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
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
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
Title | Date | PubMed |
---|---|---|
Bone marrow stem cell protection from chemotherapy by low--molecular-weight compounds. | 2001 Feb |
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Effect of three n-acetylamino acids on N-(3,5-dichlorophenyl)succinimide (NDPS) and ndps metabolite nephrotoxicity in Fischer 344 rats. | 2002 Apr 12 |
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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 |
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The LysR-type transcriptional regulator CysB controls the repression of hslJ transcription in Escherichia coli. | 2003 Dec |
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Metabolic reconstruction of sulfur assimilation in the extremophile Acidithiobacillus ferrooxidans based on genome analysis. | 2003 Dec 15 |
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Serine acetyltransferase of Escherichia coli: substrate specificity and feedback control by cysteine. | 2003 Nov 1 |
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N-acetylcysteine inhibits Na+ absorption across human nasal epithelial cells. | 2004 Oct |
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N-acetylcysteine decreases angiotensin II receptor binding in vascular smooth muscle cells. | 2005 Aug |
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O-acetylserine and the regulation of expression of genes encoding components for sulfate uptake and assimilation in potato. | 2005 May |
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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
Edited
Sat Dec 16 07:01:19 GMT 2023
by
admin
on
Sat Dec 16 07:01:19 GMT 2023
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Record UNII |
W98518XGZ3
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Record Status |
Validated (UNII)
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Record Version |
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DB02340
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