1.0 2010-04-08 22:12:23 UTC 2025-11-19 01:46:33 UTC FDB016358 Sudachiin A Isolated from Citrus sudachi peel. Sudachiin A is found in citrus. 5,7,4'-Trihydroxy-6,8,3'-trimethoxyflavone 4'-glucoside Sudachiin A C24H26O13 522.4554 522.137340918 5,7-dihydroxy-6,8-dimethoxy-2-(3-methoxy-4-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)-4H-chromen-4-one 5,7-dihydroxy-6,8-dimethoxy-2-(3-methoxy-4-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)chromen-4-one 70575-17-6 COC1=C(OC2OC(CO)C(O)C(O)C2O)C=CC(=C1)C1=CC(=O)C2=C(O)C(OC)=C(O)C(OC)=C2O1 InChI=1S/C24H26O13/c1-32-13-6-9(4-5-11(13)36-24-19(30)18(29)16(27)14(8-25)37-24)12-7-10(26)15-17(28)22(33-2)20(31)23(34-3)21(15)35-12/h4-7,14,16,18-19,24-25,27-31H,8H2,1-3H3 ZSAJLBLZRADOLX-UHFFFAOYSA-N belongs to the class of organic compounds known as flavonoid o-glycosides. Flavonoid O-glycosides are compounds containing a carbohydrate moiety which is O-glycosidically linked to the 2-phenylchromen-4-one flavonoid backbone. Flavonoid O-glycosides Organic compounds Phenylpropanoids and polyketides Flavonoids Flavonoid glycosides Aromatic heteropolycyclic compounds 3'-O-methylated flavonoids 5-hydroxyflavonoids 6-O-methylated flavonoids 7-hydroxyflavonoids 8-O-methylated flavonoids Acetals Alkyl aryl ethers Anisoles Chromones Flavones Heteroaromatic compounds Hexoses Hydrocarbon derivatives Methoxybenzenes O-glycosyl compounds Organic oxides Oxacyclic compounds Oxanes Phenolic glycosides Phenoxy compounds Polyols Primary alcohols Pyranones and derivatives Secondary alcohols Vinylogous acids 1-benzopyran 3p-methoxyflavonoid-skeleton 5-hydroxyflavonoid 6-methoxyflavonoid-skeleton 7-hydroxyflavonoid 8-methoxyflavonoid-skeleton Acetal Alcohol Alkyl aryl ether Anisole Aromatic heteropolycyclic compound Benzenoid Benzopyran Chromone Ether Flavone Flavonoid o-glycoside Flavonoid-4p-o-glycoside Glycosyl compound Heteroaromatic compound Hexose monosaccharide Hydrocarbon derivative Hydroxyflavonoid Methoxybenzene Monocyclic benzene moiety Monosaccharide O-glycosyl compound Organic oxide Organic oxygen compound Organoheterocyclic compound Organooxygen compound Oxacycle Oxane Phenol ether Phenolic glycoside Phenoxy compound Polyol Primary alcohol Pyran Pyranone Secondary alcohol Vinylogous acid logp 0.77 ALOGPS logs -2.96 ALOGPS solubility 5.67e-01 g/l ALOGPS melting_point Mp 211-213° logp -0.034 ChemAxon pka_strongest_acidic 6.63 ChemAxon pka_strongest_basic -3 ChemAxon iupac 5,7-dihydroxy-6,8-dimethoxy-2-(3-methoxy-4-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)-4H-chromen-4-one ChemAxon average_mass 522.4554 ChemAxon mono_mass 522.137340918 ChemAxon smiles COC1=C(OC2OC(CO)C(O)C(O)C2O)C=CC(=C1)C1=CC(=O)C2=C(O)C(OC)=C(O)C(OC)=C2O1 ChemAxon formula C24H26O13 ChemAxon inchi InChI=1S/C24H26O13/c1-32-13-6-9(4-5-11(13)36-24-19(30)18(29)16(27)14(8-25)37-24)12-7-10(26)15-17(28)22(33-2)20(31)23(34-3)21(15)35-12/h4-7,14,16,18-19,24-25,27-31H,8H2,1-3H3 ChemAxon inchikey ZSAJLBLZRADOLX-UHFFFAOYSA-N ChemAxon polar_surface_area 193.83 ChemAxon refractivity 124.45 ChemAxon polarizability 50.83 ChemAxon rotatable_bond_count 7 ChemAxon acceptor_count 13 ChemAxon donor_count 6 ChemAxon physiological_charge -1 ChemAxon formal_charge 0 ChemAxon Specdb::CMs 16719 Specdb::CMs 45323 Specdb::MsMs 8387 Specdb::MsMs 8388 Specdb::MsMs 8389 Specdb::MsMs 15059 Specdb::MsMs 15060 Specdb::MsMs 15061 Specdb::MsMs 2746070 Specdb::MsMs 2746071 Specdb::MsMs 2746072 Specdb::MsMs 2936779 Specdb::MsMs 2936780 Specdb::MsMs 2936781 Specdb::NmrOneD 140090 Specdb::NmrOneD 140091 Specdb::NmrOneD 140092 Specdb::NmrOneD 140093 Specdb::NmrOneD 140094 Specdb::NmrOneD 140095 Specdb::NmrOneD 140096 Specdb::NmrOneD 140097 Specdb::NmrOneD 140098 Specdb::NmrOneD 140099 Specdb::NmrOneD 140100 Specdb::NmrOneD 140101 Specdb::NmrOneD 140102 Specdb::NmrOneD 140103 Specdb::NmrOneD 140104 Specdb::NmrOneD 140105 Specdb::NmrOneD 140106 Specdb::NmrOneD 140107 Specdb::NmrOneD 140108 Specdb::NmrOneD 140109 HMDB37336 #<Reference:0x000055ce322f0ca0> Citrus Unknown generic