L-Alaninamide hydrochloride

CAS: 33208-99-0

Ref. 3D-FA38403

Produktinformation

• Name: L-Alaninamide hydrochloride
• Synonyme: (2S)-2-Aminopropanamide hydrochloride, (S)-2-Aminopropanamide hydrochloride, (S)-2-Aminopropionamide hydrochloride, (S)-Alaninamide hydrochloride, <span class="text-smallcaps">L</span>-Alaninamide hydrochloride, <span class="text-smallcaps">L</span>-Alanine amide hydrochloride, Alaninamide Hydrochloride (1:1), Alaninamide, monohydrochloride, <span class="text-smallcaps">L</span>-, Alanine amide hydrochloride, H-Ala-NH2.HCl, H-Ala-NH2・HCl, L-Alaninamide HCl, L-Alanineamidehydrochloride, Propanamide, 2-amino-, hydrochloride (1:1), (2S)-, Propanamide, 2-amino-, monohydrochloride, (2S)-, Propanamide, 2-amino-, monohydrochloride, (S)-
• CAS: 33208-99-0

Beschreibung

L-Alaninamide hydrochloride is a hydrogen bond donor that has been shown to have anti-inflammatory properties. L-Alaninamide hydrochloride is able to crosslink hyaluronic acid, which can act as an immunosuppressant and inhibit the production of proinflammatory cytokines. In addition, L-alaninamide hydrochloride has been found to be effective in the treatment of amyloid protein aggregation diseases such as Alzheimer's disease. The drug binds to amyloid proteins by binding to their receptor site and inhibits the formation of amyloid fibrils by preventing cross-linking reactions between polypeptides. L-alaninamide hydrochloride also inhibits the formation of benzimidazole compounds, which are used in the treatment of rheumatoid arthritis.br>br>
The structure of L-alaninamide hydrochloride is an intramolecular hydrogen bond donor with a carbonyl group. It

• Marke: Biosynth

Chemische Eigenschaften

• Molekulargewicht: 124.57 g/mol
• Formel: C₃H₈N₂O•HCl
• Reinheit: (Titration) Min 98%
• Farbe/Form: Powder