## L-dihydroxyphenytalanine-H3 L-tyrwsine-2HZ dopamine-H 3methoxytyramine-H3 ' H 5 and vanillylmzndetic acid H2 were prepared by hydrogen-deuterium exchange under acidic o r basic conditions. 4-hydroxy-3methoxy phenylethyleneglycol-H3 was prepared f m m vanillylman-2 2 d e t i c acid-H by reductio
Preparation of deuterium labelled catecholamines
✍ Scribed by Lakshmi D. Saraswat; Janis M. Kenny; Sharon K. Davis; Joseph B. Justice
- Publisher
- John Wiley and Sons
- Year
- 1981
- Tongue
- French
- Weight
- 308 KB
- Volume
- 18
- Category
- Article
- ISSN
- 0022-2135
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✦ Synopsis
Abstract
The preparation of deuterium labelled catecholamines and their metabolites is described. The procedures involve simple treatment of the compounds in DC1/D~2~O solution. Mass spectra of these labelled compounds — as their PFP or TFA derivative — are presented. The relative intensity of ions suitable for selective ion monitoring are given for each compound. Results are presented concerning ease or difficulty of deuteration. The compounds studied include dopamine, tyramine, 3‐methoxytyramine, norepinephrine, metanephrine, normetanephrine, homovanillic acid and dihydroxyphenylacetic acid.
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