Bluedark| GABA | |
|---|---|
 |
| Salts [] | |
|---|---|
| γ-Aminobutyric acid hydrochloride | |
|
| Molecular structure via molpic | |
|
| |
| Molecular formula | C4H9NO2 |
|---|---|
| Molecular mass | 103.12 g/mol |
| Predicted LogP | -3.2 |
| Melting point | 203 °C |
| Solubility | 1.2 [ug/mL] (The mean of the results at pH 7.4) |
| Chirality | achiral |
| Identifiers [] | |
|---|---|
| IUPAC name | 4-aminobutanoic acid |
| SMILES | C(CC(=O)O)CN |
| InChI | InChI=1S/C4H9NO2/c5-3-1-2-4(6)7/h1-3,5H2,(H,6,7) |
| InChIKey | BTCSSZJGUNDROE-UHFFFAOYSA-N |
γ-Aminobutyric acid
γ-Aminobutyric acid (also known as 4-aminobutyric acid, 4-Aminobutanoic acid, Piperidic acid, Piperidinic acid, Aminalon, Gaballon, butanoic acid, 4-amino-, γlon, γlone or γsol) is a substance of the gabapentinoid class.
Chemistry
γ-Aminobutyric acid is typically found in the form of its hydrochloride salt.
Stereochemistry
γ-Aminobutyric acid is a achiral mixtureSee also
External links
- γ-Aminobutyric acid (Wikipedia)
- γ-Aminobutyric acid (Wikidata)
- γ-Aminobutyric acid (DrugBank)
- γ-Aminobutyric acid (PubChem)
- γ-Aminobutyric acid (ChemSpider)
- γ-Aminobutyric acid (ChEMBL)
- γ-Aminobutyric acid (ChEBI)
- γ-Aminobutyric acid (Common Chemistry)
- γ-Aminobutyric acid (HMDB)
- γ-Aminobutyric acid (KEGG)
- γ-Aminobutyric acid (UNII)
- γ-Aminobutyric acid (EPA DSSTox)