DL-Homocystine CAS:870-93-9

DL-Homocystine holds important applications in biochemical and biomedical research, particularly in investigations related to homocystinuria, a genetic disorder affecting the metabolism of the amino acid methionine. It serves as an essential tool for studying the underlying biochemical mechanisms and molecular pathways associated with this condition. Research utilizing DL-Homocystine contributes to the understanding of disease pathophysiology and the development of potential therapeutic interventions. In pharmaceutical development, DL-Homocystine may be utilized in the synthesis and characterization of drug compounds targeting conditions related to homocysteine metabolism and related disorders. Its involvement in these processes supports the exploration of new treatment options and drug therapies for addressing metabolic imbalances and associated health complications. Furthermore, DL-Homocystine plays a role in clinical diagnostics and laboratory testing, particularly in the identification and quantification of homocysteine-related markers in biological samples. Its use in diagnostic assays and research assays contributes to the assessment of patient health, disease screening, and monitoring of metabolic abnormalities, aiding in the diagnosis and management of relevant medical conditions. Overall, DL-Homocystine's applications in research, pharmaceutical development, and clinical diagnostics underscore its significance in advancing our understanding of metabolic disorders and the potential development of targeted interventions for improved patient care and management.