(R)-4-Aminomethyl-thiazolidine-3-carboxylic acid tert-butyl ester (CAS 391248-13-8)

(R)-4-Aminomethyl-thiazolidine-3-carboxylic acid tert-butyl ester, referred to as AMT-B, is a molecule of interest in scientific research due to its potential applications. This chiral molecule exists in two mirror-image forms. (R)-4-Aminomethyl-thiazolidine-3-carboxylic acid tert-butyl ester is derived from thiazolidine-3-carboxylic acid, with a tert-butyl group attached to the 4-aminomethyl group. Its versatility has made it valuable in drug discovery, biochemistry, and physiology studies. Researchers have explored various scientific applications for (R)-4-Aminomethyl-thiazolidine-3-carboxylic acid tert-butyl ester, including drug discovery and biochemistry. It serves as a chiral building block for synthesizing diverse small molecules, including pharmaceuticals. (R)-4-Aminomethyl-thiazolidine-3-carboxylic acid tert-butyl ester has also contributed to studying enzyme mechanisms and developing novel drug delivery systems. Furthermore, it has aided in unraveling protein structure-function relationships and advancing peptide synthesis methodologies. The precise mechanism of action for (R)-4-Aminomethyl-thiazolidine-3-carboxylic acid tert-butyl ester remains under investigation. However, it is believed to interact selectively with proteins by binding to them and modulating their activity. These interactions are likely mediated through hydrogen bonding and hydrophobic interactions. Moreover, (R)-4-Aminomethyl-thiazolidine-3-carboxylic acid tert-butyl ester may form complexes with small molecules like amino acids, leading to the alteration of protein activity.