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Marquage par 14C DU S-Acetyl, N-Glycylcysteamine (1 102)

✍ Scribed by J. C. Madelmont; M. F. Moreau; D. Godeneche; D. Parry; J. Oiry; J. L. Imbach


Publisher
John Wiley and Sons
Year
1986
Tongue
French
Weight
298 KB
Volume
23
Category
Article
ISSN
0022-2135

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πŸ“œ SIMILAR VOLUMES


Marquage par 14C ET 13C de la N acetyl O
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## Abstract O~6~ Benzyl N acetyl guanosine a new inhibitor of O~6~ Alkyl Guanine transferase (O~6~AGT) was labelled by ^14^C and ^13^C on the benzyl methylen group in order to realize a pharmacokinetic study on nude mice grafted with human tumors. The labelling yield calculated from the precursor

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## Abstract 7‐methoxy βˆ’2‐nitro naphto [2,1‐b] furan was 14 labelled by C on two positions: on the position one of the furan ring starting with sodium formiate on the methoxy group by means of methyl iodide.

Marquage Par 14C Du[(Chloro-2-Ethyl)-3 N
✍ M. F. Moreau; J. C. Madelmont; D. Godeneche πŸ“‚ Article πŸ“… 1980 πŸ› John Wiley and Sons 🌐 French βš– 304 KB

## Abstract RPCNU was labelled with ^14^C on three positions: ‐ On the carboxyl of the acetyl groups ‐ On the carboxyl of the acetyl groups ‐ On the urea carbonyl

Marquage par 14C et 3H du 4,4-dimethyl-1
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## Abstract 4,4‐dimethyl‐1‐(3‐4‐methylenedioxyphenyl)‐1‐pentene‐3‐ol or stiripentol was labelled by ^14^C and ^3^H. ^14^C labelling was performed on the carbone 1 of the pentene group via a four steps procedure after the carbonatation. The radiochemical yield calculated from the precursor (Ba^14^C

Marquage par 35S, 14C, 3H DE LA DI [(chl
✍ J. C. Madelmont; M. F. Moreau; D. Parry; D. Godeneche; J. Duprat; G. Meyniel; J. πŸ“‚ Article πŸ“… 1983 πŸ› John Wiley and Sons 🌐 French βš– 364 KB

For disposition and metabolic study CNCC was labelled by 35S, I4C, 3H on three positions : on the two sulfur atom of the cystamine group on the urea carbonyl on the position 1 of the 2 chloro ethyl group. ## RE SLIME Dans le but de r6aliser des etudes de disposition et de 3 metabolisme le CNCC a