1.0 2010-04-08 22:12:44 UTC 2025-11-19 01:50:56 UTC FDB016924 Ganoderiol D Metabolite of Ganoderma lucidum (reishi). Ganoderiol D is found in mushrooms. 24,25,26-Tetrahydroxy-8-lanostene-3,7-dione Ganoderiol D C30H48O5 488.6991 488.350174646 2,6,6,11,15-pentamethyl-14-(5,6,7-trihydroxy-6-methylheptan-2-yl)tetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadec-1(10)-ene-5,9-dione 2,6,6,11,15-pentamethyl-14-(5,6,7-trihydroxy-6-methylheptan-2-yl)tetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadec-1(10)-ene-5,9-dione 114567-45-2 CC(CCC(O)C(C)(O)CO)C1CCC2(C)C3=C(CCC12C)C1(C)CCC(=O)C(C)(C)C1CC3=O InChI=1S/C30H48O5/c1-18(8-9-24(34)30(7,35)17-31)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/h18-19,22,24,31,34-35H,8-17H2,1-7H3 NAETYGPWGSNZTO-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 homopolycyclic compounds 3-oxosteroids 7-oxosteroids Cyclohexenones Fatty alcohols Hydrocarbon derivatives Hydroxysteroids Organic oxides Polyols Primary alcohols Secondary alcohols Tertiary alcohols Trihydroxy bile acids, alcohols and derivatives 24-hydroxysteroid 25-hydroxysteroid 26-hydroxysteroid 3-oxosteroid 7-oxosteroid Alcohol Aliphatic homopolycyclic compound Bile acid, alcohol, or derivatives Carbonyl group Cyclic ketone Cyclohexenone Fatty acyl Fatty alcohol Hydrocarbon derivative Hydroxy bile acid, alcohol, or derivatives Ketone Organic oxide Organic oxygen compound Organooxygen compound Oxosteroid Polyol Primary alcohol Secondary alcohol Steroid Tertiary alcohol Trihydroxy bile acid, alcohol, or derivatives Triterpenoid logp 4.88 ALOGPS logs -5.08 ALOGPS solubility 4.08e-03 g/l ALOGPS logp 4.42 ChemAxon pka_strongest_acidic 13.19 ChemAxon pka_strongest_basic -3.1 ChemAxon iupac 2,6,6,11,15-pentamethyl-14-(5,6,7-trihydroxy-6-methylheptan-2-yl)tetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadec-1(10)-ene-5,9-dione ChemAxon average_mass 488.6991 ChemAxon mono_mass 488.350174646 ChemAxon smiles CC(CCC(O)C(C)(O)CO)C1CCC2(C)C3=C(CCC12C)C1(C)CCC(=O)C(C)(C)C1CC3=O ChemAxon formula C30H48O5 ChemAxon inchi InChI=1S/C30H48O5/c1-18(8-9-24(34)30(7,35)17-31)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/h18-19,22,24,31,34-35H,8-17H2,1-7H3 ChemAxon inchikey NAETYGPWGSNZTO-UHFFFAOYSA-N ChemAxon polar_surface_area 94.83 ChemAxon refractivity 138.31 ChemAxon polarizability 57.49 ChemAxon rotatable_bond_count 6 ChemAxon acceptor_count 5 ChemAxon donor_count 3 ChemAxon physiological_charge 0 ChemAxon formal_charge 0 ChemAxon Specdb::CMs 20833 Specdb::CMs 45547 Specdb::CMs 171301 Specdb::MsMs 58593 Specdb::MsMs 58594 Specdb::MsMs 58595 Specdb::MsMs 114552 Specdb::MsMs 114553 Specdb::MsMs 114554 Specdb::MsMs 2407406 Specdb::MsMs 2407407 Specdb::MsMs 2407408 Specdb::MsMs 2530896 Specdb::MsMs 2530897 Specdb::MsMs 2530898 HMDB37782 #<Reference:0x000055ce304daef0> Common mushroom Type 1 specific Agaricus bisporus 5341 Mushrooms Unknown generic Oyster mushroom Type 1 specific Pleurotus ostreatus 5322