N7251
4-硝基邻苯二酚硫酸盐 二钾盐
chromogenic sulphatase substrate, crystalline
别名:
2-羟基-5-硝基苯硫酸盐, 2-羟基-5-硝基苯硫酸盐 二钾盐 一水合物, 对硝基儿茶酚硫酸盐 二钾盐
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关于此项目
线性分子式:
C6H3NO7SK2
化学文摘社编号:
分子量:
311.35
NACRES:
NA.77
PubChem Substance ID:
UNSPSC Code:
12352200
EC Number:
238-550-0
MDL number:
Beilstein/REAXYS Number:
3805018
General description
4-硝基儿茶酚硫酸盐是一种芳香族硫酸盐。
显色硫酸酯酶底物。
Application
4-硝基儿茶酚硫酸二钾盐被用作粘多糖 VI（MPS VI）分析的底物。它也被用来测量糖胺聚糖（GAG）降解酶-芳基磺化酶B和外糖苷酶的活性。
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
D B Thompson et al.
Experientia, 42(2), 150-151 (1986-02-15)
Rodent and bovine arylsulfatase B hydrolyze 4-methylumbelliferyl sulfate (4MUS) 10- to 30-fold more efficiently than arylsulfatase A. Therefore, 4MUS grossly underestimates arylsulfatase A activity in the presence of excess arylsulfatase B.
The convulsive effects of dopamine sulfate conjugates in rat brain.
N T Buu et al.
Life sciences, 29(22), 2311-2316 (1981-11-30)
Jin-Peng Sun et al.
The Journal of biological chemistry, 278(35), 33392-33399 (2003-06-18)
The pathogenic bacteria Yersinia are causative agents in human diseases ranging from gastrointestinal syndromes to bubonic plague. There is increasing risk of misuse of infectious agents, such as Yersinia pestis, as weapons of terror as well as instruments of warfare
Sandra Del Carmen Mendoza-Ruvalcaba et al.
Genetics and molecular biology, 43(1), e20180347-e20180347 (2020-02-28)
Mucopolysaccharidoses (MPS) are a group of genetic disorders, each resulting from the deficiency of one of the lysosomal enzymes that catabolizes mucopolysaccharides. For the accurate diagnosis of the disease, the quantification of a specific enzymatic activity is needed. In the
S Partanen
The Histochemical journal, 16(5), 501-506 (1984-05-01)
A new, direct-colouring, metal precipitation method for the light microscopical demonstration of arylsulphatases A and B is described. It is based on the reducing capacity of nitrocatechol liberated by arylsulphatases from p-nitrocatechol sulphate. The reaction is carried out in Karnovsky-Roots'
商品
Drug conjugate analysis and the enzymatic hydrolysis of glucuronides
实验方案
Enzymatic Assay of Sulfatase (EC 3.1.6.1.)
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