Загрузка...
A cyclic enkephalin analog with high in vitro opiate activity.
A conformationally restricted analog of [Leu5]enkephalin was synthesized by cyclization of the COOH-terminal carboxyl group of leucine to the gamma-amino moiety of alpha, gamma-diaminobutyric acid (A2bu) substituted in position 2 of the peptide. Relative to [Leu5]enkephalin, the cyclic analog with D...
Сохранить в:
| Опубликовано в: : | Proc Natl Acad Sci U S A |
|---|---|
| Главные авторы: | , |
| Формат: | Artigo |
| Язык: | Inglês |
| Опубликовано: |
National Academy of Sciences
1980
|
| Предметы: | |
| Online-ссылка: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC350461/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/6261242/ https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.77.12.7162 |
| Метки: |
Добавить метку
Нет меток, Требуется 1-ая метка записи!
|