Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C7H13NO3S |
| Molecular Weight | 191.248 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 1 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CC(=O)N[C@H](C(O)=O)C(C)(C)S
InChI
InChIKey=MNNBCKASUFBXCO-RXMQYKEDSA-N
InChI=1S/C7H13NO3S/c1-4(9)8-5(6(10)11)7(2,3)12/h5,12H,1-3H3,(H,8,9)(H,10,11)/t5-/m1/s1
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Formation and stability of a nitric oxide donor: S-nitroso-N-acetylpenicillamine. | 2006 Mar 16 |
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| Thiol-disulfide redox equilibria of glutathione metaboloma compounds investigated by tandem mass spectrometry. | 2008 Dec |
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| Novel twist on the biotin switch cracks endothelial cell S-nitrosoproteome. | 2009 Oct |
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| TRPV1 and TRPA1 mediate peripheral nitric oxide-induced nociception in mice. | 2009 Oct 29 |
|
| Formation of the distinct redox-interrelated forms of nitric oxide from reaction of dinitrosyl iron complexes (DNICs) and substitution ligands. | 2010 Jul 19 |
|
| Effect of thiol drugs on tert-butyl hydroperoxide induced luminol chemiluminescence in human erythrocytes, erythrocyte lysate, and erythrocyte membranes. | 2010 Jul 30 |
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6Q5H398H7Q
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2510-38-5
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164975
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60728
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DTXSID30947959
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admin on Sat Dec 16 08:50:08 GMT 2023 , Edited by admin on Sat Dec 16 08:50:08 GMT 2023
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SUBSTANCE RECORD
