Ethy 2 2-acetylamin0-2-carbethoq-4-cyano-3-butene oate : -3 was prepared by condensation o f trans-I-bromo-2-cymoethylene : -2 with acetamidornalonate. -3 was catalytically reduced h t h t r i t i u m followed by 3 hydrolysis giving r i s e t o (3,4,5,5-H ) DL ornithine 5\_spec. act. 103 Ci/M. L-or
Marquage A Haute Activite Specifique Par 125I, Radiolyse Et Conservation Du 3-5,3′-5′, Tetraiodo-L-Tyrosyl-L-Tyrosine
✍ Scribed by J. C. Maurizis; C. Nicolas; J. Michelot
- Book ID
- 102373739
- Publisher
- John Wiley and Sons
- Year
- 1980
- Tongue
- French
- Weight
- 312 KB
- Volume
- 17
- Category
- Article
- ISSN
- 0022-2135
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
Nous décrivons le marquage ù haute activité spécifique (1.000 – 1.200 μCi/μg) par ^125^I, la purification et l'étude des conditions de conservation du 3‐5, 3′‐5′, tetraiodo‐1‐tyrosyl‐1‐tyrosine. Mots clés: 3‐5, 3′‐5′, tetraiodo‐1‐tyrosyl‐1‐tyrosine, iodination, conservation.
📜 SIMILAR VOLUMES
Ltiamino-4-heqnoic acidwas prepared from 1, 4-dichloro-2-butyne and diethyl acetamidomlomte. Tke catalytic reduction of -$ trtth tritium led t o f4,5,6,6-RI DL-lysines) spec. act. 113 Ci/mM. Tke catalytic reduction with tritium of L-2-amino-6-t-butoqcmbonytamino-4-kelcyndc acid \_Z followed by hydro