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Details

Stereochemistry ABSOLUTE
Molecular Formula C4H8N2O3
Molecular Weight 132.1179
Optical Activity UNSPECIFIED
Defined Stereocenters 1 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of Isoasparagine

SMILES

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

InChI

InChIKey=PMLJIHNCYNOQEQ-REOHCLBHSA-N
InChI=1S/C4H8N2O3/c5-2(4(6)9)1-3(7)8/h2H,1,5H2,(H2,6,9)(H,7,8)/t2-/m0/s1

HIDE SMILES / InChI

Molecular Formula C4H8N2O3
Molecular Weight 132.1179
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 1 / 1
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

PubMed

PubMed

TitleDatePubMed
The mechanism of boron mobility in wheat and canola phloem.
2010-06
Crystal structure of the schiff base intermediate prior to decarboxylation in the catalytic cycle of aspartate alpha-decarboxylase.
2004-06-25
Crystallization and preliminary X-ray crystallographic analysis of aspartate 1-decarboxylase from Helicobacter pylori.
2002-05
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 22:01:05 GMT 2025
Edited
by admin
on Mon Mar 31 22:01:05 GMT 2025
Record UNII
L9ANT46A26
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
Isoasparagine
Common Name English
Aspartic acid ?-amide
Preferred Name English
Succinamic acid, 3-amino-, L-
Systematic Name English
L-Aspartic acid amide
Systematic Name English
L-Isoasparagine
Systematic Name English
Butanoic acid, 3,4-diamino-4-oxo-, (3S)-
Systematic Name English
Code System Code Type Description
FDA UNII
L9ANT46A26
Created by admin on Mon Mar 31 22:01:05 GMT 2025 , Edited by admin on Mon Mar 31 22:01:05 GMT 2025
PRIMARY
CHEBI
49010
Created by admin on Mon Mar 31 22:01:05 GMT 2025 , Edited by admin on Mon Mar 31 22:01:05 GMT 2025
PRIMARY
PUBCHEM
7015701
Created by admin on Mon Mar 31 22:01:05 GMT 2025 , Edited by admin on Mon Mar 31 22:01:05 GMT 2025
PRIMARY
CAS
28057-52-5
Created by admin on Mon Mar 31 22:01:05 GMT 2025 , Edited by admin on Mon Mar 31 22:01:05 GMT 2025
PRIMARY
CHEBI
21248
Created by admin on Mon Mar 31 22:01:05 GMT 2025 , Edited by admin on Mon Mar 31 22:01:05 GMT 2025
PRIMARY
Related Record Type Details
ENANTIOMER -> ENANTIOMER