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MilliporeSigma

A7009

Sigma-Aldrich

Aminoguanidine hemisulfate salt

≥98%

Sinónimos:

Guanylhydrazine hemisulfate salt

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About This Item

Fórmula lineal:
CH6N4 · 1/2H2SO4
Número de CAS:
Peso molecular:
123.12
Número CE:
Número MDL:
Código UNSPSC:
12352200
ID de la sustancia en PubChem:
NACRES:
NA.77

origen biológico

synthetic (organic)

Ensayo

≥98%

Formulario

powder

solubilidad

water: 50 mg/mL, clear to very slightly hazy, colorless

temp. de almacenamiento

room temp

cadena SMILES

NNC(N)=N.NNC(N)=N.OS(O)(=O)=O

InChI

1S/2CH6N4.H2O4S/c2*2-1(3)5-4;1-5(2,3)4/h2*4H2,(H4,2,3,5);(H2,1,2,3,4)

Clave InChI

VKGQPUZNCZPZKI-UHFFFAOYSA-N

Información sobre el gen

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Aplicación

Aminoguanidine inhibits both constitutive and inducible nitric oxide synthetase. Aminoguanidine has also been used to study the effects of nitric oxide on ovulation and ovarian steroidogenesis and prostaglandin production.

Acciones bioquímicas o fisiológicas

Inhibits both constitutive and inducible nitric oxide synthetase

Características y beneficios

This compound is featured on the Nitric Oxide Synthases page of the Handbook of Receptor Classification and Signal Transduction. To browse other handbook pages, click here.

Código de clase de almacenamiento

13 - Non Combustible Solids

Clase de riesgo para el agua (WGK)

WGK 2

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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Caroline Zanotto et al.
Molecular neurobiology, 56(5), 3538-3551 (2018-08-27)
Diabetes mellitus is a metabolic disorder that results in glucotoxicity and the formation of advanced glycated end products (AGEs), which mediate several systemic adverse effects, particularly in the brain tissue. Alterations in glutamatergic neurotransmission and cognitive impairment have been reported
Fernanda Hansen et al.
Amino acids, 48(2), 375-385 (2015-09-09)
Diabetes is a metabolic disease characterized by high fasting-glucose levels. Diabetic complications have been associated with hyperglycemia and high levels of reactive compounds, such as methylglyoxal (MG) and advanced glycation endproducts (AGEs) formation derived from glucose. Diabetic patients have a
Jong Jin Park et al.
Food chemistry, 338, 128150-128150 (2020-10-24)
This study aimed to develop efficient adsorption and desorption processes to purify phenolic compounds from Ecklonia cava. We compared the adsorption and desorption properties of five resins. HP2MG showed the highest adsorption and desorption capacities and adsorption rate; hence, it
Wei Chen et al.
Oxidative medicine and cellular longevity, 2022, 8854457-8854457 (2022-01-18)
Cerebral endothelial cells play an essential role in brain angiogenesis, and their function has been found to be impaired in diabetes. Methylglyoxal (MG) is a highly reactive dicarbonyl metabolite of glucose formed mainly during glycolysis, and its levels can be
Mikel J Rüterbusch et al.
The Journal of experimental medicine, 220(11) (2023-09-12)
CD4+ lung-resident memory T cells (TRM) generated in response to influenza infection confer effective protection against subsequent viral exposures. Whether these cells can be altered by environmental antigens and cytokines released during heterologous, antigen-independent immune responses is currently unclear. We

Artículos

Cellular oxidative stress is countered by enzymatic scavengers and antioxidant modulators against reactive oxygen species damage.

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