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  • 1965-1969  (20)
  • 1900-1904  (13)
  • Organic Chemistry  (32)
  • Chlorpromazin  (1)
  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Clinical and experimental medicine 146 (1968), S. 125-138 
    ISSN: 1591-9528
    Keywords: Thermoregulation ; Fever ; Chlorpromazine ; Thermoregulation ; Fieber ; Chlorpromazin
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Description / Table of Contents: Zusammenfassung In 160 Versuchen am Kaninchen wurde die Wirkung von Chlorpromazin, das besonders in den für die Wärmeregulation wichtigen zentralen Gebieten des Hypothalamus und der Formatio reticularis angereichert wird, auf die normale Körpertemperatur und die Fieberreaktion nach Gabe von Lipopolysacchariden gramnegativer Bakterien untersucht. Gemessen wurden die Rectal- und Ohrtemperatur, die Atem- und Herzfrequenz. Es ergab sich: 1. die Rectaltemperatur des unbeeinflußten Kaninchens wird bei einer Umgebungstemperatur von 22° C in Abhängigkeit von der Dosis gesenkt, 2. das Lipopolysaccharid-Fieber läßt sich durch Vorgabe von mehr als 1 mg/kg Chlorpromazin abschwächen oder unterdrücken, 3. die Reaktion in Empfängertieren durch Plasmaübertragung von fiebernden Spendertieren kann drei verschiedene Verlaufsformen ergeben: eingipflige, zweigipflige und afebrile. Eine Beziehung zur Größe des Spendertierfiebers bestand dabei nicht. Die Ergebnisse werden hauptsächlich durch die zentralen Angriffspunkte des Chlorpromazins erklärt.
    Notes: Summary Chlorpromazine concentrates particularly in that central regions of the CNS important for the thermoregulation, in the hypothalamus and the formatio reticularis. Therefore in 160 experiments on rabbits the effect of chlorpromazine was tested at the normal body temperature and the fever reaction after medication of lipopolysaccharides (LPS) from gramnegative bacteria. Measured were the rectal- and ear-temperature, the heart- and respiration-frequency. It resulted that: 1. the rectal temperature of untreated rabbits at environmental temperature of 22°C ± 2°C is lowered, dependant on the dose, 2. the LPS-fever is diminished or suppressed after premedication of 〉 1 mg/kg chlorpromazine, 3. the reaction in the recipient animal may proceed in three different types of fever: mono- and biphasic curves and an afebrile one. A relation to the height of fever of the donor animal was not existant. Analogue to other experiments with central acting pharmaca and local cerebral temperature-stimulations in the area of the anterior hypothalamus as well as considering the distribution of chlorpromazine in the CNS these results are explained by specific effects of chlorpromazine in the hypothalamus and the formatio reticularis.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 62 (1900), S. 134-134 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 63 (1901), S. 167-183 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 65 (1902), S. 528-533 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 67 (1903), S. 342-343 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 67 (1903), S. 433-444 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 68 (1903), S. 263-293 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 69 (1904), S. 186-186 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 70 (1904), S. 560-561 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 10
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Aus 1,2,4-Trimethoxybenzol (I) wurde das 2-Methyl-3-acetonyl-7-methoxynaphtazarin (Isojavanicin) (XIIe) synthetisiert, wobei als entscheidende Aufbaureaktion die Einführung des Acetonylrestes durch MICHAEL-Addition von Acetessigsäure-benzylester an das 2-Methyl-5,7,8-trimethoxy-1,4-naphtochinon (VIII) erfolgte. Entgegen unseren früheren Versuchen ermöglichte die analoge Anlagerungsreaktion an 3-Methyl-5,7,8-trimethoxy-1,4-naphtochinon (XVII) eine wesentliche Vereinfachung der Synthese des Javanicins (XXa). Erwartungsgemäss zeigten Javanicin (XXa) und Isojavanicin (XIIe) in UV., IR., NMR. und Massenspektrogramm keine oder nur geringe, strukturell noch nicht interpretierbare Unterschiede, während die Mischprobe der beiden Substanzen eine überraschend grosse Schmelzpunktdepression gab.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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