Similarity Study on Peptide γ-turn Conformation Mimetics
✍ Scribed by Ibon Alkorta; MariaLuisa Suarez; Rosario Herranz; Rosario González-Muñiz; M.Teresa García-López
- Book ID
- 106240854
- Publisher
- Springer-Verlag
- Year
- 1996
- Tongue
- English
- Weight
- 98 KB
- Volume
- 2
- Category
- Article
- ISSN
- 1610-2940
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
A novel ytum mimetic 2 has been prepared based on retro amide peptide design Incorporation of this mimetic into linear peptidejibritwgen receptor antagonist 7 (GPlIWIUa receptor) @rds the opportunity to test models of antagonist pharmacophore.
The solid-phase synthesis and characterization of a series of of the reverse-turn mimic. In N-acetylated tetrapeptide mimics incorporating the two different bicyclic lactams (a peptides (3-9), containing reverse-turn mimetic bicyclic lactams (1a, 1b), was reported in the preceding paper. The series
## Abstract The conformational behavior of POE‐bound model peptides Boc‐(L‐Ala)~2~‐X‐Y‐(L‐Ala)~2~‐NHPOE (X – Y = L‐Pro‐Gly (**I**), Gly‐L‐Ile (**II**); NHPOE = aminopoly(oxyethylene)) as well as of the repetitive hexapeptide of elastin, Boc‐L‐Val‐L‐Ala‐L‐Pro‐Gly‐L‐Val‐Gly‐A‐NHPOE‐M (**III**) (A = p