| Autor: |
Iskhakova FKh, Esipova OV, Zvonkova EN |
| Jazyk: |
ruština |
| Zdroj: |
Bioorganicheskaia khimiia [Bioorg Khim] 1995 Aug; Vol. 21 (8), pp. 596-603. |
| Abstrakt: |
Hydrophobic stearoyl derivatives of proline-containing di- and tripeptides and their deuterated analogs were synthesized. It was shown by NMR spectroscopy that cis-trans-equilibrium around an X-Pro peptide bond is displaced towards trans-conformers for compounds containing a Ste-Pro fragment as opposed to the compounds containing Boc-Pro or Gly-Pro fragments. |
| Databáze: |
MEDLINE |
| Externí odkaz: |
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