1.0 2010-04-08 22:14:52 UTC 2019-11-26 03:18:37 UTC FDB020209 Ganoderic acid Z Isolated from Ganoderma lucidum (reishi). Ganoderic acid Z is found in mushrooms. Anwuweizic acid Ganoderic acid Z C30H48O3 456.7003 456.360345402 (2Z)-6-{5-hydroxy-2,6,6,11,15-pentamethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadec-1(10)-en-14-yl}-2-methylhept-2-enoic acid (2Z)-6-{5-hydroxy-2,6,6,11,15-pentamethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadec-1(10)-en-14-yl}-2-methylhept-2-enoic acid 86420-19-1 CC(CC\C=C(\C)C(O)=O)C1CCC2(C)C3=C(CCC12C)C1(C)CCC(O)C(C)(C)C1CC3 InChI=1S/C30H48O3/c1-19(9-8-10-20(2)26(32)33)21-13-17-30(7)23-11-12-24-27(3,4)25(31)15-16-28(24,5)22(23)14-18-29(21,30)6/h10,19,21,24-25,31H,8-9,11-18H2,1-7H3,(H,32,33)/b20-10- KGELVXQPIUKGCO-JMIUGGIZSA-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-hydroxysteroids Carbonyl compounds Carboxylic acids Cyclic alcohols and derivatives Hydrocarbon derivatives Hydroxy fatty acids Medium-chain fatty acids Monocarboxylic acids and derivatives Monohydroxy bile acids, alcohols and derivatives Organic oxides Secondary alcohols Steroid acids Unsaturated fatty acids 3-hydroxysteroid Alcohol Aliphatic homopolycyclic compound Bile acid, alcohol, or derivatives Carbonyl group Carboxylic acid Carboxylic acid derivative Cyclic alcohol Fatty acid Fatty acyl Hydrocarbon derivative Hydroxy bile acid, alcohol, or derivatives Hydroxy fatty acid Hydroxysteroid Medium-chain fatty acid Monocarboxylic acid or derivatives Monohydroxy bile acid, alcohol, or derivatives Organic oxide Organic oxygen compound Organooxygen compound Secondary alcohol Steroid Steroid acid Triterpenoid Unsaturated fatty acid logp 7.20 ALOGPS logs -5.66 ALOGPS solubility 1.00e-03 g/l ALOGPS logp 6.9 ChemAxon pka_strongest_acidic 4.81 ChemAxon pka_strongest_basic -0.81 ChemAxon iupac (2Z)-6-{5-hydroxy-2,6,6,11,15-pentamethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadec-1(10)-en-14-yl}-2-methylhept-2-enoic acid ChemAxon average_mass 456.7003 ChemAxon mono_mass 456.360345402 ChemAxon smiles CC(CC\C=C(\C)C(O)=O)C1CCC2(C)C3=C(CCC12C)C1(C)CCC(O)C(C)(C)C1CC3 ChemAxon formula C30H48O3 ChemAxon inchi InChI=1S/C30H48O3/c1-19(9-8-10-20(2)26(32)33)21-13-17-30(7)23-11-12-24-27(3,4)25(31)15-16-28(24,5)22(23)14-18-29(21,30)6/h10,19,21,24-25,31H,8-9,11-18H2,1-7H3,(H,32,33)/b20-10- ChemAxon inchikey KGELVXQPIUKGCO-JMIUGGIZSA-N ChemAxon polar_surface_area 57.53 ChemAxon refractivity 136.26 ChemAxon polarizability 56.17 ChemAxon rotatable_bond_count 5 ChemAxon acceptor_count 3 ChemAxon donor_count 2 ChemAxon physiological_charge -1 ChemAxon formal_charge 0 ChemAxon Specdb::CMs 22556 Specdb::CMs 46779 Specdb::CMs 171491 Specdb::MsMs 316099 Specdb::MsMs 316100 Specdb::MsMs 316101 Specdb::MsMs 362263 Specdb::MsMs 362264 Specdb::MsMs 362265 Specdb::MsMs 2826511 Specdb::MsMs 2826512 Specdb::MsMs 2826513 Specdb::MsMs 2855608 Specdb::MsMs 2855609 Specdb::MsMs 2855610 HMDB40456 #<Reference:0x000055ce32d966f0> Common mushroom Type 1 specific Agaricus bisporus 5341 Mushrooms Unknown generic Oyster mushroom Type 1 specific Pleurotus ostreatus 5322