1.0 2010-04-08 22:14:45 UTC 2025-11-19 02:27:39 UTC FDB020036 Moracin O Constituent of Morus alba (white mulberry). Moracin O is found in fruits. (-)-Moracin O 5-[5,6-Dihydro-6-(1-hydroxy-1-methylethyl)benzo[1,2-b:5,4-b']difuran-2-yl]-1,3-benzenediol, 9CI C19H18O5 326.3432 326.115423686 5-[11-(2-hydroxypropan-2-yl)-4,12-dioxatricyclo[7.3.0.0³,⁷]dodeca-1(9),2,5,7-tetraen-5-yl]benzene-1,3-diol 5-[11-(2-hydroxypropan-2-yl)-4,12-dioxatricyclo[7.3.0.0³,⁷]dodeca-1(9),2,5,7-tetraen-5-yl]benzene-1,3-diol 123702-97-6 CC(C)(O)C1CC2=C(O1)C=C1OC(=CC1=C2)C1=CC(O)=CC(O)=C1 InChI=1S/C19H18O5/c1-19(2,22)18-7-11-3-10-6-15(23-16(10)9-17(11)24-18)12-4-13(20)8-14(21)5-12/h3-6,8-9,18,20-22H,7H2,1-2H3 HMTMYIWMPJSCAZ-UHFFFAOYSA-N belongs to the class of organic compounds known as 2-arylbenzofuran flavonoids. These are phenylpropanoids containing the 2-phenylbenzofuran moiety. 2-arylbenzofuran flavonoids Organic compounds Phenylpropanoids and polyketides 2-arylbenzofuran flavonoids Aromatic heteropolycyclic compounds 1-hydroxy-2-unsubstituted benzenoids 1-hydroxy-4-unsubstituted benzenoids 2-phenylbenzofurans Alkyl aryl ethers Benzene and substituted derivatives Coumarans Furans Heteroaromatic compounds Hydrocarbon derivatives Oxacyclic compounds Resorcinols Tertiary alcohols 1-hydroxy-2-unsubstituted benzenoid 1-hydroxy-4-unsubstituted benzenoid 2-arylbenzofuran flavonoid 2-phenylbenzofuran Alcohol Alkyl aryl ether Aromatic heteropolycyclic compound Benzenoid Benzofuran Coumaran Ether Furan Heteroaromatic compound Hydrocarbon derivative Monocyclic benzene moiety Organic oxygen compound Organoheterocyclic compound Organooxygen compound Oxacycle Phenol Phenylbenzofuran Resorcinol Tertiary alcohol logp 3.42 ALOGPS logs -3.49 ALOGPS solubility 1.06e-01 g/l ALOGPS logp 3.04 ChemAxon pka_strongest_acidic 8.82 ChemAxon pka_strongest_basic -3 ChemAxon iupac 5-[11-(2-hydroxypropan-2-yl)-4,12-dioxatricyclo[7.3.0.0³,⁷]dodeca-1(9),2,5,7-tetraen-5-yl]benzene-1,3-diol ChemAxon average_mass 326.3432 ChemAxon mono_mass 326.115423686 ChemAxon smiles CC(C)(O)C1CC2=C(O1)C=C1OC(=CC1=C2)C1=CC(O)=CC(O)=C1 ChemAxon formula C19H18O5 ChemAxon inchi InChI=1S/C19H18O5/c1-19(2,22)18-7-11-3-10-6-15(23-16(10)9-17(11)24-18)12-4-13(20)8-14(21)5-12/h3-6,8-9,18,20-22H,7H2,1-2H3 ChemAxon inchikey HMTMYIWMPJSCAZ-UHFFFAOYSA-N ChemAxon polar_surface_area 83.06 ChemAxon refractivity 88.67 ChemAxon polarizability 35.74 ChemAxon rotatable_bond_count 2 ChemAxon acceptor_count 4 ChemAxon donor_count 3 ChemAxon physiological_charge 0 ChemAxon formal_charge 0 ChemAxon Specdb::CMs 25827 Specdb::CMs 46731 Specdb::CMs 135754 Specdb::CMs 143488 Specdb::MsMs 323254 Specdb::MsMs 323255 Specdb::MsMs 323256 Specdb::MsMs 371365 Specdb::MsMs 371366 Specdb::MsMs 371367 Specdb::MsMs 2269249 Specdb::MsMs 2269250 Specdb::MsMs 2269251 Specdb::MsMs 3073185 Specdb::MsMs 3073186 Specdb::MsMs 3073187 HMDB40313 #<Reference:0x000055ce3231e970> Fruits Unknown generic