1.0 2010-04-08 22:11:01 UTC 2019-11-26 03:09:22 UTC FDB013983 Ganoderol B Constituent of fungus Ganoderma lucidum (reishi). Ganoderol B is found in mushrooms. (3beta,24E)-Lanosta-7,9(11),24-trien-3,26-diol (3beta,24e)-Lanosta-7,9(11),24-triene-3,26-diol 5alpha-Lanosta-7,9(11),24-triene-3beta,26-one Ganodermadiol Ganoderol B Lanosta-7,9(11),24-triene-3,26-diol Lanosta-7,9(11),24-triene-3,26-diol, (3beta,24E)- C30H48O2 440.7009 440.36543078 14-[(5E)-7-hydroxy-6-methylhept-5-en-2-yl]-2,6,6,11,15-pentamethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadeca-1(17),9-dien-5-ol 14-[(5E)-7-hydroxy-6-methylhept-5-en-2-yl]-2,6,6,11,15-pentamethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadeca-1(17),9-dien-5-ol 104700-96-1 CC(CC\C=C(/C)CO)C1CCC2(C)C3=CCC4C(C)(C)C(O)CCC4(C)C3=CCC12C InChI=1S/C30H48O2/c1-20(19-31)9-8-10-21(2)22-13-17-30(7)24-11-12-25-27(3,4)26(32)15-16-28(25,5)23(24)14-18-29(22,30)6/h9,11,14,21-22,25-26,31-32H,8,10,12-13,15-19H2,1-7H3/b20-9+ AOXXVRDKZLRGTJ-AWQFTUOYSA-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 homopolycyclic compounds 3-hydroxy delta-7-steroids Cyclic alcohols and derivatives Delta-7-steroids Dihydroxy bile acids, alcohols and derivatives Fatty alcohols Hydrocarbon derivatives Primary alcohols Secondary alcohols 26-hydroxysteroid 3-hydroxy-delta-7-steroid 3-hydroxysteroid Alcohol Aliphatic homopolycyclic compound Bile acid, alcohol, or derivatives Cholane-skeleton Cyclic alcohol Delta-7-steroid Dihydroxy bile acid, alcohol, or derivatives Fatty acyl Fatty alcohol Hydrocarbon derivative Hydroxy bile acid, alcohol, or derivatives Hydroxysteroid Organic oxygen compound Organooxygen compound Primary alcohol Secondary alcohol Steroid Triterpenoid logp 7.43 ALOGPS logs -5.57 ALOGPS solubility 1.18e-03 g/l ALOGPS melting_point Mp 171-173° logp 6.06 ChemAxon pka_strongest_acidic 16.64 ChemAxon pka_strongest_basic -0.78 ChemAxon iupac 14-[(5E)-7-hydroxy-6-methylhept-5-en-2-yl]-2,6,6,11,15-pentamethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadeca-1(17),9-dien-5-ol ChemAxon average_mass 440.7009 ChemAxon mono_mass 440.36543078 ChemAxon smiles CC(CC\C=C(/C)CO)C1CCC2(C)C3=CCC4C(C)(C)C(O)CCC4(C)C3=CCC12C ChemAxon formula C30H48O2 ChemAxon inchi InChI=1S/C30H48O2/c1-20(19-31)9-8-10-21(2)22-13-17-30(7)24-11-12-25-27(3,4)26(32)15-16-28(25,5)23(24)14-18-29(22,30)6/h9,11,14,21-22,25-26,31-32H,8,10,12-13,15-19H2,1-7H3/b20-9+ ChemAxon inchikey AOXXVRDKZLRGTJ-AWQFTUOYSA-N ChemAxon polar_surface_area 40.46 ChemAxon refractivity 137.44 ChemAxon polarizability 54.75 ChemAxon rotatable_bond_count 5 ChemAxon acceptor_count 2 ChemAxon donor_count 2 ChemAxon physiological_charge 0 ChemAxon formal_charge 0 ChemAxon Specdb::CMs 22061 Specdb::CMs 44320 Specdb::CMs 163529 Specdb::MsMs 79773 Specdb::MsMs 79774 Specdb::MsMs 79775 Specdb::MsMs 140436 Specdb::MsMs 140437 Specdb::MsMs 140438 Specdb::MsMs 2662384 Specdb::MsMs 2662385 Specdb::MsMs 2662386 Specdb::MsMs 3015690 Specdb::MsMs 3015691 Specdb::MsMs 3015692 HMDB35314 #<Reference:0x000055ce32aa9b18> Common mushroom Type 1 specific Agaricus bisporus 5341 Mushrooms Unknown generic Oyster mushroom Type 1 specific Pleurotus ostreatus 5322