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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
Toxicology studies with N-acetylglycine.
2010-05
Use of a doxycycline-enrofloxacin-metronidazole combination with/without diminazene diaceturate to treat naturally occurring canine babesiosis caused by Babesia gibsoni.
2010-04-24
Chemotherapy of human african trypanosomiasis.
2009
Substituted hippurates and hippurate analogs as substrates and inhibitors of peptidylglycine alpha-hydroxylating monooxygenase (PHM).
2008-12-01
Metabolomic profiling of a modified alcohol liquid diet model for liver injury in the mouse uncovers new markers of disease.
2008-10-15
Metabolite profiling of human amniotic fluid by hyphenated nuclear magnetic resonance spectroscopy.
2008-08-01
Syntheses of highly fluorescent GFP-chromophore analogues.
2008-03-26
Functionalizing glycine derivatives by direct C-C bond formation.
2008
Behavior of acetyl modified amino acids in reverse micelles: a non-invasive and physiochemical approach.
2007-10-15
Gas-phase ionic syntheses of amino acids: beta versus alpha.
2007-08-15
Understanding the EPR parameters of glycine-derived radicals: the case of N-acetylglycyl in the N-acetylglycine single-crystal environment.
2007-02-01
[Experimental evaluation of the effect of glycine and its phosphorylated derivative on ischemic brain injury].
2007-01-11
Spin-polarized peroxyl radical adducts formed from the addition of oxygen to amino acid radicals.
2006-12-21
Porcine eperythrozoonosis in China.
2006-10
Low molecular weight thiol amides attenuate MAPK activity and protect primary neurons from Abeta(1-42) toxicity.
2006-01-19
ORF17 from the clavulanic acid biosynthesis gene cluster catalyzes the ATP-dependent formation of N-glycyl-clavaminic acid.
2006-01-06
Reactions of 3-formylchromone with active methylene and methyl compounds and some subsequent reactions of the resulting condensation products.
2005-08-31
Efficient synthesis of tyrosine-derived marine sponge metabolites via acylation of amines with a coumarin.
2005-08-05
Enantiomer separation of a powerful chiral auxiliary, 2-methoxy-2-(1-naphthyl)propionic acid by liquid chromatography using chiral anion exchanger-type stationary phases in polar-organic mode; investigation of molecular recognition aspects.
2005
Inhibition of wortmannin activities by amino compounds.
2004-11-26
Calculation of electrostatic interaction energies in molecular dimers from atomic multipole moments obtained by different methods of electron density partitioning.
2004-05
The influence of methionine-containing peptides on the reaction of carboplatin with 5'-guanosine monophosphate: a comparison with cisplatin.
2003-12-01
Temperature dependence of the kinetics of the acylase hydrolysis reaction by differential stopped flow microcalorimetry.
2003-10-01
Single-scan longitudinal relaxation measurements in high-resolution NMR spectroscopy.
2003-10
The effects of diminazene aceturate on systemic blood pressure in clinically healthy adult dogs.
2003-09
Structural and mechanistic studies on ThiO, a glycine oxidase essential for thiamin biosynthesis in Bacillus subtilis.
2003-03-18
Recent developments in the electronic spectroscopy of amides and alpha-helical polypeptides.
2002-12-10
A competitive enzyme-linked immunosorbent assay for diminazene.
2002-11
Proximity effects in monolayer films: kinetic analysis of amide bond formation at the air-water interface using (1)H NMR spectroscopy.
2002-09-25
Importance of product inhibition in the kinetics of the acylase hydrolysis reaction by differential stopped flow microcalorimetry.
2002-09-15
Formation and stability of peptide enolates in aqueous solution.
2002-07-17
Carboxamidomethyl esters as reactive substrates for alpha-chymotrypsin. Orientational effects of hydrogen-bonding interactions.
1976-08-10
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 19:26:04 GMT 2025
Edited
by admin
on Mon Mar 31 19:26:04 GMT 2025
Record UNII
U2UT4677KR
Record Status Validated (UNII)
Record Version
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Name Type Language
ACETURIC ACID
MI  
Systematic Name English
NSC-7605
Preferred 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
Code System Code Type Description
DRUG BANK
DB02713
Created by admin on Mon Mar 31 19:26:04 GMT 2025 , Edited by admin on Mon Mar 31 19:26:04 GMT 2025
PRIMARY
PUBCHEM
10972
Created by admin on Mon Mar 31 19:26:04 GMT 2025 , Edited by admin on Mon Mar 31 19:26:04 GMT 2025
PRIMARY
CAS
543-24-8
Created by admin on Mon Mar 31 19:26:04 GMT 2025 , Edited by admin on Mon Mar 31 19:26:04 GMT 2025
PRIMARY
CHEBI
40410
Created by admin on Mon Mar 31 19:26:04 GMT 2025 , Edited by admin on Mon Mar 31 19:26:04 GMT 2025
PRIMARY
FDA UNII
U2UT4677KR
Created by admin on Mon Mar 31 19:26:04 GMT 2025 , Edited by admin on Mon Mar 31 19:26:04 GMT 2025
PRIMARY
ECHA (EC/EINECS)
208-839-6
Created by admin on Mon Mar 31 19:26:04 GMT 2025 , Edited by admin on Mon Mar 31 19:26:04 GMT 2025
PRIMARY
MERCK INDEX
m1345
Created by admin on Mon Mar 31 19:26:04 GMT 2025 , Edited by admin on Mon Mar 31 19:26:04 GMT 2025
PRIMARY Merck Index
NSC
7605
Created by admin on Mon Mar 31 19:26:04 GMT 2025 , Edited by admin on Mon Mar 31 19:26:04 GMT 2025
PRIMARY
MESH
C006368
Created by admin on Mon Mar 31 19:26:04 GMT 2025 , Edited by admin on Mon Mar 31 19:26:04 GMT 2025
PRIMARY
WIKIPEDIA
Aceturic acid
Created by admin on Mon Mar 31 19:26:04 GMT 2025 , Edited by admin on Mon Mar 31 19:26:04 GMT 2025
PRIMARY
EPA CompTox
DTXSID2043793
Created by admin on Mon Mar 31 19:26:04 GMT 2025 , Edited by admin on Mon Mar 31 19:26:04 GMT 2025
PRIMARY
CHEBI
61887
Created by admin on Mon Mar 31 19:26:04 GMT 2025 , Edited by admin on Mon Mar 31 19:26:04 GMT 2025
PRIMARY
Related Record Type Details
SALT/SOLVATE -> PARENT
SALT/SOLVATE -> PARENT