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  • 1970-1974  (2)
  • 1973  (2)
  • Chemistry  (1)
  • Intraventricular  (1)
  • Drug discrimination
  • General Chemistry
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  • 1970-1974  (2)
Year
Keywords
  • 1
    ISSN: 1432-2072
    Keywords: Nicotine ; Intraventricular ; State-Dependent Behaviour
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Rats were trained to choose between the side compartments of a three-chambered shock-escape apparatus according to whether they were injected with nicotine or saline. Half of the rats learned to discriminate between 0.4 mg/kg nicotine and saline administered subcutaneously, whereas the other half learned to differentiate between 644 ng nicotine or saline administered intraventricularly. The rats trained by the subcutaneous route of administration had the ability to discriminate between nicotine and saline given intraventricularly and the rats trained by the intraventricular route could differentiate when the two substances were injected subcutaneously. This transfer of state-dependent control of discriminative behaviour between subcutaneously and intraventricularly administered nicotine and saline is presented as evidence for the central origin of the nicotine-produced interoceptive cue.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 0030-4921
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: The chemical shifts of aromatic nitriles of the general structure para-Y—C6H4—X—CN with X = O, S, Se and N(CH3) have been investigated by the 13C NMR technique. For cyanates (X = O) the 14N shifts and for Y = F the 19F shifts were likewise measured. The chemical shifts and the corresponding 13C shift increments Δn have been found to correlate with the appropriate substituent constants σR0, σp0 and σI, as well as with the π-electron densities calculated in the PPP approximation.
    Notes: An aromatischen Nitrilverbindungen der allgemeinen Struktur para-Y—C6H4—X—CN mit X = O, S, Se und N(CH3) wurden die 13C-NMR- sowie für X = O die 14N-NMR-und für Y = F die 19F-NMR-chemischen Verschiebungen bestimmt. Die Meßergebnisse wurden in Zusammenhang mit der elektronischen Struktur der Moleküle (Substituentenkonstanten, π-Elektronendichten in PPP-Näherung) diskutiert.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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