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Merck

G2253

Sigma-Aldrich

L-谷氨酸& # 947;-单羟基己酸酯

≥97% (TLC)

别名:

-5--羟基谷氨酰胺, L-& # 947;-谷氨酰异羟肟酸

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About This Item

经验公式(希尔记法):
C5H10N2O4
CAS号:
分子量:
162.14
MDL编号:
UNSPSC代码:
12352209
PubChem化学物质编号:
NACRES:
NA.26

产品名称

L-谷氨酸& # 947;-单羟基己酸酯,

方案

≥97% (TLC)

质量水平

表单

powder

颜色

white to off-white

应用

detection

储存温度

−20°C

SMILES字符串

NC(CCC(=O)NO)C(O)=O

InChI

1S/C5H10N2O4/c6-3(5(9)10)1-2-4(8)7-11/h3,11H,1-2,6H2,(H,7,8)(H,9,10)

InChI key

YVGZXTQJQNXIAU-UHFFFAOYSA-N

应用

左旋谷氨酸γ-单异羟肟酸已用作计算谷氨酰胺转胺酶(TGase)活性的标准品。

生化/生理作用

L-谷氨酸& # 947;-单羟基肟酸盐[L-谷氨酸(γ)HXM]用作钒配体,增强钒代谢活性。L-Glu(γ)HXM也用作大肠杆菌 大肠杆菌天冬酰胺合成酶B的底物和作为ATP依赖性的大肠杆菌γ-谷氨酰半胱氨酸合成酶的不可逆抑制剂。

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

Eyeshields, Gloves, type N95 (US)


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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M Katoh et al.
Bioscience, biotechnology, and biochemistry, 62(7), 1455-1457 (1998-08-28)
Incubation of Escherichia coli gamma-glutamylcysteine synthetase with L-glutamic acid gamma-monohydroxamate and ATP caused slow but irreversible inhibition of the enzyme, and more than 90% activity was lost in three days. The enzyme was not inactivated when ATP was absent or
N Seiler et al.
Neurochemical research, 15(3), 301-305 (1990-03-01)
The method for the assay of glutamine synthetase (GlnS) relies on the gamma-glutamyl transferase reaction, i.e. the formation of glutamyl-gamma-hydroxamate from glutamine and hydroxylamine, and the chromatographic separation of the reaction product from the reactants. The method is not only
Yibin Xu et al.
Protein expression and purification, 34(1), 142-146 (2004-02-10)
A soluble N-terminal domain of the Escherichia coli adenylyl transferase (ATase) is responsible for deadenylylation activity of the intact enzyme. Previous studies of the deadenylylation activity have involved a fragment, AT-N423 (residues 1 to 423), which was extended by 17
Matteo Tegoni et al.
Dalton transactions (Cambridge, England : 2003), (9)(9), 1329-1333 (2004-07-15)
The equilibria of copper(II) with (S)-glutamic-gamma-hydroxamic acid (H2L) were investigated in aqueous solution by different techniques: glass electrode potentiometry; calorimetry; VIS and CD spectrophotometry; and ES-MS. An unexpected pentacopper(II) 12-metallacrown-4 [Cu5L4H(-4)](2-) was detected, analogous to those well known formed by
I Goldwaser et al.
Molecular pharmacology, 58(4), 738-746 (2000-09-22)
Several ligands, when complexed with vanadium, potentiate its insulinomimetic activity both in vivo and in vitro. We have recently found that L-Glu-gamma-monohydroxamate (HXM) and L-Asp(beta)HXM were especially potent in this regard. In the present study, we used vanadium-enriched adipose cells

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