Fmoc-Gly-L-Thr[PSI(Me,Me)Pro]-OH

Nom chimique: (4S,5R)-3-(N-(9-Fluorenylmethyloxycarbonyl)-glycinyl)-2,2,5-trimethyloxazolidine-4-carboxylic acid // Synonymes: Fmoc-Gly-Thr[PSI(Me,Me)Pro]-OH

  • n° Art.:PSI1180
  • n° CAS:1262308-49-5
  • Formule:C24H26N2O6
  • Storage temperature:2-8°C
  • Masse moléculaire:438,47 g/mol

from 65,00 €

Grouped product items
Nombre Unité de vente Prix SKU Disponibilité
1 g
65,00 €
PSI1180.0001
<10 jour ouvrables
5 g
205,00 €
PSI1180.0005
<10 jour ouvrables
25 g
750,00 €
PSI1180.0025
<10 jour ouvrables
Fiches de données de sécurité
description

Pseudoprolines derived from Serine and Threonine have developed to standard building blocks for peptide synthesis since their invention.


references

Pseudo-Prolines as a Molecular Hinge:  Reversible Induction of cis Amide Bonds into Peptide Backbones; P. Dumy, M. Keller, D. E. Ryan, B. Rohwedder, T. Wöhr and M. Mutter; J. Am. Chem. Soc. 1997; 119: 918-925. https://doi.org/10.1021/ja962780a


Pseudo-Prolines as a Solubilizing, Structure-Disrupting Protection Technique in Peptide Synthesis; T. Wöhr, F. Wahl, A. Nefzi, B. Rohwedder, T. Sato, X. Sun and M. Mutter; J. Am. Chem. Soc. 1996; 118: 9218-9227. https://doi.org/10.1021/ja961509q


Expediting the Fmoc solid phase synthesis of long peptides through the application of dimethyloxazolidine dipeptides; P. White, J. W. Keyte, K. Bailey and G. Bloomberg; J. Pept. Sci. 2004; 10: 18-26. https://doi.org/10.1002/psc.484


Pseudoprolines as Removable Turn Inducers: Tools for the Cyclization of Small Peptides; D. Skropeta, K. A. Jolliffe, and P. Turner; J. Org. Chem. 2004; 69: 8804-8809. https://doi.org/10.1021/jo0484732

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