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Details

Stereochemistry ACHIRAL
Molecular Formula C4H7NO3
Molecular Weight 117.1033
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of ACETURIC ACID

SMILES

CC(=O)NCC(O)=O

InChI

InChIKey=OKJIRPAQVSHGFK-UHFFFAOYSA-N
InChI=1S/C4H7NO3/c1-3(6)5-2-4(7)8/h2H2,1H3,(H,5,6)(H,7,8)

HIDE SMILES / InChI

Molecular Formula C4H7NO3
Molecular Weight 117.1033
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Formation and stability of peptide enolates in aqueous solution.
2002 Jul 17
Importance of product inhibition in the kinetics of the acylase hydrolysis reaction by differential stopped flow microcalorimetry.
2002 Sep 15
Proximity effects in monolayer films: kinetic analysis of amide bond formation at the air-water interface using (1)H NMR spectroscopy.
2002 Sep 25
Structural and mechanistic studies on ThiO, a glycine oxidase essential for thiamin biosynthesis in Bacillus subtilis.
2003 Mar 18
Inhibition of wortmannin activities by amino compounds.
2004 Nov 26
Spin-polarized peroxyl radical adducts formed from the addition of oxygen to amino acid radicals.
2006 Dec 21
Low molecular weight thiol amides attenuate MAPK activity and protect primary neurons from Abeta(1-42) toxicity.
2006 Jan 19
Understanding the EPR parameters of glycine-derived radicals: the case of N-acetylglycyl in the N-acetylglycine single-crystal environment.
2007 Feb 1
Metabolite profiling of human amniotic fluid by hyphenated nuclear magnetic resonance spectroscopy.
2008 Aug 1
Substituted hippurates and hippurate analogs as substrates and inhibitors of peptidylglycine alpha-hydroxylating monooxygenase (PHM).
2008 Dec 1
Syntheses of highly fluorescent GFP-chromophore analogues.
2008 Mar 26
Metabolomic profiling of a modified alcohol liquid diet model for liver injury in the mouse uncovers new markers of disease.
2008 Oct 15
Patents
Substance Class Chemical
Created
by admin
on Fri Dec 15 18:54:56 GMT 2023
Edited
by admin
on Fri Dec 15 18:54:56 GMT 2023
Record UNII
U2UT4677KR
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
ACETURIC ACID
MI  
Systematic Name English
N-ACETYLGLYCINE
Systematic Name English
ETHANOYLAMINOETHANOIC ACID
Systematic Name English
ACETURIC ACID [MI]
Common Name English
ACETAMIDOACETIC ACID
Systematic Name English
ACETYLAMINOACETIC ACID
Systematic Name English
ACETYLGLYCOCOLL
Common Name English
NSC-7605
Code English
Code System Code Type Description
DRUG BANK
DB02713
Created by admin on Fri Dec 15 18:54:57 GMT 2023 , Edited by admin on Fri Dec 15 18:54:57 GMT 2023
PRIMARY
PUBCHEM
10972
Created by admin on Fri Dec 15 18:54:57 GMT 2023 , Edited by admin on Fri Dec 15 18:54:57 GMT 2023
PRIMARY
CAS
543-24-8
Created by admin on Fri Dec 15 18:54:57 GMT 2023 , Edited by admin on Fri Dec 15 18:54:57 GMT 2023
PRIMARY
CHEBI
40410
Created by admin on Fri Dec 15 18:54:57 GMT 2023 , Edited by admin on Fri Dec 15 18:54:57 GMT 2023
PRIMARY
FDA UNII
U2UT4677KR
Created by admin on Fri Dec 15 18:54:57 GMT 2023 , Edited by admin on Fri Dec 15 18:54:57 GMT 2023
PRIMARY
ECHA (EC/EINECS)
208-839-6
Created by admin on Fri Dec 15 18:54:57 GMT 2023 , Edited by admin on Fri Dec 15 18:54:57 GMT 2023
PRIMARY
MERCK INDEX
m1345
Created by admin on Fri Dec 15 18:54:57 GMT 2023 , Edited by admin on Fri Dec 15 18:54:57 GMT 2023
PRIMARY Merck Index
NSC
7605
Created by admin on Fri Dec 15 18:54:57 GMT 2023 , Edited by admin on Fri Dec 15 18:54:57 GMT 2023
PRIMARY
MESH
C006368
Created by admin on Fri Dec 15 18:54:57 GMT 2023 , Edited by admin on Fri Dec 15 18:54:57 GMT 2023
PRIMARY
WIKIPEDIA
Aceturic acid
Created by admin on Fri Dec 15 18:54:57 GMT 2023 , Edited by admin on Fri Dec 15 18:54:57 GMT 2023
PRIMARY
EPA CompTox
DTXSID2043793
Created by admin on Fri Dec 15 18:54:57 GMT 2023 , Edited by admin on Fri Dec 15 18:54:57 GMT 2023
PRIMARY
CHEBI
61887
Created by admin on Fri Dec 15 18:54:57 GMT 2023 , Edited by admin on Fri Dec 15 18:54:57 GMT 2023
PRIMARY
Related Record Type Details
SALT/SOLVATE -> PARENT
SALT/SOLVATE -> PARENT