Jump to main content
Jump to site search
PLANNED MAINTENANCE Close the message box

Scheduled maintenance work on Tuesday 19th September 2017 from 8.00am to 4.00pm (BST).

During this time our website performance may be temporarily affected. If you have any questions please use the feedback button available under our menu button. We apologise for any inconvenience this might cause and thank you for your patience.


Issue 57, 2013
Previous Article Next Article

N-Triethylene glycol (N-TEG) as a surrogate for the N-methyl group: application to Sansalvamide A peptide analogs

Author affiliations

Abstract

Here we studied the N-triethylene glycol (N-TEG) group as a surrogate for the N-Me group in Sansalvamide A peptide. The five N-TEG and N-Me analogs of this cyclic pentapeptide were synthesized, and their biological activity, lipophilicity and conformational features were compared.

Graphical abstract: N-Triethylene glycol (N-TEG) as a surrogate for the N-methyl group: application to Sansalvamide A peptide analogs

Back to tab navigation

Supplementary files

Publication details

The article was received on 09 Mar 2013, accepted on 24 May 2013 and first published on 28 May 2013


Article type: Communication
DOI: 10.1039/C3CC41788C
Citation: Chem. Commun., 2013,49, 6430-6432
  •   Request permissions

    N-Triethylene glycol (N-TEG) as a surrogate for the N-methyl group: application to Sansalvamide A peptide analogs

    A. I. Fernández-Llamazares, J. García, V. Soto-Cerrato, R. Pérez-Tomás, J. Spengler and F. Albericio, Chem. Commun., 2013, 49, 6430
    DOI: 10.1039/C3CC41788C

Search articles by author

Spotlight

Advertisements