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Merck

N3877

Sigma-Aldrich

Potassium 4-nitrophenyl sulfate

sulfatase substrate, chromogenic, ≥98% (TLC), powder

Sinónimos:

4-Nitrophenyl sulfate potassium salt

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About This Item

Fórmula lineal:
NO2C6H4OSO2OK
Número de CAS:
Peso molecular:
257.26
Beilstein:
3786392
Número CE:
Número MDL:
Código UNSPSC:
12352204
ID de la sustancia en PubChem:
NACRES:
NA.32
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Nombre del producto

Potassium 4-nitrophenyl sulfate, sulfatase substrate

Nivel de calidad

Ensayo

≥98% (TLC)

Formulario

powder

mp

246-250 °C (lit.)

solubilidad

water: 50 mg/mL, clear, colorless to very faintly greenish-yellow (to Very Light Yellow)

Condiciones de envío

wet ice

temp. de almacenamiento

−20°C

cadena SMILES

[K+].[O-][N+](=O)c1ccc(OS([O-])(=O)=O)cc1

InChI

1S/C6H5NO6S.K/c8-7(9)5-1-3-6(4-2-5)13-14(10,11)12;/h1-4H,(H,10,11,12);/q;+1/p-1

Clave InChI

BITVAZYUWRLLCN-UHFFFAOYSA-M

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Aplicación

Potassium 4-nitrophenyl sulfate has been used:
  • as a substrate to measure arylsulfatase activity in cell-free coelomic fluid[1]
  • as a substrate for p-nitrophenyl glycoside-based enzyme assay[2]
  • to inhibit arylsulfatase[3]
  • as an inorganic analog of organic aryl ester sulphate[4]

Sustratos

Chromogenic sulfatase substrate.

Código de clase de almacenamiento

11 - Combustible Solids

Clase de riesgo para el agua (WGK)

WGK 3

Punto de inflamabilidad (°F)

Not applicable

Punto de inflamabilidad (°C)

Not applicable

Equipo de protección personal

Eyeshields, Gloves, type N95 (US)


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J O Falkinham
International journal of systematic bacteriology, 40(1), 66-70 (1990-01-01)
A rapid (3-h) arylsulfatase assay for cell suspensions of mycobacteria, in which p-nitrophenyl sulfate is used as the substrate, was developed. Arylsulfatase activity was found in cell suspensions of representative strains of Mycobacterium avium, Mycobacterium intracellulare, and Mycobacterium scrofulaceum grown
N Sakuma-Sawada et al.
Research communications in molecular pathology and pharmacology, 97(2), 131-138 (1997-08-01)
Hepatic uptake of the sulfate conjugate of p-nitrophenol (p-NPsul) has been studied. Uptake clearance of p-NPsul by isolated rat hepatocytes was dependent on p-NPsul concentration, suggesting carrier-mediated transport. The uptake of p-NPsul by isolated rat hepatocytes was inhibited by acetaminophen
M P Kung et al.
Endocrinology, 122(4), 1195-1200 (1988-04-01)
Subcellular preparations from rat liver, brain, and kidney and from human liver were tested for their ability to desulfate T3 sulfate (T3SO4). Activity was found associated with the microsomal fraction: rat liver was the most active, hydrolyzing 76 pmol/min.mg protein
H X Zhang et al.
Drug metabolism and disposition: the biological fate of chemicals, 19(2), 473-477 (1991-03-01)
Although numerous previous reports have characterized the mammalian biotransformation of the organophosphorus insecticides parathion and methyl parathion, questions still remain regarding the toxicological significance of certain metabolic pathways in vivo. The present study utilized rat liver perfusions in order to
M D Burkart et al.
Analytical biochemistry, 274(1), 131-137 (1999-10-21)
We have developed a continuous spectrophotometric coupled-enzyme assay for sulfotransferase activity. This assay is based on the regeneration of 3'-phosphoadenosine-5'-phosphosulfate (PAPS) from the desulfated 3'-phosphoadenosine-5'-phosphate (PAP) by a recombinant aryl sulfotransferase using p-nitrophenyl sulfate as the sulfate donor and visible

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