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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
Bone marrow stem cell protection from chemotherapy by low--molecular-weight compounds.
2001 Feb
Effect of three n-acetylamino acids on N-(3,5-dichlorophenyl)succinimide (NDPS) and ndps metabolite nephrotoxicity in Fischer 344 rats.
2002 Apr 12
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 Feb
The LysR-type transcriptional regulator CysB controls the repression of hslJ transcription in Escherichia coli.
2003 Dec
Metabolic reconstruction of sulfur assimilation in the extremophile Acidithiobacillus ferrooxidans based on genome analysis.
2003 Dec 15
Serine acetyltransferase of Escherichia coli: substrate specificity and feedback control by cysteine.
2003 Nov 1
N-acetylcysteine inhibits Na+ absorption across human nasal epithelial cells.
2004 Oct
N-acetylcysteine decreases angiotensin II receptor binding in vascular smooth muscle cells.
2005 Aug
O-acetylserine and the regulation of expression of genes encoding components for sulfate uptake and assimilation in potato.
2005 May
Cationic liposomes induce apoptosis through p38 MAP kinase-caspase-8-Bid pathway in macrophage-like RAW264.7 cells.
2006 Jan
Possible bioactivation pathways of lamotrigine.
2007 Jul
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 Oct
Substance Class Chemical
Created
by admin
on Sat Dec 16 07:01:19 GMT 2023
Edited
by admin
on Sat Dec 16 07:01:19 GMT 2023
Record UNII
W98518XGZ3
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
N-ACETYLSERINE
Systematic Name English
N-ACETYL-L-SERINE
Systematic Name English
ACETYLSERINE
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 Sat Dec 16 07:01:19 GMT 2023 , Edited by admin on Sat Dec 16 07:01:19 GMT 2023
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FDA UNII
W98518XGZ3
Created by admin on Sat Dec 16 07:01:19 GMT 2023 , Edited by admin on Sat Dec 16 07:01:19 GMT 2023
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CHEBI
45441
Created by admin on Sat Dec 16 07:01:19 GMT 2023 , Edited by admin on Sat Dec 16 07:01:19 GMT 2023
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PUBCHEM
65249
Created by admin on Sat Dec 16 07:01:19 GMT 2023 , Edited by admin on Sat Dec 16 07:01:19 GMT 2023
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EPA CompTox
DTXSID30167615
Created by admin on Sat Dec 16 07:01:19 GMT 2023 , Edited by admin on Sat Dec 16 07:01:19 GMT 2023
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DRUG BANK
DB02340
Created by admin on Sat Dec 16 07:01:19 GMT 2023 , Edited by admin on Sat Dec 16 07:01:19 GMT 2023
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