GLPBio

Nitrosoglutathione (GSNO)

Catalog No.: GC11815Purity:>98.00%Synonyms: S-Nitroso-L-glutathione
SNOG (GSNO), ein exogener NO-Donor und ein Substrat fÜr das Alkoholdehydrogenase-Klasse-III-Isoenzym der Ratte, hemmt zerebrovaskulÄre Angiotensin-II-abhÄngige und -unabhÄngige AT1-Rezeptorantworten.

Die Produkte sind ausschließlich für Forschungszwecke bestimmt. Nicht zur Anwendung am Menschen. Wir verkaufen nicht an Patienten.


Nitrosoglutathione (GSNO)
Cas No.: 57564-91-7
1mgIn Stock
$16.00
1
5mgIn Stock
$42.00
1
10mgIn Stock
$67.00
1
50mgIn Stock
$196.00
1
100mgIn Stock
$280.00
1

Zitate (Citations)

Für dieses Produkt sind derzeit keine Zitate verfügbar. Nachfolgend finden Sie ausgewählte Publikationen, die GlpBio-Produkte zitieren.
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    641, 529–536 (2025)
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    632, 686–694 (2024)
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    Nature
    618, 1017–1023 (2023)
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    Nature
    610, 366–372 (2022)
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    Cell
    187(9):2288-2304 (2024)
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    Cell
    183(7):1867-1883 (2020)
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    Science
    388(6745) (2025)
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    387(6734) (2025)
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    35, 97–116 (2025)
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    34, 683–706 (2024)
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    31, 1291–1307 (2021)

Beschreibung (Description)

Nitrosoglutathione (GSNO) is an S-nitrosylthiol NO donor based on natural glutathione [1]. Nitrosoglutathione is an effective smooth muscle relaxant and platelet aggregation inhibitor, capable of inhibiting the AT1 receptor responses dependent and independent of brain vascular angiotensin II [2]. Nitrosoglutathione selectively inhibits platelet and NF-κB activation [3].

In vitro, Nitrosoglutathione (1-100μM; 5h) can activate Ras, Src and ERK1/2 MAP kinases and promote HeLa cell proliferation. However, when HeLa cells are exposed to 1mM Nitrosoglutathione, cell proliferation is inhibited [4]. Nitrosoglutathione (500μM; 2h) treatment of neutrophils reduces TNFα-induced NF-κB activity and inhibits IκBα degradation [5].

In vivo, Nitrosoglutathione (8mg/kg/day; 7d; i.v.) significantly reduces systolic blood pressure, diastolic blood pressure and mean arterial pressure in rats with preeclampsia (PE) from day 14 to day 20 [6]. Nitrosoglutathione (0.2 and 0.6mg/kg; single administration; i.v.) significantly inhibits the production of superoxide in rats with ischemia/reperfusion injury models and inhibits NF-κB activation, iNOS induction and 3-nitrotyrosine expression, and upregulats the expression of endothelial NOS in flap vessels [7].

References:
[1] Bouressam ML, Lecat S, Raoul A, et al. S-nitrosoglutathione inhibits cerebrovascular angiotensin II-dependent and -independent AT receptor responses: A possible role of S-nitrosation. Br J Pharmacol. 2019;176(12):2049-2062.
[2] Jensen DE, Belka GK, Du Bois GC. S-Nitrosoglutathione is a substrate for rat alcohol dehydrogenase class III isoenzyme. Biochem J. 1998;331 (Pt 2) (Pt 2):659-668.
[3] Fortenberry J D, Owens M L, Brown L A S. S-nitrosoglutathione enhances neutrophil DNA fragmentation and cell death[J]. American Journal of Physiology-Lung Cellular and Molecular Physiology, 1999, 276(3): L435-L442.
[4] Batista W L, Ogata F T, Curcio M F, et al. S-nitrosoglutathione and endothelial nitric oxide synthase-derived nitric oxide regulate compartmentalized ras S-nitrosylation and stimulate cell proliferation[J]. Antioxidants & redox signaling, 2013, 18(3): 221-238. 
[5] Fortenberry J D, Owens M L, Chen N X, et al. S-nitrosoglutathione inhibits TNF-α-induced NF κ B activation in neutrophils[J]. Inflammation Research, 2001, 50(2): 89-95.
[6] Brown, Caneta et al. “The effects of S-nitrosoglutathione and S-nitroso-N-acetyl-D, L-penicillamine in a rat model of pre-eclampsia.” Journal of natural science, biology, and medicine vol. 4,2 (2013): 330-5.
[7] Kuo YR, Wang FS, Jeng SF, Lutz BS, Huang HC, Yang KD. Nitrosoglutathione promotes flap survival via suppression of reperfusion injury-induced superoxide and inducible nitric oxide synthase induction. J Trauma. 2004;57(5):1025-1031.

Protokoll (Protocol)

Cell experiment [1]:

Cell lines

HeLa cells

Preparation Method

HeLa cells (8×103) were seeded in a 96-well culture plate and subjected to a 24-h period of starvation with MEM 0.5% FBS at 37°C, 5% CO2 . Cells were exposed to different concentrations of Nitrosoglutathione for 5h. In the assay that was used, PP2 (a Src kinase inhibitor) or BIBX1382 (an EGFR inhibitor) or LY294002 (PI3K inhibitor) or PD98059 (MEK inhibitor) was added 30min before stimulation with Nitrosoglutathione, EGF, Bk, or FBS. Cells were washed and subsequently incubated with MTT (0.5mg/ml) reagent at 37°C, 5% CO2, for 2h to measure the daily proliferation rate. The medium was discarded, and 100μl of cold isopropanol was added to monitor the absorbance spectrophotometrically at 570nm. The experiment was repeated three times. Cell pro-liferation was evaluated by a cell count assay. Cells were cultured in six-well plates to attain 40%–50% confluence and stimulated during 5h with Nitrosoglutathione or FBS in a culture medium without supplements. After 24–48h stimulation, cells were trypsinized and counted using an inverted microscope

Reaction Conditions

0, 0.1, 1, 10, 50, 100, and 1000μM; 5h

Applications

Cells pretreated with low concentrations (1.0-100μM) of Nitrosoglutathione showed significant stimulation and proliferation at 24 and 48 hours. However, exposing HeLa cells to 1.0 millimole of Nitrosoglutathioneinhibited cell proliferation.
Animal experiment [2]:

Animal models

Sprague-Dawley rats

Preparation Method

On day 14 of gestation, female Sprague-Dawley rats were separated into five groups and treated intravenously for 7 days as follows: (i) 0.3mL 0.9% saline (control, n = 11); (ii) 50mg/kg Body Weight (BW) N-nitro-L-arginine methyl ester (L-NAME) in 0.3mL saline (n = 10); (iii) 50mg/kg BW L-NAME and 8mg/kg BW Nitrosoglutathione in 0.15mL saline (n = 6); (iv) 50 mg/kg BW L-NAME in 0.15mL saline and 8mg/kg BW SNAP in 0.15mL DMSO (n = 9); and (v) 0.15mL DMSO and 0.15mL saline (SNAP control, n = 7). Blood pressures were measured on day 14 through day 20, a 4-h urine sample was taken on day 20, and animals were sacrificed on day 21. Pups were counted and weighed individually.

Dosage form

8mg/kg/day; 7d; i.v.

Applications

Nitrosoglutathione significantly decreased systolic, diastolic, and mean arterial pressures in Pre-eclampsia (PE)-induced rats from day 14 through day 20.

References:
 [1] Batista W L, Ogata F T, Curcio M F, et al. S-nitrosoglutathione and endothelial nitric oxide synthase-derived nitric oxide regulate compartmentalized ras S-nitrosylation and stimulate cell proliferation[J]. Antioxidants & redox signaling, 2013, 18(3): 221-238.
[2] Brown, Caneta et al. “The effects of S-nitrosoglutathione and S-nitroso-N-acetyl-D, L-penicillamine in a rat model of pre-eclampsia.” Journal of natural science, biology, and medicine vol. 4,2 (2013): 330-5. 

Produktdokumente (Product Documents)

Purity:>98.00%Appearance:A solid

Chemische Eigenschaften (Chemical Properties)

CAS-Nr.
57564-91-7
Synonyme
S-Nitroso-L-glutathione
Chemischer Name
(S)-2-amino-5-(((R)-1-((carboxymethyl)amino)-3-(nitrosothio)-1-oxopropan-2-yl)amino)-5-oxopentanoic acid
SMILES
O=C(CC[C@@H](C(O)=O)N)N[C@H](C(NCC(O)=O)=O)CSN=O
Summenformel
C10H16N4O7S
Molekulargewicht
336.32
Löslichkeit
DMSO:67mg/ml
Lagerung
Store at -20°C, protect from light
Allgemeine Hinweise
Wählen Sie anhand der Löslichkeitsdaten des Produkts ein geeignetes Lösungsmittel. Aliquotieren Sie die Stammlösung nach der Herstellung, um wiederholte Gefrier-Auftau-Zyklen zu vermeiden.
Verwenden Sie Stammlösungen bei Lagerung bei -80°C innerhalb von 6 Monaten bzw. bei -20°C innerhalb von 1 Monat.
Zur Verbesserung der Löslichkeit das Röhrchen auf 37°C erwärmen und für eine angemessene Dauer beschallen.
Versandbedingungen
Evaluierungsmuster werden mit Kühlakkus versandt. Andere verfügbare Größen werden bei Raumtemperatur oder auf Anfrage mit Kühlakkus versandt.

Rechner (Calculators)Molarität / Verdünnung / Molekulargewicht / Einheitenumrechnung / In-vivo-Formulierung / Löslichkeit

g/mol

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