## Abstract The precursor peptides H‐Phe(I)‐Pro‐Gly‐OH (III) and H‐Tyr(I~2~)‐Pro‐Phe(I)‐pyrrolidide (VIII) were synthesized by stepwise elongation from the C‐terminal end and by coupling of Boc‐Tyr(I~2~)‐Pro‐OH with H‐Phe(I)‐pyrrolidide and following deprotection of the Boc‐residue respectively. Ca
Synthesis of a tritium labeled rat enterostatin, Val-[3,4-3H-Pro]-Gly-[3,4-3H-Pro]-Arg-Oh
✍ Scribed by Edward S. Kozlowski; Douglas D. Dischino; Graham Johnson
- Publisher
- John Wiley and Sons
- Year
- 1995
- Tongue
- French
- Weight
- 251 KB
- Volume
- 36
- Category
- Article
- ISSN
- 0022-2135
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✦ Synopsis
Abstract
A tritium labeled rat Enterostatin, Val‐[3,4‐^3^H‐Pro]‐Gly‐[3,4‐^3^H‐Pro]‐Arg‐OH, was prepared by the catalytic tritiation of the didehydroproline analog of rat Enterostatin, Val‐[3,4‐dehydroPro]‐Gly‐[3,4‐dehydroPro]‐Arg‐OH, over Pd/C in methanol. The product had a specific activity of 59.2 Ci/mmol and a radiochemical purity of greater than 99%.
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