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A0737

N-acetylcysteine amide

≥98% (HPLC), lyophilized powder, antioxidant

Sinonimo/i:

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

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Cambia visualizzazione
Voi/SKUDisponibilitàPrezzo
5 mg
Per conoscere la disponibilità, visualizza il carrello
CHF 144.00
25 mg
Per conoscere la disponibilità, visualizza il carrello
CHF 580.00

Informazioni su questo articolo

Formula empirica (notazione di Hill):
C5H10N2O2S
Numero CAS:
Peso molecolare:
162.21
UNSPSC Code:
12352209
PubChem Substance ID:
NACRES:
NA.25
MDL number:
Assay:
≥98% (HPLC)
Form:
powder
Storage condition:
desiccated

CHF 144.00


Per conoscere la disponibilità, visualizza il carrello

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Nome del prodotto

N-acetylcysteine amide, ≥98% (HPLC)

Quality Segment

assay

≥98% (HPLC)

form

powder

storage condition

desiccated

color

white to off-white

solubility

H2O: ≥20 mg/mL, DMSO: >40 mg/mL

storage temp.

−20°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.

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S8825S9318SML1065
Salermide ≥98% (HPLC)

Sigma-Aldrich

S8825

Salermide

Sandoz 58-035 >98% (HPLC), powder

Sigma-Aldrich

S9318

Sandoz 58-035

TR100 ≥98% (HPLC)

Sigma-Aldrich

SML1065

TR100

description

≥98% (HPLC)

description

≥98% (HPLC)

description

>98% (HPLC), powder

description

≥98% (HPLC)

form

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.

−20°C

storage temp.

2-8°C

storage temp.

2-8°C

storage temp.

2-8°C

storage condition

desiccated

storage condition

desiccated

storage condition

-

storage condition

-

solubility

H2O: ≥20 mg/mL, DMSO: >40 mg/mL

solubility

DMSO: >10 mg/mL

solubility

H2O: insoluble, DMSO: 16 mg/mL

solubility

DMSO: 5 mg/mL, clear (warmed)


pictograms

Exclamation mark

signalword

Warning

hcodes

Hazard Classifications

Acute Tox. 4 Oral

Classe di stoccaggio

11 - Combustible Solids

flash_point_f

Not applicable

flash_point_c

Not applicable



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