Conformational studies of C2 symmetric peptidomimetics based on 2,5-anhydro sugar diacid and 2,5-anhydro sugar diamine scaffolds

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

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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

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