EMBL-EBI | Chemical Biology | ChEBI
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| Formula | C4H9NO5S |
| Net Charge | 0 |
| Average Mass | 183.185 |
| Monoisotopic Mass | 183.02014 |
| SMILES | N[C@H](CCS(=O)(=O)O)C(=O)O |
| InChI | InChI=1S/C4H9NO5S/c5-3(4(6)7)1-2-11(8,9)10/h3H,1-2,5H2,(H,6,7)(H,8,9,10)/t3-/m1/s1 |
| InChIKey | VBOQYPQEPHKASR-GSVOUGTGSA-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). |
| Biological Role: | metabotropic glutamate receptor agonist An agonist that selectively binds to and activates a metabotropic glutamate receptor. |
| ChEBI Ontology |
|---|
| Outgoing Relation(s) |
| D-homocysteic acid (CHEBI:132225) has role metabotropic glutamate receptor agonist (CHEBI:61966) |
| D-homocysteic acid (CHEBI:132225) is a homocysteic acid (CHEBI:90324) |
| D-homocysteic acid (CHEBI:132225) is enantiomer of L-homocysteic acid (CHEBI:132223) |
| Incoming Relation(s) |
| DL-homocysteic acid (CHEBI:132221) has part D-homocysteic acid (CHEBI:132225) |
| L-homocysteic acid (CHEBI:132223) is enantiomer of D-homocysteic acid (CHEBI:132225) |
| IUPAC Name |
|---|
| (2R)-2-amino-4-sulfobutanoic acid |
| Synonyms | Source |
|---|---|
| (2R)-2-amino-4-sulfobutyric acid | ChEBI |
| (R)-2-amino-4-sulfobutyric acid | ChEBI |
| (R)-2-amino-4-sulfobutanoic acid | ChEBI |
| Registry Numbers | Sources |
|---|---|
| Reaxys:6582338 | Reaxys |
| CAS:56892-03-6 | ChemIDplus |
| Citations |
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