7606-79-3Relevant articles and documents
Ivanov et al.
, (1971)
Adamantyl amino acid as γ-turn inducer for peptide
Kuroda, Yasuhisa,Ueda, Hiroshi,Nozawa, Hiroshi,Ogoshi, Hisanobu
, p. 7901 - 7904 (2007/10/03)
The structures of six peptide mimics having different bulkiness and/or rigidity of the amino acids were investigated spectroscopically. Comparison of H NMR, IR spectra and H-D exchangerate of the amide protons reveals that 2-amino-2-carboxyadamantane induces the high population of γ-turn conformation in the room temperature region and may be utilized as a promising γ-turn inducer for synthetic peptides.
Aqueous Solutions Containing Amino Acids and Peptides. Part 16. --Solute-Solute Interactions in Solutions Containing some N-Acetyl-N'-methylamino Acid Amides
Blackburn, G. Michael,Lilley, Terence H.,Milburn, Peter J.
, p. 2191 - 2206 (2007/10/02)
The energetics of the interactions occuring between some N-acetyl-N'-methylamino acid amides in aqueous solutions at 25 deg C have been investigated.Osmotic coefficients and enthalpies of dilution have been obtained for single-component and two-component