Enhancing the proline effect: Pseudo-prolines for tailoring Cis/ trans isomerization
Cis-trans isomerization of proline-like oxazolidines and thiazolidines, denoted pseudo-prolines, is investigated spectrophotometrically with a chymotrypsin coupled assay and by 1H NMR. A series of peptides carrying substituents of varying stere
Pseudo-prolines as a molecular hinge: Reversible induction of cis amide bonds into peptide backbones
Serine, threonine-derived (4S)-oxazolidine-4-carboxylic acid, and cysteine-derived (4R)-thiazolidinecarboxylic acid, denoted pseudo-proline (Xaa[Ψ(R1,R2)pro]), serve as structure disrupting, solubilizing building blocks in peptide sy
Get Best Price for186023-46-1((S)-2-Methyl-1-{(S)-4-[(S)-1-(4-nitro-phenylcarbamoyl)-2-phenyl-ethylcarbamoyl]-oxazolidine-3-carbonyl}-propyl)-carbamic acid 9H-fluoren-9-ylmethyl ester