1.0 2010-04-08 22:11:46 UTC 2019-11-26 03:11:26 UTC FDB015323 Lucidenic acid F Constituent of Ganoderma lucidum (reishi). Lucidenic acid F is found in mushrooms. 25,26,27-Trinor-3,7,11,15-tetraoxolanost-8-en-24-oic acid 4,4,14-Trimethyl-3,7,11,15-tetraoxochol-8-en-24-oic acid Lucidenic acid F C27H36O6 456.5711 456.251188884 4-{2,6,6,11,15-pentamethyl-5,9,12,17-tetraoxotetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadec-1(10)-en-14-yl}pentanoic acid 4-{2,6,6,11,15-pentamethyl-5,9,12,17-tetraoxotetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadec-1(10)-en-14-yl}pentanoic acid 98665-18-0 CC(CCC(O)=O)C1CC(=O)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(=O)C(C)(C)C1CC3=O InChI=1S/C27H36O6/c1-14(7-8-21(32)33)15-11-20(31)27(6)23-16(28)12-18-24(2,3)19(30)9-10-25(18,4)22(23)17(29)13-26(15,27)5/h14-15,18H,7-13H2,1-6H3,(H,32,33) GLUXWRYPXYKXKV-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-oxosteroids 7-oxosteroids Bile acids, alcohols and derivatives Carboxylic acids Cyclohexenones Hydrocarbon derivatives Monocarboxylic acids and derivatives Organic oxides 11-oxosteroid 15-oxosteroid 3-oxosteroid 7-oxosteroid Aliphatic homopolycyclic compound Bile acid, alcohol, or derivatives Carbonyl group Carboxylic acid Carboxylic acid derivative Cyclic ketone Cyclohexenone Hydrocarbon derivative Ketone Monocarboxylic acid or derivatives Organic oxide Organic oxygen compound Organooxygen compound Oxosteroid Steroid Triterpenoid logp 3.64 ALOGPS logs -4.99 ALOGPS solubility 4.71e-03 g/l ALOGPS logp 4.18 ChemAxon pka_strongest_acidic 4.19 ChemAxon pka_strongest_basic -7.1 ChemAxon iupac 4-{2,6,6,11,15-pentamethyl-5,9,12,17-tetraoxotetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadec-1(10)-en-14-yl}pentanoic acid ChemAxon average_mass 456.5711 ChemAxon mono_mass 456.251188884 ChemAxon smiles CC(CCC(O)=O)C1CC(=O)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(=O)C(C)(C)C1CC3=O ChemAxon formula C27H36O6 ChemAxon inchi InChI=1S/C27H36O6/c1-14(7-8-21(32)33)15-11-20(31)27(6)23-16(28)12-18-24(2,3)19(30)9-10-25(18,4)22(23)17(29)13-26(15,27)5/h14-15,18H,7-13H2,1-6H3,(H,32,33) ChemAxon inchikey GLUXWRYPXYKXKV-UHFFFAOYSA-N ChemAxon polar_surface_area 105.58 ChemAxon refractivity 122.87 ChemAxon polarizability 49.53 ChemAxon rotatable_bond_count 4 ChemAxon acceptor_count 6 ChemAxon donor_count 1 ChemAxon physiological_charge -1 ChemAxon formal_charge 0 ChemAxon Specdb::MsMs 64653 Specdb::MsMs 64654 Specdb::MsMs 64655 Specdb::MsMs 121881 Specdb::MsMs 121882 Specdb::MsMs 121883 Specdb::MsMs 2441899 Specdb::MsMs 2441900 Specdb::MsMs 2441901 Specdb::MsMs 2519909 Specdb::MsMs 2519910 Specdb::MsMs 2519911 Specdb::CMs 23433 Specdb::CMs 44872 Specdb::CMs 134268 Specdb::CMs 142002 HMDB36436 #<Reference:0x000055ce30641910> Common mushroom Type 1 specific Agaricus bisporus 5341 Mushrooms Unknown generic Oyster mushroom Type 1 specific Pleurotus ostreatus 5322