𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Comparison of proline and N-methylnorleucine induced conformational equilibria in cyclic pentapeptides

✍ Scribed by Hardy Weiβhoff; Torsten Wieprecht; Peter Henklein; Cornelius Frömmel; Christof Antz; Clemens Mügge

Book ID
115932419
Publisher
Elsevier Science
Year
1996
Tongue
English
Weight
625 KB
Volume
387
Category
Article
ISSN
0014-5793

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Can N-methylated amino acids serve as su
Can N-methylated amino acids serve as substitutes for prolines in conformational design of cyclic pentapeptides?
✍ Burkhardt Laufer; Jayanta Chatterjee; Andreas O. Frank; Horst Kessler 📂 Article 📅 2009 🏛 John Wiley and Sons 🌐 English ⚖ 207 KB

## Abstract The incorporation of proline into cyclic peptides seems to be the most promising way to induce β‐turn structures. Recently, however, it was shown that __N__‐methylated amino acids might be even better suited than proline for introducing turn structures. Another property of proline, the