10-​b-​D-​Glucopyranosyl-​1,​8-​dihydroxy-​3-​(hydroxymethyl)​-anthrone heptaacetate

• CAT Number: C000671
• CAS Number: 13928-72-8
• Molecular Formula: C₃₅H₃₆O₁₆
• Molecular Weight: 712.66
• Purity: ≥95%
• Synonyms: Barbaloin, heptaacetate
• Solubility: Chloroform (Slightly), DMSO (Slightly)
• Appearance: Pale Yellow to Light Yellow Solid
• Storage: -20°C, Inert atmosphere
• IUPAC Name: [3,4,5-triacetyloxy-6-[4,5-diacetyloxy-2-(acetyloxymethyl)-10-oxo-9H-anthracen-9-yl]oxan-2-yl]methyl acetate
• InChI: InChI=1S/C35H36O16/c1-15(36)44-13-22-11-24-28(23-9-8-10-25(46-17(3)38)29(23)31(43)30(24)26(12-22)47-18(4)39)33-35(50-21(7)42)34(49-20(6)41)32(48-19(5)40)27(51-33)14-45-16(2)37/h8-12,27-28,32-35H,13-14H2,1-7H3
• InChIKey: BCGOCQLKVPJNOS-UHFFFAOYSA-N
• SMILES: CC(=O)OCC1C(C(C(C(O1)C2C3=C(C(=CC=C3)OC(=O)C)C(=O)C4=C2C=C(C=C4OC(=O)C)COC(=O)C)OC(=O)C)OC(=O)C)OC(=O)C

10-β-D-Glucopyranosyl-1,8-dihydroxy-3-(hydroxymethyl)-anthrone heptaacetate (Cat No.:C000671) is a complex compound consisting of a glucopyranosyl group attached to a 1,8-dihydroxy-3-(hydroxymethyl)anthrone core, further acetylated with seven acetate groups. This structure suggests potential applications in medicinal and synthetic chemistry. Anthrone derivatives have been explored for various biological activities, and the addition of a glucopyranosyl group may influence its interactions with cellular systems.

Reference

Kay, A.G., et al.: Curr. Med. Res. Opin., 6, 548 (1980), Raimondi, L., et al.: Pharmacol. Res. Commun., 14, 103 (1982), Adami, S., et al.: Clin. Ter., 112, 439 (1985),