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Merck

M6885

Sigma-Aldrich

1-Methyluric acid

Sinónimos:

1-Methyl-2,6,8-trihydroxypurine, 1-U, 1MUA

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About This Item

Fórmula empírica (notación de Hill):
C6H6N4O3
Número de CAS:
Peso molecular:
182.14
Beilstein:
195190
Número CE:
Número MDL:
Código UNSPSC:
41106305
ID de la sustancia en PubChem:
NACRES:
NA.51

Ensayo

≥98% (HPLC)

Formulario

powder

solubilidad

1 M NaOH: 20 mg/mL, clear to slightly hazy

cadena SMILES

CN1C(=O)NC2=C(NC(=O)N2)C1=O

InChI

1S/C6H6N4O3/c1-10-4(11)2-3(9-6(10)13)8-5(12)7-2/h1H3,(H,9,13)(H2,7,8,12)

Clave InChI

QFDRTQONISXGJA-UHFFFAOYSA-N

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Aplicación

1-Methyluric acid has been used:
  • for the determination of uric acid in stool samples by liquid chromatography and tandem mass spectrometry
  • in turbidimetric assay of synthetic urine samples
  • as a substrate for CYP1A2(cytochrome P450 family 1 subfamily A member 2) assay

Acciones bioquímicas o fisiológicas

1-Methyluric acid (1-U) is a major metabolite of caffeine and theophylline with antioxidant activity that protects molecules such as low density lipoproteins (LDL) from oxidative modifications. 1-Methyluric acid may be used in studies aimed at differentiating the activities of caffeine and theophylline metabolites.

Envase

Bottomless glass bottle. Contents are inside inserted fused cone.

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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Effects of peppermint tea consumption on the activities of CYP1A2, CYP2A6, Xanthine Oxidase, N-acetyltranferase-2 and UDP-glucuronosyltransferases-1A1/1A6 in healthy volunteers
Begas E, et al.
Food And Chemical Toxicology, 100, 80-89 (2017)
Theophano A Psarra et al.
Fundamental & clinical pharmacology, 22(5), 537-547 (2008-10-11)
The present study, aimed to clarify whether the gastrointestinal adverse effects following administration of the bronchodilator theophylline are owing to the action of the drug itself or its metabolites, investigates the pharmacodymanic effects of theophylline's metabolites on the spontaneous contractility
C Lee
Clinica chimica acta; international journal of clinical chemistry, 295(1-2), 141-154 (2000-04-18)
Although caffeine has been suggested as an antioxidant at millimolar concentrations, little information is available about the antioxidant activity of caffeine and its metabolites at physiological concentrations. Antioxidant activity was measured by oxygen-radical absorbing capacity (ORAC) using 2, 2'-azobis(2-amidinopropane) dihydrochloride
M Boda et al.
Journal of pediatric gastroenterology and nutrition, 29(5), 546-550 (1999-11-30)
The xanthine oxidoreductase system has been identified as one of the main sources of free radicals responsible for various forms of tissue injury. Because the intestinal villi are an important location of this enzyme, it was of interest to study
Klaus Abraham et al.
Clinical pharmacology and therapeutics, 72(2), 163-174 (2002-08-22)
The correct in vivo quantification of aryl hydrocarbon receptor-mediated induction of cytochrome P450 1A2 (CYP1A2) in humans is a long-standing question. We compared the performance of several modifications of the caffeine test for measurement of CYP1A2 activity in subjects with

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