G0903
γ-Glu-Cys
≥80% (HPLC), suitable for ligand binding assays
别名:
γ-L-谷氨酰基-L半胱氨酸, 去甘氨酸-谷胱甘肽的还原形式
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关于此项目
经验公式（希尔记法）:
C8H14N2O5S
化学文摘社编号:
分子量:
250.27
MDL编号:
UNSPSC代码:
12352209
PubChem化学物质编号:
NACRES:
NA.26
产品名称
γ-Glu-Cys, ≥80% (HPLC)
质量水平
方案
≥80% (HPLC)
表单
powder
组成
Peptide content, ≥60% elemental analysis
技术
ligand binding assay: suitable
颜色
white to off-white
储存温度
−20°C
SMILES字符串
N[C@@H](CCC(=O)N[C@@H](CS)C(O)=O)C(O)=O
InChI
1S/C8H14N2O5S/c9-4(7(12)13)1-2-6(11)10-5(3-16)8(14)15/h4-5,16H,1-3,9H2,(H,10,11)(H,12,13)(H,14,15)/t4-,5-/m0/s1
InChI key
RITKHVBHSGLULN-WHFBIAKZSA-N
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Amino Acid Sequence
Glu-Cys
应用
γ-Glu-Cys可用于研究谷胱甘肽合成酶的活性位点和动力学。它也被用于从拟南芥 组织中提取和量化低分子量硫醇。
生化/生理作用
γ-L-谷氨酰基-L-半胱氨酸（γ-Glu-Cys）是用于通过谷胱甘肽合成酶生物合成L-谷胱甘肽的底物。γ-Glu-Cys通过裂解谷胱甘肽的Cys-Gly肽键而产生。它对植物螯合素的形成也是必需的，植物螯合素是富含半胱氨酸的硫醇反应性肽。
外形
从0.1％TFA中冻干获得。
警示用语：
Warning
危险声明
危险分类
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
靶器官
Respiratory system
储存分类代码
11 - Combustible Solids
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
dust mask type N95 (US), Eyeshields, Gloves
T Hara et al.
Protein engineering, 8(7), 711-716 (1995-07-01)
Lys18, Arg86, Asn283, Ser286, Thr288 and Glu292 of glutathione synthetase from Escherichia coli B are presumed to be highly concerned with the substrate, gamma-L-glutamyl-L-cysteine (gamma-Glu-Cys), binding by X-ray crystallography and affinity labeling studies. Using site-directed mutagenesis, we investigated functional roles
Method for determination of free and total glutathione and gamma-glutamylcysteine concentrations in human leukocytes and plasma.
J Mårtensson
Journal of chromatography, 420(1), 152-157 (1987-09-04)
Helmut Schweikl et al.
Dental materials : official publication of the Academy of Dental Materials, 37(1), 175-190 (2020-12-12)
The release of inflammatory cytokines from antigen-stimulated cells of the immune system is inhibited by resin monomers such as 2-hydroxyethyl methacrylate (HEMA). Although the formation of oxidative stress in cells exposed to HEMA is firmly established, the mechanism behind the
Jan Stout et al.
Journal of molecular biology, 416(4), 486-494 (2012-01-10)
Glutathione is an intracellular redox-active tripeptide thiol with a central role in cellular physiology across all kingdoms of life. Glutathione biosynthesis has been traditionally viewed as a conserved process relying on the sequential activity of two separate ligases, but recently
Naser A. Anjum, Sarvajeet Singh Gill, Ritu Gill
Plant Adaptation to Environmental Change: Significance of Amino Acids and their Derivatives (2014)
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