(S)-3-Thienylglycine (CAS 1194-87-2)

(S)-3-Thienylglycine, known as thioproline, has gained increasing popularity in scientific research due to its wide range of potential applications. This thiol-containing amino acid possesses a chiral secondary structure, with a distinctive thiophene ring attached to the carboxyl group. (S)-3-Thienylglycine serves as a valuable reagent in organic synthesis and a significant biomarker in biomedical research. It also acts as a precursor to other thiophenyl compounds and functions as a ligand in metal-catalyzed organic reactions. The versatility of (S)-3-Thienylglycine extends to various disciplines within biochemistry and biophysics, contributing to critical aspects such as protein folding and enzyme catalysis. As a result, (S)-3-Thienylglycine has been extensively employed in numerous scientific studies, harnessing its unique properties. In protein folding studies, (S)-3-Thienylglycine has demonstrated its remarkable ability to stabilize the tertiary structure of proteins. Furthermore, it has exhibited effectiveness as a ligand in metal-catalyzed organic reactions and as a reagent in organic synthesis. (S)-3-Thienylglycine employs diverse mechanisms of action, each playing a role in its multifaceted applications. It serves as a stabilizing agent, promoting protein folding and contributing to the maintenance of proper protein structures. Additionally, (S)-3-Thienylglycine functions as a ligand, facilitating metal-catalyzed organic reactions. Its biomarker properties allow for the detection of specific diseases, enabling diagnostic advancements. Moreover, (S)-3-Thienylglycine has been recognized as a modulator of signal transduction pathways and an inhibitor of specific enzymes, further broadening its scope of impact.