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  • 1
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Clinical and experimental pharmacology and physiology 14 (1987), S. 0 
    ISSN: 1440-1681
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: 1. The influence of two angiotensin-converting enzyme inhibitors, captopril and enalapril, on the cAMP content of microdissected brain areas was examined in spontaneously hypertensive rats. Both drugs depleted systolic arterial blood pressure significantly.2. Captopril and enalapril increased the level of cAMP in catecholaminergic cell groups in the lower brain-stem. Captopril was more effective in the substantia nigra, while enalapril treatment resulted in high cAMP levels in the ventrolateral medulla oblongata (A1 catecholaminergic cell group).3. Both drugs, especially captopril, depleted cAMP content in the cingulate cortex.4. No changes in cAMP levels were measured in the primary baroreceptor centre (nucleus of the solitary tract) following either captopril or enalapril treatment.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1365-2826
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: The concentration of cyclic AMP (cAMP) and the activity of sodium-fluoride-stimulated adenylate cyclase was measured in 29 microdissected brain areas of homozygous Brattleboro rats and their Long-Evans control rats. In ten of the investigated brain areas a decreased cAMP level was measured in Brattleboro rats. It was particularly decreased in the supraoptic nucleus, cingulate and parietal cortex, hippocampus, habenula and organum vasculosum laminae terminalis. Significantly lower cAMP levels were also found in the periventricular nucleus, bed nucleus of the stria terminalis, area postrema and locus coeruleus. An increased cAMP concentration was detected only in the subcommissural organ of Brattleboro rats. In most brain areas, where cAMP was decreased, sodium fluoride-stimulated adenylate cyclase activity was significantly increased (supraoptic nucleus, parietal cortex, periventricular nucleus, bed nucleus of the stria terminalis, locus coeruleus) or unchanged (hippocampus, habenula, organum vasculosum laminae terminalis). The coincidence of alterations in cAMP concentration and adenylate cyclase activity in brain areas of Brattleboro rats with relatively dense vasopressinergic innervation and/or vasopressin receptor population in control rats, suggests an influence of brain vasopressin on the cAMP-adenylate cyclase second messenger system.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 628 (1959), S. 75-83 
    ISSN: 0075-4617
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Aufgrund der in der IX. bis XI. Mitteilung enthaltenen Erfahrungen und Ergebnisse wird ein Chemismus der oxydativen Kupplung aufgestellt. Die kuppelnde Oxydationsstufe der heterocyclischen Hydrazone stellt das Ion X dar, welches mit der Kupplungskomponente unter elektrophiler Substitution zum Leukofarbstoff reagiert. Die Reaktion entspricht der Indanilinkupplung. Der Weg über eine Diazoniumstufe konnte ausgeschlossen werden.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 697 (1966), S. 116-139 
    ISSN: 0075-4617
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Azoquartärsalze vom Typ 4 sind auf verschiedenen Wegen darstellbar. Sie lassen sich glatt zu Sulfonylhydrazonen 2 reduzieren sowie mit Phenolen und aromatischen Aminen zu Farbstoffen (47  -  51; 54  -  55) kuppeln. Die Azogruppe addiert Sulfinat-Ionen zu Bis-sulfonylhydrazonen (z. B. 26), deren thermisch beschleunigter rückläufiger Zerfall u. a. durch eine neuartige Kupplungsreaktion nachgewiesen wird. Die Reaktionen mit Natriumazid (z. B. zu 31 und 32) und mit nucleophilen Carbenen (zu Azinen 41) werden ebenfalls aufgeklärt.
    Additional Material: 3 Tab.
    Type of Medium: Electronic Resource
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