CHEBI:231977 - D-allylglycine

ChEBI IDCHEBI:231977
ChEBI NameD-allylglycine
Stars
ASCII NameD-allylglycine
DefinitionThe D-enantiomer of allylglycine.
Last Modified19 September 2024
SubmitterAdnan
DownloadsMolfile
FormulaC5H9NO2
Net Charge0
Average Mass115.132
Monoisotopic Mass115.06333
SMILESC=CC[C@@H](N)C(=O)O
InChIInChI=1S/C5H9NO2/c1-2-3-4(6)5(7)8/h2,4H,1,3,6H2,(H,7,8)/t4-/m1/s1
InChIKeyWNNNWFKQCKFSDK-SCSAIBSYSA-N
Roles Classification
Chemical Roles:
Bronsted base  A molecular entity capable of accepting a hydron from a donor (Brønsted acid).
Bronsted acid  A molecular entity capable of donating a hydron to an acceptor (Brønsted base).
Bronsted base  A molecular entity capable of accepting a hydron from a donor (Brønsted acid).
Bronsted acid  A molecular entity capable of donating a hydron to an acceptor (Brønsted base).
Biological Role:
EC 4.1.1.15 (glutamate decarboxylase) inhibitor  An EC 4.1.1.* (carboxy-lyase) inhibitor that interferes with the action of glutamate decarboxylase (EC 4.1.1.15).
ChEBI Ontology
Outgoing Relation(s)
D-allylglycine (CHEBI:231977) is a allylglycine (CHEBI:231976)
D-allylglycine (CHEBI:231977) is enantiomer of L-allylglycine (CHEBI:230523)
Incoming Relation(s)
DL-allylglycine (CHEBI:231241) has part D-allylglycine (CHEBI:231977)
L-allylglycine (CHEBI:230523) is enantiomer of D-allylglycine (CHEBI:231977)
IUPAC Name 
(2R)-2-aminopent-4-enoic acid
Synonyms  Source
(D)-2-amino-4-pentenoic acidChEBI
D-2-amino-4-pentenoic acidChEBI
H-D-allylgly-OHChEBI
(R)-(+)-2-amino-4-pentenoic acidChEBI
(R)-2-aminopent-4-enoic acidChEBI
(R)-2-amino-4-pentenoic acidChEBI
Manual XrefsDatabases
DYLPDBeChem
Registry NumbersSources
Reaxys:1721511Reaxys
CAS:54594-06-8ChEBI
Citations