Saltar al contenido
Merck

Saltar a

A0737

N-acetylcysteine amide

≥98% (HPLC), lyophilized powder, antioxidant

Sinónimos:

(R)- 2-(Acetylamino)-3-mercapto-Propanamide, AD4, N-Acetyl-L-cysteinamide, NACA, acetylcysteinamide

Iniciar sesión para ver los precios por organización y contrato.

Seleccione un Tamaño

Cambiar Vistas
A ustedes/SKUDisponibilidadPrecio

Acerca de este artículo

Fórmula empírica (notación de Hill):
C5H10N2O2S
Número CAS:
Peso molecular:
162.21
UNSPSC Code:
12352209
PubChem Substance ID:
NACRES:
NA.25
MDL number:
Assay:
≥98% (HPLC)
Form:
lyophilized powder
Storage condition:
desiccated
En este momento no podemos mostrarle ni los precios ni la disponibilidad
Servicio técnico
¿Necesita ayuda? Nuestro equipo de científicos experimentados está aquí para ayudarle.
Permítanos ayudarle


Nombre del producto

N-acetylcysteine amide, ≥98% (HPLC)

Quality Segment

assay

≥98% (HPLC)

form

lyophilized powder

storage condition

desiccated

color

white to off-white

solubility

H2O: ≥20 mg/mL, DMSO: >40 mg/mL

storage temp.

2-8°C

SMILES string

CC(=O)N[C@@H](CS)C(N)=O

InChI

1S/C5H10N2O2S/c1-3(8)7-4(2-10)5(6)9/h4,10H,2H2,1H3,(H2,6,9)(H,7,8)/t4-/m0/s1

InChI key

UJCHIZDEQZMODR-BYPYZUCNSA-N

Application

N-acetylcysteine amide has been used:
  • to protect retinal pigment epithelium (RPE) from oxidative stress
  • to show that increased expression of cell adhesion molecule 4 (CADM4) in oligodendrocytes inhibits myelination
  • to protect cells from apoptosis induced by shikonin plus erlotinib/gefitinib
  • as a component in various culture media

as an antioxidant to reduce oxidative stress in brains of homozygous Drosophila spermine synthase (dSms e/e) mutant flies and melanoma cells.

Biochem/physiol Actions

N-acetylcysteine amide is a membrane penetrating antioxidant with antiinflamatory activity through regulation of activation of NF-κB and HIF-1α as well as modulation of ROS.
N-acetylcysteine amide is a membrane penetrating antioxidant with antiinflamatory activity through regulation of activation of NF-κB and HIF-1α as well as modulation of ROS. The compound readily crosses cell membranes, replenishes intracellular GSH, and defends the cell from oxidative stress. In contrast to DTT, AD4 is able to directly reduce intracellularl GSSG to GSH without the involvement of glutathione peroxidase. Such direct thiol exchange might have a protective effect. This compound has a potential in research and exploration for treatment of neurodegeneration, radiation exposure, and other oxidation-mediated disorders.

Other Notes

This product is hydroscopic and air sensitive.

Comparar elementos similares

Ver comparación completa

Mostrar Diferencias

1 of 1

Este artículo
S8825S9318SML1065
form

lyophilized powder

form

powder

form

powder

form

powder

assay

≥98% (HPLC)

assay

≥98% (HPLC)

assay

>98% (HPLC)

assay

≥98% (HPLC)

Quality Level

100

Quality Level

100

Quality Level

100

Quality Level

100

storage temp.

2-8°C

storage temp.

2-8°C

storage temp.

2-8°C

storage temp.

2-8°C

solubility

H2O: ≥20 mg/mL, DMSO: >40 mg/mL

solubility

DMSO: >10 mg/mL

solubility

DMSO: 16 mg/mL, H2O: insoluble

solubility

DMSO: 5 mg/mL, clear (warmed)

storage condition

desiccated

storage condition

desiccated

storage condition

-

storage condition

-


pictograms

Exclamation mark

signalword

Warning

hcodes

Hazard Classifications

Acute Tox. 4 Oral

Clase de almacenamiento

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable



Elija entre una de las versiones más recientes:

Certificados de análisis (COA)

Lot/Batch Number

It looks like we've run into a problem, but you can still download Certificates of Analysis from our Documentos section.

Si necesita más asistencia, póngase en contacto con Atención al cliente

¿Ya tiene este producto?

Encuentre la documentación para los productos que ha comprado recientemente en la Biblioteca de documentos.

Visite la Librería de documentos



Questions

Reviews

No rating value

Active Filters