
CAS 40964-56-5
:Sortieren nach
Reinheit (%)
0
100
|
0
|
50
|
90
|
95
|
100
5 Produkte.
1H-1,2,3-Triazole, 4-bromo-
CAS:Formel:C2H2BrN3Reinheit:98%Farbe und Form:SolidMolekulargewicht:147.96144-Bromo-1H-1,2,3-triazole
CAS:4-Bromo-1H-1,2,3-triazoleReinheit:97%Farbe und Form:SolidMolekulargewicht:147.96g/mol4-BROMO-1H-1,2,3-TRIAZOLE
CAS:Formel:C2H2BrN3Reinheit:95%Farbe und Form:SolidMolekulargewicht:147.9634-Bromo-1H-1,2,3-triazole
CAS:Kontrolliertes Produkt<p>Applications 4-Bromo-1H-1,2,3-triazoleare an important class of organic compounds, playing an important role in modern medicinal chemistry. Compounds with 1,2,3-triazole moieties are known to possess fungicidal, antimicrobial, antidepressant, antibacterial, anti-inflammatory, analgesic and antitumor activities.<br>References Sibgatulin, D. A., et al.: Synthesis, No. 7, 1075 (2010); Karivopalov, V. P., et al.: Chem. Rev. (Engl. Trans), 74, 339 (2005);<br></p>Formel:C2H2BrN3Farbe und Form:NeatMolekulargewicht:147.9614-Bromo-1,2,3-triazole
CAS:4-Bromo-1,2,3-triazole is an organic solvent that belongs to the group of phenyl groups. 4-Bromo-1,2,3-triazole has been found to have antibacterial and antifungal properties. It has also been shown to inhibit protease activity in mollusca, as well as insulin resistance in mammals. This compound is used as a structural formula for the synthesis of replication inhibitors and is a serine protease inhibitor. The structure of this compound was determined using X-ray crystallography on 5-membered heteroaryl rings. 4-Bromo-1,2,3-triazole inhibits serine proteases by binding to their active site and blocking access to the catalytic triad consisting of Ser195 (aspartate), His57 (histidine), and Glu194 (glutamic acid). Structural analysis revealed that 4-bromoFormel:C2H2BrN3Reinheit:Min. 95%Molekulargewicht:147.96 g/mol




