1.0 2010-04-08 22:11:28 UTC 2019-11-26 03:10:45 UTC FDB014792 Ganoderic acid K Constituent of Ganoderma lucidum (reishi). Ganoderic acid K is found in mushrooms. (+)-Ganoderic acid K Ganoderic acid K C32H46O9 574.7022 574.31418307 6-[16-(acetyloxy)-5,9-dihydroxy-2,6,6,11,15-pentamethyl-12,17-dioxotetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadec-1(10)-en-14-yl]-2-methyl-4-oxoheptanoic acid 6-[16-(acetyloxy)-5,9-dihydroxy-2,6,6,11,15-pentamethyl-12,17-dioxotetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadec-1(10)-en-14-yl]-2-methyl-4-oxoheptanoic acid 104700-95-0 CC(CC(=O)CC(C)C(O)=O)C1CC(=O)C2(C)C3=C(C(=O)C(OC(C)=O)C12C)C1(C)CCC(O)C(C)(C)C1CC3O InChI=1S/C32H46O9/c1-15(11-18(34)12-16(2)28(39)40)19-13-23(37)32(8)24-20(35)14-21-29(4,5)22(36)9-10-30(21,6)25(24)26(38)27(31(19,32)7)41-17(3)33/h15-16,19-22,27,35-36H,9-14H2,1-8H3,(H,39,40) OEHYQHPDUCRLMW-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 11-oxosteroids 3-hydroxysteroids 7-hydroxysteroids Alpha-acyloxy ketones Carboxylic acid esters Carboxylic acids Cyclic alcohols and derivatives Cyclohexenones Dicarboxylic acids and derivatives Dihydroxy bile acids, alcohols and derivatives Gamma-keto acids and derivatives Hydrocarbon derivatives Medium-chain keto acids and derivatives Organic oxides Secondary alcohols Steroid acids Steroid esters 11-oxosteroid 15-oxosteroid 23-oxosteroid 3-hydroxysteroid 7-hydroxysteroid Alcohol Aliphatic homopolycyclic compound Alpha-acyloxy ketone Bile acid, alcohol, or derivatives Carbonyl group Carboxylic acid Carboxylic acid derivative Carboxylic acid ester Cyclic alcohol Cyclohexenone Dicarboxylic acid or derivatives Dihydroxy bile acid, alcohol, or derivatives Gamma-keto acid Hydrocarbon derivative Hydroxy bile acid, alcohol, or derivatives Hydroxysteroid Keto acid Ketone Medium-chain keto acid Organic oxide Organic oxygen compound Organooxygen compound Oxosteroid Secondary alcohol Steroid Steroid acid Steroid ester Triterpenoid logp 3.36 ALOGPS logs -4.80 ALOGPS solubility 9.01e-03 g/l ALOGPS logp 3.03 ChemAxon pka_strongest_acidic 4.16 ChemAxon pka_strongest_basic -0.81 ChemAxon iupac 6-[16-(acetyloxy)-5,9-dihydroxy-2,6,6,11,15-pentamethyl-12,17-dioxotetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadec-1(10)-en-14-yl]-2-methyl-4-oxoheptanoic acid ChemAxon average_mass 574.7022 ChemAxon mono_mass 574.31418307 ChemAxon smiles CC(CC(=O)CC(C)C(O)=O)C1CC(=O)C2(C)C3=C(C(=O)C(OC(C)=O)C12C)C1(C)CCC(O)C(C)(C)C1CC3O ChemAxon formula C32H46O9 ChemAxon inchi InChI=1S/C32H46O9/c1-15(11-18(34)12-16(2)28(39)40)19-13-23(37)32(8)24-20(35)14-21-29(4,5)22(36)9-10-30(21,6)25(24)26(38)27(31(19,32)7)41-17(3)33/h15-16,19-22,27,35-36H,9-14H2,1-8H3,(H,39,40) ChemAxon inchikey OEHYQHPDUCRLMW-UHFFFAOYSA-N ChemAxon polar_surface_area 155.27 ChemAxon refractivity 149.42 ChemAxon polarizability 61.72 ChemAxon rotatable_bond_count 8 ChemAxon acceptor_count 8 ChemAxon donor_count 3 ChemAxon physiological_charge -1 ChemAxon formal_charge 0 ChemAxon Specdb::MsMs 7850 Specdb::MsMs 7851 Specdb::MsMs 7852 Specdb::MsMs 14522 Specdb::MsMs 14523 Specdb::MsMs 14524 Specdb::MsMs 2773031 Specdb::MsMs 2773032 Specdb::MsMs 2773033 Specdb::MsMs 2909669 Specdb::MsMs 2909670 Specdb::MsMs 2909671 Specdb::CMs 9585 Specdb::CMs 44672 Specdb::CMs 282413 Specdb::CMs 373166 Specdb::CMs 373167 Specdb::CMs 373168 Specdb::CMs 373169 Specdb::CMs 373170 Specdb::CMs 373171 Specdb::CMs 373172 Specdb::CMs 373173 Specdb::CMs 373174 Specdb::CMs 373175 Specdb::CMs 373176 Specdb::CMs 373177 Specdb::CMs 373178 Specdb::CMs 373179 Specdb::CMs 373180 Specdb::CMs 373181 Specdb::CMs 373182 Specdb::CMs 373183 Specdb::CMs 373184 Specdb::CMs 373185 Specdb::CMs 373186 Specdb::CMs 373187 HMDB35986 #<Reference:0x000055ce307613b8> Common mushroom Type 1 specific Agaricus bisporus 5341 Mushrooms Unknown generic Oyster mushroom Type 1 specific Pleurotus ostreatus 5322