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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
Structure of ACETYLPENICILLAMINE

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

HIDE SMILES / InChI

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

PubMed

TitleDatePubMed
Pretreatment with the nitric oxide donor SNAP or nerve transection blocks humoral preconditioning by remote limb ischemia or intra-arterial adenosine.
2010-11
N-acetylpenicillamine inhibits the replication of porcine reproductive and respiratory syndrome virus in vitro.
2010-10
Effect of thiol drugs on tert-butyl hydroperoxide induced luminol chemiluminescence in human erythrocytes, erythrocyte lysate, and erythrocyte membranes.
2010-07-30
Formation of the distinct redox-interrelated forms of nitric oxide from reaction of dinitrosyl iron complexes (DNICs) and substitution ligands.
2010-07-19
TRPV1 and TRPA1 mediate peripheral nitric oxide-induced nociception in mice.
2009-10-29
Novel twist on the biotin switch cracks endothelial cell S-nitrosoproteome.
2009-10
Thiol-disulfide redox equilibria of glutathione metaboloma compounds investigated by tandem mass spectrometry.
2008-12
Determination of thiolic compounds as mercury complexes by cold vapor atomic absorption spectrometry and its application to wines.
2008-01-15
Reductive nitrosylation of water-soluble iron porphyrins by S-nitroso-N-acetylpenicillamine: rate constants and EPR characterization.
2006-11
Formation and stability of a nitric oxide donor: S-nitroso-N-acetylpenicillamine.
2006-03-16
Synthesis, characterization, and controlled nitric oxide release from S-nitrosothiol-derivatized fumed silica polymer filler particles.
2005-03-15
Characterization of the disulfides of bio-thiols by electrospray ionization and triple-quadrupole tandem mass spectrometry.
2004-12
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.
2004-09-06
Inhibition of SARS-coronavirus infection in vitro by S-nitroso-N-acetylpenicillamine, a nitric oxide donor compound.
2004-07
Molecular characterization of homo- and heterodimeric mercury(II)-bis-thiolates of some biologically relevant thiols by electrospray ionization and triple quadrupole tandem mass spectrometry.
2004-03
Inhibition of nitric oxide enhances ovine lentivirus replication in monocyte-derived macrophages.
2002-12
Nitric oxide and iron overload. Limitations of ESR detection by DETC.
2001-10-30
Induction of a non-rhythmic motor pattern by nitric oxide in hatchling Rana temporaria embryos.
2001-04
NO donors inhibit Leishmania infantum cysteine proteinase activity.
2001-02-09
Substance Class Chemical
Created
by admin
on Mon Mar 31 22:19:59 GMT 2025
Edited
by admin
on Mon Mar 31 22:19:59 GMT 2025
Record UNII
6Q5H398H7Q
Record Status Validated (UNII)
Record Version
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Name Type Language
ACETYLPENICILLAMINE
Systematic Name English
L-N-ACETYL-.BETA.-MERCAPTOVALINE
Preferred Name English
L-VALINE, N-ACETYL-3-MERCAPTO-
Systematic Name English
N-ACETYLPENICILLAMINE, (L)-
Common Name English
NAPA
Common Name English
NAP
Common Name English
Code System Code Type Description
FDA UNII
6Q5H398H7Q
Created by admin on Mon Mar 31 22:19:59 GMT 2025 , Edited by admin on Mon Mar 31 22:19:59 GMT 2025
PRIMARY
CAS
2510-38-5
Created by admin on Mon Mar 31 22:19:59 GMT 2025 , Edited by admin on Mon Mar 31 22:19:59 GMT 2025
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PUBCHEM
164975
Created by admin on Mon Mar 31 22:19:59 GMT 2025 , Edited by admin on Mon Mar 31 22:19:59 GMT 2025
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CHEBI
60728
Created by admin on Mon Mar 31 22:19:59 GMT 2025 , Edited by admin on Mon Mar 31 22:19:59 GMT 2025
PRIMARY
EPA CompTox
DTXSID30947959
Created by admin on Mon Mar 31 22:19:59 GMT 2025 , Edited by admin on Mon Mar 31 22:19:59 GMT 2025
PRIMARY