7-[(2-O-D-Apio-β-D-furanosyl-β-D-glucopyranosyl)oxy]-5-hydroxy-3-(4-methoxyphenyl)-4H-1-benzopyran-4

• CAT Number: M082970
• CAS Number: 15914-68-8
• Molecular Formula: C27H30O14
• Molecular Weight: 578.52
• Purity: ≥95%
• Storage: Store at -20°C
• IUPAC Name: 7-[(2S,3R,4S,5S,6R)-6-[[(2R,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxy-5-hydroxy-3-(4-methoxyphenyl)chromen-4-one
• InChI: InChI=1S/C27H30O14/c1-36-13-4-2-12(3-5-13)15-8-37-17-7-14(6-16(29)19(17)20(15)30)40-25-23(33)22(32)21(31)18(41-25)9-38-26-24(34)27(35,10-28)11-39-26/h2-8,18,21-26,28-29,31-35H,9-11H2,1H3/t18-,21-,22+,23-,24+,25-,26-,27-/m1/s1
• InChIKey: VGKGODYADVWBQB-NRIIMPDMSA-N
• SMILES: COC1=CC=C(C=C1)C2=COC3=CC(=CC(=C3C2=O)O)OC4C(C(C(C(O4)COC5C(C(CO5)(CO)O)O)O)O)O

7-[(2-O-D-Apio-β-D-furanosyl-β-D-glucopyranosyl)oxy]-5-hydroxy-3-(4-methoxyphenyl)-4H-1-benzopyran-4-one（Cat No.:M082970） is a complex flavonoid glycoside. This molecule features a benzopyran core, a typical structure found in flavonoids, which are known for their antioxidant properties. It is further modified with hydroxy and methoxy groups that enhance its biological activity and solubility. The presence of sugar moieties like apiose and glucose in glycosidic linkage extends its role in medicinal chemistry, often impacting its bioavailability and metabolic stability. Such compounds are studied for their potential benefits in reducing inflammation, combating oxidative stress, and modulating various biological pathways.