1.0 2010-04-08 22:09:35 UTC 2025-11-18 23:26:16 UTC FDB011320 Kuwanon Y Constituent of Morus alba (white mulberry). Kuwanon Y is found in fruits. C34H30O9 582.5966 582.188982558 2-[6-(2,4-dihydroxybenzoyl)-5-(2,4-dihydroxyphenyl)-3-methylcyclohex-2-en-1-yl]-5-[(E)-2-(2,4-dihydroxyphenyl)ethenyl]benzene-1,3-diol 2-[6-(2,4-dihydroxybenzoyl)-5-(2,4-dihydroxyphenyl)-3-methylcyclohex-2-en-1-yl]-5-[(E)-2-(2,4-dihydroxyphenyl)ethenyl]benzene-1,3-diol 105016-28-2 CC1=CC(C(C(C1)C1=C(O)C=C(O)C=C1)C(=O)C1=C(O)C=C(O)C=C1)C1=C(O)C=C(\C=C\C2=C(O)C=C(O)C=C2)C=C1O InChI=1S/C34H30O9/c1-17-10-25(23-8-6-21(36)15-28(23)39)32(34(43)24-9-7-22(37)16-29(24)40)26(11-17)33-30(41)12-18(13-31(33)42)2-3-19-4-5-20(35)14-27(19)38/h2-9,11-16,25-26,32,35-42H,10H2,1H3/b3-2+ YYUHPJKWIHNMSV-NSCUHMNNSA-N belongs to the class of organic compounds known as linear diarylheptanoids. These are diarylheptanoids with an open heptane chain. The two aromatic rings are linked only by the heptane chain. Linear diarylheptanoids Organic compounds Phenylpropanoids and polyketides Diarylheptanoids Linear diarylheptanoids Aromatic homomonocyclic compounds 1-hydroxy-2-unsubstituted benzenoids 1-hydroxy-4-unsubstituted benzenoids Alkyl-phenylketones Aryl alkyl ketones Benzoyl derivatives Hydrocarbon derivatives Organic oxides Resorcinols Stilbenes Styrenes Vinylogous acids 1-hydroxy-2-unsubstituted benzenoid 1-hydroxy-4-unsubstituted benzenoid Alkyl-phenylketone Aromatic homomonocyclic compound Aryl alkyl ketone Aryl ketone Benzenoid Benzoyl Hydrocarbon derivative Ketone Linear 1,7-diphenylheptane skeleton Monocyclic benzene moiety Organic oxide Organic oxygen compound Organooxygen compound Phenol Phenylketone Resorcinol Stilbene Styrene Vinylogous acid logp 4.33 ALOGPS logs -5.14 ALOGPS solubility 4.18e-03 g/l ALOGPS logp 6.93 ChemAxon pka_strongest_acidic 7.8 ChemAxon pka_strongest_basic -3.9 ChemAxon iupac 2-[6-(2,4-dihydroxybenzoyl)-5-(2,4-dihydroxyphenyl)-3-methylcyclohex-2-en-1-yl]-5-[(E)-2-(2,4-dihydroxyphenyl)ethenyl]benzene-1,3-diol ChemAxon average_mass 582.5966 ChemAxon mono_mass 582.188982558 ChemAxon smiles CC1=CC(C(C(C1)C1=C(O)C=C(O)C=C1)C(=O)C1=C(O)C=C(O)C=C1)C1=C(O)C=C(\C=C\C2=C(O)C=C(O)C=C2)C=C1O ChemAxon formula C34H30O9 ChemAxon inchi InChI=1S/C34H30O9/c1-17-10-25(23-8-6-21(36)15-28(23)39)32(34(43)24-9-7-22(37)16-29(24)40)26(11-17)33-30(41)12-18(13-31(33)42)2-3-19-4-5-20(35)14-27(19)38/h2-9,11-16,25-26,32,35-42H,10H2,1H3/b3-2+ ChemAxon inchikey YYUHPJKWIHNMSV-NSCUHMNNSA-N ChemAxon polar_surface_area 178.91 ChemAxon refractivity 163.65 ChemAxon polarizability 60.9 ChemAxon rotatable_bond_count 6 ChemAxon acceptor_count 9 ChemAxon donor_count 8 ChemAxon physiological_charge 0 ChemAxon formal_charge 0 ChemAxon Specdb::MsMs 101283 Specdb::MsMs 101284 Specdb::MsMs 101285 Specdb::MsMs 166875 Specdb::MsMs 166876 Specdb::MsMs 166877 Specdb::MsMs 2699192 Specdb::MsMs 2699193 Specdb::MsMs 2699194 Specdb::MsMs 3005691 Specdb::MsMs 3005692 Specdb::MsMs 3005693 Specdb::CMs 15012 Specdb::CMs 43210 Specdb::CMs 282596 Specdb::CMs 404554 Specdb::CMs 404555 Specdb::CMs 404556 Specdb::CMs 404557 Specdb::CMs 404558 Specdb::CMs 404559 Specdb::CMs 404560 Specdb::CMs 404561 Specdb::CMs 404562 Specdb::CMs 404563 Specdb::CMs 404564 Specdb::CMs 404565 Specdb::CMs 404566 Specdb::CMs 404567 Specdb::CMs 404568 Specdb::CMs 404569 Specdb::CMs 404570 Specdb::CMs 404571 Specdb::CMs 404572 Specdb::CMs 404573 Specdb::CMs 404574 Specdb::CMs 404575 HMDB33296 #<Reference:0x000055ce31f24ec8> Fruits Unknown generic