CAS 157843-41-9
:2-cloro-4-nitrofenil-alfa-L-fucopiranósido
- Cnp-Afu
- 2-Chloro-4-nitrophenyl-α-L-fucopyranoside
α-L-Galactopyranoside, 2-chloro-4-nitrophenyl 6-deoxy-
CAS:Fórmula:C12H14ClNO7Pureza:%Forma y color:SolidPeso molecular:319.69512-Chloro-4-Nitrophenyl-α-L-Fucopyranoside
CAS:2-Chloro-4-Nitrophenyl-α-L-FucopyranosidePureza:98%Peso molecular:319.7g/mol2-Chloro-4-nitrophenyl a-L-fucopyranoside
CAS:Fórmula:C12H14ClNO7Pureza:≥ 98.0%Forma y color:White to off-white powderPeso molecular:319.692-Chloro-4-nitrophenyl-alpha-L-fucopyranoside
CAS:Alternative chromogenic substrate for alpha-D-galactosidase
Fórmula:C12H14ClNO7Pureza:Min. 98 Area-%Forma y color:White PowderPeso molecular:319.69 g/mol2-Chloro-4-Nitrophenyl a-L-Fucopyranoside (CNPF) extrapure, 98%
CAS:Fórmula:C12H14ClNO7Peso molecular:319.7CNP-AFU
CAS:CNP-AFU (2-Chloro-4-nitrophenyl α-L-fucopyranoside) is the substrate of alpha-L-fucosidase.Fórmula:C12H14ClNO7Pureza:99.55%Forma y color:White To Off-White SolidPeso molecular:319.72-Chloro-4-nitrophenyl-α-L-fucopyranoside
CAS:2-Chloro-4-nitrophenyl-alpha-L-fucopyranoside is a compound that is commonly used as an enzyme substrate for glycogen synthase kinase (GSK). It is activated by GSK-3β and has been shown to inhibit the activity of this enzyme. This compound has also been found to have inhibitory effects on other enzymes such as carbonic anhydrase and lactate dehydrogenase. Additionally, 2-Chloro-4-nitrophenyl-alpha-L-fucopyranoside exhibits antifungal activity against various fungi, including those resistant to other antifungal agents such as fluopyram and prothioconazole. Its mechanism of action involves interfering with ergosterol biosynthesis, an essential component of fungal cell membranes. Furthermore, this compound has potential applications in the development of new drugs targeting GSK-3β and β-catenin signaling pathways, which are implicated in various diseases including cancer and neuro
Fórmula:C12H14ClNO7Pureza:Min. 98 Area-%Peso molecular:319.7 g/mol






