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  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Journal of agricultural and food chemistry 36 (1988), S. 384-390 
    ISSN: 1520-5118
    Source: ACS Legacy Archives
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition , Process Engineering, Biotechnology, Nutrition Technology
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Journal of agricultural and food chemistry 36 (1988), S. 390-392 
    ISSN: 1520-5118
    Source: ACS Legacy Archives
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition , Process Engineering, Biotechnology, Nutrition Technology
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Journal of computer aided molecular design 4 (1990), S. 355-367 
    ISSN: 1573-4951
    Keywords: Urease active site ; Substrates ; Inhibitors ; Molecular modeling ; Urea hydrolysis
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary These studies are an attempt to gain better insight into the pharmacophore requirements of urease. On the basis of published information on this enzyme (EXAFS, amino acid sequence, essential groups at the active site) a hypothetical nickel-tripeptide complex, as preliminary substitute for the urease active site was modeled using computer-aided molecular modeling techniques. The results suggest two alternative docking modes of urea and reaction intermediates, corresponding to two different reaction mechanisms. Both binding modes are compatible with the docking of known potent inhibitors such as selected hydroxamic acids and phosphorodiamides. The results can be used to help in the design of new potential inhibitors of urease.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 112 (1979), S. 1835-1840 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Aromatic Diazonium Salts, IX. The Nα, Nβ-Interchange in Aromatic Diazonium Salts during SolvolysisThe Nα, Nβ-interchange during the solvolysis of [β-15N]benzenediazonium tetrafluoroborate in 2,2,2-trifluoroethanol under N2 was inhibited by less than 4% when the free radical inhibitors bromotrichloromethane, 1,1-diphenylethylene or methyl acrylate were added. Under an air atmosphere the N-inversion was increased by 8%. The main part of the N-inversion under solvolysis conditions is therefore not occurring via reversible addition of phenyl radicals to the diazonium salt.
    Notes: Der Nα, Nβ-Austausch in [β-15N] Benzoldiazonium-tetrafluoroborat bei der Solvolyse in 2,2,2-Trifluorethanol unter N2 wurde durch Zusatz der Radikalinhibitoren Bromtrichlormethan, 1,1-Diphenylethylen und Acrylsäure-methylester nur um maximal 4% erniedrigt. Unter Luftatmosphäre stieg die N-Inversion um 8% an. Eine umkehrbare Addition von Phenyl-Radikalen an das Diazoniumsalz ist daher als Hauptweg der N-Inversion unter Solvolysebedingungen ausgeschlossen.
    Additional Material: 1 Tab.
    Type of Medium: Electronic Resource
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