CAS 626-72-2
:L-Homocystine
Description:
L-Homocystine is a naturally occurring amino acid derivative, specifically a dimer of homocysteine, which is an important intermediate in the metabolism of sulfur-containing amino acids. It is characterized by the presence of two homocysteine molecules linked by a disulfide bond, resulting in a compound that contains both amino and thiol functional groups. L-Homocystine is typically found in biological systems and plays a role in various metabolic pathways, including the synthesis of cysteine and methionine. It is soluble in water and exhibits a crystalline structure. The compound is of interest in medical research due to its association with cardiovascular diseases and other health conditions linked to elevated homocysteine levels. Additionally, L-homocystine can be involved in the formation of protein structures and may influence cellular signaling pathways. Its CAS number, 626-72-2, is used for identification in chemical databases and regulatory contexts. Overall, L-homocystine is significant in both biochemistry and clinical research.
Formula:C8H16N2O4S2
InChI:InChI=1S/C8H16N2O4S2/c9-5(7(11)12)1-3-15-16-4-2-6(10)8(13)14/h5-6H,1-4,9-10H2,(H,11,12)(H,13,14)/t5-,6-/m0/s1
InChI key:InChIKey=ZTVZLYBCZNMWCF-WDSKDSINSA-N
SMILES:C([C@@H](C(O)=O)N)CSSCC[C@@H](C(O)=O)N
Synonyms:- (2S,2′S)-4,4′-Dithiobis[2-aminobutanoic acid]
- (H-HoCys-OH)2
- <span class="text-smallcaps">L</span>-Homocystine
- Butanoic acid, 4,4′-dithiobis[2-amino-, (2S,2′S)-
- Butanoic acid, 4,4′-dithiobis[2-amino-, [S-(R*,R*)]-
- Butyric acid, 4,4′-dithiobis[2-amino-, <span class="text-smallcaps">L</span>-
- L-Homocystine
- Butyric acid, 4,4′-dithiobis[2-amino-, L-
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Found 11 products.
(H-Homocys-OH)₂
CAS:The spontaneous oxidation of plasma homocysteine yields homocystine, which is scarcely soluble at neutral pH. The homocystine microcrystals damage the endothelial tissue which increases the risk of vascular diseases.Formula:C8H16N2O4S2Purity:> 99%Color and Shape:White PowderMolecular weight:268.36(2S)-2-Amino-4-[[(3S)-3-amino-4-hydroxy-4-oxo-butyl]disulfanyl]butanoic acid
CAS:<p>(2S)-2-Amino-4-[[(3S)-3-amino-4-hydroxy-4-oxo-butyl]disulfanyl]butanoic acid</p>Formula:C8H16N2O4S2Purity:98%Color and Shape: off-white to light yellow solidMolecular weight:268.35g/molL-Homocystine
CAS:<p>Homocystine briefly forms before turning into cystathionine via vitamin B6; linked to schizophrenia and neural tube defects; folic acid lowers risk.</p>Formula:C8H16N2O4S2Purity:99.79%Color and Shape:SolidMolecular weight:268.35L-Homocystine
CAS:Controlled Product<p>Applications Increased levels lead to hyperhomocysteinemia; a cardiovascular risk factor in prediction of coronary heart disease as well as being associated with congenital birth defects, pregnancy complications and cancer.<br>References Geisel, J. et al.: Clin. Chem. Lab. Med., 41, 1513 (2003); Geisel, J. et al.: Clin. Chem. Lab. Med., 41, 1513 (2003);<br></p>Formula:C8H16N2O4S2Color and Shape:NeatMolecular weight:268.35L-Homocystine
CAS:<p>L-Homocystine is a chemical compound that is used as a research chemical and a speciality chemical. It is an amino acid that can be obtained from the degradation of methionine, cysteine, and serine. L-Homocystine has been found to have many uses in the pharmaceutical industry, including as a building block or intermediate for complex compounds such as antibiotics, antihypertensive drugs, and anticonvulsants. L-Homocystine can also be used as a reagent in organic synthesis reactions. This compound is not only useful for research purposes but can also be used in the manufacturing of high quality products.</p>Formula:C8H16N2O4S2Molecular weight:268.36 g/molL-Homocystine
CAS:<p>Oxidized member of L-homocysteine/L-homocystine pair</p>Formula:C8H16N2O4S2Purity:(Nitrogen Content) Min. 98%Color and Shape:PowderMolecular weight:268.36 g/molH-HoCys-OH
CAS:<p>M06106 - H-HoCys-OH</p>Formula:C8H16N2O4S2Purity:95%Color and Shape:SolidMolecular weight:268.35








