Oxalyldiaminopropionic acid

Oxalyldiaminopropionic acid
Names

IUPAC name 3-[(Carboxycarbonyl)amino]alanine
Other names Dencichin β-Oxalylaminoalanine β-N-Oxalyl-α,β-diaminopropionic acid
Identifiers
3DMet	B00693
Abbreviations	BOAA ODAP β-ODAP
CAS Registry Number	7554-90-7^N 5302-45-4 (S)^N
ChEBI	CHEBI:16399^N
ChemSpider	389238^N
InChI InChI=1S/C5H8N2O5/c6-2(4(9)10)1-7-3(8)5(11)12/h2H,1,6H2,(H,7,8)(H,9,10)(H,11,12)/t2-/m0/s1^N Key: NEEQFPMRODQIKX-REOHCLBHSA-N^N InChI=1/C5H8N2O5/c6-2(4(9)10)1-7-3(8)5(11)12/h2H,1,6H2,(H,7,8)(H,9,10)(H,11,12)/t2-/m0/s1 Key: NEEQFPMRODQIKX-REOHCLBHBZ
Jmol-3D images	Image
KEGG	C04209^N
MeSH	oxalyldiaminopropionic+acid
PubChem	2360 440259 (S)
SMILES C([C@@H](C(=O)O)N)NC(=O)C(=O)O
Properties
Molecular formula	C₅H₈N₂O₅
Molar mass	176.13 g·mol⁻¹
Related compounds
Related compounds	Beta-Methylamino-L-alanine
Except where noted otherwise, data is given for materials in their standard state (at 25 °C (77 °F), 100 kPa)
N verify (what is: Y/N?)
Infobox references

Oxalyldiaminopropionic acid (ODAP), a structural analogue of the neurotransmitter glutamate, is the neurotoxin responsible for lathyrism.^[1]

References

↑ Ravindranath, V. (2002). "Neurolathyrism: Mitochondrial dysfunction in excitotoxicity mediated by L-β-oxalyl aminoalanine". Neurochemistry International 40 (6): 505–509. doi:10.1016/S0197-0186(01)00121-8. PMID 11850107.