1.0 2010-04-08 22:13:41 UTC 2019-11-26 03:16:06 UTC FDB018397 Ramontoside Isolated from Flacourtia ramontchii (governor's plum). Ramontoside is found in herbs and spices and fruits. Ramontoside C34H38O16 702.6559 702.215985168 9-(2H-1,3-benzodioxol-5-yl)-4-[(3,4-dimethoxy-5-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}oxan-2-yl)oxy]-6,7-dimethoxy-1H,3H-naphtho[2,3-c]furan-1-one 9-(2H-1,3-benzodioxol-5-yl)-4-[(3,4-dimethoxy-5-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}oxan-2-yl)oxy]-6,7-dimethoxy-3H-naphtho[2,3-c]furan-1-one 133882-75-4 COC1C(COC(OC2=C3COC(=O)C3=C(C3=CC4=C(OCO4)C=C3)C3=CC(OC)=C(OC)C=C23)C1OC)OC1OC(CO)C(O)C(O)C1O InChI=1S/C34H38O16/c1-40-19-8-15-16(9-20(19)41-2)29(17-11-44-32(39)25(17)24(15)14-5-6-18-21(7-14)47-13-46-18)50-34-31(43-4)30(42-3)23(12-45-34)49-33-28(38)27(37)26(36)22(10-35)48-33/h5-9,22-23,26-28,30-31,33-38H,10-13H2,1-4H3 DDUSFSKGAHCYFG-UHFFFAOYSA-N belongs to the class of organic compounds known as lignan glycosides. These are aromatic polycyclic compounds containing a carbohydrate component glycosidically linked to a lignan moiety. They include 1-aryltetralin lactones. Lignan glycosides Organic compounds Lignans, neolignans and related compounds Lignan glycosides Aromatic heteropolycyclic compounds Acetals Alkyl aryl ethers Anisoles Arylnaphthalene lignans Benzodioxoles Carboxylic acid esters Dialkyl ethers Disaccharides Hydrocarbon derivatives Lactones Lignan lactones Monocarboxylic acids and derivatives Naphthalenes Naphthofurans O-glycosyl compounds Organic oxides Oxacyclic compounds Oxanes Phenolic glycosides Phthalides Polyols Primary alcohols Secondary alcohols Acetal Alcohol Alkyl aryl ether Anisole Aromatic heteropolycyclic compound Arylnaphthalene lignan skeleton Benzenoid Benzodioxole Carboxylic acid derivative Carboxylic acid ester Dialkyl ether Disaccharide Ether Glycosyl compound Hydrocarbon derivative Isobenzofuranone Isocoumaran Lactone Lignan glycoside Lignan lactone Monocarboxylic acid or derivatives Naphthalene Naphthofuran O-glycosyl compound Organic oxide Organic oxygen compound Organoheterocyclic compound Organooxygen compound Oxacycle Oxane Phenolic glycoside Phthalide Polyol Primary alcohol Secondary alcohol logp 1.41 ALOGPS logs -3.10 ALOGPS solubility 5.52e-01 g/l ALOGPS melting_point Mp 140-142° logp 1.05 ChemAxon pka_strongest_acidic 12.21 ChemAxon pka_strongest_basic -3 ChemAxon iupac 9-(2H-1,3-benzodioxol-5-yl)-4-[(3,4-dimethoxy-5-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}oxan-2-yl)oxy]-6,7-dimethoxy-1H,3H-naphtho[2,3-c]furan-1-one ChemAxon average_mass 702.6559 ChemAxon mono_mass 702.215985168 ChemAxon smiles COC1C(COC(OC2=C3COC(=O)C3=C(C3=CC4=C(OCO4)C=C3)C3=CC(OC)=C(OC)C=C23)C1OC)OC1OC(CO)C(O)C(O)C1O ChemAxon formula C34H38O16 ChemAxon inchi InChI=1S/C34H38O16/c1-40-19-8-15-16(9-20(19)41-2)29(17-11-44-32(39)25(17)24(15)14-5-6-18-21(7-14)47-13-46-18)50-34-31(43-4)30(42-3)23(12-45-34)49-33-28(38)27(37)26(36)22(10-35)48-33/h5-9,22-23,26-28,30-31,33-38H,10-13H2,1-4H3 ChemAxon inchikey DDUSFSKGAHCYFG-UHFFFAOYSA-N ChemAxon polar_surface_area 199.52 ChemAxon refractivity 167 ChemAxon polarizability 70.63 ChemAxon rotatable_bond_count 10 ChemAxon acceptor_count 15 ChemAxon donor_count 4 ChemAxon physiological_charge 0 ChemAxon formal_charge 0 ChemAxon Specdb::MsMs 101361 Specdb::MsMs 101362 Specdb::MsMs 101363 Specdb::MsMs 166974 Specdb::MsMs 166975 Specdb::MsMs 166976 Specdb::MsMs 2745845 Specdb::MsMs 2745846 Specdb::MsMs 2745847 Specdb::MsMs 2936536 Specdb::MsMs 2936537 Specdb::MsMs 2936538 Specdb::CMs 70062 Specdb::CMs 749578 Specdb::CMs 749579 Specdb::CMs 749580 Specdb::CMs 749581 Specdb::CMs 749582 Specdb::CMs 749583 Specdb::CMs 749584 Specdb::CMs 749585 Specdb::CMs 749586 Specdb::CMs 749587 Specdb::CMs 749588 Specdb::CMs 749589 Specdb::CMs 749590 Specdb::CMs 749591 HMDB38929 #<Reference:0x000055ce320713f8> Fruits Unknown generic Herbs and Spices Unknown generic