1.0 2016-09-30 23:18:50 UTC 2020-05-11 20:24:34 UTC BMDB0005810 BMDB05810 Eriodictyol (S)-2-(3,4-Dihydroxyphenyl)-2,3-dihydro-5,7-dihydroxy-4-benzopyrone (S)-Eriodictyol Eriodictiol (+)-Eriodictyol (2S)-Eriodictyol (S)-2,3-Dihydroluteolin (S)-3',4',5,7-Tetrahydroxyflavanone (S)-3’,4’,5,7-Tetrahydroxyflavanone 3',4',5,7-Tetrahydroxyflavanone 3’,4’,5,7-Tetrahydroxyflavanone (2S)-2-(3,4-Dihydroxyphenyl)-2,3-dihydro-5,7-dihydroxy-4H-1-benzopyran-4-one (2S)-2-(3,4-Dihydroxyphenyl)-5,7-dihydroxy-2,3-dihydrochromen-4-one Huazhongilexone C15H12O6 288.2522 288.063388116 (2S)-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3,4-dihydro-2H-1-benzopyran-4-one eriodictyol 552-58-9 OC1=CC(O)=C2C(=O)C[C@H](OC2=C1)C1=CC=C(O)C(O)=C1 InChI=1S/C15H12O6/c16-8-4-11(19)15-12(20)6-13(21-14(15)5-8)7-1-2-9(17)10(18)3-7/h1-5,13,16-19H,6H2/t13-/m0/s1 SBHXYTNGIZCORC-ZDUSSCGKSA-N belongs to the class of organic compounds known as flavanones. Flavanones are compounds containing a flavan-3-one moiety, with a structure characterized by a 2-phenyl-3,4-dihydro-2H-1-benzopyran bearing a ketone at the carbon C3. Organic compounds Phenylpropanoids and polyketides Flavonoids Flavans Flavanones 1-hydroxy-2-unsubstituted benzenoids 1-hydroxy-4-unsubstituted benzenoids 3'-hydroxyflavonoids 4'-hydroxyflavonoids 5-hydroxyflavonoids 7-hydroxyflavonoids Alkyl aryl ethers Aryl alkyl ketones Benzene and substituted derivatives Catechols Chromones Hydrocarbon derivatives Organic oxides Oxacyclic compounds Vinylogous acids 1-benzopyran 1-hydroxy-2-unsubstituted benzenoid 1-hydroxy-4-unsubstituted benzenoid 3'-hydroxyflavonoid 4'-hydroxyflavonoid 5-hydroxyflavonoid 7-hydroxyflavonoid Alkyl aryl ether Aromatic heteropolycyclic compound Aryl alkyl ketone Aryl ketone Benzenoid Benzopyran Catechol Chromane Chromone Ether Flavanone Hydrocarbon derivative Hydroxyflavonoid Ketone Monocyclic benzene moiety Organic oxide Organic oxygen compound Organoheterocyclic compound Organooxygen compound Oxacycle Phenol Vinylogous acid Aromatic heteropolycyclic compounds 3'-hydroxyflavanones Flavanones flavanones tetrahydroxyflavanone Solid melting_point 269 - 270 °C water_solubility 0.07 mg/mL at 20 °C logp 2.02 PERRISSOUD,D & TESTA,B (1986) logp 2.15 ALOGPS logs -2.90 ALOGPS logp 2.53 ChemAxon pka_strongest_acidic 7.85 ChemAxon pka_strongest_basic -5 ChemAxon iupac (2S)-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3,4-dihydro-2H-1-benzopyran-4-one ChemAxon average_mass 288.2522 ChemAxon mono_mass 288.063388116 ChemAxon smiles OC1=CC(O)=C2C(=O)C[C@H](OC2=C1)C1=CC=C(O)C(O)=C1 ChemAxon formula C15H12O6 ChemAxon inchi InChI=1S/C15H12O6/c16-8-4-11(19)15-12(20)6-13(21-14(15)5-8)7-1-2-9(17)10(18)3-7/h1-5,13,16-19H,6H2/t13-/m0/s1 ChemAxon inchikey SBHXYTNGIZCORC-ZDUSSCGKSA-N ChemAxon polar_surface_area 107.22 ChemAxon refractivity 73.27 ChemAxon polarizability 27.33 ChemAxon rotatable_bond_count 1 ChemAxon acceptor_count 6 ChemAxon donor_count 4 ChemAxon physiological_charge 0 ChemAxon formal_charge 0 ChemAxon number_of_rings 3 ChemAxon bioavailability 1 ChemAxon rule_of_five Yes ChemAxon ghose_filter Yes ChemAxon veber_rule Yes ChemAxon mddr_like_rule Yes ChemAxon Specdb::CMs 16521 Specdb::CMs 38901 Specdb::CMs 102694 Specdb::CMs 102695 Specdb::CMs 172021 Specdb::NmrOneD 317681 Specdb::NmrOneD 317682 Specdb::NmrOneD 317683 Specdb::NmrOneD 317684 Specdb::NmrOneD 317685 Specdb::NmrOneD 317686 Specdb::NmrOneD 317687 Specdb::NmrOneD 317688 Specdb::NmrOneD 317689 Specdb::NmrOneD 317690 Specdb::NmrOneD 317691 Specdb::NmrOneD 317692 Specdb::NmrOneD 317693 Specdb::NmrOneD 317694 Specdb::NmrOneD 317695 Specdb::NmrOneD 317696 Specdb::NmrOneD 317697 Specdb::NmrOneD 317698 Specdb::NmrOneD 317699 Specdb::NmrOneD 317700 Specdb::MsMs 71934 Specdb::MsMs 71935 Specdb::MsMs 71936 Specdb::MsMs 130716 Specdb::MsMs 130717 Specdb::MsMs 130718 Specdb::MsMs 285775 Specdb::MsMs 285776 Specdb::MsMs 285777 Specdb::MsMs 285778 Specdb::MsMs 285779 Specdb::MsMs 285780 Specdb::MsMs 373831 Specdb::MsMs 373832 Specdb::MsMs 373833 Specdb::MsMs 373834 Specdb::MsMs 373835 Specdb::MsMs 373836 Specdb::MsMs 438936 Specdb::MsMs 438937 Specdb::MsMs 438938 Specdb::MsMs 438939 Specdb::MsMs 439134 Specdb::MsMs 447839 Specdb::MsMs 447840 Kidney Wishart DS, Feunang YD, Marcu A, Guo AC, Liang K, Vazquez-Fresno R, Sajed T, Johnson D, Li C, Karu N, Sayeeda Z, Lo E, Assempour N, Berjanskii M, Singhal S, Arndt D, Liang Y, Badran H, Grant J, Serra-Cayuela A, Liu Y, Mandal R, Neveu V, Pon A, Knox C, Wilson M, Manach C, Scalbert A: HMDB 4.0: the human metabolome database for 2018. Nucleic Acids Res. 2018 Jan 4;46(D1):D608-D617. doi: 10.1093/nar/gkx1089. 29140435 Liver Wishart DS, Feunang YD, Marcu A, Guo AC, Liang K, Vazquez-Fresno R, Sajed T, Johnson D, Li C, Karu N, Sayeeda Z, Lo E, Assempour N, Berjanskii M, Singhal S, Arndt D, Liang Y, Badran H, Grant J, Serra-Cayuela A, Liu Y, Mandal R, Neveu V, Pon A, Knox C, Wilson M, Manach C, Scalbert A: HMDB 4.0: the human metabolome database for 2018. Nucleic Acids Res. 2018 Jan 4;46(D1):D608-D617. doi: 10.1093/nar/gkx1089. 29140435 FDB011936 389606 C00000960 440735 C05631 202 28412 CPD-7671 Eriodictyol 3415 Powers, Fred B.; Tutin, Frank. Chemical Examination of Eriodictyon. Pharmaceutical Review (1907), 24 301.