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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Naunyn-Schmiedeberg's archives of pharmacology 262 (1969), S. 124-134 
    ISSN: 1432-1912
    Keywords: Prostaglandins ; Guinea-Pig Lung ; Phospholipase A ; Cobra Venom ; Biosynthesis ; Prostaglandine ; Meerschweinchenlunge ; Phospholipase A ; Kobragift ; Biosynthese
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Description / Table of Contents: Zusammenfassung SRS-C tritt in Perfusaten von Meerschweinchenlungen auf, wenn Phospholipase A-haltige Gifte einwirken. Sie wurde aus den Perfusaten angereichert. Die Wirkung von SRS-C beruht im wesentlichen auf Prostaglandinen, z.T. auf Peroxyden. Beide stammen von mehrfach ungesättigten Fettsäuren ab. Die freigesetzten Prostaglandine sind nur z. T. im Gewebe vorgebildet, der größere Teil entsteht neu nach Abspaltung der als Vorstufen dienenden Fettsäuren aus Phosphatiden. In den Lungenphosphatiden selbst wurde Prostaglandin als Bestandteil nicht gefunden.
    Notes: Summary SRS-C appears in perfusates of guinea-pig lungs when the lungs are treated with phospholipase A or venoms containing this enzyme. SRS-C has been concentrated and purified from such perfusates. The biological activity of SRS-C depends mainly on the presence of prostaglandins and to a minor degree also on peroxides. Both compounds originate from unsaturated fatty acids. The liberated prostaglandins are only partially preformed. The bulk of them is formed after cleavage of the precursor acids from tissue phosphatides. Prostaglandins have not been detected as constituents of lung phosphatides.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-1: Polymer Chemistry 5 (1967), S. 1289-1296 
    ISSN: 0449-296X
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: From the conversion-composition data of Gruber and Elias, the reactivity ratios of styrene (M1) and methyl methacrylate (M2) were calculated to be r1 = 0.55 ± 0.02 and r2 = 0.58 ± 0.06 at 90°C. The least-squares method was then used on these and literature values at other temperatures to obtain the Arrhenius expressions: In r1 = 0.04736 - (235.45/T), and ln r2 = 0.1183 - (285.36/T). Using literature values for the homopolymerization steps, A11 = 2.2 × 107l./mole-sec., E11 = 7.8 kcal./mole, and A22 = 0.51 × 107 l./mole-sec.-1, E22 = 6.3 kcal./mole, activation energies and frequency factors were then calculated for the cross-polymerization steps: A12 = 2.1 × 107 l./mole-sec., E12 = 7.3 kcal./mole, and A21 = 0.45 × 107 l./mole-sec., E21 = 5.7 kcal./mole.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-1: Polymer Chemistry 4 (1966), S. 2819-2830 
    ISSN: 0449-296X
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A method for the determination of reactivity ratios from conversion-composition data has been outlined. The conversion-composition changes during the copolymerization of styrene (M1) and methyl methacrylate (M2) have been studied at 60°C. By a method of graphical intersection, the integrated form of Skeist's equation has been used to determine the reactivity ratios (r1 = 0.54 ± 0.02 and r2 = 0.50 ± 0.06) in reasonably good agreement with values reported in the literature. The area of intersection was used as a measure of the precision of the data.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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