Galactosamine
| Names | |
|---|---|
| IUPAC name 2-Amino-2-deoxy-D-galactose | |
| Other names α-D-galactosamine | |
| Identifiers | |
| 3D model (JSmol) | |
| ChEBI | |
| ChEMBL | |
| ChemSpider | |
| PubChem CID | |
| UNII | |
| 
 | |
| 
 | |
| Properties | |
| C6H13NO5 | |
| Molar mass | 179.172 g·mol−1 | 
| Melting point | 180 °C (356 °F; 453 K) (HCl salt) | 
| Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references | |
Galactosamine is a hexosamine derived from galactose with the molecular formula C6H13NO5. This amino sugar is a constituent of some glycoprotein hormones such as follicle-stimulating hormone (FSH) and luteinizing hormone (LH).
Precursors such as uridine diphosphate (UDP), UDP-N-acetyl-D-glucosamine, or glucosamine are used to synthesize galactosamine in the human body. A derivative of this compound is N-acetyl-D-galactosamine.
Galactosamine is a hepatotoxic, or liver-damaging, agent that is sometimes used in animal models of liver failure.