1.0 2010-04-08 22:11:29 UTC 2019-11-26 03:10:47 UTC FDB014809 Epoxyganoderiol B Metabolite of Ganoderma lucidum (reishi). Epoxyganoderiol B is found in mushrooms. 24S,25S-Epoxy-26-hydroxylanosta-7,9(11)-dien-3-one Epoxyganoderiol B C30H46O3 454.6844 454.344695338 14-{4-[3-(hydroxymethyl)-3-methyloxiran-2-yl]butan-2-yl}-2,6,6,11,15-pentamethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadeca-1(17),9-dien-5-one 14-{4-[3-(hydroxymethyl)-3-methyloxiran-2-yl]butan-2-yl}-2,6,6,11,15-pentamethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadeca-1(17),9-dien-5-one 114020-57-4 CC(CCC1OC1(C)CO)C1CCC2(C)C3=CCC4C(C)(C)C(=O)CCC4(C)C3=CCC12C InChI=1S/C30H46O3/c1-19(8-11-25-30(7,18-31)33-25)20-12-16-29(6)22-9-10-23-26(2,3)24(32)14-15-27(23,4)21(22)13-17-28(20,29)5/h9,13,19-20,23,25,31H,8,10-12,14-18H2,1-7H3 XOBQAKLXNUVCPN-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-oxo delta-7-steroids Cyclic ketones Delta-7-steroids Dialkyl ethers Epoxides Hydrocarbon derivatives Hydroxysteroids Monohydroxy bile acids, alcohols and derivatives Organic oxides Oxacyclic compounds Primary alcohols 26-hydroxysteroid 3-oxo-delta-7-steroid 3-oxosteroid Alcohol Aliphatic heteropolycyclic compound Bile acid, alcohol, or derivatives Carbonyl group Cholane-skeleton Cyclic ketone Delta-7-steroid Dialkyl ether Ether Hydrocarbon derivative Hydroxy bile acid, alcohol, or derivatives Ketone Monohydroxy bile acid, alcohol, or derivatives Organic oxide Organic oxygen compound Organoheterocyclic compound Organooxygen compound Oxacycle Oxirane Oxosteroid Primary alcohol Steroid Triterpenoid logp 6.60 ALOGPS logs -5.67 ALOGPS solubility 9.72e-04 g/l ALOGPS logp 5.88 ChemAxon pka_strongest_acidic 14.29 ChemAxon pka_strongest_basic -3.1 ChemAxon iupac 14-{4-[3-(hydroxymethyl)-3-methyloxiran-2-yl]butan-2-yl}-2,6,6,11,15-pentamethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadeca-1(17),9-dien-5-one ChemAxon average_mass 454.6844 ChemAxon mono_mass 454.344695338 ChemAxon smiles CC(CCC1OC1(C)CO)C1CCC2(C)C3=CCC4C(C)(C)C(=O)CCC4(C)C3=CCC12C ChemAxon formula C30H46O3 ChemAxon inchi InChI=1S/C30H46O3/c1-19(8-11-25-30(7,18-31)33-25)20-12-16-29(6)22-9-10-23-26(2,3)24(32)14-15-27(23,4)21(22)13-17-28(20,29)5/h9,13,19-20,23,25,31H,8,10-12,14-18H2,1-7H3 ChemAxon inchikey XOBQAKLXNUVCPN-UHFFFAOYSA-N ChemAxon polar_surface_area 49.83 ChemAxon refractivity 135.22 ChemAxon polarizability 54.77 ChemAxon rotatable_bond_count 5 ChemAxon acceptor_count 3 ChemAxon donor_count 1 ChemAxon physiological_charge 0 ChemAxon formal_charge 0 ChemAxon Specdb::CMs 21770 Specdb::CMs 44679 Specdb::CMs 157206 Specdb::MsMs 78108 Specdb::MsMs 78109 Specdb::MsMs 78110 Specdb::MsMs 138372 Specdb::MsMs 138373 Specdb::MsMs 138374 Specdb::MsMs 2393818 Specdb::MsMs 2393819 Specdb::MsMs 2393820 Specdb::MsMs 2572658 Specdb::MsMs 2572659 Specdb::MsMs 2572660 HMDB36000 #<Reference:0x000055ce2b7edb88> Common mushroom Type 1 specific Agaricus bisporus 5341 Mushrooms Unknown generic Oyster mushroom Type 1 specific Pleurotus ostreatus 5322