๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

Fate of3H- and14C-labelled A-4166 in pancreatic islets

โœ 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.


๐Ÿ“œ SIMILAR VOLUMES


Radiolysis of 14C- and 3H-labelled thymi
โœ J. Kopoldovรก; V. Dedkว’vรก ๐Ÿ“‚ Article ๐Ÿ“… 1975 ๐Ÿ› John Wiley and Sons ๐ŸŒ French โš– 519 KB

## Abstract 10^โˆ’3^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

Synthesis of 3H and 14C labelled SCH 484
โœ D. Hesk; C. Bowlen; S. Hendershot; D. Koharski; P. McNamara; D. Rettig; S. Saluj ๐Ÿ“‚ Article ๐Ÿ“… 1996 ๐Ÿ› John Wiley and Sons ๐ŸŒ French โš– 404 KB ๐Ÿ‘ 1 views

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

Preparation of 3H- and 14C-labelled cont
โœ Kenyu Shibata; Yoshio Osawa; Avery A. Sandberg ๐Ÿ“‚ Article ๐Ÿ“… 1975 ๐Ÿ› John Wiley and Sons ๐ŸŒ French โš– 236 KB

## Abstract ^3^Hโ€ and ^14^Cโ€Labelled 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

Reparation of 3H-, and 14C-labeled ethyl
โœ Yul Yost; Jordan L. Holtzman ๐Ÿ“‚ Article ๐Ÿ“… 1981 ๐Ÿ› John Wiley and Sons ๐ŸŒ French โš– 179 KB

## Abstract 7,8โ€Didehydroโ€4,5โ€epoxyโ€3โ€ethoxyโ€17โ€methyl(^3^H)โ€, and โˆ’17โ€methyl (^14^C)morphinanโ€6โ€ol were prepared by substituting the Nโ€methyl group with/^a^carbphenoxy group which was then either reduced with LiAl^3^H~4~ or removed to remethylate the Nโ€atom with ^14^CH~3~I.