metabolites. This observation highlighted the need to conduct adequate control experiments to ensure that artifacts from the FAB process, as well as from the incubation procedures, were distinguished from ions attributable to metabolites.
    Additional Material: 10 Ill.
    Type of Medium: Electronic Resource
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