𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Synthesis of high specific activity tritiated dihydropyridines: Nicardipine-3H

✍ Scribed by Howard Parnes; Glenn T. Huan


Publisher
John Wiley and Sons
Year
1991
Tongue
French
Weight
296 KB
Volume
29
Category
Article
ISSN
0022-2135

No coin nor oath required. For personal study only.


πŸ“œ SIMILAR VOLUMES


Tritiated guanethidine of high specific
✍ Steven D. Wyrick; A. Wayne Pittman; Larry J. Loeffler πŸ“‚ Article πŸ“… 1983 πŸ› John Wiley and Sons 🌐 French βš– 310 KB

Due to the desire for biological assay techniques of greater sensitivity and specificity than presently exist for the antihypertensive drug guanethidine, tritium labeled guanethidine of high specific activity was prepared for use in radioimmunoassay procedures. This drug has been labeled in other po

The synthesis of tritiated methoxamine w
✍ R. M. Demarinis; A. J. Villani; D. Brungard; J. Meier πŸ“‚ Article πŸ“… 1982 πŸ› John Wiley and Sons 🌐 French βš– 153 KB

## Abstract Tritiated methoxamine with a specific activity of 28.5 Ci/mmol was prepared by iodination of methoxamine followed by catalytic tritiation.

Synthesis of tritiated threonine with a
✍ Jean-Michel Delacotte; HervΓ© Galons; Dominique Schott; Jean-Louis Morgat πŸ“‚ Article πŸ“… 1991 πŸ› John Wiley and Sons 🌐 French βš– 294 KB

## Abstract The synthesis of the trichloromethyl analogue of benzyloxycarbonyl‐threonine is described. This precursor was reduced by tritium gas to give [methyl‐^3^H~3~]‐threonine and its allo isomer. They were separated by HPLC using a chiral stationnary phase. They have a molar specific activity

Synthesis and 3H NMR of 3H-alaproclate o
✍ Stefan Bengtsson; Lars Gawell; Thomas HΓΆgberg; Christer Sahlberg πŸ“‚ Article πŸ“… 1985 πŸ› John Wiley and Sons 🌐 French βš– 310 KB

The antidepressant alaproclate (IJ i s a selective i n h i b i t o r o f neuronal serotonin reuptake w i t h 1 ow aff i n i t y f o r other receptor sites. (2, 2-( [ 2,5-3H2]-4-chl orophenyl)-2-methyl-2-propyl 2-aminopropanoate) with high specific a c t i v i t y (38 C i / m o l ) was prepared by h