1.0 2010-04-08 22:11:28 UTC 2019-11-26 03:10:44 UTC FDB014777 Lucidenic acid M Constituent of Ganoderma lucidum (reishi). Lucidenic acid M is found in mushrooms. 11-Oxo-3beta,7alpha,15alpha-trihydroxy-5alpha-lanost-8-en-24-oic acid 3b,7a,15a-Trihydroxy-11-oxo-25,26,27-trisnorlanost-8-en-24-oic acid 3b,7a,15a-Trihydroxy-4,4,14a-trimethyl-11-oxo-5a-chol-8-en-24-oic acid, 9CI C27H42O6 462.6188 462.298139076 4-{5,9,12-trihydroxy-2,6,6,11,15-pentamethyl-17-oxotetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadec-1(10)-en-14-yl}pentanoic acid 4-{5,9,12-trihydroxy-2,6,6,11,15-pentamethyl-17-oxotetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadec-1(10)-en-14-yl}pentanoic acid 110241-33-3 CC(CCC(O)=O)C1CC(O)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(O)C(C)(C)C1CC3O InChI=1S/C27H42O6/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/h14-16,18-20,28,30-31H,7-13H2,1-6H3,(H,32,33) DPRVTGUHOBXEIW-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 Carboxylic acids Cyclic alcohols and derivatives Cyclohexenones Hydrocarbon derivatives Monocarboxylic acids and derivatives Organic oxides Polyols Secondary alcohols Trihydroxy bile acids, alcohols and derivatives 11-oxosteroid 15-hydroxysteroid 3-hydroxysteroid 7-hydroxysteroid Alcohol Aliphatic homopolycyclic compound Bile acid, alcohol, or derivatives Carbonyl group Carboxylic acid Carboxylic acid derivative Cyclic alcohol Cyclohexenone Hydrocarbon derivative Hydroxy bile acid, alcohol, or derivatives Hydroxysteroid Ketone Monocarboxylic acid or derivatives Organic oxide Organic oxygen compound Organooxygen compound Oxosteroid Polyol Secondary alcohol Steroid Trihydroxy bile acid, alcohol, or derivatives Triterpenoid logp 3.05 ALOGPS logs -4.04 ALOGPS solubility 4.24e-02 g/l ALOGPS logp 2.49 ChemAxon pka_strongest_acidic 4.3 ChemAxon pka_strongest_basic -0.81 ChemAxon iupac 4-{5,9,12-trihydroxy-2,6,6,11,15-pentamethyl-17-oxotetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadec-1(10)-en-14-yl}pentanoic acid ChemAxon average_mass 462.6188 ChemAxon mono_mass 462.298139076 ChemAxon smiles CC(CCC(O)=O)C1CC(O)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(O)C(C)(C)C1CC3O ChemAxon formula C27H42O6 ChemAxon inchi InChI=1S/C27H42O6/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/h14-16,18-20,28,30-31H,7-13H2,1-6H3,(H,32,33) ChemAxon inchikey DPRVTGUHOBXEIW-UHFFFAOYSA-N ChemAxon polar_surface_area 115.06 ChemAxon refractivity 125.33 ChemAxon polarizability 52.39 ChemAxon rotatable_bond_count 4 ChemAxon acceptor_count 6 ChemAxon donor_count 4 ChemAxon physiological_charge -1 ChemAxon formal_charge 0 ChemAxon Specdb::CMs 19478 Specdb::CMs 44664 Specdb::CMs 135401 Specdb::CMs 143135 Specdb::MsMs 79194 Specdb::MsMs 79195 Specdb::MsMs 79196 Specdb::MsMs 139734 Specdb::MsMs 139735 Specdb::MsMs 139736 Specdb::MsMs 2841609 Specdb::MsMs 2841610 Specdb::MsMs 2841611 Specdb::MsMs 2864253 Specdb::MsMs 2864254 Specdb::MsMs 2864255 HMDB35973 #<Reference:0x000055ce2eacf650> Common mushroom Type 1 specific Agaricus bisporus 5341 Mushrooms Unknown generic Oyster mushroom Type 1 specific Pleurotus ostreatus 5322