Positive-ion fast atom bombardment maw spectrometry appears to be a useful method for the differentiation of anomeric C-glycosides. The mass-analysed ion kinetic energy (MIKE) and collision-activated dissociation (CAD) MIKE spectra of selected positive ions can be used as fingerprints of the a-or /$
Identification of butyryl derivatives of cyclic nucleotides by positive ion fast atom bombardment mass spectrometry and mass-analysed ion kinetic energy spectrometry
β Scribed by Russell P. Newton; Terence J. Walton; Salem A. Basaif; Andrea M. Jenkins; A. Gareth Brenton; Dipankar Ghosh; Frank M. Harris
- Publisher
- John Wiley and Sons
- Year
- 1989
- Tongue
- English
- Weight
- 887 KB
- Volume
- 24
- Category
- Article
- ISSN
- 1076-5174
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β¦ Synopsis
The syntheses of the dibutyryl derivatives of the 3',5'cyclic monophosphates of adenosine, guanosine and cytidine are described. The fast atom bombardment mass spectra of these compounds are discussed, together with the mass-analysed ion kinetic energy spectra of their protonated molecular ions and of diagnostic fragments. A protocol for the identification of the derivatives is reported which includes criteria for confirming retention of the cyclic phosphodiester moiety, substitution of both heterocyclic base and ribose ring, and butyrylation of the 2'-O-position. The origins of significant fragments in the spectra are discussed.
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Two enzymes, cyclic CMP-specific phosphodiesterase and multifunctional phosphodiesterase, are responsible for the hydrolysis of cytidine 3',5'-cyclic monophosphate in living cells. Quantitation of both enzymes has been carried out by positive-ion fast-atom bombardment mass spectrometric analysis of
The syntheses of 2'-O-snccinyl, 2'-O-succinyltyrosinyl methyl ester and 2'-O-succinyliodotyrosinyl methyl ester derivatives of a cyclic nucleotide, derivatives necessary for the successful development of a specific radioimmunoassay, are described. Fast atom bombardment with collision-induced dissoci
## Abstract A new technique using negativeβion fast atom bombardment mass spectrometry for the analysis of xanthates and related compounds is described. Electron impact and positiveβion fast atom bombardment mass spectrometry produced no structurally related fragment ions or observable molecular io