Ah&act: Dolastatin 3, a unique cyclic peptide, was synthesised in hi h yield. Its minimum energy conformation in solution was established by NMR spectroscopy and force ield calculations, and is character&d k by three intramolecular hydrogen bonds.
β¦ LIBER β¦
Nuclear magnetic resonance and conformational energy calculations of repeat peptides of elastin. Conformational characterization of cyclopentadecapeptide cyclo-(L-Val-L-Pro-Gly-L-Val-Gly)3
β Scribed by Venkatachalam, C. M.; Khaled, M. A.; Sugano, H.; Urry, D. W.
- Book ID
- 126416922
- Publisher
- American Chemical Society
- Year
- 1981
- Tongue
- English
- Weight
- 895 KB
- Volume
- 103
- Category
- Article
- ISSN
- 0002-7863
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## Abstract The cyclic peptide cyclo[βLβProβLβLeuβDβ(Gln)Thzβ(Gly)ThzβLβValβ] (1a), which is a diastereomer of the antineoplastic agent dolastatin 3 (1b), and contains the unusual thiazole amino acids, was synthesized. All the peptide bonds of the cyclic peptide 1a are __trans__ in solution, and th
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