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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Cellular and molecular life sciences 11 (1955), S. 314-315 
    ISSN: 1420-9071
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary In synthesizing 6-(4′-pyridyl)-3-mercapto-1,2,4-tria-zin-5-one from the oxime of 4-pyridyl-glyoxylic acid, isonicotinaldehyde-thiosemicarbazone is obtained through decarboxilation as a by-product, which is mainly responsible for the tuberculostatic properties.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Cellular and molecular life sciences 10 (1954), S. 62-63 
    ISSN: 1420-9071
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary From thiosemicarbazones of aromatic and heterocyclic α-ketoacids, a number of aromatically and heterocyclically substituted mercapto-triazinones were prepared, some of which, especially 6-(γ-pyridyl)-3-mercap-to-1,2,4-triazin-5-one, show definite antitubercular properties and low mammalian toxicity.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Cellular and molecular life sciences 8 (1952), S. 184-185 
    ISSN: 1420-9071
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary Description of 30 thiosemicarbazones of heterocyclic Aldehydes. Some of these compounds show tuberculostatic activityin vivo superior to p-Acetylaminobenzal-dehyde-thiosemicarbazone which statement was already made independently by French and American research groups. In the series of heterocyclic thiosemicarbazones very small changes in the molecular structure may cause a total loss of the tuberculostatic properties.
    Type of Medium: Electronic Resource
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