1.0 2010-04-08 22:09:35 UTC 2019-11-26 03:04:49 UTC FDB011332 Moracin J Isolated from Morus alba (white mulberry) infected with Fusarium solani. Moracin J is found in fruits. 2-(3,5-Dihydroxyphenyl)-5-hydroxy-6-methoxybenzofuran Moracin J C15H12O5 272.2528 272.068473494 5-(5-hydroxy-6-methoxy-1-benzofuran-2-yl)benzene-1,3-diol 5-(5-hydroxy-6-methoxy-1-benzofuran-2-yl)benzene-1,3-diol 73338-89-3 COC1=C(O)C=C2C=C(OC2=C1)C1=CC(O)=CC(O)=C1 InChI=1S/C15H12O5/c1-19-15-7-14-9(4-12(15)18)5-13(20-14)8-2-10(16)6-11(17)3-8/h2-7,16-18H,1H3 UUWOGANMKVBGHH-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-phenylbenzofurans Alkyl aryl ethers Anisoles Benzene and substituted derivatives Furans Heteroaromatic compounds Hydrocarbon derivatives Oxacyclic compounds Resorcinols 1-hydroxy-2-unsubstituted benzenoid 1-hydroxy-4-unsubstituted benzenoid 2-arylbenzofuran flavonoid 2-phenylbenzofuran Alkyl aryl ether Anisole Aromatic heteropolycyclic compound Benzenoid Benzofuran Ether Furan Heteroaromatic compound Hydrocarbon derivative Monocyclic benzene moiety Organic oxygen compound Organoheterocyclic compound Organooxygen compound Oxacycle Phenol Phenylbenzofuran Resorcinol logp 2.68 ALOGPS logs -2.89 ALOGPS solubility 3.51e-01 g/l ALOGPS logp 2.63 ChemAxon pka_strongest_acidic 8.66 ChemAxon pka_strongest_basic -2.9 ChemAxon iupac 5-(5-hydroxy-6-methoxy-1-benzofuran-2-yl)benzene-1,3-diol ChemAxon average_mass 272.2528 ChemAxon mono_mass 272.068473494 ChemAxon smiles COC1=C(O)C=C2C=C(OC2=C1)C1=CC(O)=CC(O)=C1 ChemAxon formula C15H12O5 ChemAxon inchi InChI=1S/C15H12O5/c1-19-15-7-14-9(4-12(15)18)5-13(20-14)8-2-10(16)6-11(17)3-8/h2-7,16-18H,1H3 ChemAxon inchikey UUWOGANMKVBGHH-UHFFFAOYSA-N ChemAxon polar_surface_area 83.06 ChemAxon refractivity 72.32 ChemAxon polarizability 28.16 ChemAxon rotatable_bond_count 2 ChemAxon acceptor_count 4 ChemAxon donor_count 3 ChemAxon physiological_charge 0 ChemAxon formal_charge 0 ChemAxon Specdb::CMs 10240 Specdb::CMs 43222 Specdb::CMs 146455 Specdb::MsMs 99333 Specdb::MsMs 99334 Specdb::MsMs 99335 Specdb::MsMs 164466 Specdb::MsMs 164467 Specdb::MsMs 164468 Specdb::MsMs 2412403 Specdb::MsMs 2412404 Specdb::MsMs 2412405 Specdb::MsMs 2549832 Specdb::MsMs 2549833 Specdb::MsMs 2549834 HMDB33308 #<Reference:0x000055ce316ba080> Fruits Unknown generic