Abstract
A novo trifunctional EDTA-like peptidomimetic amino acid is described. This unique building block, which is prepared in a straightforward manner from commercialized starting materials, contains three moieties: a hexadentate chelating unit similar to that present in EDTA, and amino and carboxylic groups, which facilitate its introduction into the backbone of peptides using conventional SPPS. As a proof of concept, this building block is introduced into a cyclic peptide inspired from the family of Gratisin analogues. The designed peptide contains the amino acid analogue in one of the turns, and chelates Ca2+ with nanomolar affinity at physiological pH.
| Original language | English |
|---|---|
| Pages (from-to) | 2634-2636 |
| Number of pages | 3 |
| Journal | Chemical Communications |
| Volume | 53 |
| Issue number | 17 |
| DOIs | |
| State | Published - 2017 |
Bibliographical note
Publisher Copyright:© The Royal Society of Chemistry.
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