67776-06-1
67776-06-1
Chemical Structure
S-Nitroso-N-acetyl-DL-penicillamine
Synonym(s): SNAP
- CAS No.: 67776-06-1
- Formula:C7H12N2O4S
- Molecular Weight:220.25
IUPAC Name: 2-acetamido-3-methyl-3-(nitrosothio)butanoic acid
InChIKey: ZIIQCSMRQKCOCT-UHFFFAOYSA-N
SMILES: O=NSC(C)(C(C(O)=O)NC(C)=O)C
Biological Activity: S-Nitroso-N-acetyl-DL-penicillamine (SNAP) is a nitric oxide donor and acts as a stable inhibitor of platelet aggregation[1][2][3][4].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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S-Nitroso-N-acetyl-DL-penicillamine | 98.76% | S-Nitroso-N-acetyl-DL-penicillamine (SNAP) is a nitric oxide donor and acts as a stable inhibitor of platelet aggregation. | ||||||||||||||||||||
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References
- [1]. E. Salas, 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. [Content Brief]
- [2]. Ioannidis I, et al. Enhanced release of nitric oxide causes increased cytotoxicity of S-nitroso-N-acetyl-DL-penicillamine and sodium nitroprusside under hypoxic conditions. Biochem J. 1996 Sep 15;318 ( Pt 3):789-95. [Content Brief]
- [3]. Pravdic D, 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. [Content Brief]
- [4]. Mang CF, et al. 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. [Content Brief]
