1.0 2010-04-08 22:15:33 UTC 2019-11-26 03:20:03 UTC FDB021213 Moracin K Production by Morus alba (white mulberry) infected with Fusarium solani. Moracin K is found in mulberry and fruits. C19H16O5 324.3273 324.099773622 5-{5-hydroxy-7,7-dimethyl-7H-furo[2,3-f]chromen-2-yl}benzene-1,3-diol 5-{5-hydroxy-7,7-dimethylfuro[2,3-f]chromen-2-yl}benzene-1,3-diol 73338-90-6 CC1(C)OC2=C(O)C=C3C=C(OC3=C2C=C1)C1=CC(O)=CC(O)=C1 InChI=1S/C19H16O5/c1-19(2)4-3-14-17-11(7-15(22)18(14)24-19)8-16(23-17)10-5-12(20)9-13(21)6-10/h3-9,20-22H,1-2H3 HRYWITBPMMQCBB-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 2,2-dimethyl-1-benzopyrans 2-phenylbenzofurans Alkyl aryl ethers Benzene and substituted derivatives Furans Heteroaromatic compounds Hydrocarbon derivatives Oxacyclic compounds Resorcinols 1-benzopyran 1-hydroxy-2-unsubstituted benzenoid 1-hydroxy-4-unsubstituted benzenoid 2,2-dimethyl-1-benzopyran 2-arylbenzofuran flavonoid 2-phenylbenzofuran Alkyl aryl ether Aromatic heteropolycyclic compound Benzenoid Benzofuran Benzopyran Ether Furan Heteroaromatic compound Hydrocarbon derivative Monocyclic benzene moiety Organic oxygen compound Organoheterocyclic compound Organooxygen compound Oxacycle Phenol Phenylbenzofuran Resorcinol logp 3.82 ALOGPS logs -3.60 ALOGPS solubility 8.09e-02 g/l ALOGPS logp 3.69 ChemAxon pka_strongest_acidic 8.63 ChemAxon pka_strongest_basic -3 ChemAxon iupac 5-{5-hydroxy-7,7-dimethyl-7H-furo[2,3-f]chromen-2-yl}benzene-1,3-diol ChemAxon average_mass 324.3273 ChemAxon mono_mass 324.099773622 ChemAxon smiles CC1(C)OC2=C(O)C=C3C=C(OC3=C2C=C1)C1=CC(O)=CC(O)=C1 ChemAxon formula C19H16O5 ChemAxon inchi InChI=1S/C19H16O5/c1-19(2)4-3-14-17-11(7-15(22)18(14)24-19)8-16(23-17)10-5-12(20)9-13(21)6-10/h3-9,20-22H,1-2H3 ChemAxon inchikey HRYWITBPMMQCBB-UHFFFAOYSA-N ChemAxon polar_surface_area 83.06 ChemAxon refractivity 90.25 ChemAxon polarizability 34.81 ChemAxon rotatable_bond_count 1 ChemAxon acceptor_count 4 ChemAxon donor_count 3 ChemAxon physiological_charge 0 ChemAxon formal_charge 0 ChemAxon Specdb::CMs 16708 Specdb::CMs 47238 Specdb::CMs 154697 Specdb::MsMs 8081 Specdb::MsMs 8082 Specdb::MsMs 8083 Specdb::MsMs 14753 Specdb::MsMs 14754 Specdb::MsMs 14755 Specdb::MsMs 2372730 Specdb::MsMs 2372731 Specdb::MsMs 2372732 Specdb::MsMs 2565575 Specdb::MsMs 2565576 Specdb::MsMs 2565577 HMDB41296 #<Reference:0x000055ce305c3600> Fruits Unknown generic Mulberry Type 1 specific Morus 3497