1.0 2010-04-08 22:12:49 UTC 2019-11-26 03:14:10 UTC FDB017078 Aureol Isolated from Phaseolus aureus (mung bean) and other Phaseolus subspecies Aureol is found in many foods, some of which are scarlet bean, pulses, gram bean, and mung bean. 1,3,9-Trihydroxy-6H-benzofuro[3,2-c]benzopyran-6-one, 9CI Aureol Aureol? C15H8O6 284.2204 284.032087988 3,5,14-trihydroxy-8,17-dioxatetracyclo[8.7.0.0²,⁷.0¹¹,¹⁶]heptadeca-1(10),2,4,6,11(16),12,14-heptaen-9-one aureol 88478-03-9 OC1=CC2=C(C=C1)C1=C(O2)C2=C(O)C=C(O)C=C2OC1=O InChI=1S/C15H8O6/c16-6-1-2-8-10(4-6)20-14-12(8)15(19)21-11-5-7(17)3-9(18)13(11)14/h1-5,16-18H WIRRQLQRDSREEG-UHFFFAOYSA-N belongs to the class of organic compounds known as coumestans. These are polycyclic aromatic compounds containing a coumestan moiety, which consists of a benzoxole fused to a chromen-2-one to form 1-Benzoxolo[3,2-c]chromen-6-one. They are oxidation products of pterocarpan. Coumestans Organic compounds Phenylpropanoids and polyketides Isoflavonoids Coumestans Aromatic heteropolycyclic compounds 1-benzopyrans 1-hydroxy-2-unsubstituted benzenoids 1-hydroxy-4-unsubstituted benzenoids Angular furanocoumarins Benzofurans Furans Furopyrans Heteroaromatic compounds Hydrocarbon derivatives Lactones Organic oxides Oxacyclic compounds Polyols Pyranones and derivatives 1-benzopyran 1-hydroxy-2-unsubstituted benzenoid 1-hydroxy-4-unsubstituted benzenoid Angular furanocoumarin Aromatic heteropolycyclic compound Benzenoid Benzofuran Benzopyran Coumarin Coumestan Furan Furanocoumarin Furopyran Heteroaromatic compound Hydrocarbon derivative Lactone Organic oxide Organic oxygen compound Organoheterocyclic compound Organooxygen compound Oxacycle Polyol Pyran Pyranone Coumestan flavonoids logp 2.64 ALOGPS logs -2.55 ALOGPS solubility 7.96e-01 g/l ALOGPS logp 2.09 ChemAxon pka_strongest_acidic 6.6 ChemAxon pka_strongest_basic -4.5 ChemAxon iupac 3,5,14-trihydroxy-8,17-dioxatetracyclo[8.7.0.0²,⁷.0¹¹,¹⁶]heptadeca-1(10),2,4,6,11(16),12,14-heptaen-9-one ChemAxon average_mass 284.2204 ChemAxon mono_mass 284.032087988 ChemAxon smiles OC1=CC2=C(C=C1)C1=C(O2)C2=C(O)C=C(O)C=C2OC1=O ChemAxon formula C15H8O6 ChemAxon inchi InChI=1S/C15H8O6/c16-6-1-2-8-10(4-6)20-14-12(8)15(19)21-11-5-7(17)3-9(18)13(11)14/h1-5,16-18H ChemAxon inchikey WIRRQLQRDSREEG-UHFFFAOYSA-N ChemAxon polar_surface_area 100.13 ChemAxon refractivity 71.6 ChemAxon polarizability 27.22 ChemAxon rotatable_bond_count 0 ChemAxon acceptor_count 4 ChemAxon donor_count 3 ChemAxon physiological_charge -1 ChemAxon formal_charge 0 ChemAxon Specdb::CMs 9421 Specdb::CMs 45591 Specdb::CMs 153749 Specdb::MsMs 6701 Specdb::MsMs 6702 Specdb::MsMs 6703 Specdb::MsMs 13373 Specdb::MsMs 13374 Specdb::MsMs 13375 Specdb::MsMs 2356026 Specdb::MsMs 2356027 Specdb::MsMs 2356028 Specdb::MsMs 2609153 Specdb::MsMs 2609154 Specdb::MsMs 2609155 HMDB37921 #<Reference:0x000055ce30cf15f8> Gram bean Type 1 specific Vigna mungo 3915 Mung bean Type 1 specific Vigna radiata 157791 Pulses Unknown generic Scarlet bean Type 1 specific Phaseolus coccineus 3886