1.0 2010-04-08 22:11:15 UTC 2019-11-26 03:10:00 UTC FDB014419 Lucidenic acid J Constituent of Ganoderma lucidum (reishi). Lucidenic acid J is found in mushrooms. 3b,12b-Dihydroxy-4a-hydroxymethyl-4b,14a-dimethyl-7,11,15-trioxo-5a-chol-8-en-24-oic acid, 9CI 3b,12b,28-Trihydroxy-7,11,15-trioxo-25,26,27-trisnorlanost-8-en-24-oic acid Lucidenic acid J C27H38O8 490.5858 490.256668192 4-[5,16-dihydroxy-6-(hydroxymethyl)-2,6,11,15-tetramethyl-9,12,17-trioxotetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadec-1(10)-en-14-yl]pentanoic acid 4-[5,16-dihydroxy-6-(hydroxymethyl)-2,6,11,15-tetramethyl-9,12,17-trioxotetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadec-1(10)-en-14-yl]pentanoic acid CC(CCC(O)=O)C1CC(=O)C2(C)C3=C(C(=O)C(O)C12C)C1(C)CCC(O)C(C)(CO)C1CC3=O InChI=1S/C27H38O8/c1-13(6-7-19(32)33)14-10-18(31)27(5)20-15(29)11-16-24(2,9-8-17(30)25(16,3)12-28)21(20)22(34)23(35)26(14,27)4/h13-14,16-17,23,28,30,35H,6-12H2,1-5H3,(H,32,33) HAVMVUFJSIMVDG-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 12-hydroxysteroids 3-hydroxysteroids 7-oxosteroids Carboxylic acids Cyclic alcohols and derivatives Cyclohexenones Hydrocarbon derivatives Monocarboxylic acids and derivatives Organic oxides Primary alcohols Secondary alcohols Short-chain hydroxy acids and derivatives Trihydroxy bile acids, alcohols and derivatives 11-oxosteroid 12-hydroxysteroid 15-oxosteroid 2-hydroxysteroid 3-hydroxysteroid 7-oxosteroid 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 Primary alcohol Secondary alcohol Short-chain hydroxy acid Steroid Trihydroxy bile acid, alcohol, or derivatives Triterpenoid logp 1.90 ALOGPS logs -3.16 ALOGPS solubility 3.39e-01 g/l ALOGPS logp 1.62 ChemAxon pka_strongest_acidic 4.1 ChemAxon pka_strongest_basic -2.8 ChemAxon iupac 4-[5,16-dihydroxy-6-(hydroxymethyl)-2,6,11,15-tetramethyl-9,12,17-trioxotetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadec-1(10)-en-14-yl]pentanoic acid ChemAxon average_mass 490.5858 ChemAxon mono_mass 490.256668192 ChemAxon smiles CC(CCC(O)=O)C1CC(=O)C2(C)C3=C(C(=O)C(O)C12C)C1(C)CCC(O)C(C)(CO)C1CC3=O ChemAxon formula C27H38O8 ChemAxon inchi InChI=1S/C27H38O8/c1-13(6-7-19(32)33)14-10-18(31)27(5)20-15(29)11-16-24(2,9-8-17(30)25(16,3)12-28)21(20)22(34)23(35)26(14,27)4/h13-14,16-17,23,28,30,35H,6-12H2,1-5H3,(H,32,33) ChemAxon inchikey HAVMVUFJSIMVDG-UHFFFAOYSA-N ChemAxon polar_surface_area 149.2 ChemAxon refractivity 126.8 ChemAxon polarizability 52.59 ChemAxon rotatable_bond_count 5 ChemAxon acceptor_count 8 ChemAxon donor_count 4 ChemAxon physiological_charge -1 ChemAxon formal_charge 0 ChemAxon Specdb::CMs 21914 Specdb::CMs 44512 Specdb::CMs 166910 Specdb::MsMs 79341 Specdb::MsMs 79342 Specdb::MsMs 79343 Specdb::MsMs 139908 Specdb::MsMs 139909 Specdb::MsMs 139910 Specdb::MsMs 2334613 Specdb::MsMs 2334614 Specdb::MsMs 2334615 Specdb::MsMs 2628098 Specdb::MsMs 2628099 Specdb::MsMs 2628100 HMDB35700 #<Reference:0x000055ce32c7faf0> Common mushroom Type 1 specific Agaricus bisporus 5341 Mushrooms Unknown generic Oyster mushroom Type 1 specific Pleurotus ostreatus 5322