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Atomfair DL-Homocysteine thiolactone C4H7NOS

Description DL-Homocysteine thiolactone (CAS No. 6038-19-3) is a high-purity biochemical compound with the molecular formula C4H7NOS and the IUPAC name 3-aminothiolan-2-one . This heterocyclic thiolactone derivative is widely utilized in biochemical and pharmaceutical research due to its role as a reactive intermediate in homocysteine metabolism. Our product is rigorously tested for purity and stability, ensuring optimal performance in sensitive applications. It is supplied as a crystalline solid with excellent solubility in polar solvents, making it suitable for a variety of experimental protocols. DL-Homocysteine thiolactone is an essential reagent for studying cardiovascular diseases, oxidative stress, and metabolic disorders linked to homocysteine…

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Description

Description

DL-Homocysteine thiolactone (CAS No. 6038-19-3) is a high-purity biochemical compound with the molecular formula C4H7NOS and the IUPAC name 3-aminothiolan-2-one. This heterocyclic thiolactone derivative is widely utilized in biochemical and pharmaceutical research due to its role as a reactive intermediate in homocysteine metabolism. Our product is rigorously tested for purity and stability, ensuring optimal performance in sensitive applications. It is supplied as a crystalline solid with excellent solubility in polar solvents, making it suitable for a variety of experimental protocols. DL-Homocysteine thiolactone is an essential reagent for studying cardiovascular diseases, oxidative stress, and metabolic disorders linked to homocysteine dysregulation.

  • CAS No: 6038-19-3
  • Molecular Formula: C4H7NOS
  • Molecular Weight: 117.17
  • Exact Mass: 117.02483502
  • Monoisotopic Mass: 117.02483502
  • IUPAC Name: 3-aminothiolan-2-one
  • SMILES: C1CSC(=O)C1N
  • Synonyms: DL-Homocysteine thiolactone, 3-aminothiolan-2-one, 3-AMINODIHYDROTHIOPHEN-2-ONE, 10593-85-8, 14007-10-4

Application

DL-Homocysteine thiolactone is primarily used in biochemical research to investigate homocysteine-related metabolic pathways and their association with cardiovascular and neurodegenerative diseases. It serves as a key precursor in the synthesis of homocysteine derivatives for studying protein N-homocysteinylation, a post-translational modification linked to cellular dysfunction. Researchers also employ this compound to explore oxidative stress mechanisms and endothelial cell toxicity. Additionally, it finds applications in pharmaceutical development for designing inhibitors targeting homocysteine metabolism enzymes.

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