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
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10mgIn Stock
$35.00
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25mgIn Stock
$70.00
1
50mgIn Stock
$122.00
1
100mgIn Stock
$212.00
1

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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.

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.

Product Documents

Purity:>98.00%Appearance:A solid

Chemical Properties

CAS No.
67776-06-1
Synonyms
SNitrosoNAcetylD,LPenicillamine
Chemical Name
(R)-2-acetamido-3-methyl-3-(nitrosothio)butanoic acid
SMILES
OC([C@H](C(C)(C)SN=O)NC(C)=O)=O
Molecular Formula
C7H12N2O4S
Molecular Weight
220.24
Solubility
<22.02mg/ml in DMSO
Storage
Store at -20°C
General tips
Select a suitable solvent according to the product solubility data. Once prepared, aliquot the stock solution to avoid repeated freeze-thaw cycles.
Use stock solutions within 6 months when stored at -80°C or within 1 month when stored at -20°C.
To improve solubility, warm the tube to 37°C and sonicate it for an appropriate period.
Shipping Condition
Evaluation samples are shipped with blue ice. Other available sizes are shipped at room temperature or with blue ice upon request.

CalculatorsMolarity / Dilution / Molecular Weight / Unit Conversion / In Vivo Formulation / Solubility

g/mol

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