CAS 157843-41-9
:2-Chloro-4-nitrophenyl-alpha-L-fucopyranoside
- Cnp-Afu
- 2-Chloro-4-nitrophenyl-α-L-fucopyranoside
α-L-Galactopyranoside, 2-chloro-4-nitrophenyl 6-deoxy-
CAS:Formula:C12H14ClNO7Purity:%Color and Shape:SolidMolecular weight:319.69512-Chloro-4-Nitrophenyl-α-L-Fucopyranoside
CAS:2-Chloro-4-Nitrophenyl-α-L-FucopyranosidePurity:98%Molecular weight:319.7g/mol2-Chloro-4-nitrophenyl a-L-fucopyranoside
CAS:Formula:C12H14ClNO7Purity:≥ 98.0%Color and Shape:White to off-white powderMolecular weight:319.692-Chloro-4-nitrophenyl-alpha-L-fucopyranoside
CAS:Alternative chromogenic substrate for alpha-D-galactosidase
Formula:C12H14ClNO7Purity:Min. 98 Area-%Color and Shape:White PowderMolecular weight:319.69 g/mol2-Chloro-4-Nitrophenyl a-L-Fucopyranoside (CNPF) extrapure, 98%
CAS:Formula:C12H14ClNO7Molecular weight:319.7CNP-AFU
CAS:CNP-AFU (2-Chloro-4-nitrophenyl α-L-fucopyranoside) is the substrate of alpha-L-fucosidase.Formula:C12H14ClNO7Purity:99.55%Color and Shape:White To Off-White SolidMolecular weight: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
Formula:C12H14ClNO7Purity:Min. 98 Area-%Molecular weight:319.7 g/mol






