The commercially available preparation of the naturally occurring diterpene ester ryanodine contains several compounds in addition to ryanodine. In the present study these compounds were separated and purified using high performance liquid chromatography. The two major components, ryanodine and dehy
The preparation of tritium-labelled ryanodine
β Scribed by Alan S. Fairhurst
- Publisher
- John Wiley and Sons
- Year
- 1971
- Tongue
- French
- Weight
- 203 KB
- Volume
- 7
- Category
- Article
- ISSN
- 0022-2135
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β¦ Synopsis
Abstract
A method for preparing tritiumβlabelled ryanodine is described. The alkaloid was first brominated, and the bromoryanodines were separated from the reaction mixture by thin layer chromatography; NMR analysis at this stage showed substitution of pyrrole protons by bromine. Bromoryanodine was first hydrogenated, and the product was purified and characterized as ryanodine, to establish the feasibility of the method. Tritium was then reacted with bromoryanodine to yield labelled ryanodine with a specific activity of 2.85 Ci/mmole. No detectable isotope exchange occurred when the labelled alkaloid was incubated in aqueous media at pH 7.0 and 30Β° C.
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