GLPBio

SNAP

Catalog No.: GC10767Purity:>98.00%Synonyms: SNitrosoNAcetylD,LPenicillamine
SNAP is a nitric oxide (NO) donor, commonly used as a tool compound for studying the physiological and pharmacological roles of nitric oxide.

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SNAP
Cas No.: 67776-06-1
5mgIn Stock
$23.00
1
10mgIn Stock
$35.00
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25mgIn Stock
$70.00
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50mgIn Stock
$122.00
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100mgIn Stock
$212.00
1

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    618, 1017–1023 (2023)
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    610, 366–372 (2022)
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    Cell
    187(9):2288-2304 (2024)
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    183(7):1867-1883 (2020)
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Beschreibung (Description)

SNAP is a nitric oxide (NO) donor, commonly used as a tool compound for studying the physiological and pharmacological roles of nitric oxide[1]. SNAP decomposes spontaneously or under the influence of light, heat, or metal ions to release nitric oxide, while generating the corresponding disulfide[2]. SNAP is widely employed to investigate the mechanisms of cardiovascular regulation, neurotransmission, and immune responses[3-4].

In vitro, treatment of Fu5 rat hepatoma cells with SNAP (1mM) for 8 hours significantly induced cytotoxicity[5]. Exposure of Lewis lung carcinoma cells (LLC-F6) and B16 melanoma cells (B16-4A5-F6) to SNAP (2mM) for 24 hours markedly reduced the viability of both cell types[6].

In vivo, a single intramuscular injection of SNAP (1.0mg/kg) administered 3 hours after the induction of critical limb ischemia (CLI) in SD rats significantly increased the ischemic-to-normal limb blood flow (INBF) ratio on day 14 and enhanced microvessel density in the ischemic area[7]. Continuous intracerebroventricular infusion of SNAP (0.1μM; 2μL) over 6 days in P2X7R+/+ and P2X7R−/− mice significantly elevated S-nitrosylation of protein disulfide isomerase (SNO-PDI) in the hippocampus and enhanced phosphorylation of NF-κB p65 at serine 276 in microglia[8].

References:
[1] Salas E, Moro MA, Askew S, et al. Comparative pharmacology of analogues of S-nitroso-N-acetyl-DL-penicillamine on human platelets. Br J Pharmacol. 1994 Aug;112(4):1071-6.
[2] Pravdic D, Vladic N, Cavar I, et al. Effect of nitric oxide donors S-nitroso-N-acetyl-DL-penicillamine, spermine NONOate and propylamine propylamine NONOate on intracellular pH in cardiomyocytes. Clin Exp Pharmacol Physiol. 2012 Sep;39(9):772-8.
[3] Mang CF, Kilbinger H. Modulation of acetylcholine release in the guinea-pig trachea by the nitric oxide donor, S-nitroso-N-acetyl-DL-penicillamine (SNAP). Br J Pharmacol. 2000 Sep;131(1):94-8.
[4] Lu J, Katano T, Okuda-Ashitaka E, et al. Involvement of S-nitrosylation of actin in inhibition of neurotransmitter release by nitric oxide. Mol Pain. 2009 Sep 29;5:58.
[5] Ioannidis I, de Groot H. Cytotoxicity of nitric oxide in Fu5 rat hepatoma cells: evidence for co-operative action with hydrogen peroxide. Biochem J. 1993 Dec 1;296 ( Pt 2)(Pt 2):341-5.
[6] Hirano S. In vitro and in vivo cytotoxic effects of nitric oxide on metastatic cells. Cancer Lett. 1997 May 1;115(1):57-62.
[7] Yeh JN, Yip HK, Shao PL, et al. Combination of melatonin-delivered endothelial progenitor cells with S-nitroso-N-acetyl-DL-penicillamine for improving critical limb ischemia in the rat. Am J Transl Res. 2024 Sep 15;16(9):5020-5037.
[8] Kim JE, Wang SH, Lee DS, et al. Protein disulfide isomerase integrates toll-like receptor 4 and P2X7 receptor signaling pathways during lipopolysaccharide-induced neuroinflammation. Sci Rep. 2025 Mar 6;15(1):7906.

Protokoll (Protocol)

Cell experiment [1]:

Cell lines

Fu5 rat hepatoma cells (rat hepatoma cell line)

Preparation Method

Fu5 cells were maintained in Dulbecco's Modified Eagle Medium/Nutrient Mix F12 (1:1) supplemented with 2mM L-glutamine, 50μg/mL gentamycin, and 10% fetal-calf serum at 37°C under 5% CO₂. Cells were treated with SNAP at a concentration of 1mM for 8 hours.

Reaction Conditions

1mM; 8h

Applications

SNAP induced significant cytotoxicity in Fu5 cells. When combined with xanthine oxidase (20m-units/mL), SNAP synergistically enhanced cytotoxicity. The cytotoxic effects were mediated by nitric oxide (NO) release, independent of superoxide anion (O₂⁻) or peroxynitrite (ONOO⁻) pathways.

Animal experiment [2]:

Animal models

SD rats

Preparation Method

Rats were intramuscularly administered a single dose of SNAP (1.0mg/kg) at 3 hours after critical limb ischemia (CLI) induction. Rats were sacrificed at day 14 for quadriceps muscle analysis.

Dosage form

1.0mg/kg; i.m.; 14 days

Applications

SNAP administration significantly increased the ischemic-to-normal blood flow (INBF) ratio and enhanced small vessel density in the ischemic limb. SNAP upregulated endothelial cell surface markers (CD31/vWF/eNOS) and angiogenesis factors, while reducing oxidative stress, apoptosis, and inflammatory biomarkers.

References:
[1] Ioannidis I, de Groot H. Cytotoxicity of nitric oxide in Fu5 rat hepatoma cells: evidence for co-operative action with hydrogen peroxide. Biochem J. 1993 Dec 1;296 ( Pt 2)(Pt 2):341-5.
[2] Yeh JN, Yip HK, Shao PL, et al. Combination of melatonin-delivered endothelial progenitor cells with S-nitroso-N-acetyl-DL-penicillamine for improving critical limb ischemia in the rat. Am J Transl Res. 2024 Sep 15;16(9):5020-5037.

Produktdokumente (Product Documents)

Purity:>98.00%Appearance:A solid

Chemische Eigenschaften (Chemical Properties)

CAS-Nr.
67776-06-1
Synonyme
SNitrosoNAcetylD,LPenicillamine
Chemischer Name
(R)-2-acetamido-3-methyl-3-(nitrosothio)butanoic acid
SMILES
OC([C@H](C(C)(C)SN=O)NC(C)=O)=O
Summenformel
C7H12N2O4S
Molekulargewicht
220.24
Löslichkeit
<22.02mg/ml in DMSO
Lagerung
Store at -20°C
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

Reviews

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