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
| Molecular Formula | C7H13NO3S |
| Molecular Weight | 191.248 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ABSOLUTE |
| Additional Stereochemistry | No |
| Defined Stereocenters | 1 / 1 |
| E/Z Centers | 0 |
| Optical Activity | UNSPECIFIED |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| NO donors inhibit Leishmania infantum cysteine proteinase activity. | 2001 Feb 9 |
|
| Nitric oxide and iron overload. Limitations of ESR detection by DETC. | 2001 Oct 30 |
|
| Inhibition of nitric oxide enhances ovine lentivirus replication in monocyte-derived macrophages. | 2002 Dec |
|
| Characterization of the disulfides of bio-thiols by electrospray ionization and triple-quadrupole tandem mass spectrometry. | 2004 Dec |
|
| Inhibition of SARS-coronavirus infection in vitro by S-nitroso-N-acetylpenicillamine, a nitric oxide donor compound. | 2004 Jul |
|
| Molecular characterization of homo- and heterodimeric mercury(II)-bis-thiolates of some biologically relevant thiols by electrospray ionization and triple quadrupole tandem mass spectrometry. | 2004 Mar |
|
| Syntheses, structures, and reactivities of (Fe-NO)6 nitrosyls derived from polypyridine-carboxamide ligands: photoactive NO-donors and reagents for S-nitrosylation of alkyl thiols. | 2004 Sep 6 |
|
| Synthesis, characterization, and controlled nitric oxide release from S-nitrosothiol-derivatized fumed silica polymer filler particles. | 2005 Mar 15 |
|
| Formation and stability of a nitric oxide donor: S-nitroso-N-acetylpenicillamine. | 2006 Mar 16 |
|
| Reductive nitrosylation of water-soluble iron porphyrins by S-nitroso-N-acetylpenicillamine: rate constants and EPR characterization. | 2006 Nov |
|
| Thiol-disulfide redox equilibria of glutathione metaboloma compounds investigated by tandem mass spectrometry. | 2008 Dec |
|
| Determination of thiolic compounds as mercury complexes by cold vapor atomic absorption spectrometry and its application to wines. | 2008 Jan 15 |
|
| 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 |
|
| Pretreatment with the nitric oxide donor SNAP or nerve transection blocks humoral preconditioning by remote limb ischemia or intra-arterial adenosine. | 2010 Nov |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 08:50:08 GMT 2023
by
admin
on
Sat Dec 16 08:50:08 GMT 2023
|
| Record UNII |
6Q5H398H7Q
|
| Record Status |
Validated (UNII)
|
| Record Version |
|
-
Download
| Name | Type | Language | ||
|---|---|---|---|---|
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English |
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
6Q5H398H7Q
Created by
admin on Sat Dec 16 08:50:08 GMT 2023 , Edited by admin on Sat Dec 16 08:50:08 GMT 2023
|
PRIMARY | |||
|
2510-38-5
Created by
admin on Sat Dec 16 08:50:08 GMT 2023 , Edited by admin on Sat Dec 16 08:50:08 GMT 2023
|
PRIMARY | |||
|
164975
Created by
admin on Sat Dec 16 08:50:08 GMT 2023 , Edited by admin on Sat Dec 16 08:50:08 GMT 2023
|
PRIMARY | |||
|
60728
Created by
admin on Sat Dec 16 08:50:08 GMT 2023 , Edited by admin on Sat Dec 16 08:50:08 GMT 2023
|
PRIMARY | |||
|
DTXSID30947959
Created by
admin on Sat Dec 16 08:50:08 GMT 2023 , Edited by admin on Sat Dec 16 08:50:08 GMT 2023
|
PRIMARY |