286964-96-3Relevant academic research and scientific papers
Effect of progressive benzyl substitution on the conformations of aminocaproic acid-cyclized dipeptides
MacDonald,Vander Velde,Aube
, p. 2636 - 2642 (2007/10/03)
The constraint of dipeptides into a β-turn conformation can be accomplished by linking the two ends of a standard dipeptide with a linker derived from aminocaproic acid (aca). To elucidate the possibility of using substituted Aca linkers in peptidomimetic design, a series of five macrocycles composed of a monobenzylated Aca linker (containing the benzyl group on each of the five methylene groups of the parent linker) and Gly-gly were synthesized. The requisite linkers were made by regiochemically controlled ring expansion techniques (for substitution on Aca positions C-3, C-4, or C-5), an Evans alkylation route (for C-2), or by chain extension of L-phenylalanal (for C-6). The solution-phase conformations of the macrocycles were examined by Nmr and Cd techniques; in addition, crystal structures of the C-4- and C-6-benzyl-substituted linkers were obtained. Four out of the five macrocycles were found to exist with the dipeptide portion taking up either a type Ii or Ii′ β-turn conformation, but the Gly-gly unit in the compound derived from 4-benzyl-aca did not correspond to one of the standard β-turn types.
Synthesis and conformation of Gly-Gly dipeptides constrained with phenylalanine-like aminocaproic acid linkers.
MacDonald,Vander Velde,Aube
, p. 1653 - 1655 (2007/10/03)
[structure: see text] The constraint of dipeptides with linkers derived from 6-aminocaproic acid (Aca) is a useful means of constructing a beta-turn peptidomimetic. The extension of this concept to the mimicry of a tripeptide entails the incorporation of a side chain moiety on either end of the Aca chain. The synthesis and conformational analysis of two exemplary compounds is discussed.
