1.0 2010-04-08 22:12:04 UTC 2019-11-26 03:12:16 UTC FDB015821 Marasmal Metabolite of Marasmius oreades (fairy ring mushroom). Marasmal is found in mushrooms. Marasmal C15H20O6 296.3157 296.125988372 (3S,8R,10S,10aR,10bS)-3,8,10-trihydroxy-7,7-dimethyl-1-oxo-1H,3H,6H,6aH,7H,8H,9H,10H,10bH-naphtho[1,8a-c]furan-4-carbaldehyde (3S,8R,10S,10aR,10bS)-3,8,10-trihydroxy-7,7-dimethyl-1-oxo-3H,6H,6aH,8H,9H,10H,10bH-naphtho[1,8a-c]furan-4-carbaldehyde 124869-10-9 [H][C@@]12[C@@H](O)OC(=O)[C@@]11[C@@H](O)C[C@@H](O)C(C)(C)C1CC=C2C=O InChI=1S/C15H20O6/c1-14(2)8-4-3-7(6-16)11-12(19)21-13(20)15(8,11)10(18)5-9(14)17/h3,6,8-12,17-19H,4-5H2,1-2H3/t8?,9-,10+,11-,12+,15+/m1/s1 OLGMJXURWXVYKR-JAIRQZCISA-N belongs to the class of organic compounds known as naphthofurans. Naphthofurans are compounds containing a furan ring fused to a naphthalene moiety. Furan is a 5 membered- ring aromatic ring with four carbon and one oxygen atoms. Naphthalene is a polycyclic aromatic hydrocarbon made up of two fused benzene rings. Naphthofurans Organic compounds Organoheterocyclic compounds Naphthofurans Aliphatic heteropolycyclic compounds Aldehydes Carboxylic acid esters Cyclic alcohols and derivatives Gamma butyrolactones Hemiacetals Hydrocarbon derivatives Monocarboxylic acids and derivatives Organic oxides Oxacyclic compounds Polyols Secondary alcohols Tetrahydrofurans Alcohol Aldehyde Aliphatic heteropolycyclic compound Carbonyl group Carboxylic acid derivative Carboxylic acid ester Cyclic alcohol Gamma butyrolactone Hemiacetal Hydrocarbon derivative Lactone Monocarboxylic acid or derivatives Naphthofuran Organic oxide Organic oxygen compound Organooxygen compound Oxacycle Polyol Secondary alcohol Tetrahydrofuran logp 0.50 ALOGPS logs -1.07 ALOGPS solubility 2.50e+01 g/l ALOGPS melting_point Mp 195-200° logp -0.76 ChemAxon pka_strongest_acidic 5.27 ChemAxon pka_strongest_basic -3 ChemAxon iupac (3S,8R,10S,10aR,10bS)-3,8,10-trihydroxy-7,7-dimethyl-1-oxo-1H,3H,6H,6aH,7H,8H,9H,10H,10bH-naphtho[1,8a-c]furan-4-carbaldehyde ChemAxon average_mass 296.3157 ChemAxon mono_mass 296.125988372 ChemAxon smiles [H][C@@]12[C@@H](O)OC(=O)[C@@]11[C@@H](O)C[C@@H](O)C(C)(C)C1CC=C2C=O ChemAxon formula C15H20O6 ChemAxon inchi InChI=1S/C15H20O6/c1-14(2)8-4-3-7(6-16)11-12(19)21-13(20)15(8,11)10(18)5-9(14)17/h3,6,8-12,17-19H,4-5H2,1-2H3/t8?,9-,10+,11-,12+,15+/m1/s1 ChemAxon inchikey OLGMJXURWXVYKR-JAIRQZCISA-N ChemAxon polar_surface_area 104.06 ChemAxon refractivity 72.49 ChemAxon polarizability 28.87 ChemAxon rotatable_bond_count 1 ChemAxon acceptor_count 5 ChemAxon donor_count 3 ChemAxon physiological_charge 0 ChemAxon formal_charge 0 ChemAxon Specdb::CMs 9774 Specdb::CMs 45090 Specdb::CMs 147259 Specdb::MsMs 101913 Specdb::MsMs 101914 Specdb::MsMs 101915 Specdb::MsMs 167607 Specdb::MsMs 167608 Specdb::MsMs 167609 Specdb::MsMs 2674576 Specdb::MsMs 2674577 Specdb::MsMs 2674578 Specdb::MsMs 3034643 Specdb::MsMs 3034644 Specdb::MsMs 3034645 Specdb::NmrOneD 137230 Specdb::NmrOneD 137231 Specdb::NmrOneD 137232 Specdb::NmrOneD 137233 Specdb::NmrOneD 137234 Specdb::NmrOneD 137235 Specdb::NmrOneD 137236 Specdb::NmrOneD 137237 Specdb::NmrOneD 137238 Specdb::NmrOneD 137239 Specdb::NmrOneD 137240 Specdb::NmrOneD 137241 Specdb::NmrOneD 137242 Specdb::NmrOneD 137243 Specdb::NmrOneD 137244 Specdb::NmrOneD 137245 Specdb::NmrOneD 137246 Specdb::NmrOneD 137247 Specdb::NmrOneD 137248 Specdb::NmrOneD 137249 HMDB36867 #<Reference:0x000055ce318f52c8> Common mushroom Type 1 specific Agaricus bisporus 5341 Mushrooms Unknown generic Oyster mushroom Type 1 specific Pleurotus ostreatus 5322