Informations sur le produit
- L-Leucine Amide Hydrochloride
- (2S)-1-amino-4-methyl-1-oxopentan-2-aminium
- (S)-2-Amino-4-methylpentanamide hydrochloride
- (S)-Leucinamide hydrochloride
- 211-696-2
- <span class="text-smallcaps">L</span>-Leucinamide hydrochloride
- <span class="text-smallcaps">L</span>-Leucinamide monohydrochloride
- H-Leu-NH2・HCl
- L-leucinamide
- L-leucinamide hydrochloride
- Voir d'autres synonymes
- Leucinamide hydrochloride
- Leucinamide, monohydrochloride, <span class="text-smallcaps">L</span>-
- Leucine amide hydrochloride
- NSC 83635
- Pentanamide, 2-Amino-4-Methyl-, Chloride
- Pentanamide, 2-amino-4-methyl-, hydrochloride (1:1), (2S)-
- Pentanamide, 2-amino-4-methyl-, monohydrochloride, (2S)-
- Pentanamide, 2-amino-4-methyl-, monohydrochloride, (S)-
- pentanamide, 2-amino-4-methyl-, (2S)-
Leu-NH2 • HCl is an imidazolidinone that has been shown to have anti-inflammatory properties. The compound is a highly selective, full agonist at the CB1 receptor and has been shown to be effective in animal models of inflammatory diseases, such as collagen-induced arthritis. Leu-NH2 • HCl also has been shown to inhibit the enzymatic activity of cb1 receptor in food chemistry and c1-6 alkyl atrial receptors. Leu-NH2 • HCl binds to the same site on the receptor as THC (Δ9-tetrahydrocannabinol) and is used in research on Alzheimer's disease. This drug has also been shown to inhibit the enzymatic activity of hyaluronic acid synthetase, which may be related to its pharmacokinetic study.
Propriétés chimiques
Question d’ordre technique sur : 3D-SLN-3027 Leu-NH2 • HCl
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