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  • 1965-1969  (2)
  • 1
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Young plants of Digitalis lanata were fed by the vick technique with ammonium mevalonate-[3-14C]. The isolation from the leaves of pure digitoxigenin and gitoxigenin (without dilution) was described formerly [5]. We describe here the isolation from the same plants of the four pure spirostanols: tigogenin (5), digalogenin (6), gitogenin (7) and digitogenin (8), again without dilution. These spirostanols contained about 3-5 times more radioactivity per Mol than the cardenolides.
    Additional Material: 4 Tab.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Helvetica Chimica Acta 49 (1966), S. 1475-1483 
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Strongly radioactive digitoxin (6) could be isolated (without dilution) in crystalline form from young plants of Digitalis lanata after their inoculation with D-Glucose-[6-14C] using the wick method. Hydrolytic cleavage of this digitoxin gave digitoxigenin (11) and D-digitoxose (7), both being isolated in crystalline form (without dilution). The genin was found to be 4 times more active, pro mole, than the digitoxose. This can be best explained when one assumes that the plant converts 1 mole of D-glucose into 3 moles of acetic acid. After degradation of the digitoxose using NaJO4, acetaldehyde (as the crystalline p-nitrophenylhydrazone) and formic acid (as the Pb salt) could be isolated. The acetaldehyde carried 65% and the formic acid 8,45% of the activity of the digitoxose. This is compatible with the assumption that digitoxose is formed in the plant from D-glucose without re-arrangement of the carbon chain. The appreciable activity of the formic acid could be derived from the relatively large proportion of radioactivity lost (ca. 38,9%), partly in the form of C1-subunits, in the transformation of the intermediary lanosterol into digitoxigenin. This lost activity may be incorporated in unspecifically labelled D-glucose which then re-enters the biosynthetic pathway.
    Additional Material: 3 Tab.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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