S-Nitroso-N-acetylpenicillamine

S-Nitroso-N-acetylpenicillamine
Names
	IUPAC name S-Nitroso-N-acetylpenicillamine
	Other names N-Acetyl-3-(nitrosothio)-DL-valine; S-Nitroso-N-acetylpenicillamine
Identifiers
CAS Number	79032-48-7 ;
3D model (JSmol)	Interactive image;
Abbreviations	SNAP
ChEBI	CHEBI:77702 ;
ChEMBL	ChEMBL73188 ;
ChemSpider	5036251 ;
PubChem CID	6603945;
CompTox Dashboard (EPA)	DTXSID80897531 ;
	InChI InChI=1S/C7H12N2O4S/c1-4(10)8-5(6(11)12)7(2,3)14-9-13/h5H,1-3H3,(H,8,10)(H,11,12)/t5-/m0/s1 Key: ZIIQCSMRQKCOCT-YFKPBYRVSA-N ; InChI=1/C7H12N2O4S/c1-4(10)8-5(6(11)12)7(2,3)14-9-13/h5H,1-3H3,(H,8,10)(H,11,12)/t5-/m0/s1 Key: ZIIQCSMRQKCOCT-YFKPBYRVBE;
	SMILES O=C(N[C@@H](C(=O)O)C(SN=O)(C)C)C;
Properties
Chemical formula	C7H12N2O4S
Molar mass	220.25 g/mol
Hazards
	GHS labelling:
Pictograms
Signal word	Warning
Hazard statements	H315, H319, H335
Precautionary statements	P261, P264, P271, P280, P302+P352, P305+P351+P338
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
	(what is ?)
	Infobox references

S-Nitroso-N-acetylpenicillamine (SNAP) is the chemical compound with the formula ON S C(CH₃)₂C H(N HAc)CO₂H. SNAP is an S-nitrosothiol and is used as a model for the general class of S-nitrosothiols which have received much attention in biochemistry because nitric oxide and some organic nitroso derivatives serve as signaling molecules in living systems, especially related to vasodilation.^[2] SNAP is derived from the amino acid penicillamine. S-Nitrosoglutathione is a related agent.

References[]

^ "N3398 h S-Nitroso-N-acetyl-DL-penicillamine". Sigma-Aldric. Retrieved 13 December 2021.
^ Zhang Y.; Hogg, N. (2005). "S-Nitrosothiols: Cellular Formation and Transport". Free Radical Biology and Medicine. 38 (7): 831–838. doi:10.1016/j.freeradbiomed.2004.12.016. PMID 15749378.

[1] "N3398 h S-Nitroso-N-acetyl-DL-penicillamine". Sigma-Aldric. Retrieved 13 December 2021.

[2] Zhang Y.; Hogg, N. (2005). "S-Nitrosothiols: Cellular Formation and Transport". Free Radical Biology and Medicine. 38 (7): 831–838. doi:10.1016/j.freeradbiomed.2004.12.016. PMID 15749378.

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