1.0 2010-04-08 22:11:01 UTC 2019-11-26 03:09:25 UTC FDB014001 Ganoderic acid Md Metabolite of Ganoderma lucidum (reishi). Ganoderic acid Md is found in mushrooms. 3a,22-Diacetoxy-7a-methoxylanosta-8,24E-dien-26-oic acid Ganoderic acid Md C35H54O7 586.7991 586.386954082 (2Z)-5-(acetyloxy)-6-[5-(acetyloxy)-9-methoxy-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)-5-(acetyloxy)-6-[5-(acetyloxy)-9-methoxy-2,6,6,11,15-pentamethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadec-1(10)-en-14-yl]-2-methylhept-2-enoic acid COC1CC2C(C)(C)C(CCC2(C)C2=C1C1(C)CCC(C(C)C(C\C=C(\C)C(O)=O)OC(C)=O)C1(C)CC2)OC(C)=O InChI=1S/C35H54O7/c1-20(31(38)39)11-12-26(41-22(3)36)21(2)24-13-18-35(9)30-25(14-17-34(24,35)8)33(7)16-15-29(42-23(4)37)32(5,6)28(33)19-27(30)40-10/h11,21,24,26-29H,12-19H2,1-10H3,(H,38,39)/b20-11- UBGHTOOEMRLEGM-JAIQZWGSSA-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 Bile acids, alcohols and derivatives Carbonyl compounds Carboxylic acid esters Carboxylic acids Dialkyl ethers Hydrocarbon derivatives Organic oxides Steroid acids Steroid esters Tricarboxylic acids and derivatives Aliphatic homopolycyclic compound Bile acid, alcohol, or derivatives Carbonyl group Carboxylic acid Carboxylic acid derivative Carboxylic acid ester Dialkyl ether Ether Hydrocarbon derivative Organic oxide Organic oxygen compound Organooxygen compound Steroid Steroid acid Steroid ester Tricarboxylic acid or derivatives Triterpenoid logp 6.40 ALOGPS logs -6.13 ALOGPS solubility 4.37e-04 g/l ALOGPS melting_point Mp 181-182° logp 5.88 ChemAxon pka_strongest_acidic 4.56 ChemAxon pka_strongest_basic -4.2 ChemAxon iupac (2Z)-5-(acetyloxy)-6-[5-(acetyloxy)-9-methoxy-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 586.7991 ChemAxon mono_mass 586.386954082 ChemAxon smiles COC1CC2C(C)(C)C(CCC2(C)C2=C1C1(C)CCC(C(C)C(C\C=C(\C)C(O)=O)OC(C)=O)C1(C)CC2)OC(C)=O ChemAxon formula C35H54O7 ChemAxon inchi InChI=1S/C35H54O7/c1-20(31(38)39)11-12-26(41-22(3)36)21(2)24-13-18-35(9)30-25(14-17-34(24,35)8)33(7)16-15-29(42-23(4)37)32(5,6)28(33)19-27(30)40-10/h11,21,24,26-29H,12-19H2,1-10H3,(H,38,39)/b20-11- ChemAxon inchikey UBGHTOOEMRLEGM-JAIQZWGSSA-N ChemAxon polar_surface_area 99.13 ChemAxon refractivity 162.42 ChemAxon polarizability 68.05 ChemAxon rotatable_bond_count 10 ChemAxon acceptor_count 5 ChemAxon donor_count 1 ChemAxon physiological_charge -1 ChemAxon formal_charge 0 ChemAxon Specdb::CMs 20577 Specdb::CMs 44334 Specdb::CMs 282784 Specdb::CMs 411175 Specdb::MsMs 91377 Specdb::MsMs 91378 Specdb::MsMs 91379 Specdb::MsMs 154752 Specdb::MsMs 154753 Specdb::MsMs 154754 Specdb::MsMs 2265570 Specdb::MsMs 2265571 Specdb::MsMs 2265572 Specdb::MsMs 3076455 Specdb::MsMs 3076456 Specdb::MsMs 3076457 HMDB35331 #<Reference:0x000055ce32fd7388> Common mushroom Type 1 specific Agaricus bisporus 5341 Mushrooms Unknown generic Oyster mushroom Type 1 specific Pleurotus ostreatus 5322