Literature DB >> 526557

Cardenolide analogues: 10--characterization of cardiac glycosides by chemical ionization mass spectrometry.

J Vine, L Brown, J Boutagy, R Thomas, D Nelson.   

Abstract

The potential of chemical ionization mass spectrometry for the characterization of naturally occurring and semi-synthetic cardiac glycosides has been investigated. Methane, isobutane and ammonia were used as reactant gases. With the exception of ouabain, the ammonia chemical ionization mass spectra of the cardiac glycosides examined in this work contained abundant [M + NH4]+ions and abundant fragment ions formed by cleavage of glycoside bonds. Ammonia chemical ionization mass spectrometry was found to provide a rapid and sensitive method for the characterization of the products of glycosidation reactions. In contrast, the methane and isobutane chemical ionization mass spectra of the cardiac glycosides, with the exception of ouabain, did not contain protonated molecular ions and did not contain abundant fragment ions above m/z 400.

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Year:  1979        PMID: 526557     DOI: 10.1002/bms.1200061002

Source DB:  PubMed          Journal:  Biomed Mass Spectrom        ISSN: 0306-042X


  3 in total

1.  Mechanistic considerations of the protonation and fragmentation of highly functionalized molecules in fast atom bombardment: High resolution mass spectrometry and tandem mass spectrometry analysis of the ions formed by fast atom bombardment of digoxin and related cardiac glycosides.

Authors:  K J Light; J Allison
Journal:  J Am Soc Mass Spectrom       Date:  1990-11       Impact factor: 3.109

2.  Identification of steroids by chemical ionization mass spectrometry.

Authors:  Y Y Lin
Journal:  Lipids       Date:  1980-09       Impact factor: 1.880

3.  Cardiac glycosides with non-rotating steroid to sugar linkages: tools for the study of digitalis structure-activity relationships.

Authors:  L Brown; R Thomas; T Watson
Journal:  Naunyn Schmiedebergs Arch Pharmacol       Date:  1986-01       Impact factor: 3.000

  3 in total

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