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Details

Stereochemistry ABSOLUTE
Molecular Formula C5H9NO4
Molecular Weight 147.1293
Optical Activity UNSPECIFIED
Defined Stereocenters 1 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of N-ACETYLSERINE

SMILES

CC(=O)N[C@@H](CO)C(O)=O

InChI

InChIKey=JJIHLJJYMXLCOY-BYPYZUCNSA-N
InChI=1S/C5H9NO4/c1-3(8)6-4(2-7)5(9)10/h4,7H,2H2,1H3,(H,6,8)(H,9,10)/t4-/m0/s1

HIDE SMILES / InChI

Molecular Formula C5H9NO4
Molecular Weight 147.1293
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 1 / 1
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

PubMed

PubMed

TitleDatePubMed
Mechanism for the direct synthesis of tryptophan from indole and serine: a useful NMR technique for the detection of a reactive intermediate in the reaction mixture.
2010-10
Toxicology studies with N-acetyl-L-serine.
2010-02-09
Proteomic profiling of L-cysteine induced selenite resistance in Enterobacter sp. YSU.
2009-08-28
Rapid changes in gene expression dynamics in response to superoxide reveal SoxRS-dependent and independent transcriptional networks.
2007-11-14
Possible bioactivation pathways of lamotrigine.
2007-07
Intracerebroventricular injection of L-serine analogs and derivatives induces sedative and hypnotic effects under an acute stressful condition in neonatal chicks.
2006-06-03
Cationic liposomes induce apoptosis through p38 MAP kinase-caspase-8-Bid pathway in macrophage-like RAW264.7 cells.
2006-01
N-acetylcysteine decreases angiotensin II receptor binding in vascular smooth muscle cells.
2005-08
Impact of elevated H(2)S on metabolite levels, activity of enzymes and expression of genes involved in cysteine metabolism.
2005-05
O-acetylserine and the regulation of expression of genes encoding components for sulfate uptake and assimilation in potato.
2005-05
N-acetylcysteine inhibits Na+ absorption across human nasal epithelial cells.
2004-10
Metabolic reconstruction of sulfur assimilation in the extremophile Acidithiobacillus ferrooxidans based on genome analysis.
2003-12-15
The LysR-type transcriptional regulator CysB controls the repression of hslJ transcription in Escherichia coli.
2003-12
Serine acetyltransferase of Escherichia coli: substrate specificity and feedback control by cysteine.
2003-11-01
Effect of three n-acetylamino acids on N-(3,5-dichlorophenyl)succinimide (NDPS) and ndps metabolite nephrotoxicity in Fischer 344 rats.
2002-04-12
Cysteine synthase of an extremely thermophilic bacterium, Thermus thermophilus HB8.
2002-03
Oxidative stress is involved in the heat stress-induced downregulation of TCR zeta chain expression and TCR/CD3-mediated [Ca(2+)](i) response in human T-lymphocytes.
2002-02
Crystallization of full-length CysB of Klebsiella aerogenes, a LysR-type transcriptional regulator.
2001-02
Bone marrow stem cell protection from chemotherapy by low--molecular-weight compounds.
2001-02
Functional dissection of the LysR-type CysB transcriptional regulator. Regions important for DNA binding, inducer response, oligomerization, and positive control.
2001-01-19
Liquid chromatographic-mass spectrometric analysis of N-acetylamino acids in human urine.
1994-07-01
Substance Class Chemical
Created
by admin
on Mon Mar 31 21:39:44 GMT 2025
Edited
by admin
on Mon Mar 31 21:39:44 GMT 2025
Record UNII
W98518XGZ3
Record Status Validated (UNII)
Record Version
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Name Type Language
ACETYLSERINE
Preferred Name English
N-ACETYLSERINE
Systematic Name English
N-ACETYL-L-SERINE
Systematic Name English
L-SERINE, N-ACETYL-
Systematic Name English
N-ACETYL-SERINE
Systematic Name English
Code System Code Type Description
CAS
16354-58-8
Created by admin on Mon Mar 31 21:39:44 GMT 2025 , Edited by admin on Mon Mar 31 21:39:44 GMT 2025
PRIMARY
FDA UNII
W98518XGZ3
Created by admin on Mon Mar 31 21:39:44 GMT 2025 , Edited by admin on Mon Mar 31 21:39:44 GMT 2025
PRIMARY
CHEBI
45441
Created by admin on Mon Mar 31 21:39:44 GMT 2025 , Edited by admin on Mon Mar 31 21:39:44 GMT 2025
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PUBCHEM
65249
Created by admin on Mon Mar 31 21:39:44 GMT 2025 , Edited by admin on Mon Mar 31 21:39:44 GMT 2025
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EPA CompTox
DTXSID30167615
Created by admin on Mon Mar 31 21:39:44 GMT 2025 , Edited by admin on Mon Mar 31 21:39:44 GMT 2025
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DRUG BANK
DB02340
Created by admin on Mon Mar 31 21:39:44 GMT 2025 , Edited by admin on Mon Mar 31 21:39:44 GMT 2025
PRIMARY