Informations sur le produit
- (Methyl{[(2-methyl-2-propanyl)oxy]carbonyl}amino)acetic acid
- (t-Butoxycarbonyl)sarcosine
- (tert-Butoxycarbonyl)sarcosine
- (tert-Butyloxycarbonyl)sarcosine
- 2-((t-Butoxycarbonyl)(methyl)amino)acetic acid
- 2-[(tert-Butoxycarbonyl)(methyl)amino]acetic acid
- 2-[Methyl-[(2-methylpropan-2-yl)oxycarbonyl]amino]acetic acid
- Boc-N-Me-Gly-OH
- Boc-N-methylglycine
- Boc-Sar
- Voir d'autres synonymes
- Boc-Sar-OH
- N-(tert-Butoxycarbonyl)-N-methylglycine
- N-(tert-Butoxycarbonyl)sarcosine
- N-(tert-Butyloxycarbonyl)sarcosine
- N-Methyl-N-Boc-glycine
- N-Methyl-N-{[(2-methyl-2-propanyl)oxy]carbonyl}glycine
- N-[(1,1-Dimethylethoxy)carbonyl]-N-methylglycine
- Sarcosine, N-carboxy-, N-tert-butyl ester
- [(Tert-Butoxycarbonyl)(Methyl)Amino]Acetate
- [(tert-Butoxycarbonyl)(methyl)amino]acetic acid
- [N-(tert-Butoxycarbonyl)-N-methylamino]acetic acid
- glycine, N-[(1,1-dimethylethoxy)carbonyl]-N-methyl-
BOC-Sarcosine is a monomer that belongs to the class of organic compounds called amides. It is synthesized from dopamine and potassium ion, which are readily available in nature. The triazole antifungal activity of BOC-Sarcosine has been shown to be due to its ability to inhibit ergosterol synthesis by binding competitively to the d4 receptor in the cell membrane. This chemical compound is synthesized by solid phase synthesis on a cellulose support with chloroformate as a coupling agent and magnesium as a catalyst. BOC-Sarcosine also has the ability to induce fibrinogen production and inhibit chloride transport across the cell membrane, which may contribute to its anti-cancer properties.