EMBL-EBI | Chemical Biology | ChEBI
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| Formula | C5H9NO2 |
| Net Charge | 0 |
| Average Mass | 115.132 |
| Monoisotopic Mass | 115.06333 |
| SMILES | C=CC[C@@H](N)C(=O)O |
| InChI | InChI=1S/C5H9NO2/c1-2-3-4(6)5(7)8/h2,4H,1,3,6H2,(H,7,8)/t4-/m1/s1 |
| InChIKey | WNNNWFKQCKFSDK-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 acid | ChEBI |
| D-2-amino-4-pentenoic acid | ChEBI |
| H-D-allylgly-OH | ChEBI |
| (R)-(+)-2-amino-4-pentenoic acid | ChEBI |
| (R)-2-aminopent-4-enoic acid | ChEBI |
| (R)-2-amino-4-pentenoic acid | ChEBI |
| Manual Xrefs | Databases |
|---|---|
| DYL | PDBeChem |
| Registry Numbers | Sources |
|---|---|
| Reaxys:1721511 | Reaxys |
| CAS:54594-06-8 | ChEBI |
| Citations |
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