Edwards, Alison A., Fleet, George W.J., Mayes, Benjamin A., Hunter, Stuart J., Tranter, George E. (2004) Circular dichroism studies of carbopeptoid-cyclodextrins. Chirality, 17 (S1). S114-S119. ISSN 0899-0042. (doi:10.1002/chir.20117) (Access to this publication is currently restricted. You may be able to access a copy if URLs are provided) (KAR id:4887)
PDF
Language: English Restricted to Repository staff only |
|
|
|
Official URL: https://doi.org/10.1002/chir.20117 |
Abstract
A series of sugar amino acids, based on open chain sugars, have been oligomerised and cyclised. The resulting cyclic carbopeptoids have been examined for desirable properties such as host–guest chemistry (as in cyclodextrins) or self-assembling properties (e.g., peptide nanotubes). Initial studies of these systems, by circular dichroism and X-ray crystallography, have given valuable insight into their
stability and properties. One of the four cyclic species studied was found to interact with ion/molecular probes.
Item Type: | Article |
---|---|
DOI/Identification number: | 10.1002/chir.20117 |
Subjects: |
Q Science Q Science > QD Chemistry |
Divisions: | Divisions > Division of Natural Sciences > Medway School of Pharmacy |
Funders: |
Engineering and Physical Sciences Research Council (https://ror.org/0439y7842)
Biotechnology and Biological Sciences Research Council (https://ror.org/00cwqg982) Smith & Nephew (United Kingdom) (https://ror.org/03agge938) |
Depositing User: | Alison Edwards |
Date Deposited: | 08 Sep 2008 14:58 UTC |
Last Modified: | 05 Nov 2024 09:36 UTC |
Resource URI: | https://kar.kent.ac.uk/id/eprint/4887 (The current URI for this page, for reference purposes) |
- Export to:
- RefWorks
- EPrints3 XML
- BibTeX
- CSV
- Depositors only (login required):