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Antibacterial agents based on the cyclic d,l-α-peptide architecture

✍ Scribed by Fernandez-Lopez, Sara; Kim, Hui-Sun; Choi, Ellen C.; Delgado, Mercedes; Granja, Juan R.; Khasanov, Alisher; Kraehenbuehl, Karin; Long, Georgina; Weinberger, Dana A.; Wilcoxen, Keith M.; Ghadiri, M. Reza

Book ID
109775415
Publisher
Nature Publishing Group
Year
2001
Tongue
English
Weight
248 KB
Volume
412
Category
Article
ISSN
0028-0836

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Designed Beta-Turn Mimic Based on the Al
Designed Beta-Turn Mimic Based on the Allylic-Strain Concept: Evaluation of Structural and Biological Features by Incorporation into a Cyclic RGD Peptide (Cyclo(-L-arginylglycyl-L-α-aspartyl-))
✍ Martin Sukopp; Luciana Marinelli; Markus Heller; Trixi Brandl; Simon L. Goodman; 📂 Article 📅 2002 🏛 John Wiley and Sons 🌐 German ⚖ 144 KB

## Abstract The (3__R__,5__S__,6__E__,8__S__,10__R__)‐11‐amino‐3,5,8,10‐tetramethylundec‐6‐enoic acid (ATUA; **1**), which was designed as a __β__II′‐turn mimic according to the concepts of allylic strain and 2,4‐dimethylpentane units, was incorporated into a cyclic RGD peptide. The three‐dimension