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Structural biochemistry. 26. Antineoplastic agents. 111. Synthesis of the modified dolastatin 3 sequence cyclo-[L-Val-L-Leu-L-Pro-(R,S)-(gln)Thz-(gly)Thz]

✍ Scribed by Pettit, George R.; Holzapfel, Cedric W.


Book ID
127251634
Publisher
American Chemical Society
Year
1986
Tongue
English
Weight
531 KB
Volume
51
Category
Article
ISSN
0022-3263

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πŸ“œ SIMILAR VOLUMES


The synthesis and conformation in soluti
✍ Cedric W. Holzapfel; Wynand J. van Zyl; Marita Roos πŸ“‚ Article πŸ“… 1990 πŸ› Elsevier Science 🌐 French βš– 788 KB

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.

The synthesis and analysis of the confor
✍ Bredenkamp, Martin W. ;Holzapfel, Cedric W. ;van Zyl, Wynand J. πŸ“‚ Article πŸ“… 1990 πŸ› John Wiley and Sons 🌐 English βš– 525 KB

## Abstract The cyclic peptide cyclo[‐L‐Pro‐L‐Leu‐D‐(Gln)Thz‐(Gly)Thz‐L‐Val‐] (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