1.0 2019-09-16 21:23:36 UTC 2025-11-19 03:06:37 UTC FDB093565 Dulcisisoflavone C25H26O5 406.478 406.178023937 9-(2,2-dimethyl-3,4-dihydro-2H-1-benzopyran-6-yl)-5-hydroxy-2,2-dimethyl-2H,3H,4H,10H-pyrano[2,3-f]chromen-10-one 9-(2,2-dimethyl-3,4-dihydro-1-benzopyran-6-yl)-5-hydroxy-2,2-dimethyl-3H,4H-pyrano[2,3-f]chromen-10-one CC1(C)CCC2=C(O1)C=CC(=C2)C1=COC2=C(C1=O)C1=C(CCC(C)(C)O1)C(O)=C2 InChI=1S/C25H26O5/c1-24(2)9-7-15-11-14(5-6-19(15)29-24)17-13-28-20-12-18(26)16-8-10-25(3,4)30-23(16)21(20)22(17)27/h5-6,11-13,26H,7-10H2,1-4H3 AAVIPCXEXKHNTR-UHFFFAOYSA-N belongs to the class of organic compounds known as 6-prenylated isoflavanones. These are isoflavanones featuring a C5-isoprenoid unit at the 6-position. 6-prenylated isoflavanones Organic compounds Phenylpropanoids and polyketides Isoflavonoids Isoflavans Aromatic heteropolycyclic compounds 1-hydroxy-2-unsubstituted benzenoids 2,2-dimethyl-1-benzopyrans Alkyl aryl ethers Chromones Heteroaromatic compounds Hydrocarbon derivatives Hydroxyisoflavonoids Isoflavones Organic oxides Oxacyclic compounds Pyranoisoflavonoids Pyranones and derivatives Vinylogous esters 1-benzopyran 1-hydroxy-2-unsubstituted benzenoid 2,2-dimethyl-1-benzopyran 6-prenylated isoflavanone Alkyl aryl ether Aromatic heteropolycyclic compound Benzenoid Benzopyran Chromane Chromone Ether Heteroaromatic compound Hydrocarbon derivative Hydroxyisoflavonoid Isoflavone Organic oxide Organic oxygen compound Organoheterocyclic compound Organooxygen compound Oxacycle Pyran Pyranoisoflavonoid Pyranone Vinylogous ester logp 5.51 ALOGPS logs -5.27 ALOGPS solubility 2.19e-03 g/l ALOGPS logp 5.08 ChemAxon pka_strongest_acidic 6.83 ChemAxon pka_strongest_basic -4.5 ChemAxon iupac 9-(2,2-dimethyl-3,4-dihydro-2H-1-benzopyran-6-yl)-5-hydroxy-2,2-dimethyl-2H,3H,4H,10H-pyrano[2,3-f]chromen-10-one ChemAxon average_mass 406.478 ChemAxon mono_mass 406.178023937 ChemAxon smiles CC1(C)CCC2=C(O1)C=CC(=C2)C1=COC2=C(C1=O)C1=C(CCC(C)(C)O1)C(O)=C2 ChemAxon formula C25H26O5 ChemAxon inchi InChI=1S/C25H26O5/c1-24(2)9-7-15-11-14(5-6-19(15)29-24)17-13-28-20-12-18(26)16-8-10-25(3,4)30-23(16)21(20)22(17)27/h5-6,11-13,26H,7-10H2,1-4H3 ChemAxon inchikey AAVIPCXEXKHNTR-UHFFFAOYSA-N ChemAxon polar_surface_area 64.99 ChemAxon refractivity 114.58 ChemAxon polarizability 45.28 ChemAxon rotatable_bond_count 1 ChemAxon acceptor_count 5 ChemAxon donor_count 1 ChemAxon physiological_charge -1 ChemAxon formal_charge 0 ChemAxon Specdb::MsMs 1257895 Specdb::MsMs 1257896 Specdb::MsMs 1257897 Specdb::MsMs 1373053 Specdb::MsMs 1373054 Specdb::MsMs 1373055 Specdb::MsMs 3609430 Specdb::MsMs 3609431 Specdb::MsMs 3609432 Specdb::MsMs 3609433 Specdb::MsMs 3609434 Specdb::MsMs 3609435 Mundu Type 1 Garcinia dulcis