𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Studies related to the metabolism of anabolic steriods in the horse: The metabolism of 1-dehydrotestosterone and the use of fast atom bombardment mass spectrometry in the identification of steroid conjugates

✍ Scribed by M. C. Dumasia; E. Houghton; Carol V. Bradley; D. H. Williams

Publisher
John Wiley and Sons
Year
1983
Tongue
English
Weight
625 KB
Volume
10
Category
Article
ISSN
1076-5174

No coin nor oath required. For personal study only.

πŸ“œ SIMILAR VOLUMES

Studies related to the metabolism of ana
Studies related to the metabolism of anabolic steroids in the horse: A gas chromatographic mass spectrometric method to confirm the administration of 19-nortestosterone or its esters to horses
✍ E. Houghton; G. A. Oxley; M. S. Moss; S. Evans πŸ“‚ Article πŸ“… 1978 πŸ› John Wiley and Sons 🌐 English βš– 316 KB πŸ‘ 2 views

A method is described to confirm the presence of 19-nortestosterone metabolites in urine after the administration of veterinary preparations of this anabolic steroid to horses. The method is based upon the detection, by gas chromatography mass spectrometry or selected ion monitoring, of an isomer of

Application of fast atom bombardment and
Application of fast atom bombardment and tandem mass spectrometry to the identification of organic micropollutants in water
✍ J. Rivera; J. Caixach; A. Figueras; D. Fraisse; F. Ventura πŸ“‚ Article πŸ“… 1988 πŸ› John Wiley and Sons 🌐 English βš– 399 KB πŸ‘ 2 views

Organic compounds in raw and drinking water, not amenable to gas chromatogaphy/mass spectrometry, were characterized by fast atom bombardment (FAB) and collision-induced decomposition/mass-analysed ion kinetic energy (CID/MIKE) spectrometry. Anionic, cationic and non-ionic surfactants were successfu

Fast-atom-bombardment mass spectrometry
Fast-atom-bombardment mass spectrometry and 1H-NMR spectrometry in studies of the transformations of thiamine in strongly basic solutions
✍ Ian Horman πŸ“‚ Article πŸ“… 1984 πŸ› John Wiley and Sons 🌐 German βš– 341 KB

## Abstract Fast‐atom‐bombardment (FAB) mass spectra have been used to establish or confirm the nature of the yellow‐product and open‐chain forms of thiamine produced in the presence of excess (5 mol‐equivb.) of strong base. Time‐dependent changes in ^1^H‐NMR spectra show that the rates of disappea