Synthesis of constrained bicyclic dipeptide mimetics
✍ Scribed by M.Arshad Siddiqui; Patrice Préville; Micheline Tarazi; Scott E. Warder; Paul Eby; Elise Gorseth; Karen Puumala; John DiMaio
- Publisher
- Elsevier Science
- Year
- 1997
- Tongue
- French
- Weight
- 198 KB
- Volume
- 38
- Category
- Article
- ISSN
- 0040-4039
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✦ Synopsis
An efficient synthesis of constrained bicyclic peptidomimetics of (R)-Phe-Pro dipeptide is described. Such mimetics may provide an opportunity to develop inhibitors of thrombin possessing the desired pharmacological features.
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Peptide side chains play critical roles in the event of molecular recognition. In order to study the bioactive conformation of parent peptides, a concise and straightforward five-step synthesis of [5.5]-bicyclic reverse turn dipeptide mimetic scaffolds with side chain functionality at the i+1 and i
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