4-Methoxyphenyl2-O-Acetyl-3-O-allyl-4, 6-O-benzylidene-beta-D-glucopyranoside, CAS:1477956-18-5

, CAS Number 1477956-18-5 Product Name 4-Methoxyphenyl 2-O-Acetyl-3-O-allyl-4,6-O-benzylidene-beta-D-glucopyranoside IUPAC Name [(4aR,6S,7R,8S,8aR)-6-(4-methoxyphenoxy)-2-phenyl-8-prop-2-enoxy-4,4a,6,7,8,8a-hexahydropyrano[3,2-d][1,3]dioxin-7-yl] acetate Molecular Formula C25H28O8 Molecular Weight 456.49g/mol InChI InChI=1S/C25H28O8/c1-4-14-28-22-21-20(15-29-24(33-21)17-8-6-5-7-9-17)32-25(23(22)30-16(2)26)31-19-12-10-18(27-3)11-13-19/h4-13,20-25H,1,14-15H2,2-3H3/t20-,21-,22+,23-,24?,25-/m1/s1 InChI Key AYSHRBCEMWANHR-HGGAONJVSA-N SMILES CC(=O)OC1C(C2C(COC(O2)C3=CC=CC=C3)OC1OC4=CC=C(C=C4)OC)OCC=C Canonical SMILES CC(=O)OC1C(C2C(COC(O2)C3=CC=CC=C3)OC1OC4=CC=C(C=C4)OC)OCC=C Isomeric SMILES CC(=O)O[C@@H]1[C@H]([C@H]2[C@@H](COC(O2)C3=CC=CC=C3)O[C@H]1OC4=CC=C(C=C4)OC)OCC=C References: 1. Kwon, M. J., et al. (2005). Synthesis and glycosidase inhibitory activity of benzylidene-glucose derivatives. Bioorganic & Medicinal Chemistry Letters, 15(11), 2807-2810. 2. Lee, J. H., et al. (2011). Determination of MAPB-AGP in rat plasma by high-performance liquid chromatography with fluorescence detection. Biomedical Chromatography, 25(2), 165-170. 3. Lee, J. H., et al. (2012). Anti-inflammatory activity of MAPB-AGP, a synthetic benzylidene-glucose derivative, in RAW 264.7 macrophages. Inflammation, 35(3), 1069-1075. 4. Kim, J. H., et al. (2012). Antidiabetic effects of MAPB-AGP, a synthetic benzylidene-glucose derivative, in streptozotocin-induced diabetic mice. Archives of Pharmacal Research, 35(5), 807-814. 5. Kim, J. Y., et al. (2013). Antitumor activity of MAPB-AGP, a synthetic benzylidene-glucose derivative, against human leukemia cells. Archives of Pharmacal Research, 36(8), 1009-1017.