1.0 2010-04-08 22:11:29 UTC 2019-11-26 03:10:47 UTC FDB014810 Epoxyganoderiol A Metabolite of Ganoderma lucidum (reishi). Epoxyganoderiol A is found in mushrooms. Epoxyganoderiol A C30H48O4 472.6997 472.355260024 9-hydroxy-14-{4-[3-(hydroxymethyl)-3-methyloxiran-2-yl]butan-2-yl}-2,6,6,11,15-pentamethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadec-1(10)-en-5-one 9-hydroxy-14-{4-[3-(hydroxymethyl)-3-methyloxiran-2-yl]butan-2-yl}-2,6,6,11,15-pentamethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadec-1(10)-en-5-one 114020-56-3 CC(CCC1OC1(C)CO)C1CCC2(C)C3=C(CCC12C)C1(C)CCC(=O)C(C)(C)C1CC3O InChI=1S/C30H48O4/c1-18(8-9-24-30(7,17-31)34-24)19-10-15-29(6)25-20(11-14-28(19,29)5)27(4)13-12-23(33)26(2,3)22(27)16-21(25)32/h18-19,21-22,24,31-32H,8-17H2,1-7H3 XRLVMZVXPMYCSF-UHFFFAOYSA-N belongs to the class of organic compounds known as triterpenoids. These are terpene molecules containing six isoprene units. Triterpenoids Organic compounds Lipids and lipid-like molecules Prenol lipids Triterpenoids Aliphatic heteropolycyclic compounds 3-oxosteroids 7-hydroxysteroids Cyclic ketones Dialkyl ethers Dihydroxy bile acids, alcohols and derivatives Epoxides Hydrocarbon derivatives Organic oxides Oxacyclic compounds Primary alcohols Secondary alcohols 26-hydroxysteroid 3-oxosteroid 7-hydroxysteroid Alcohol Aliphatic heteropolycyclic compound Bile acid, alcohol, or derivatives Carbonyl group Cyclic ketone Dialkyl ether Dihydroxy bile acid, alcohol, or derivatives Ether Hydrocarbon derivative Hydroxy bile acid, alcohol, or derivatives Hydroxysteroid Ketone Organic oxide Organic oxygen compound Organoheterocyclic compound Organooxygen compound Oxacycle Oxirane Oxosteroid Primary alcohol Secondary alcohol Steroid Triterpenoid logp 5.25 ALOGPS logs -5.19 ALOGPS solubility 3.07e-03 g/l ALOGPS logp 5.01 ChemAxon pka_strongest_acidic 14.29 ChemAxon pka_strongest_basic -0.73 ChemAxon iupac 9-hydroxy-14-{4-[3-(hydroxymethyl)-3-methyloxiran-2-yl]butan-2-yl}-2,6,6,11,15-pentamethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadec-1(10)-en-5-one ChemAxon average_mass 472.6997 ChemAxon mono_mass 472.355260024 ChemAxon smiles CC(CCC1OC1(C)CO)C1CCC2(C)C3=C(CCC12C)C1(C)CCC(=O)C(C)(C)C1CC3O ChemAxon formula C30H48O4 ChemAxon inchi InChI=1S/C30H48O4/c1-18(8-9-24-30(7,17-31)34-24)19-10-15-29(6)25-20(11-14-28(19,29)5)27(4)13-12-23(33)26(2,3)22(27)16-21(25)32/h18-19,21-22,24,31-32H,8-17H2,1-7H3 ChemAxon inchikey XRLVMZVXPMYCSF-UHFFFAOYSA-N ChemAxon polar_surface_area 70.06 ChemAxon refractivity 135.62 ChemAxon polarizability 56.52 ChemAxon rotatable_bond_count 5 ChemAxon acceptor_count 4 ChemAxon donor_count 2 ChemAxon physiological_charge 0 ChemAxon formal_charge 0 ChemAxon Specdb::CMs 11555 Specdb::CMs 44680 Specdb::CMs 148596 Specdb::MsMs 49125 Specdb::MsMs 49126 Specdb::MsMs 49127 Specdb::MsMs 174012 Specdb::MsMs 174013 Specdb::MsMs 174014 Specdb::MsMs 3036644 Specdb::MsMs 3036645 Specdb::MsMs 3036646 Specdb::MsMs 3106328 Specdb::MsMs 3106329 Specdb::MsMs 3106330 HMDB36001 #<Reference:0x000055ce31ff6400> Common mushroom Type 1 specific Agaricus bisporus 5341 Mushrooms Unknown generic Oyster mushroom Type 1 specific Pleurotus ostreatus 5322