Chakraborty, T. K. ; Ghosh, Subhash ; Ramana Rao, M. H. V. ; Kunwar, A. C. (2005) Conformational studies of C2 symmetric peptidomimetics based on 2,5-anhydro sugar diacid and 2,5-anhydro sugar diamine scaffolds Arkivoc, 2005 (xi). pp. 89-101. ISSN 1424-6376
![[img]](https://repository.ias.ac.in/style/images/fileicons/application_pdf.png)
|
PDF
- Publisher Version
292kB |
Official URL: http://www.arkat-usa.org/get-file/20551
Abstract
Conformational studies of C2 symmetric peptidomimetics with identical peptide strands attached on both sides of 2,5-anhydro sugar diacid and 2,5-anhydro sugar diamine scaffolds revealed the presence of nine-membered pseudo β-turns in the sugar diacid based molecules consisting of identical intramolecular hydrogen bonds at the two ends between the AA2NH and sugarOH.
| Item Type: | Article |
|---|---|
| Source: | Copyright of this article belongs to Arkat USA Inc. |
| Keywords: | C2 Symmetry; Peptidomimetics; NMR; Roesy; Molecular Dynamics Introduction |
| ID Code: | 20544 |
| Deposited On: | 20 Nov 2010 14:20 |
| Last Modified: | 17 May 2016 04:51 |
Repository Staff Only: item control page
