
CAS 98942-06-4
:Formel:C33H40O18
InChl:InChI=1S/C33H40O18/c1-44-19-10-16(4-7-18(19)36)5-9-25(38)49-31-28(41)23(14-35)50-33(31,51-32-30(43)29(42)27(40)22(13-34)48-32)15-47-24(37)8-6-17-11-20(45-2)26(39)21(12-17)46-3/h4-12,22-23,27-32,34-36,39-43H,13-15H2,1-3H3/b8-6+,9-5+/t22-,23-,27-,28-,29+,30-,31+,32-,33-/m1/s1
InChI Key:LHGNBKKPEPCPCT-MAPAUBAGSA-N
SMILES:COC1=CC(=CC(=C1O)OC)/C=C/C(=O)OC[C@]2([C@H]([C@@H]([C@H](O2)CO)O)OC(=O)/C=C/C3=CC(=C(C=C3)O)OC)O[C@@H]4[C@@H]([C@H]([C@@H]([C@H](O4)CO)O)O)O
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3-Feruloyl-1-Sinapoyl sucrose
CAS:3-Feruloyl-1-Sinapoyl sucroseFormel:C33H40O18Reinheit:HP≥90%Molekulargewicht:724.663-Feruloyl-1-Sinapoyl sucrose
CAS:3-Feruloyl-1-Sinapoyl sucrose (Feruloyl Sinapoyl sucrose) is a glycoside isolated from Polygala chamaebuxus.Formel:C33H40O18Reinheit:98%Farbe und Form:SolidMolekulargewicht:724.663-Feruloyl-1-sinapoyl sucrose
CAS:3-Feruloyl-1-sinapoyl sucrose is a specialized type of phenolic compound known as a derivative of sucrose. It is primarily sourced from certain plant species, where it naturally occurs as part of the plant's secondary metabolite repertoire. The mode of action of 3-Feruloyl-1-sinapoyl sucrose is largely attributed to its antioxidant properties. This involves the scavenging of free radicals through electron donation, which can mitigate oxidative stress in biological systems.
Formel:C33H40O18Reinheit:Min. 95%Molekulargewicht:724.7 g/mol







