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Merck
CN

00251

Supelco

Fumarylacetone

≥95.0% (GC)

别名:

(2E)-4,6-Dioxo-2-heptenoic acid

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关于此项目

经验公式(希尔记法):
C7H8O4
化学文摘社编号:
分子量:
156.14
Beilstein:
1907125
UNSPSC代码:
41116107
NACRES:
NA.24
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质量水平

方案

≥95.0% (GC)

应用

clinical testing

包装形式

neat

储存温度

2-8°C

SMILES字符串

CC(CC(/C=C/C(O)=O)=O)=O

InChI

1S/C7H6O3/c8-5-1-2-6(9)4-7(10)3-5/h1-2H,3-4H2

InChI key

LRBCDZWXQXOVTN-UHFFFAOYSA-N

生化/生理作用

Metabolite of tyrosine catabolic pathway

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Inactivation of polymorphic variants of human glutathione transferase zeta (hGSTZ1-1) by maleylacetone and fumarylacetone.
H B Lantum et al.
Advances in experimental medicine and biology, 500, 339-342 (2002-01-05)
Albert L Shroads et al.
Journal of chromatography. B, Analytical technologies in the biomedical and life sciences, 808(2), 153-161 (2004-07-21)
Tyrosine and many of its catabolites play significant roles in the in the toxicity associated with acquired and congenital forms of hypertyrosinemia. We now report a specific and sensitive GC/MS method for the simultaneous determination of tyrosine metabolites maleylacetone (MA)
C Laberge et al.
Advances in experimental medicine and biology, 206, 209-221 (1986-01-01)
Review of the literature of the past 40 years on tyrosine and its toxicity shows that no direct link between this aromatic amino acid and carcinogenesis has been well established. Ten years ago, studies of tyrosine toxicity in mice suggested
Hoffman B M Lantum et al.
Chemical research in toxicology, 15(5), 707-716 (2002-05-23)
Glutathione transferase zeta (GSTZ1-1) catalyzes the cis-trans isomerization of maleylacetoacetate or maleylacetone (MA) to fumarylacetoacetate or fumarylacetone (FA), respectively. GSTZ1-1 also catalyzes the glutathione-dependent biotransformation of a range of alpha-haloacids, including dichloroacetic acid. The objective of this study was to
J M Fernández-Cañón et al.
The Journal of biological chemistry, 273(1), 329-337 (1998-02-07)
We have previously used Aspergillus nidulans as a fungal model for human phenylalanine catabolism. This model was crucial for our characterization of the human gene involved in alcaptonuria. We use here an identical approach to characterize at the cDNA level

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