物质信息

ID:37

名称和标识
IUPAC标准名
(2R)-2-amino-3-sulfanylpropanoic acid
IUPAC传统名
L-cysteine
别名
2-Amino-3-mercaptopropionic acidL-CysteineL-CysL-(+)-Cysteineb-MercaptoalanineL-2-Amino-3-mercaptopropionic acid3-mercapto-L-AlanineCyscarbocysteineCysteinHalf-cystineThioserine(R)-Cysteine(R)-2-Amino-3-mercaptopropanoic acid
数据登录号
CAS号
PubChem CID
PubChem SID
化合物性质
理化性质
疏水性(logP)
-2.6
溶解度
277 mg/mL at 25 oC [BEILSTEIN]
描述信息
Drug Groups
approved; nutraceutical
Description
A thiol-containing non-essential amino acid that is oxidized to form cystine. [PubChem]
Indication
For the prevention of liver damage and kidney damage associated with overdoses of acetaminophen
Pharmacology
Due to this ability to undergo redox reactions, cysteine has antioxidant properties. Cysteine is an important source of sulfur in human metabolism, and although it is classified as a non-essential amino acid, cysteine may be essential for infants, the elderly, and individuals with certain metabolic disease or who suffer from malabsorption syndromes. Cysteine may at some point be recognized as an essential or conditionally essential amino acid.
Affected Organisms
Humans and other mammals
References
• Bulaj G, Kortemme T, Goldenberg DP: Ionization-reactivity relationships for cysteine thiols in polypeptides. Biochemistry. 1998 Jun 23;37(25):8965-72. [Pubmed]
• Baker DH, Czarnecki-Maulden GL: Pharmacologic role of cysteine in ameliorating or exacerbating mineral toxicities. J Nutr. 1987 Jun;117(6):1003-10. [Pubmed]
External Links
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参考文献
• Bulaj G, Kortemme T, Goldenberg DP: Ionization-reactivity relationships for cysteine thiols in polypeptides. Biochemistry. 1998 Jun 23;37(25):8965-72. Pubmed
• Baker DH, Czarnecki-Maulden GL: Pharmacologic role of cysteine in ameliorating or exacerbating mineral toxicities. J Nutr. 1987 Jun;117(6):1003-10. Pubmed