The mass spectrometric behaviour of four new macrocyclic compounds, all containing the 13,Striazine moiety, was studied with the aid of different ionization methods and mass-analysed ion kinetic energy spectrometry. Extensive fragmentation of the oligoethylene glycol side-chains is observed, with th
Electron impact ionization and fast atom bombardment mass spectrometry of some 3,3-dimethyl-1-(isoxazol-3-yl)triazenes, a new class of potential anticancer agents
✍ Scribed by Laura Orsatti; Roberta Seraglia; Pietro Traldi; Giuseppe Diamantini; Giorgio Tarzia; Andrea Tontini
- Publisher
- John Wiley and Sons
- Year
- 1995
- Tongue
- English
- Weight
- 423 KB
- Volume
- 30
- Category
- Article
- ISSN
- 1076-5174
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✦ Synopsis
Abstract
A series of 3,3‐dimethyl‐1‐(isoxazol‐3‐yl)triazenes, potential anticancer agents, were studied by electron impact (EI) ionization and fast atom bombardment mass spectrometry. Their behaviour was compared with that of dacarbazine, 5‐(3,3‐dimethyl‐1‐triazenyl)‐(1__H__)‐imidazole‐4‐carboxamide, which is employed in the treatment of several neoplastic conditions. An interesting EI‐generated decomposition pathway was observed, consisting in the primary formation of [NH~2~CH~3~]^+^ cations, involved in the metabolic pathway of triazenes, as the alkylating agent responsible for the anticancer properties of the drug. A higher thermodynamic stability of the examined compounds than decarbazine was observed, which reasonably reflects the higher chemical stability.
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