## Abstract 10^โ3^M oxygenated aqueous solutions of thymidine preparations, labelled with ^14^C and ^3^H in various positions were gammairradiated. Radiation produats formed were followed in dependenae of irradiation doses. Their yields were confronted with produats formed during the autoradiolysis
Fate of3H- and14C-labelled A-4166 in pancreatic islets
โ Scribed by F. Malaisse-Lagae; W. J. Malaisse
- Publisher
- Springer
- Year
- 1996
- Tongue
- English
- Weight
- 580 KB
- Volume
- 33
- Category
- Article
- ISSN
- 0940-5429
No coin nor oath required. For personal study only.
๐ SIMILAR VOLUMES
3H-Sch 47949, racemic 3H-Sch 48461, was prepared at a specific activity of 40 mCi/mmole by Pt catalysed exchange with tritiated water. 3H-Sch 48461 was prepared at a specific activity of 64.6 Ci/mmole by a Pd/C catalysed reduction of an olefinic intermediate. 14C-Sch 48461 was prepared in 8 steps fr
## Abstract ^3^Hโ and ^14^CโLabelled ethynodiol diacetate, chlormadinone acetate, and medroxyprogesterone acetate with one label at the steroid nucleus and the other at the acetoxy group were prepared for use in studies of regioโ and stereospecificity of metabolic hydrolysis of the steroid contrace
## Abstract 7,8โDidehydroโ4,5โepoxyโ3โethoxyโ17โmethyl(^3^H)โ, and โ17โmethyl (^14^C)morphinanโ6โol were prepared by substituting the Nโmethyl group with/^a^carbphenoxy group which was then either reduced with LiAl^3^H~4~ or removed to remethylate the Nโatom with ^14^CH~3~I.